User:Darafsh Kaviyani/test

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Contents

Selenocysteine[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=458287647
|Reference=<ref>''[[Merck Index]]'', 12th Edition, '''8584'''</ref>
|ImageFileL1=L-selenocysteine-2D-skeletal.png
|ImageSizeL1=120px
|ImageFileR1=Selenocysteine-3D-vdW.png
|ImageSizeR1=120px
|IUPACName=3-Selanyl-2-aminopropanoic acid
|OtherNames=<small>L</small>-Selenocysteine; 3-Selanyl-<small>L</small>-alanine; Selenium cysteine
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=23436
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=109962
|KEGG_Ref={{keggcite|correct|kegg}}
|KEGG=C05688
|InChI=1/C3H7NO2Se/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m0/s1
|InChIKey=ZKZBPNGNEQAJSX-REOHCLBHBZ
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C3H7NO2Se/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m0/s1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=ZKZBPNGNEQAJSX-REOHCLBHSA-N
|CASNo_Ref={{cascite|changed|??}}
|CASNo=10236-58-5
|PubChem=25076
|DrugBank_Ref={{drugbankcite|correct|drugbank}}
|DrugBank=DB02345
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=16633
|SMILES=O=C(O)[C@@H](N)C[SeH]
}}
|Section2={{Chembox Properties
|C=3|H=7|N=1|O=2|Se=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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Retinol[edit]

{{chembox
|verifiedrevid=464381333
|ImageFile=All-trans-Retinol2.svg
|ImageSize=250px
|ImageName=Retinol
|ImageFile2=Retinol 3D balls.png
|ImageSize2=200px
|ImageName2=Stick model of retinol
|ImageFile3=Retinol 3D ball.png
|ImageSize3=200px
|ImageName3=Ball model of retinol
|IUPACName=(2''E'',4''E'',6''E'',8''E'')-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,4,6,8-tetraen-1-ol
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=393012
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=81G40H8B0T
|InChI1=1/C20H30O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,21H,7,10,14-15H2,1-5H3/b9-6+,12-11+,16-8+,17-13+
|InChIKey1=FPIPGXGPPPQFEQ-OVSJKPMPBW
|CASNo=68-26-8
|CASNo_Ref={{cascite|correct|CAS}}
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=986
|PubChem=1071
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=17336
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C20H30O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,21H,7,10,14-15H2,1-5H3/b9-6+,12-11+,16-8+,17-13+
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=FPIPGXGPPPQFEQ-OVSJKPMPSA-N
|SMILES=OC/C=C(/C=C/C=C(/C=C/C1=C(/CCCC1(C)C)C)C)C
|MeSHName=
|ATCCode_prefix=A11
|ATCCode_suffix=CA01
|ATC_Supplemental={{ATC|D10|AD02}}, {{ATC|R01|AX02}}, {{ATC|S01|XA02}}
  }}
|Section2={{Chembox Properties
|C=20|H=30|O=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
  }}
|Section3={{Chembox Hazards
|Solubility=
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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Uridine[edit]

{{chembox
|Verifiedfields=changed
|Watchedfields=changed
|verifiedrevid=459510448
|ImageFile=Uridin.svg
|ImageSize=150px
|IUPACName=1-[(3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
|OtherNames=uridine
|Section1={{Chembox Identifiers
|CASNo=58-96-8
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=100259
|DrugBank_Ref={{drugbankcite|correct|drugbank}}
|DrugBank=DB02745
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=WHI7HQ7H85
|SMILES=O=C1NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O
|MeSHName=Uridine
  }}
|Section2={{Chembox Properties
|C=9|H=12|N=2|O=6
|MolarMass=244.20
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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Thujone[edit]

{{Chembox
|verifiedrevid=450658404
|Name=Thujone
|ImageFileL1=(-)-alpha-Thujon.svg
|ImageSizeL1=120px
|ImageCaptionL1=(−)-α-Thujone
|ImageFileR1=(+)-beta-Thujon.svg
|ImageSizeR1=120px
|ImageCaptionR1=(+)-β-Thujone
|IUPACName=α:  (1''S'',4''R'',5''R'')-4-Methyl-1-(propan-2-yl)bicyclo[3.1.0]hexan-3-one<br>β:  (1''S'',4''S'',5''R'')-4-methyl-1-propan-2-ylbicyclo[3.1.0]hexan-3-one
|OtherNames=
|Section1={{Chembox Identifiers
|InChI=1/C10H16O/c1-6(2)10-4-8(10)7(3)9(11)5-10/h6-8H,4-5H2,1-3H3/t7-,8-,10+/m1/s1
|InChIKey=USMNOWBWPHYOEA-MRTMQBJTBZ
|InChI1=1S/C10H16O/c1-6(2)10-4-8(10)7(3)9(11)5-10/h6-8H,4-5H2,1-3H3/t7-,8-,10+/m1/s1
|InChIKey1=USMNOWBWPHYOEA-MRTMQBJTSA-N
|PubChem=261491
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=546-80-5
|CASNo_Comment=(α-thujone)
|CASNo1=471-15-8 
|CASNo1_Comment=(β-thujone)
|PubChem1=11027
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=229574
|ChemSpiderID_Comment=(α-thujone)
|ChemSpiderID1=82583
|ChemSpiderID1_Comment=(β-thujone)
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=9577
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=USMNOWBWPHYOEA-MRTMQBJTSA-N
|SMILES=O=C1[C@H](C)[C@@H]2[C@](C(C)C)(C1)C2
|SMILES_Comment=(α-thujone)
|SMILES1=C[C@@H]([C@@H](C2)[C@]2([C@@H](C)C)C1)C1=O 
|SMILES1_Comment=(β-thujone)
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C10H16O/c1-6(2)10-4-8(10)7(3)9(11)5-10/h6-8H,4-5H2,1-3H3/t7-,8-,10+/m1/s1
  }}
|Section2={{Chembox Properties
|C=10|H=16|O=1
|Appearance=
|Density=0.92 g/cm³ (β-thujone)
|MeltingPt=
|BoilingPt=201 °C (β-thujone)
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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Sodium cyclamate[edit]

{{chembox
|Verifiedfields=changed
|UNII_Ref={{fdacite|changed|FDA}}
|UNII=1I6F42RME1
|verifiedrevid=477163337
|ImageFile=Cyclamate Structural Formulae .V.1.svg
|ImageSize=
|IUPACName=sodium N-cyclohexylsulfamate
|OtherNames=
|Section1={{Chembox Identifiers
|InChIKey=UDIPTWFVPPPURJ-REWHXWOFAV
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C6H13NO3S.Na/c8-11(9,10)7-6-4-2-1-3-5-6;/h6-7H,1-5H2,(H,8,9,10);/q;+1/p-1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=UDIPTWFVPPPURJ-UHFFFAOYSA-M
|CASNo_Ref={{cascite|correct|??}}
|CASNo=
|PubChem=8751
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=273977
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=8421
|SMILES=[Na+].O=S([O-])(=O)NC1CCCCC1
|InChI=1/C6H13NO3S.Na/c8-11(9,10)7-6-4-2-1-3-5-6;/h6-7H,1-5H2,(H,8,9,10);/q;+1/p-1
}}
|Section2={{Chembox Properties
|C=6 |H=12 |N=1 |Na=1 |O=3 |S=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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Resveratrol[edit]

{{chembox
|Watchedfields=changed
|verifiedrevid=477172311
|Name=Resveratrol
|ImageFile=resveratrol.svg
|ImageSize=250px
|ImageName=Chemical 9–69 structure of ''trans''-resveratrol
|ImageFile1=Resveratrol3d.png
|ImageSize1=180px
|ImageName1=Chemical structure of ''trans''-resveratrol
|ImageFile2=Cis_and_trans_resveratrol.PNG
|ImageSize2=250px
|ImageName2=Chemical structures of ''cis-'' and ''trans''-resveratrols
|ImageCaption2=Chemical structures of ''cis-'' ((Z)-resveratrol, left) and ''trans''-resveratrol ((E)-resveratrol, right)<ref name=Camont>Simple spectrophotometric assessment of the trans-/cis-resveratrol ratio in aqueous solutions. Laurent Camont, Charles-Henry Cottart, Yara Rhayem, Valérie Nivet-Antoine, Raja Djelidi, Fabrice Collin, Jean-Louis Beaudeux and Dominique Bonnefont-Rousselot, Analytica Chimica Acta, 2009, 634, pages 121–128, {{doi|10.1016/j.aca.2008.12.003}}</ref>
|OtherNames=''trans''-3,5,4'-Trihydroxystilbene;<br />3,4',5-Stilbenetriol;<br />''trans''-Resveratrol;<br />(''E'')-5-(''p''-Hydroxystyryl)resorcinol;<br />(''E'')-5-(4-hydroxystyryl)benzene-1,3-diol
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=501-36-0
|PubChem=445154
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=392875
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=165
|DrugBank_Ref={{drugbankcite|correct|drugbank}}
|DrugBank=DB02709
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=Q369O8926L
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=45713
|KEGG_Ref={{keggcite|correct|kegg}}
|KEGG=C03582
|RTECS=CZ8987000
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=LUKBXSAWLPMMSZ-OWOJBTEDSA-N
|SMILES=Oc2ccc(C=Cc1cc(O)cc(O)c1)cc2
|InChI=1/C14H12O3/c15-<br />12-5-3-10(4-6-12)<br />1-2-11-7-13(16)9-<br />14(17)8-11/h1-9,15-<br />17H/b2-1+
 }}
|Section2={{Chembox Properties
|C=14
|H=12
|O=3
|ExactMass=228.078644 u
|Appearance=white powder with<br /> slight yellow cast
|MeltingPt=261 - 263°C / 501.8 - 505.4°F<ref name=FisherScientificMSDS>[http://www.fishersci.com/ecomm/servlet/msdsproxy?productName=AC430075000&productDescription=RESVERATROL+99%25+500MG&catNo=AC43007-5000&vendorId=VN00032119&s Resveratrol MSDS on Fisher Scientific website]</ref>
|Solubility1=0.03 g/L
|Solvent1=water
|Solubility2=16 g/L
|Solvent2=Dimethyl sulfoxide{{!}}DMSO
|Solubility3=50 g/L
|Solvent3=ethanol
|LambdaMax=304nm (trans-resveratrol, in water)<br>286nm (cis-resveratrol, in water)<ref name=Camont/>
 }}
|Section7={{Chembox Hazards
|ExternalMSDS=Fisher Scientific<ref name=FisherScientificMSDS/><br>Sigma Aldrich<ref name=SigmaAldrichMSDS>[http://www.sigmaaldrich.com/catalog/DisplayMSDSContent.do Resveratrol MSDS on www.sigmaaldrich.com]</ref>
|EUClass=
|EUIndex=
|MainHazards=
|NFPA-H=
|NFPA-F=
|NFPA-R=
|NFPA-O=
|RPhrases={{R36}} (irritating to eyes)<ref name=SigmaAldrichMSDS/>
|SPhrases={{S26}} (in case of contact with eyes, rinse immediately with plenty of water and 
seek medical advice)<ref name=SigmaAldrichMSDS/>
|RSPhrases=
|FlashPt=
|Autoignition=
|ExploLimits=
|LD50=23.2 µM (5,29 g)<ref>Resveratrol amplifies profibrogenic effects of free fatty acids on human hepatic stellate cells. Bechmann LP, Zahn D, Gieseler RK, Fingas CD, Marquitan G, Jochum C, Gerken G, Friedman SL and Canbay A, Hepatol Res., 2009 Jun, volume 39, issue 6, pages 601-608, {{PMID|19207580}}, {{doi|10.1111/j.1872-034X.2008.00485.x}}</ref>
|PEL=
   }}
}}

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Silanol[edit]

{{Chembox
|verifiedrevid=410336390
|ImageFileL1=Silanol.svg
|ImageFileL1_Ref={{Chemboximage|correct|??}}
|ImageSizeL1=
|ImageNameL1=Stereo structural formula of silanol with explicit hydrogens
|ImageFileR1=Silanol-Spartan-MP2-3D-balls.png
|IUPACName=Silanol
|SystematicName=Silanol<ref>http://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:37173</ref> (substitutive)
|OtherNames=Hydroxysilane<br />
Silicol<br />
Silinic acid<br />
Silinol<br />
Silyl alcohol<br />
Silyl hydrate
|Section1={{Chembox Identifiers
|CASNo=14475-38-8
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=142154
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=125395
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=37173
|Gmelin=384
|SMILES=O[SiH3]
|StdInChI=1S/H4OSi/c1-2/h1H,2H3
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|InChI=1/H4OSi/c1-2/h1H,2H3
|StdInChIKey=SCPYDCQAZCOKTP-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|InChIKey=SCPYDCQAZCOKTP-UHFFFAOYAI
}}
|Section2={{Chembox Properties
|H=4
|O=1
|Si=1
|ExactMass=48.003141283 g mol<sup>-1</sup>
|Appearance=Colorless liquid}}
}}

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Thymol[edit]

{{chembox
|verifiedrevid=470609679
|ImageFile=Thymol2.svg
|ImageSize=150
|ImageFile2=Thymol3D.png
|ImageName=Thymol
|IUPACName=2-Isopropyl-5-methylphenol
|Section1={{Chembox Identifiers
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=3J50XA376E
|KEGG_Ref={{keggcite|correct|kegg}}
|KEGG=D01039
|InChI=1/C10H14O/c1-7(2)9-5-4-8(3)6-10(9)11/h4-7,11H,1-3H3
|InChIKey=MGSRCZKZVOBKFT-UHFFFAOYAS
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=29411
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C10H14O/c1-7(2)9-5-4-8(3)6-10(9)11/h4-7,11H,1-3H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=MGSRCZKZVOBKFT-UHFFFAOYSA-N
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=89-83-8
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=21105998
|DrugBank_Ref={{drugbankcite|correct|drugbank}}
|DrugBank=DB02513
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=27607
|SMILES=CC(C)c1ccc(C)cc1O
|ATCvet=yes
|ATCCode_prefix=P53
|ATCCode_suffix=AX22

  }}
|Section2={{Chembox Properties
|C=10|H=14|O=1
|Density=0.96 g/cm<sup>3</sup>
<!--|MeltingPtC=49-->
|MeltingPtC=51
|BoilingPtC=232
|Solubility=Insoluble in water<ref>''CRC Handbook of Chemistry and Physics'', 1977</ref>
  }}
}}

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Sodium amide[edit]

{{Chembox
|Verifiedfields=changed
|Watchedfields=changed
|verifiedrevid=265528656
|ImageFile=Sodium-amide-2D-ionic.svg
|ImageFile_Ref={{Chemboximage|correct|??}}
|ImageSize=
|ImageName=Structural formula of sodium amide
|ImageFile1=Sodium-amide-3D-balls-B.png
|ImageFile1_Ref={{Chemboximage|correct|??}}
|ImageSize1=
|ImageName1=Ball and stick, unit cell model of sodium amide
|IUPACName=Sodium amide
|SystematicName=
|OtherNames=Sodamide
|Section1={{Chembox Identifiers
|CASNo=7782-92-5
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=24533
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=22940
|ChemSpiderID_Ref={{chemspidercite|changed|chemspider}}
|EINECS=231-971-0
|UNNumber=1390
|SMILES=[NH2-].[Na+]
|StdInChI=1S/H2N.Na/h1H2;/q-1;+1
|StdInChI_Ref={{stdinchicite|changed|chemspider}}
|StdInChIKey=ODZPKZBBUMBTMG-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|changed|chemspider}}}}

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Pyroglutamic acid[edit]

{{Chembox
|Verifiedfields=changed
|verifiedrevid=464377606
|ImageFile=(S)-Pyroglutamic acid Structural Formulae.png
|ImageName=Stereo structural formula of (2''S'')-pyroglutamic acid
|PIN=Pidolic acid
|SystematicName=5-Oxopyrrolidine-2-carboxylic acid
|OtherNames=5-Oxoproline<br />
5-Oxo-proline
|Section1={{Chembox Identifiers
|Abbreviations=Glp
|InChI=1S/C5H7NO3/c7-4-2-1-3(6-4)5(8)9/h3H,1-2H2,(H,6,7)(H,8,9)/t3-/m0/s1
|InChIKey1=ODHCTXKNWHHXJC-VKHMYHEASA-N
|InChI1=1S/C5H7NO3/c7-4-2-1-3(6-4)5(8)9/h3H,1-2H2,(H,6,7)(H,8,9)/t3-/m0/s1
|CASNo2=149-87-1
|CASNo2_Ref={{cascite|changed|??}}
|CASNo1=4042-36-8
|CASNo1_Comment=(2''R'')
|CASNo=98-79-3
|CASNo_Comment=(2''S'')
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem2=499
|PubChem2_Ref={{Pubchemcite|correct|PubChem}}
|PubChem1=439685
|PubChem1_Comment=(2''R'')
|PubChem1_Ref={{Pubchemcite|correct|PubChem}}
|PubChem=7405
|PubChem_Comment=(2''S'')
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|PubChem3=10534703
|PubChem3_Comment=(2''S'')(3,4-<sup>3</sup>''H''<sub>2</sub>)
|PubChem3_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=7127
|ChemSpiderID_Comment=(2''S'')
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID1=388752
|ChemSpiderID1_Comment=(2''R'')
|ChemSpiderID1_Ref={{Chemspidercite|correct|ChemSpider}}
|ChemSpiderID2=485
|ChemSpiderID2_Ref={{Chemspidercite|correct|ChemSpider}}
|ChemSpiderID3=8710094
|ChemSpiderID3_Comment=(2''S'')(3,4-<sup>3</sup>''H''<sub>2</sub>)
|ChemSpiderID3_Ref={{Chemspidercite|correct|ChemSpider}}
|UNII=SZB83O1W42
|UNII_Ref={{fdacite|correct|FDA}}
|EINECS=205-748-3
|DrugBank_Ref={{drugbankcite|changed|drugbank}}
|DrugBank=DB03088
|KEGG_Ref={{keggcite|changed|kegg}}
|KEGG=C02237
|MeSHName=Pyrrolidonecarboxylic+acid
|ChEBI_Ref={{ebicite|changed|EBI}}
|ChEBI=16010
|RTECS=TW3710000
|SMILES=O=C(O)[C@H]1NC(=O)CC1
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=284718
|StdInChI_Ref={{stdinchicite|changed|chemspider}}
|StdInChI=1S/C5H7NO3/c7-4-2-1-3(6-4)5(8)9/h3H,1-2H2,(H,6,7)(H,8,9)
|StdInChIKey_Ref={{stdinchicite|changed|chemspider}}
|StdInChIKey=ODHCTXKNWHHXJC-UHFFFAOYSA-N
|Gmelin=1473408
|Beilstein=82134
|3DMet=B01549}}
|Section2={{Chembox Properties
|C=5
|H=7
|N=1
|O=3
|ExactMass=129.042593095 g mol<sup>-1</sup>
|MeltingPtC=184
|LogP=-0.89
|pKa=-1.76, 3.48, 12.76
|pKb=15.76, 10.52, 1.24
|IsoelectricPt=0.94}}
}}

@@@

@@@

Sphingosine[edit]

{{Chembox
|Verifiedfields=changed
|verifiedrevid=433061503
|ImageFile=Sphingosine structure.svg
|ImageSize=200px
|ImageName=Sphingosine
|IUPACName=(2''S'',3''R'')-2-aminooctadec-4-ene-1,3-diol
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=4444047
|InChI=1/C18H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)17(19)16-20/h14-15,17-18,20-21H,2-13,16,19H2,1H3/b15-14+/t17-,18+/m0/s1
|InChIKey=WWUZIQQURGPMPG-KRWOKUGFBW
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C18H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)17(19)16-20/h14-15,17-18,20-21H,2-13,16,19H2,1H3/b15-14+/t17-,18+/m0/s1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=WWUZIQQURGPMPG-KRWOKUGFSA-N
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=123-78-4
|PubChem=1104
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=67166
|ChEBI_Ref={{ebicite|changed|EBI}}
|ChEBI=16393
|SMILES=CCCCCCCCCCCCC/C=C/[C@H]([C@H](CO)N)O
}}
|Section2={{Chembox Properties
|C=18 |H=37 |N=1 |O=2
|Formula=
|MolarMass=
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
}}
}}

@@@

@@@

Rhodinol[edit]

{{chembox
|verifiedrevid=388367131
|Reference=<ref>[http://www.sigmaaldrich.com/catalog/search/ProductDetail/ALDRICH/W298018 Rhodinol] at [[Sigma-Aldrich]]</ref>
|ImageFile=Rhodinol.png
|ImageSize=200px
|IUPACName=(3''S'')-3,7-Dimethyloct-7-en-1-ol
|OtherNames=
|Section1={{Chembox Identifiers
|CASNo=6812-78-8
|PubChem=81263
|SMILES=CC(CCCC(=C)C)CCO
  }}
|Section2={{Chembox Properties
|C=10|H=20|O=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=68-70 °C at 1.8 mmHg
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Silylene[edit]

{{Chembox
|Watchedfields=changed
|verifiedrevid=404979853
|IUPACName=Silylene
|SystematicName=Silylidene{{citation needed|date=March 2011}}
|OtherNames=Hydrogen silicide(-II)<br />
Silicene<br />
|Section1={{Chembox Identifiers
|PubChem=6327230
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=4885758
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|SMILES=[SiH2]
|StdInChI=1S/H2Si/h1H2
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=XMIJDTGORVPYLW-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
}}
|Section2={{Chembox Properties
|H=2
|Si=1
|ExactMass=29.992576597 g mol<sup>-1</sup>
}}
}}

@@@

@@@

T-2 mycotoxin[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=438853897
|Name=T-2
|Reference=<ref>[http://www.cbwinfo.com/Biological/Toxins/T2.html T-2 Toxin: essential data]</ref>
|ImageFile1=T-2 mycotoxin.png
|ImageSize1=150px
|ImageFile2=T-2 mycotoxin flat.png
|ImageSize2=200px
|IUPACName=(2α,3α,4β,8α)-4,15-bis(acetyloxy)-3-hydroxy-12,13-epoxytrichothec-9-en-8-yl 3-methylbutanoate
|OtherNames=T-2 Toxin<br>Fusariotoxin T 2<br>Insariotoxin<br>Mycotoxin T 2 
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=4447526
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=152423
|InChI=1/C24H34O9/c1-12(2)7-18(27)32-16-9-23(10-29-14(4)25)17(8-13(16)3)33-21-19(28)20(31-15(5)26)22(23,6)24(21)11-30-24/h8,12,16-17,19-21,28H,7,9-11H2,1-6H3/t16-,17+,19+,20+,21+,22+,23+,24-/m0/s1
|InChIKey=BXFOFFBJRFZBQZ-QYWOHJEZBH
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C24H34O9/c1-12(2)7-18(27)32-16-9-23(10-29-14(4)25)17(8-13(16)3)33-21-19(28)20(31-15(5)26)22(23,6)24(21)11-30-24/h8,12,16-17,19-21,28H,7,9-11H2,1-6H3/t16-,17+,19+,20+,21+,22+,23+,24-/m0/s1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=BXFOFFBJRFZBQZ-QYWOHJEZSA-N
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=21259-20-1
|RTECS=YD0100000
|PubChem=5284461
|SMILES=O=C(O[C@@H]4C(=C/[C@H]3O[C@H]2[C@]1(OC1)[C@]([C@H](OC(=O)C)[C@H]2O)([C@@]3(COC(=O)C)C4)C)\C)CC(C)C
}}
|Section2={{Chembox Properties
|C=24 |H=34 |O=9
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=Insoluble
}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=}}
}}

@@@

@@@

Silicic acid[edit]

{{Chembox
|Verifiedfields=changed
|verifiedrevid=476994660
|IUPACName=Silicic acid
|OtherNames=Monosilicic acid<br />Orthosilicic acid
|ImageFile=Kyselina křemičitá.PNG
|Section1={{Chembox Identifiers
|InChI1=1/H4O4Si/c1-5(2,3)4/h1-4H
|InChIKey1=RMAQACBXLXPBSY-UHFFFAOYAS
|CASNo=10193-36-9
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=14942
|PubChem_Ref={{Pubchemcite}}
|ChemSpiderID=14236
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|EINECS=233-477-0
|ChEBI_Ref={{ebicite|changed|EBI}}
|ChEBI=26675
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/H4O4Si/c1-5(2,3)4/h1-4H
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=RMAQACBXLXPBSY-UHFFFAOYSA-N
|SMILES=O[Si](O)(O)O
|InChI=1S/H4O4Si/c1-5(2,3)4/h1-4H
|InChIKey=RMAQACBXLXPBSY-UHFFFAOYSA-N
|Gmelin=2009}}
|Section2={{Chembox Properties
|H=4
|O=4
|Si=1
|ExactMass=95.987885149 g mol<sup>-1</sup>
|pKa=9.84, 13.2}}
|Section3={{Chembox Related
|OtherCpds=[[Orthocarbonic acid]]}}
}}

@@@

@@@

Tetrabutylammonium hydroxide[edit]

{{chembox
|verifiedrevid=444217565
|ImageFile=TBAH.PNG
|ImageSize=
|IUPACName=tetrabutylammonium hydroxide
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=2005872
|InChI=1/C16H36N.H2O/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H2/q+1;/p-1
|InChIKey=VDZOOKBUILJEDG-REWHXWOFAE
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C16H36N.H2O/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H2/q+1;/p-1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=VDZOOKBUILJEDG-UHFFFAOYSA-M
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=2052-49-5
|PubChem=2723671
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=1078154
|SMILES=[OH-].CCCC[N+](CCCC)(CCCC)CCCC
}}
|Section2={{Chembox Properties
|C=16 |H=37 |N=1 |O=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Thiazole[edit]

{{chembox
|verifiedrevid=470606357
|ImageFileL1=Thiazole_numbering.png
|ImageSizeL1=100px
|ImageFileR1=Thiazole3d.png
|ImageSizeR1=125px
|IUPACName=1,3-Thiazole
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=8899
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=320RCW8PEF
|InChI=1/C3H3NS/c1-2-5-3-4-1/h1-3H
|InChIKey=FZWLAAWBMGSTSO-UHFFFAOYAI
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=15605
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C3H3NS/c1-2-5-3-4-1/h1-3H
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=FZWLAAWBMGSTSO-UHFFFAOYSA-N
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=288-47-1
|PubChem=9256
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=43732
|SMILES=n1ccsc1
}}
|Section2={{Chembox Properties
|C=3 |H=3 |N=1 |S=1 
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=116-118 °C
|Solubility=
|pKb=2.5
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Spilanthol[edit]

{{Chembox
|ImageFile=Spilanthol skeletal.svg
|ImageSize=200px
|IUPACName=(2''E'',6''Z'',8''E'')-''N''-Isobutyl-2,6,8-decatrienamide
|OtherNames=Affinin
|Section1={{Chembox Identifiers
|CASNo=25394-57-4
|PubChem=5353001
|ChemSpiderID=4509783
|SMILES=O=C(/C=C/CC/C=C\C=C\C)NCC(C)C
|InChI=1/C14H23NO/c1-4-5-6-7-8-9-10-11-14(16)15-12-13(2)3/h4-7,10-11,13H,8-9,12H2,1-3H3,(H,15,16)/b5-4+,7-6-,11-10+
|InChIKey=BXOCHUWSGYYSFW-HVWOQQCMBC
|StdInChI=1S/C14H23NO/c1-4-5-6-7-8-9-10-11-14(16)15-12-13(2)3/h4-7,10-11,13H,8-9,12H2,1-3H3,(H,15,16)/b5-4+,7-6-,11-10+
|StdInChIKey=BXOCHUWSGYYSFW-HVWOQQCMSA-N
  }}
|Section2={{Chembox Properties
|C=14|H=23|N=1|O=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Ribulose[edit]

{{chembox
|verifiedrevid=450937939
|Name=<small>D</small>-Ribulose
|ImageFileL1=D-Ribulose.svg
|ImageSizeL1=88px
|ImageFileR1=Ribulose.svg
|ImageSizeR1=150px
|IUPACName=(''3R,4R'')-1,3,4,5-Tetrahydroxypentan-2-one
|OtherNames=<small>D</small>-erythro-2-Pentulose<br>Adonose<br>Arabinulose<br>Araboketose<br>Ribosone
|Section1={{Chembox Identifiers
|CASNo=488-84-6
|CASOther=(D)<br>2042027-5 (L)<br>5556-48-9 (DL)
|PubChem=151261
|SMILES=D: C([C@H]([C@H](C(=O)CO)O)O)O<br>L: OCC([C@@H](O)[C@@H](O)CO)=O
  }}
|Section2={{Chembox Properties
|C=5|H=10|O=5
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Tetrasodium pyrophosphate[edit]

{{chembox
|verifiedrevid=443823619
|ImageFile=Sodium pyrophosphate.png
|ImageSize=200px
|IUPACName=Tetrasodium diphosphate
|OtherNames=
|Section1={{Chembox Identifiers
|CASNo=7722-88-5
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo2=13472-36-1 
|CASNo2_Comment=(decahydrate)
|PubChem=
  }}
|Section2={{Chembox Properties
|Na=4|P=2|O=7
|Appearance=Colorless crystals
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|ExternalMSDS=
|EUIndex=Not listed
|MainHazards=
|FlashPt=Non-flammable
  }}
|Section8={{Chembox Related
|OtherAnions=[[Trisodium phosphate]]<br/>[[Pentasodium triphosphate]]<br/>[[Hexasodium metaphosphate]]
|OtherCations=[[Tetrapotassium pyrophosphate]]
|OtherCpds=[[Disodium pyrophosphate]]
  }}
}}

@@@

@@@

Sodium orthophenyl phenol[edit]

{{Chembox
|verifiedrevid=444111037
|ImageFile=Sodium orthophenyl phenol.svg
|ImageSize=200px
|ImageAlt=
|IUPACName=Sodium [1,1'-biphenyl]-2-olate
|OtherNames=(1,1'-Biphenyl)-2-ol, sodium salt; 2-Hydroxydiphenyl sodium; ''o''-Phenylphenol sodium; ''o''-Phenylphenol, sodium; Sodium ''o''-phenylphenol; Sodium 2-phenylphenolate; Sodium ''o''-phenylphenate
|Section1={{Chembox Identifiers
|CASNo=132-27-4
|CASNo_Ref={{cascite|correct|??}}
|PubChem=23675735
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C12H10O.Na/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;/h1-9,13H;/q;+1
|SMILES=[O-]C1=C(C2=CC=CC=C2)C=CC=C1.[Na+]
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=10764729
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=KSQXVLVXUFHGJQ-UHFFFAOYSA-N
|InChI=InChI=1S/C12H10O.Na/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;/h1-9,13H;/q;+1
}}
|Section2={{Chembox Properties
|C=12|H=9|Na=1|O=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=}}
}}

@@@

@@@

Trigonelline[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=470614745
|Name=Trigonelline
|ImageFile=Trigonelline.png
<!-- |ImageSize=120px -->
|ImageName=
|IUPACName=1-Methylpyridinium- 3-carboxylate
|OtherNames=Nicotinic acid N- methylbetaine<br />Coffearine<br />Caffearine<br />Gynesine<br />Trigenolline
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=5369
|PubChem=5570
|InChI=1/C7H7NO2/c1-8-4-2-3-6(5-8)7(9)10/h2-5H,1H3
|InChIKey=WWNNZCOKKKDOPX-UHFFFAOYAV
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=350675
|ChEMBL2=489961
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C7H7NO2/c1-8-4-2-3-6(5-8)7(9)10/h2-5H,1H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=WWNNZCOKKKDOPX-UHFFFAOYSA-N
|CASNo_Ref={{cascite|changed|??}}
|CASNo=535-83-1
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=18123
|SMILES=O=C([O-])c1ccc[n+](c1)C
}}
|Section2={{Chembox Properties
|C=7|H=7|O=2|N=1
|Density=? g/cm<sup>3</sup>
|MeltingPt=230–233 °C (monohydrate)<br />258–259 °C (hydrochloride)
  }}
}}

@@@

@@@

Trimethylsilyl[edit]

{{Chembox
|Name=Trimethylsilyl radical
|ImageFile=Trimethylsilyl group.PNG
|ImageSize=121
|ImageName=Skeletal formula of tetramethylsilane with some implicit hydrogens shown
|IUPACName=Trimethylsilyl
|OtherNames=Trimethyl-λ<sup>3</sup>-silyl
|Section1={{Chembox Identifiers
|CASNo=16571-41-8
|PubChem=123362
|PubChem_Ref={{Pubchemcite|correct|pubchem}}
|ChemSpiderID=109962
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|SMILES=C[Si](C)C
|StdInChI=1S/C3H9Si/c1-4(2)3/h1-3H3
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=DCERHCFNWRGHLK-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
}}
|Section2={{Chembox Properties
|C=3
|H=9
|Si=1
|ExactMass=73.047351821 g mol<sup>-1</sup>
}}
|Section3={{Chembox Related
|Function=silyls
|OtherFunctn=[[Disilyne]]<br />
== [[Silylene]] ==
}}
}}

@@@

@@@

Triphenylene[edit]

{{chembox
|verifiedrevid=450122676
|ImageFile=Triphenylene_chemical_structure.png
|ImageSize=180px
|ImageName=Skeletal formula with numbering convention
|ImageFile1=Triphenylene-3D-balls.png
|ImageSize1=180px
|ImageName1=Ball-and-stick model
|IUPACName=triphenylene
|OtherNames=benzo[''l'']phenanthrene, 9,10-benzophenanthrene, 1,2,3,4-dibenznaphthalene, isochrysene
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite}}
|CASNo=217-59-4
|PubChem=9170
|InChI=1/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H
|KEGG_Ref={{keggcite|correct|kegg}}
|KEGG=C19541
|SMILES=C1(C=CC=C3)=C3C(C=CC=C4)=C4C2=C1C=CC=C2
}}
|Section2={{Chembox Properties
|C=18|H=12
|Appearance=
|Density=
|MeltingPtK=471
|BoilingPtK=711
|Solubility=}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=}}
}}

@@@

@@@

Thorin (chemistry)[edit]

{{Chembox
|Verifiedfields=changed
|verifiedrevid=470609258
|ImageFile=Thorin.png
|ImageSize=244
|ImageName=Structural formula of ((4''E'')-4-hydrazin-1-ylidene)-thorin
|PIN=Disodium 3-hydroxy-4-[(2-arsonophenyl)diazenyl]naphthalene-2,7-disulfonate
|SystematicName=Disodium 4-[2-(2-arsonophenyl)hydrazin-1-ylidene]-3-oxo-3,4-dihydronaphthalene-2,7-disulfonate
|OtherNames=Disodium 4-[2-(2-arsonophenyl)hydrazin-1-ylidene]-3-oxonaphthalene-2,7-disulfonate<br />
2-(3,6-Disulfo-2-hydroxy-1-naphthylazo)benzenearsonic acid disodium salt<br />
Thoron<br />
Thoronol
|Section1={{Chembox Identifiers
|CASNo=3688-92-4
|CASNo_Comment=(4''E'')-4-hydrazin-1-ylidene
|CASNo_Ref={{cascite|changed|??}}
|PubChem=6364518
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|PubChem1=6537679
|PubChem1_Comment=(4''E'')-4-hydrazin-1-ylidene
|PubChem1_Ref={{Pubchemcite|correct|PubChem}}
<!--|ChemSpiderID=4895471-->
|ChemSpiderID=5020708
|ChemSpiderID_Comment=(4''E'')-4-hydrazin-1-ylidene
|ChemSpiderID_Ref={{chemspidercite|changed|chemspider}}
|EINECS=222-993-1
|UNNumber=1557
|Beilstein=2957648
|SMILES=[Na+].[Na+].O[As](O)(=O)c3ccccc3/N=N/c1c2ccc(cc2cc(c1O)S([O-])(=O)=O)S([O-])(=O)=O
|SMILES1=[Na+].[Na+].O[As](O)(=O)C1=CC=CC=C1NN=C1C(=O)C(=CC2=C1C=CC(=C2)S([O-])(=O)=O)S([O-])(=O)=O
|StdInChI=1S/C16H13AsN2O10S2.2Na/c20-16-14(31(27,28)29)8-9-7-10(30(24,25)26)5-6-11(9)15(16)19-18-13-4-2-1-3-12(13)17(21,22)23;;/h1-8,18H,(H2,21,22,23)(H,24,25,26)(H,27,28,29);;/q;2*+1/p-2
|StdInChI_Ref={{stdinchicite|changed|chemspider}}
|InChI1=1/C16H13AsN2O10S2.2Na/c20-16-14(31(27,28)29)8-9-7-10(30(24,25)26)5-6-11(9)15(16)19-18-13-4-2-1-3-12(13)17(21,22)23;;/h1-8,20H,(H2,21,22,23)(H,24,25,26)(H,27,28,29);;/q;2*+1/p-2/b19-18+;;
|StdInChIKey=ZQMPNLOZJUWHSA-UHFFFAOYSA-L
|StdInChIKey_Ref={{stdinchicite|changed|chemspider}}
|InChIKey=DCSRPHQBFSYJNN-GJLVVKPQBS}}
|Section2={{Chembox Properties
|C=16
|H=11
|As=1
|N=2
|O=10
|S=2
|ExactMass=575.886646729 g mol<sup>-1</sup>
|Appearance=Orange-yellow crystals
|MeltingPtC=300}}
|Section3={{Chembox Hazards
|MainHazards=Toxic ('''T'''), Dangerous for the environment ('''N''')
|RPhrases={{R23/25}}, {{R50/53}}
|SPhrases={{S20/21}}, {{S28}}, {{S45}}, {{S60}}, {{S61}}
|NFPA-H=3
|NFPA-F=0
|NFPA-R=0}}
}}

@@@

@@@

Trimethyl borate[edit]

{{chembox
|verifiedrevid=444236768
|ImageFileL1_Ref={{chemboximage|correct|??}}
|ImageFileL1=Trimethyl-borate-2D.png
|ImageFileR1=Trimethyl-borate-3D-vdW.png
|ImageSize=
|IUPACName=
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=8157
|InChI=1/C3H9BO3/c1-5-4(6-2)7-3/h1-3H3
|InChIKey=WRECIMRULFAWHA-UHFFFAOYAY
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C3H9BO3/c1-5-4(6-2)7-3/h1-3H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=WRECIMRULFAWHA-UHFFFAOYSA-N
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=121-43-7
|PubChem=8470
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=38913
|SMILES=O(B(OC)OC)C
|EINECS=204-468-9
}}
|Section2={{Chembox Properties
|C=3 |H=9 |O=3 |B=1
|Appearance=clear liquid
|Density=0.932 g/ml
|MeltingPt=−34
|BoilingPtC=68
|BoilingPtCH=69
|Solubility=decomposes
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Tris-(Benzyltriazolylmethyl)amine[edit]

{{Chembox
|verifiedrevid=470617490
|ImageFile=Tris(benzyltriazolylmethyl)amine.png
|ImageSize=
|IUPACName=1-(1-benzyltriazol-4-yl)-N,N-bis[(1-benzyltriazol-4-yl)methyl]methanamine
|OtherNames=
|Section1={{Chembox Identifiers
|InChI=1S/C30H30N10/c1-4-10-25(11-5-1)16-38-22-28(31-34-38)19-37(20-29-23-39(35-32-29)17-26-12-6-2-7-13-26)21-30-24-40(36-33-30)18-27-14-8-3-9-15-27/h1-15,22-24H,16-21H2
|InChIKey1=WKGZJBVXZWCZQC-UHFFFAOYSA-N
|InChI1=1S/C30H30N10/c1-4-10-25(11-5-1)16-38-22-28(31-34-38)19-37(20-29-23-39(35-32-29)17-26-12-6-2-7-13-26)21-30-24-40(36-33-30)18-27-14-8-3-9-15-27/h1-15,22-24H,16-21H2
|CASNo_Ref={{cascite|correct|??}}
|CASNo=
|PubChem=11203363
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=9378431
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=WKGZJBVXZWCZQC-UHFFFAOYSA-N
|SMILES=c1ccc(cc1)Cn2cc(nn2)CN(Cc3cn(nn3)Cc4ccccc4)Cc5cn(nn5)Cc6ccccc6
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C30H30N10/c1-4-10-25(11-5-1)16-38-22-28(31-34-38)19-37(20-29-23-39(35-32-29)17-26-12-6-2-7-13-26)21-30-24-40(36-33-30)18-27-14-8-3-9-15-27/h1-15,22-24H,16-21H2
  }}
|Section2={{Chembox Properties
|C=30 |H=30 |N=10
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Triamcinolone acetonide[edit]

{{chembox
|verifiedrevid=434949825
|ImageFile_Ref={{chemboximage|correct|??}}
|ImageFile=Triamcinolone acetonide.png
|ImageSize=200px
|IUPACName=(4a''S'',4b''R'',5''S'',6a''S'',6b''S'',9a''R'',10a''S'',10b''S'')-4b-fluoro-6b-glycoloyl-5-hydroxy-4a,6a,8,8-tetramethyl-4a,4b,5,6,6a,6b,9a,10,10a,10b,11,12-dodecahydro-2''H''-naphtho[2',1':4,5]indeno[1,2-''d''][1,3]dioxol-2-one
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=6196
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=F446C597KA
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=1504
|InChI=1/C24H31FO6/c1-20(2)30-19-10-16-15-6-5-13-9-14(27)7-8-21(13,3)23(15,25)17(28)11-22(16,4)24(19,31-20)18(29)12-26/h7-9,15-17,19,26,28H,5-6,10-12H2,1-4H3/t15-,16-,17-,19+,21-,22-,23-,24+/m0/s1
|InChIKey=YNDXUCZADRHECN-JNQJZLCIBL
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C24H31FO6/c1-20(2)30-19-10-16-15-6-5-13-9-14(27)7-8-21(13,3)23(15,25)17(28)11-22(16,4)24(19,31-20)18(29)12-26/h7-9,15-17,19,26,28H,5-6,10-12H2,1-4H3/t15-,16-,17-,19+,21-,22-,23-,24+/m0/s1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=YNDXUCZADRHECN-JNQJZLCISA-N
|CASNo=76-25-5
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=6436
|SMILES=O=C\1\C=C5/[C@@](/C=C/1)(C)[C@]2(F)[C@H]([C@H]3[C@](C[C@@H]2O)([C@@]4(OC(O[C@@H]4C3)(C)C)C(=O)CO)C)CC5
}}
|Section2={{Chembox Properties
|C=24|H=31|F=1|O=6
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Sumanene[edit]

{{chembox
|verifiedrevid=435704948
|ImageFile=Sumanene.svg
|ImageSize=156px
|ImageFile1=Sumanene3D.png
|ImageSize1=180px
|IUPACName=4,7-Dihydro-1H-tricyclopenta[def,jkl,pqr]triphenylene
|OtherNames=
|Section1={{Chembox Identifiers
|CASNo=151253-59-7
|PubChem=
|SMILES=C16=C5C4=C3C2=C1C7=CC=C2 CC3=CC=C4CC5=CC=C6C7
  }}
|Section2={{Chembox Properties
|C=21|H=12
|MolarMass=264.32
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Sodium selenite[edit]

{{chembox
|verifiedrevid=464403878
|ImageFile=Natriumseleniet t.png
|ImageSize=
|IUPACName=
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=23308
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=HIW548RQ3W
|InChI=1/2Na.H2O3Se/c;;1-4(2)3/h;;(H2,1,2,3)/q2*+1;/p-2
|InChIKey=BVTBRVFYZUCAKH-NUQVWONBAC
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=48843
|SMILES=[Na+].[Na+].[O-][Se]([O-])=O
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/2Na.H2O3Se/c;;1-4(2)3/h;;(H2,1,2,3)/q2*+1;/p-2
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=BVTBRVFYZUCAKH-UHFFFAOYSA-L
|CASNo=10102-18-8
|CASNo_Ref={{cascite|correct|CAS}}
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=112302
|PubChem=24934
|EINECS=233-267-9
|RTECS=VS7350000
|UNNumber=2630
|ATCCode_prefix=A12
|ATCCode_suffix=CE02
 }}
|Section2={{Chembox Properties
|Na=2 |Se=1 |O=3
|Appearance=colourless solid
|Density=
|MeltingPt=320 °C (decomp.)
|BoilingPt=
|Solubility=850 g/L (20 °C)
 }}
|Section7={{Chembox Hazards
|ExternalMSDS=[http://www.inchem.org/documents/icsc/icsc/eics0698.htm ICSC 0698]
|EUIndex=034-003-00-3
|EUClass=Very toxic ('''T+''')<br/>Dangerous for the environment ('''N''')
|RPhrases={{R23}}, {{R28}}, {{R31}}, {{R43}}, {{R51/53}}
|SPhrases={{S1/2}}, {{S28}}, {{S36/37}}, {{S45}}, {{S61}}
|NFPA-H=3
|NFPA-F=0
|NFPA-R=0
|FlashPt=
 }}
|Section8={{Chembox Related
|OtherCpds=[[سدیم سولفیت]] <br> [[Sodium selenate]] <br> [[Sodium selenide]]
 }}
}}

@@@

@@@

Secoisolariciresinol[edit]

{{chembox
|Verifiedfields=changed
|Watchedfields=changed
|verifiedrevid=414643352
|Name=Secoisolariciresinol
|ImageFile=Secoisolariciresinol.PNG
|ImageSize=200px
|ImageName=Chemical structure of secoisolariciresinol
|IUPACName=(2''R'',3''R'')-2,3-bis[(4-hydroxy-3-methoxyphenyl)methyl]butane-1,4-diol
|OtherNames=(−)-Secoisolariciresinol<!-- <br> -->
|Section1={{Chembox Identifiers
|CASNo=29388-59-8
|CASNo_Ref={{cascite|correct|??}}
|CASOther=
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=368347
|PubChem=65373
|SMILES=COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O
|InChI=
|MeSHName=
}}
|Section2={{Chembox Properties
|C=20|H=26|O=6
|ExactMass=362.172939 u
|Appearance=
|Density=
|MeltingPt=<!-- °C -->
|BoilingPt=<!-- °C -->
|Solubility=
}}
}}

@@@

@@@

Sodium monofluorophosphate[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=464402436
|ImageFile=Sodium monofluorophosphate.PNG
|ImageSize=
|IUPACName=Disodium phosphorofluoridate
|OtherNames=Sodium fluorophosphate, disodium monofluorophosphate
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=22686
|InChI=1/FH2O3P.2Na/c1-5(2,3)4;;/h(H2,2,3,4);;/q;2*+1/p-2
|InChIKey=BFDWBSRJQZPEEB-NUQVWONBAA
|SMILES=[Na+].[Na+].[O-]P([O-])(F)=O
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/FH2O3P.2Na/c1-5(2,3)4;;/h(H2,2,3,4);;/q;2*+1/p-2
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=BFDWBSRJQZPEEB-UHFFFAOYSA-L
|CASNo=10163-15-2
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=1200892
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=24266
|ATCCode_prefix=A01
|ATCCode_suffix=AA02
|ATC_Supplemental={{ATC|A12|CD02}} }}

@@@

@@@

Trans-2-Phenyl-1-cyclohexanol[edit]

{{chembox
|verifiedrevid=401639290
|Name=(1''S'',2''R'')-2-phenylcyclohexanol
|ImageFile=(1S,2R)-2-phenylcyclohexanol-2D-skeletal.png
|ImageSize=
|IUPACName=(1S,2R)-2-phenyl-1-cyclohexanol
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=8074632
|InChI=1/C12H16O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-3,6-7,11-13H,4-5,8-9H2/t11-,12+/m1/s1
|InChIKey=AAIBYZBZXNWTPP-NEPJUHHUBI
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C12H16O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-3,6-7,11-13H,4-5,8-9H2/t11-,12+/m1/s1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=AAIBYZBZXNWTPP-NEPJUHHUSA-N
|CASNo=34281-92-0
|PubChem=9898975
|SMILES=O[C@@H]2[C@@H](c1ccccc1)CCCC2
}}
|Section2={{Chembox Properties
|C=12|H=16|O=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Triplet oxygen[edit]

{{Chembox
|PIN=Triplet oxygen{{Citation needed|date=July 2011}}
|SystematicName=Dioxidanediyl<ref name="Triplet Dioxygen (CHEBI:27140)">{{Cite web|url=http://www.ebi.ac.uk/chebi/searchId.do;jsessionid=365B584AEF7AC9DBA25DFB67350F6CAF?chebiId=CHEBI%3A27140|title=Triplet Dioxygen (CHEBI:27140)|work=Chemical Entities of Biological Interest (ChEBI)|location=UK|publisher=European Bioinformatics Institute}}</ref> (substitutive)<br />
dioxygen(2•)(triplet)<ref name="Triplet Dioxygen (CHEBI:27140)" /> (additive)
|Section1={{Chembox Identifiers
|CASNo=7782-44-7
|CASNo_Ref={{cascite|correct|CAS}}
|EINECS=231-956-9
|UNNumber=1072
|KEGG=D00003
|KEGG_Ref={{keggcite|correct|kegg}}
|MeSHName=Oxygen
|ChEBI=27140
|RTECS=RS2060000
|Gmelin=492
|ATCCode_prefix=V03
|ATCCode_suffix=AN01
|SMILES=[O]#[O]
|SMILES1=o:o
|SMILES2=[O][O]
|StdInChI=1S/O2/c1-2
|StdInChIKey=MYMOFIZGZYHOMD-UHFFFAOYSA-N
}}
|Section2={{Chembox Properties
|O=2
|ExactMass=31.989829244 g mol<sup>-1</sup>
|Appearance=Colorless gas
|MeltingPtK=55
|BoilingPtK=90
}}
|Section3={{Chembox Structure
|MolShape=Linear
|Dipole=0 D
}}
|Section4={{Chembox Thermochemistry
|DeltaHf=0 kJ mol<sup>-1</sup>
|Entropy=205.152 J K<sup>-1</sup> mol<sup>-1</sup>
}}
|Section5={{Chembox Hazards
|EUClass={{Hazchem O}}
|RPhrases={{R8}}
|SPhrases={{S17}}
|NFPA-F=0
|NFPA-H=0
|NFPA-R=0
|NFPA-O=Ox
}}
}}

@@@

@@@

Triphosphoric acid[edit]

{{Chembox
|verifiedrevid=446484776
|ImageFile=Triphosphorsäure.svg
|ImageSize=
|ImageAlt=
|ImageFile1=Tripolyphosphoric-acid-3D-vdW.png
|ImageSize1=
|ImageAlt1=Structure of triphosphoric acid
|IUPACName=Triphosphoric acid
|PIN=
|OtherNames=
|Section1={{Chembox Identifiers
|CASNo=10380-08-2
|CASNo_Ref={{cascite|correct|??}}
|PubChem=
|SMILES=}}
|Section2={{Chembox Properties
|Formula=
|MolarMass=257.95 g/mol
|pKa=small; small; 2.30; 6.50; 9.24
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=}}
|Section3={{Chembox Hazards
|MainHazards=Corrosive ('''C''')
|FlashPt=
|Autoignition=}}
}}

@@@

@@@

Trimethylsilyldiazomethane[edit]

{{Chembox
|verifiedrevid=404978232
|ImageFile=Trimethylsilyldiazomethane.png
|ImageSize=150
|IUPACName=(Diazomethyl)trimethylsilane
|OtherNames=Trimethylsilyldiazomethane<br />Diazo(trimethylsilyl)methane
|Section1={{Chembox Identifiers
|CASNo=18107-18-1
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=167693
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=146699
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|MeSHName=Trimethylsilyldiazomethane
|SMILES=C[Si](C)(C)[CH-][N+]#N
|SMILES1=[N-]=[N+]=C[Si](C)(C)C
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C4H10N2Si/c1-7(2,3)4-6-5/h4H,1-3H3
|InChI1=1/C4H10N2Si/c1-7(2,3)4-6-5/h4H,1-3H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=ONDSBJMLAHVLMI-UHFFFAOYSA-N
|InChIKey1=ONDSBJMLAHVLMI-UHFFFAOYAN
|Beilstein=1902903}}
|Section2={{Chembox Properties
|C=4
|H=10
|N=2
|Si=1
|ExactMass=114.061324863 g mol<sup>-1</sup>
|Appearance=greenish-yellow liquid<ref>{{ cite journal |doi=10.1021/ja01006a055 |title=Trimethylsilyldiazomethane and trimethylsilylcarbene |year=1968 |last1=Seyferth |first1=Dietmar. |last2=Dow |first2=Alan W. |last3=Menzel |first3=Horst. |last4=Flood |first4=Thomas C. |journal=[[J. Am. Chem. Soc.]] |volume=90 |issue=4 |pages=1080–1082 }}</ref><ref>{{cite journal |doi=10.1016/S0022-328X(00)82916-2 |title=Trimethylsilyl-substituted diazoalkanes I. Trimethylsilyldiazomethane |year=1972 |last1=Seyferth |first1=Dietmar |last2=Menzel |first2=Horst |last3=Dow |first3=Alan W. |last4=Flood |first4=Thomas C. |journal=[[J. Organomet. Chem.]] |volume=44 |issue=2 |pages=279–290 }}</ref> }}

@@@

@@@

Ricinolein[edit]

{{Chembox
|ImageFile=Ricinolein.svg
|ImageSize=200px
|IUPACName=Propane-1,2,3-triyl (9''Z'',12''R'',9′''Z'',12′''R'',9′′''Z'',12′′''R'')tris(12-hydroxyoctadec-9-enoate)
|OtherNames=Glycerin triricinoleate; Glycerol triricinoleate; Glyceryl triricinoleate; Ricinoleic acid triglyceride; Ricinoleic triglyceride; Triricinolein
|Section1={{Chembox Identifiers
|CASNo=2540-54-7
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=11764524
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=9939216
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|EINECS=219-817-0
|SMILES=O=C(CCCCCCC/C=C\C[C@H](O)CCCCCC)OCC(OC(CCCCCCC/C=C\C[C@H](O)CCCCCC)=O)COC(CCCCCCC/C=C\C[C@H](O)CCCCCC)=O
|InChI=InChI=1S/C57H104O9/c1-4-7-10-31-40-51(58)43-34-25-19-13-16-22-28-37-46-55(61)64-49-54(66-57(63)48-39-30-24-18-15-21-27-36-45-53(60)42-33-12-9-6-3)50-65-56(62)47-38-29-23-17-14-20-26-35-44-52(59)41-32-11-8-5-2/h25-27,34-36,51-54,58-60H,4-24,28-33,37-50H2,1-3H3/b34-25-,35-26-,36-27-/t51-,52-,53-/m1/s1
}}
|Section2={{Chembox Properties
|C=57
|H=104
|O=9
|ExactMass=932.768034926 g mol<sup>-1</sup>
}}
}}

@@@

@@@

Triazene[edit]

{{Chembox
|ImageFile=Triazene.svg
|ImageSize=150px
|IUPACName=Triazene
|SystematicName=Triaz-1-ene<ref>[http://www.ebi.ac.uk/chebi/searchFreeText.do?searchString=15056-34-5 triazene], Chemical Entities of Biological Interest</ref>
|Section1={{Chembox Identifiers
|CASNo=15056-34-5
|CASNo_Ref={{cascite|correct|??}}
|PubChem=115034
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=102956
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChEBI=35468
|Gmelin=49028
|SMILES=NN=N
|StdInChI=1S/H3N3/c1-3-2/h(H3,1,2)
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=AYNNSCRYTDRFCP-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
}}
|Section2={{Chembox Properties
|H=3
|N=3
|ExactMass=45.032697111 gmol<sup>-1</sup>
}}
|Section3={{Chembox Hazards
|NFPA-H=3
|NFPA-F=4
|NFPA-R=4
}}
}}

@@@

@@@

Quinizarine Green SS[edit]

{{chembox
|verifiedrevid=401038222
|Name=Quinizarine Green SS
|ImageFile=Quinizarine Green SS.png
|Image Size=200px
|Image Name=Quinizarine Green SS
|IUPAC Name=Quinizarine Green SS
|Other Names=C.I. Solvent Green 3;
1,4-bis[(4-methylphenyl)amino]-9,10-Anthracenedione; D & C Green No.6; 1,4-Bis(p-tolylamino)anthraquinone; 1,4-Bis(p-toluidino)anthraquinone; C.I. 61565; Oil Green G;
|Section1={{Chembox Identifiers
|SMILES=O=C2c1ccccc1C(=O)c3c2c(ccc3Nc4ccc(cc4)C)Nc5ccc(cc5)C
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=29146
|PubChem=31416
|InChI=1/C28H22N2O2/c1-17-7-11-19(12-8-17)29-23-15-16-24(30-20-13-9-18(2)10-14-20)26-25(23)27(31)21-5-3-4-6-22(21)28(26)32/h3-16,29-30H,1-2H3
|InChIKey=TVRGPOFMYCMNRB-UHFFFAOYAN
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C28H22N2O2/c1-17-7-11-19(12-8-17)29-23-15-16-24(30-20-13-9-18(2)10-14-20)26-25(23)27(31)21-5-3-4-6-22(21)28(26)32/h3-16,29-30H,1-2H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=TVRGPOFMYCMNRB-UHFFFAOYSA-N
|CASNo_Ref=
|CASNo=128-80-3
|RTECS=
  }}
|Section2={{Chembox Properties
|C=28|H=22|N=2|O=2
|Appearance=Black Powder
|Density=
|Solubility=Insoluble
|MeltingPt=220-221 °C
|BoilingPt=
}}
|Section7={{Chembox Hazards
|MainHazards=
|FlashPt=
|RPhrases={{R36/37/38}}
|SPhrases={{S26}}, {{S36}}
  }}
|Section8={{Chembox Related
|OtherCpds=
  }}
}}

@@@

@@@

Solvent Yellow 124[edit]

{{Chembox
|verifiedrevid=446992534
|ImageFile=Solvent Yellow 124.svg
|ImageSize=200px
|IUPACName=''N''-Ethyl-''N''-[2-[1-(2-methylpropoxy)ethoxy]ethyl]-4-phenyldiazenylaniline
|OtherNames=SY124; Sudan 455; Somalia Yellow; T10 Yellow LBN; C.I. 111155
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=105606
|InChI=1/C22H31N3O2/c1-5-25(15-16-26-19(4)27-17-18(2)3)22-13-11-21(12-14-22)24-23-20-9-7-6-8-10-20/h6-14,18-19H,5,15-17H2,1-4H3/b24-23+
|InChIKey=BATVZJPOLFSGTD-WCWDXBQEBJ
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C22H31N3O2/c1-5-25(15-16-26-19(4)27-17-18(2)3)22-13-11-21(12-14-22)24-23-20-9-7-6-8-10-20/h6-14,18-19H,5,15-17H2,1-4H3/b24-23+
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=BATVZJPOLFSGTD-WCWDXBQESA-N
|CASNo_Ref={{cascite|correct|??}}
|CASNo=34432-92-3
|PubChem=118170
|SMILES=N(=N/c1ccc(N(CCOC(OCC(C)C)C)CC)cc1)\c2ccccc2
}}
|Section2={{Chembox Properties
|C=22 |H=31 |N=3 |O=2
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Red-Al[edit]

{{Chembox
|ImageFile=Red-Al.png
|ImageFile_Ref={{Chemboximage|correct|??}}
|ImageSize=244
|ImageName=Structural formula of red-Al with explicit hydrogens
|IUPACName=Sodium bis(2-methoxyethoxy)aluminumhydride
|OtherNames=Vitride
|Section1={{Chembox Identifiers
|Abbreviations=SMEAH
|CASNo=22722-98-1
|CASNo_Ref={{cascite|changed|??}}
|PubChem=16684438
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=21169529
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|SMILES=[Na+].COCCO[AlH2-]OCCOC
|SMILES1=[H][Al-](OCCOC)([H])OCCOC.[Na+]
|StdInChI=1S/2C3H7O2.Al.Na.2H/c2*1-5-3-2-4;;;;/h2*2-3H2,1H3;;;;/q2*-1;2*+1;;
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=XJIQVZMZXHEYOY-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
}}
|Section2={{Chembox Properties
|C=6
|H=16
|Al=1
|Na=1
|O=4
|ExactMass=202.076167116 g mol<sup>-1</sup>
|Appearance=Transparent crystals
}}
|Section3={{Chembox Hazards
|MainHazards=Unstable toward water
}}
}}

@@@

@@@

TSQ[edit]

{{chembox
|verifiedrevid=401616778
|ImageFile=TSQ.png
|ImageSize=120px
|IUPACName=''N''-(6-Methoxy-8-quinolyl)-4-toluenesulfonamide
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=115530
|InChI=1/C17H16N2O3S/c1-12-5-7-15(8-6-12)23(20,21)19-16-11-14(22-2)10-13-4-3-9-18-17(13)16/h3-11,19H,1-2H3
|InChIKey=HKRNYOZJJMFDBV-UHFFFAOYAJ
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C17H16N2O3S/c1-12-5-7-15(8-6-12)23(20,21)19-16-11-14(22-2)10-13-4-3-9-18-17(13)16/h3-11,19H,1-2H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=HKRNYOZJJMFDBV-UHFFFAOYSA-N
|CASNo=109628-27-5
|PubChem=130606
|SMILES=O=S(=O)(c1ccc(cc1)C)Nc2cc(OC)cc3cccnc23
}}
|Section2={{Chembox Properties
|C=17|H=16|N=2|O=3|S=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Sudan Red 7B[edit]

{{Chembox
|verifiedrevid=434011492
|ImageFile1=Sudan Red 7B.png
|ImageSize1=200px
|ImageFile2=Sudan-Red-7B-3D-balls.png
|ImageSize2=200px
|ImageAlt=
|IUPACName=''N''-Ethyl-1-((4-phenyldiazenyl)phenyl)diazenyl)naphthalen-2-amine
|OtherNames=Solvent Red 19; Ceres Red 7B; Fat Red 7B; Hexatype carmine B; Lacquer red V3B; Oil violet; Organol bordeaux B; Sudanrot 7B; Typogen carmine; C.I. 26050; ''N''-ethyl-1-[[''p''-(phenylazo)phenyl]azo]-2-naphthalenamine
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=55325
|InChI1=1/C24H21N5/c1-2-25-23-17-12-18-8-6-7-11-22(18)24(23)29-28-21-15-13-20(14-16-21)27-26-19-9-4-3-5-10-19/h3-17,25H,2H2,1H3/b27-26+,29-28+
|InChIKey1=VKWNTWQXVLKCSG-ZDXBJJIEBU
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C24H21N5/c1-2-25-23-17-12-18-8-6-7-11-22(18)24(23)29-28-21-15-13-20(14-16-21)27-26-19-9-4-3-5-10-19/h3-17,25H,2H2,1H3/b27-26+,29-28+
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=VKWNTWQXVLKCSG-ZDXBJJIESA-N
|CASNo=6368-72-5
|PubChem=61396
|KEGG_Ref={{keggcite|correct|kegg}}
|KEGG=C19529
|SMILES=N(=N/c3ccc(/N=N/c1c2c(ccc1NCC)cccc2)cc3)\c4ccccc4
}}
|Section2={{Chembox Properties
|C=24|H=21|N=5
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=}}
}}

@@@

@@@

Vat Yellow 4[edit]

{{Chembox
|Watchedfields=changed
|verifiedrevid=444502525
|ImageFile=Vat Yellow 4.png
|ImageSize=190
|ImageName=Skeletal formula
|ImageFile1=Vat-yellow-4-3D-balls.png
|ImageSize1=210
|ImageName1=Ball-and-stick model
|IUPACName=
|PIN=
|OtherNames=Golden Yellow GK<br>Dibenzochrysenedione<br>Dibenzpyrenequinone<br>Tyrian Yellow I-GOK<br>C.I. 59100<br>Dibenzo[b,def]chrysene-7,14-dione<br>3,4:8,9-dibenzopyrene-5,10-dione
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=29142
|InChI=1/C24H12O2/c25-23-17-7-3-1-5-13(17)15-9-11-20-22-16(10-12-19(23)21(15)22)14-6-2-4-8-18(14)24(20)26/h1-12H
|InChIKey=ZTWQZJLUUZHJGS-UHFFFAOYAD
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C24H12O2/c25-23-17-7-3-1-5-13(17)15-9-11-20-22-16(10-12-19(23)21(15)22)14-6-2-4-8-18(14)24(20)26/h1-12H
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=ZTWQZJLUUZHJGS-UHFFFAOYSA-N
|CASNo_Ref={{cascite|correct|??}}
|CASNo=128-66-5
|PubChem=31412
|KEGG_Ref={{keggcite|correct|kegg}}
|KEGG=C19545
|SMILES=O=C2c1ccccc1c6c5c2ccc4c3ccccc3C(=O)c(c45)cc6
}}
|Section2={{Chembox Properties
|C=24 |H=12 |O=2
|MolarMass=
|Appearance=viscous orange liquid
|Density=1.418g/cm3 
|MeltingPt=
|BoilingPt=606.7 °C @ 760mmHg 
|Solubility=soluble }}
|Section3={{Chembox Hazards
|MainHazards=Possible carcinogen
|FlashPt=219.93 
|Autoignition=}}
}}

@@@

@@@

Solvent Violet 13[edit]

{{Chembox
|Verifiedimages=changed
|verifiedrevid=444112202
|ImageFile_Ref={{chemboximage|changed|??}}
|ImageFile=Solvent Violet 13.png
|ImageSize=
|IUPACName=1-hydroxy-4-(p-tolylamino)anthracene-9,10-dione
|OtherNames=
|Section1={{Chembox Identifiers
|InChI=1/C21H15NO3/c1-12-6-8-13(9-7-12)22-16-10-11-17(23)19-18(16)20(24)14-4-2-3-5-15(14)21(19)25/h2-11,22-23H,1H3
|InChIKey=LJFWQNJLLOFIJK-UHFFFAOYAI
|InChI1=1S/C21H15NO3/c1-12-6-8-13(9-7-12)22-16-10-11-17(23)19-18(16)20(24)14-4-2-3-5-15(14)21(19)25/h2-11,22-23H,1H3
|InChIKey1=LJFWQNJLLOFIJK-UHFFFAOYSA-N
|CASNo=
|PubChem=6680
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=6428
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=LJFWQNJLLOFIJK-UHFFFAOYSA-N
|SMILES=O=C2c1ccccc1C(=O)c3c2c(ccc3O)Nc4ccc(cc4)C
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C21H15NO3/c1-12-6-8-13(9-7-12)22-16-10-11-17(23)19-18(16)20(24)14-4-2-3-5-15(14)21(19)25/h2-11,22-23H,1H3
  }}
|Section2={{Chembox Properties
|C=21 |H=15 |N=1 |O=3
|Appearance=
|Density=
|MeltingPt=142-143 °C
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Ranelic acid[edit]

{{chembox
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=K9CCS0RIBT
|ImageFile=Ranelic acid.png
|ImageFile_Ref={{Chemboximage|correct|??}}
|ImageSize=244
|ImageName=Structural formula of ranelic acid
|IUPACName=5-(Bis(carboxymethyl)amino)-3-(carboxymethyl)-4-cyano-2-thiophenecarboxylic acid
|SystematicName=5-[Bis(carboxymethyl)amino]-3-(carboxymethyl)-4-cyanothiophene-2-carboxylic acid<ref>{{PubChem|3052774}}</ref>
|Section1={{Chembox Identifiers
|CASNo=135459-90-4
|CASNo_Ref={{cascite|correct|??}}
|CASNo1=5459-90-4
|CASNo1_Ref={{cascite|changed|??}}
|PubChem=3052774
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=2314551
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|KEGG=D08467
|KEGG_Ref={{keggcite|correct|kegg}}
|SMILES=OC(=O)CN(CC(O)=O)C1=C(C#N)C(CC(O)=O)=C(S1)C(O)=O
|SMILES1=C(C1=C(SC(=C1C#N)N(CC(=O)O)CC(=O)O)C(=O)O)C(=O)O
|StdInChI=1S/C12H10N2O8S/c13-2-6-5(1-7(15)16)10(12(21)22)23-11(6)14(3-8(17)18)4-9(19)20/h1,3-4H2,(H,15,16)(H,17,18)(H,19,20)(H,21,22)
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=DJSXNILVACEBLP-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
}}
|Section2={{Chembox Properties
|C=12
|H=10
|N=2
|O=8
|S=1
|ExactMass=342.015785996 g mol<sup>-1</sup>
}}
}}

@@@

@@@

Sodium ascorbate[edit]

{{chembox
|Verifiedfields=changed
|UNII_Ref={{fdacite|changed|FDA}}
|UNII=S033EH8359
|verifiedrevid=414219642
|Reference=<ref>[http://www.sigmaaldrich.com/catalog/ProductDetail.do?lang=en&N4=268550|ALDRICH&N5=SEARCH_CONCAT_PNO|BRAND_KEY&F=SPEC (+)-Sodium L-ascorbate] at [[Sigma-Aldrich]]</ref>
|Name=Sodium <small>L</small>-ascorbate
|ImageFile=sodium ascorbate.png
|ImageSize=200px
|IUPACName=Sodium (2''R'')-2-[(1''S'')-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2''H''-furan-3-olate
|OtherNames=Sodascorbate; Monosodium ascorbate; E301
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=134-03-2
|PubChem=23667548
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=591665
|SMILES=OC1=C([O-])[C@]([C@@H](O)CO)([H])OC1=O.[Na+]
}}
|Section2={{Chembox Properties
|C=6|H=7|Na=1|O=6 
|Appearance=
|Density=
|MeltingPt=220 °C (dec.)
|BoilingPt=
|Solubility=}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=}}
}}

@@@

@@@

Rubidium-82 chloride[edit]

{{Chembox
|IUPACName=Rubidium-82 chloride
|SystematicName=(<sup>82</sup>''Rb'')Rubidium chloride
|Section1={{Chembox Identifiers
|CASNo=132486-03-4
|CASNo_Ref={{cascite|correct|??}}
|PubChem=71357
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=64457
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|KEGG=D05773
|KEGG_Ref={{Keggcite|correct|kegg}}
|SMILES=[Cl-].[82Rb+]
|StdInChI=1S/ClH.Rb/h1H;/q;+1/p-1/i;1-3
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=FGDZQCVHDSGLHJ-RYDPDVNUSA-M
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}}}

@@@

@@@

Sodium cobaltinitrite[edit]

{{chembox
|verifiedrevid=447351420
|ImageFile=Sodium cobaltinitrite.png
|ImageSize=
|IUPACName=sodium hexanitritocobaltate(III)
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=13198283
|InChI=1/Co.6NO2.3Na/c;6*2-1-3;;;/q-3;;;;;;;3*+1/rCoN6O12.3Na/c8-2(9)1(3(10)11,4(12)13,5(14)15,6(16)17)7(18)19;;;/q-3;3*+1
|InChIKey=IMBXIBFCGMYSME-PEVTYUNUAJ
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/Co.6NO2.3Na/c;6*2-1-3;;;/q-3;;;;;;;3*+1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=IMBXIBFCGMYSME-UHFFFAOYSA-N
|CASNo=13600-98-1
|PubChem=16211641
|SMILES=[Na+].[Na+].[Na+].O=[N+]([O-])[Co-3]([N+]([O-])=O)([N+](=O)[O-])([N+]([O-])=O)([N+]([O-])=O)[N+]([O-])=O
}}
|Section2={{Chembox Properties
|Co=1 |N=6 |Na=3 |O=12
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|ExternalMSDS=[http://hazard.com/msds/mf/baker/baker/files/s3434.htm JT Baker MSDS]
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Seliciclib[edit]

{{chembox
|Verifiedfields=changed
|UNII_Ref={{fdacite|changed|FDA}}
|UNII=0ES1C2KQ94
|verifiedrevid=377431079
|ImageFile=Seliciclib.PNG
|ImageSize=200px
|IUPACName=2-(''R'')-(1-Ethyl-2-hydroxyethylamino)-6-benzylamino-9-isopropylpurine
|OtherNames=Roscovitine; CYC202
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite|correct|??}}
|CASNo=186692-46-6
|PubChem=160355
|SMILES=CC[C@H](CO)NC1=NC2=C(C(=N1)NCC3=CC=CC=C3)N=CN2C(C)C
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=14762
|MeSHName=roscovitine
  }}
|Section2={{Chembox Properties
|C=19|H=26|N=6|O=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
  }}
|Section3={{Chembox Hazards
|Solubility=
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Trimethylsilyl cyanide[edit]

{{chembox
|Watchedfields=changed
|verifiedrevid=412009295
|ImageFileL1=Trimethylsilyl-cyanide-skeletal.png
|ImageSizeL1=120px
|ImageFileR1=Trimethylsilyl-cyanide-3D-vdW.png
|ImageSizeR1=120px
|IUPACName=trimethylsilylformonitrile
|OtherNames=Cyanotrimethylsilane; TMS cyanide; Trimethylsilylnitrile; Trimethylsilanecarbonitrile' Trimethylsilylcarbonitrile
|Section1={{Chembox Identifiers
|Abbreviations=TMSCN
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=74110
|InChI=1/C4H9NSi/c1-6(2,3)4-5/h1-3H3
|InChIKey=LEIMLDGFXIOXMT-UHFFFAOYAM
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C4H9NSi/c1-6(2,3)4-5/h1-3H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=LEIMLDGFXIOXMT-UHFFFAOYSA-N
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=7677-24-9
|EINECS=
|PubChem=82115
|SMILES=C[Si](C)(C)C#N
|RTECS=
|MeSHName=
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=
|KEGG_Ref={{keggcite|correct|kegg}}
|KEGG=
|ATCCode=}}
|Section2={{Chembox Properties
|C=4|H=9|Si=1|N=1
|Appearance=
|Density=0.793 g/mL at 20 °C
|MeltingPtC=8
|MeltingPtCH=11
|Melting_notes=
|BoilingPtC=114
|BoilingPtCH=117
|Boiling_notes=
|Solubility=organic solvents
|SolubleOther=reacts with water
|Solvent=
|pKa=
|pKb=
|IsoelectricPt=
|SpecRotation=
|RefractIndex=1.392
|Viscosity=
|Dipole=}}
|Section3={{Chembox Structure
|CrystalStruct=
|Coordination=
|MolShape=
|Dipole=}}
|Section7={{Chembox Hazards
|ExternalMSDS=
|EUClass=
|EUIndex=
|MainHazards=
|NFPA-H=
|NFPA-F=
|NFPA-R=
|NFPA-O=
|RPhrases={{R11}} {{R26/27/28}} {{R29}}
|SPhrases={{S16}} {{S36/37/39}} {{S45}}
|RSPhrases=
|FlashPt={{convert|1|C|F}}
|Autoignition=
|ExploLimits=
|PEL=}}
|Section8={{Chembox Related
|OtherAnions=
|OtherCations=
|OtherFunctn=
|Function=
|OtherCpds=}}
}}

@@@

@@@

Titanium(II) chloride[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=477000010
|ImageFile=Kristallstruktur Cadmiumiodid.png
|ImageSize=200px
|IUPACName=
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=8466246
|InChI=1/2ClH.Ti/h2*1H;/q;;+2/p-2
|InChIKey=ZWYDDDAMNQQZHD-NUQVWONBAH
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/2ClH.Ti/h2*1H;/q;;+2/p-2
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=ZWYDDDAMNQQZHD-UHFFFAOYSA-L
|CASNo_Ref={{cascite|changed|??}}
|CASNo=10049-06-6
|PubChem=66228
|SMILES=[Ti+2].[Cl-].[Cl-]
}}
|Section2={{Chembox Properties
|Ti=1 |Cl=2
|Appearance=black [[دستگاه بلوری هگزاگونال]] crystals
|Density=3.13 g/cm<sup>3</sup>
|MeltingPt=1035°C
|BoilingPt=1500°C<ref name="hand">
{{Cite book
 |last=Lide
 |first=David R.
 |author-link=
 |last2=
 |first2=
 |author2-link=
 |publication-date=
 |date=
 |year=1998
 |title=Handbook of Chemistry and Physics
 |edition=87
 |volume=
 |series=
 |publication-place=Boca Raton, FL
 |place=
 |publisher=CRC Press
 |id=
 |isbn=0-8493-0594-2
 |doi=
 |oclc=
 |pages=491
 |url=
 |accessdate=
 |postscript=<!--None-->
}}</ref>
|Solubility=
  }}

@@@

@@@

Voacangine[edit]

{{Chembox
|Verifiedfields=changed
|Watchedfields=changed
|verifiedrevid=399125860
|ImageFile=Voacangine.svg
|ImageFile_Ref={{Chemboximage|correct|??}}
|ImageSize=244
|ImageName=Stereo structural formula of voacangine ((1S,17S)-17-ethyl,-1-carboxyl)
|IUPACName=12-Methoxyibogamine-18-carboxylic acid, methyl ester
|SystematicName=Methyl 17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.0<sup>2,10</sup>.0<sup>4,9</sup>.0<sup>13,18</sup>] nonadeca-2(10),4,6,8-tetraene-1-carboxylate<ref>{{ cite web |url=https://www.ebi.ac.uk/chembldb/index.php/compound/inspect/407575 |title=Compound Report Card CHEMBL182120 - Voacangine |publisher=ChEMBL }}</ref>
|Section1={{Chembox Identifiers
|CASNo=510-22-5
|CASNo_Ref={{cascite|correct|??}}
|PubChem=363270
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|PubChem1=261793
|PubChem1_Ref={{Pubchemcite|correct|PubChem}}
|PubChem1_Comment=<small>(15''S'',17''R'')-17-ethyl,-15-nonadeca</small>
|PubChem2=10451681
|PubChem2_Ref={{Pubchemcite|correct|PubChem}}
|PubChem2_Comment=<small>(1''S'',15''S'',18''S'')-15,18-nonadeca,-1-carboxyl</small>
|PubChem3=21598350
|PubChem3_Ref={{Pubchemcite|correct|PubChem}}
|PubChem3_Comment=<small>(1''R'',15''S'',17''R'',18''R'')-17-ethyl,-15,18-nonadeca,-1-carboxyl</small>
|PubChem4=10361692
|PubChem4_Ref={{Pubchemcite|correct|PubChem}}
|PubChem4_Comment=<small>(1''S'',15''R'',17''S'',18''S'')-17-ethyl,-15,18-nonadeca,-1-carboxyl</small>
|PubChem5=73255
|PubChem5_Ref={{Pubchemcite|correct|PubChem}}
|PubChem5_Comment=<small>(1''S'',15''S'',17''S'',18''S'')-17-ethyl,-15,18-nonadeca,-1-carboxyl</small>
|ChemSpiderID=322451
|ChemSpiderID_Ref={{chemspidercite|changed|chemspider}}
|ChemSpiderID1=229858
|ChemSpiderID1_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID1_Comment=<small>(15''S'',17''R'')-17-ethyl,-15-nonadeca</small>
|ChemSpiderID2=8627098
|ChemSpiderID2_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID2_Comment=<small>(1''S'',15''S'',18''S'')-15,18-nonadeca,-1-carboxyl</small>
|ChemSpiderID3=10225658
|ChemSpiderID3_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID3_Comment=<small>(1''R'',15''S'',17''R'',18''R'')-17-ethyl,-15,18-nonadeca,-1-carboxyl</small>
|ChemSpiderID4=8537141
|ChemSpiderID4_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID4_Comment=<small>(1''S'',15''R'',17''S'',18''S'')-17-ethyl,-15,18-nonadeca,-1-carboxyl</small>
|ChemSpiderID5=66007
|ChemSpiderID5_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID5_Comment=<small>(1''S'',15''S'',17''S'',18''S'')-17-ethyl,-15,18-nonadeca,-1-carboxyl</small>
|MeSHName=Voacangine
|ChEBI_Ref={{ebicite|changed|EBI}}
|ChEBI=407575
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=182120
|SMILES=CCC1CC2CN3CCC4=C(NC5=C4C=C(OC)C=C5)C(C2)(C13)C(=O)OC
|SMILES1=CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC
|StdInChI=1S/C22H28N2O3/c1-4-14-9-13-11-22(21(25)27-3)19-16(7-8-24(12-13)20(14)22)17-10-15(26-2)5-6-18(17)23-19/h5-6,10,13-14,20,23H,4,7-9,11-12H2,1-3H3
|StdInChI_Ref={{stdinchicite|changed|chemspider}}
|StdInChIKey=MMAYTCMMKJYIAM-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|changed|chemspider}}
}}
|Section2={{Chembox Properties
|C=22
|H=28
|N=2
|O=3
|ExactMass=368.209992772 g mol<sup>-1</sup>
|MeltingPtC=136
|MeltingPtCH=137
|LogP=3.748
}}
}}

@@@

@@@

Tetramethylammonium hydroxide[edit]

{{chembox
|verifiedrevid=470604806
|ImageFile=TMAH.svg
|ImageSize=
|IUPACName=tetramethylammonium hydroxide
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=54928
|InChI=1/C4H12N.H2O/c1-5(2,3)4;/h1-4H3;1H2/q+1;/p-1
|InChIKey=WGTYBPLFGIVFAS-REWHXWOFAQ
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C4H12N.H2O/c1-5(2,3)4;/h1-4H3;1H2/q+1;/p-1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=WGTYBPLFGIVFAS-UHFFFAOYSA-M
|CASNo=75-59-2
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=60966
|SMILES=C[N+](C)(C)C.[OH-]
  }}
|Section2={{Chembox Properties
|C=4 |H=13 |N=1 |O=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
|Section8={{Chembox Related
|OtherAnions=[[tetramethylammonium chloride]]
|OtherCations=[[tetraethylammonium hydroxide]]
  }}
}}

@@@

@@@

Vinylsilane[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=470630766
|ImageFile=vinylsilane.png
|ImageFile_Ref={{chemboximage|correct|??}}
|ImageSize=100
|ImageName=Skeletal formula of vinylsilane
|PIN=Vinylsilane{{Citation needed|date=October 2011}}
|SystematicName=Ethenylsilane<ref>{{Cite web|title=Ethenylsilane - Compound Summary|url=http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=81714|work=PubChem Compound|publisher=National Center for Biotechnology Information|accessdate=20 October 2011|location=USA|date=27 March 2005|at=Identification and Related Records}}</ref>
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite|changed|??}}
|CASNo=7291-09-0
|PubChem=81714
|PubChem_Ref={{Pubchemcite|correct|Pubchem}}
|ChemSpiderID=73732
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|SMILES=[SiH3]C=C
|StdInChI=1S/C2H6Si/c1-2-3/h2H,1H2,3H3
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=UKRDPEFKFJNXQM-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
}}
|Section2={{Chembox Properties
|Si=1|C=2|H=6
|MolarMass=58.1545 g mol<sup>-1</sup>
|ExactMass=58.023876725 g mol<sup>-1</sup>
}}
}}

@@@

@@@

Zeise's salt[edit]

{{chembox
|verifiedrevid=398682803
|Reference=<ref>[http://www.sigmaaldrich.com/catalog/search/ProductDetail/ALDRICH/244953 Aldrich datasheet]</ref>
|ImageFile=Zeise's-salt-anion-from-xtal-3D-balls.png
|ImageSize=200px
|IUPACName=Potassium trichloro(ethene)platinate(II)
|OtherNames=
|Section1={{Chembox Identifiers
|CASNo=16405-35-9
|PubChem=16211684
|SMILES=
  }}
|Section2={{Chembox Properties
|K=1 |Pt=1 |Cl=3 |C=2 |H=4
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|EUClass={{Hazchem Xi}}
|RPhrases={{R36/37/38}}
|SPhrases={{S26}}-{{S37/39}}
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Trioxidane[edit]

{{Chembox
|Verifiedfields=changed
|verifiedrevid=477175194
|ImageFile=Trioxidan.svg
|ImageSize=121
|ImageName=Structural formula of trioxidane with explicit hydrogens
|IUPACName=Trioxidane
|OtherNames=Dihydrogen trioxide<br>Hydrogen trioxide<br>Water-Air
|Section1={{Chembox Identifiers
|CASNo=14699-99-1
|CASNo_Ref={{cascite|changed|??}}
|PubChem=166717
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=145859
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=46736
|Gmelin=200290
|SMILES=OOO
|StdInChI=1S/H2O3/c1-3-2/h1-2H
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|InChI=1/H2O3/c1-3-2/h1-2H
|StdInChIKey=JSPLKZUTYZBBKA-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|InChIKey=JSPLKZUTYZBBKA-UHFFFAOYAV}}
|Section2={{Chembox Properties
|H=2
|O=3
|ExactMass=50.000393930 g mol<sup>-1</sup>}}
}}

@@@

@@@

Triethyloxonium tetrafluoroborate[edit]

{{Chembox
|Verifiedfields=changed
|Watchedfields=changed
|verifiedrevid=409427530
|ImageFile=Triethyloxonium tetrafluoroborate.png
|ImageFile_Ref={{chemboximage|correct|??}}
|ImageSize=121
|ImageName=Skeletal formula of triethyloxonium tetrafluoroborate
|ImageFileL1=Triethyloxonium-3D-balls.png
|ImageFileL1_Ref={{chemboximage|correct|??}}
|ImageSizeL1=121
|ImageNameL1=Ball and stick model of the triethyloxonium cation
|ImageFileR1=Tetrafluoroborate-ion-3D-balls.png
|ImageFileR1_Ref={{chemboximage|correct|??}}
|ImageSizeR1=121
|ImageNameR1=Ball and stick model of the tetrafluoroborate anion
|IUPACName=Triethyloxonium tetrafluoroborate
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite|correct|??}}
|CASNo=368-39-8
|PubChem=2723982
|PubChem_Ref={{Pubchemcite|correct|pubchem}}
|ChemSpiderID=2006158
|ChemSpiderID_Ref={{chemspidercite|changed|chemspider}}
|UNNumber=3261
|Beilstein=3598090
|SMILES=F[B-](F)(F)F.CC[O+](CC)CC
|StdInChI=1S/C6H15O.BF4/c1-4-7(5-2)6-3;2-1(3,4)5/h4-6H2,1-3H3;/q+1;-1
|StdInChI_Ref={{stdinchicite|changed|chemspider}}
|StdInChIKey=IYDQMLLDOVRSJJ-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|changed|chemspider}}
}}
|Section2={{Chembox Properties
|C=6
|H=15
|B=1
|F=4
|O=1
|ExactMass=190.115208388 g mol<sup>-1</sup>
|MeltingPtC=91
|MeltingPtCH=92
|Solubility=Reacts
}}
|Section3={{Chembox Hazards
|EUClass={{Hazchem C}}
|RPhrases={{R14}}, {{R34}}
|SPhrases={{S22}}, {{S26}}, {{S36/37/39}}
}}
}}

@@@

@@@

Thorium(IV) orthosilicate[edit]

{{Chembox
|verifiedrevid=429359792
|PIN=Thorium(IV) orthosilicate
|SystematicNames=Thorium(4+) silicate
|OtherNames=Thorite<br />
Thorium(4+) orthosilicate
|Section1={{Chembox Identifiers
|CASNo=15501-85-6
|CASNo_Ref={{cascite|correct|??}}
|PubChem=186011
|PubChem_Ref={{PubChemcite|correct|PubChem}}
|ChemSpiderID=161685
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|SMILES=[Th+4].[O-][Si]([O-])([O-])[O-]
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/O4Si.Th/c1-5(2,3)4;/q-4;+4
|InChI=1/O4Si.Th/c1-5(2,3)4;/q-4;+4
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=XSSPKPCFRBQLBU-UHFFFAOYSA-N
|InChIKey=XSSPKPCFRBQLBU-UHFFFAOYAP}}
|Section2={{Chembox Properties
|O=4
|Si=1
|Th=1
|ExactMass=323.994635381 g mol<sup>-1</sup>
|Appearance=Brown crystals
|Density=6.7 g cm<sup>-3</sup>}}
|Section3={{Chembox Structure
|CrystalStruct=tetragonal cubic
  }}<!--

|[[Soluble|Solubility]]
|?
|-

|[[سختی موس]]
|4.8
|-
|[[ضریب شکست]]
|1.8 (n<sub>a</sub>)
|-
 -->
|Section7={{Chembox Hazards
|EUClass=not listed
  }}
}}

@@@

@@@

Thiepine[edit]

{{Chembox
|verifiedrevid=439653460
|ImageFile=Thiepine.png
|ImageFile_Ref={{Chemboximage|correct|??}}
|ImageSize=121
|ImageName=Structural formula of thiepine
|IUPACName=Thiepine
|SystematicName=<!-- Thienpine -->
|OtherNames=Thiatropilidene<br />
Thiepin
|Section1={{Chembox Identifiers
|CASNo=291-72-5
|CASNo_Ref={{cascite|??|??}}
|PubChem=12444286
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=13299847
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|SMILES=S1C=CC=CC=C1
|StdInChI=1S/C6H6S/c1-2-4-6-7-5-3-1/h1-6H
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=BISQTCXKVNCDDA-UHFFFAOYSA-N
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
}}
|Section2={{Chembox Properties
|C=6
|H=6
|S=1
|ExactMass=110.019020882 g mol<sup>-1</sup>}}
}}

@@@

@@@

Thioxanthene[edit]

{{Chembox
|Verifiedfields=changed
|verifiedrevid=470609193
|ImageFile=Thioxanthene.png
|ImageSize=200px
|IUPACName=9''H''-thioxanthene
|OtherNames=10''H''-dibenzo(''b'',''e'')thiin
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=60819
|InChI=1/C13H10S/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-8H,9H2
|InChIKey=PQJUJGAVDBINPI-UHFFFAOYAP
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=79451
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C13H10S/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-8H,9H2
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=PQJUJGAVDBINPI-UHFFFAOYSA-N
|CASNo_Ref={{cascite|changed|??}}
|CASNo=261-31-4
|PubChem=67495
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=51055
|SMILES=S2c1ccccc1Cc3c2cccc3
}}
|Section2={{Chembox Properties
|C=13 |H=10 |S=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Swainsonine[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=470475299
|ImageFile=Swainsonine structure.png
|ImageSize=200px
|IUPACName=(''1S,2R,8R,8aR'')-1,2,3,5,6,7,8,8a-Octahydroindolizine-
1,2,8-triol
|OtherNames=Tridolgosir
|Section1={{Chembox Identifiers
|InChI=1/C8H15NO3/c10-5-2-1-3-9-4-6(11)8(12)7(5)9/h5-8,10-12H,1-4H2/t5-,6-,7-,8-/m1/s1
|InChIKey=FXUAIOOAOAVCGD-WCTZXXKLBP
|InChI1=1S/C8H15NO3/c10-5-2-1-3-9-4-6(11)8(12)7(5)9/h5-8,10-12H,1-4H2/t5-,6-,7-,8-/m1/s1
|InChIKey1=FXUAIOOAOAVCGD-WCTZXXKLSA-N
|CASNo_Ref={{cascite|changed|??}}
|CASNo=72741-87-8
|PubChem=51683
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=46788
|DrugBank_Ref={{drugbankcite|correct|drugbank}}
|DrugBank=DB02034
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=RSY4RK37KQ
|KEGG_Ref={{keggcite|correct|kegg}}
|KEGG=C10173
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=FXUAIOOAOAVCGD-WCTZXXKLSA-N
|SMILES=C1C[C@H]([C@@H]2[C@@H]([C@@H](CN2C1)O)O)O
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=371197
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C8H15NO3/c10-5-2-1-3-9-4-6(11)8(12)7(5)9/h5-8,10-12H,1-4H2/t5-,6-,7-,8-/m1/s1
  }}
|Section2={{Chembox Properties
|C=8 |H=15 |N=1 |O=3
|MolarMass=173.2
|Appearance=
|Density=
|MeltingPt=143-144 °C
|BoilingPt=
|Solubility=10 mg/1 mL
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Usnic acid[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=477867469
|Name=Usnic acid
|ImageFile=Usnic acid.svg
<!-- |ImageSize=200px -->
|ImageName=Chemical structure of usnic acid
|IUPACName=2,6-Diacetyl-7,9-dihydroxy-8,9b-dimethyl-1,3(2H,9bh)<br />-dibenzofurandione
|OtherNames=usneine, usninic acid, usniacin
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite|correct|??}}
|CASNo=125-46-2<ref name="AshAsh2004">{{cite book
|author1=Michael Ash
|author2=Irene Ash
|title=Handbook of preservatives
|url=http://books.google.com/books?id=XZ2QB7bu5LwC&pg=PA670
|accessdate=5 August 2010
|year=2004
|publisher=Synapse Info Resources
|isbn=9781890595661
|page=5856}}</ref>
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=242022
|SMILES=CC1=C(C(=C2C(=C1O)C3(C(=CC(=O)C(C3=O)C(=O)C)O2)C)C(=O)C)O
|PubChem=5646
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=5444
|InChI=1/C18H16O7/c1-6-14(22)12(8(3)20)16-13(15(6)23)18(4)10(25-16)5-9(21)11(7(2)19)17(18)24/h5,11,22-23H,1-4H3
|InChIKey=CUCUKLJLRRAKFN-UHFFFAOYAS
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C18H16O7/c1-6-14(22)12(8(3)20)16-13(15(6)23)18(4)10(25-16)5-9(21)11(7(2)19)17(18)24/h5,11,22-23H,1-4H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=CUCUKLJLRRAKFN-UHFFFAOYSA-N
  }}

@@@

@@@

Sec-Butyllithium[edit]

{{Chembox
|verifiedrevid=464388187
|Name=''sec''-Butyllithium
|ImageFile=Sec-butyllithium-monomer-2D-skeletal.png
|ImageFile_Ref={{chemboximage|correct|??}}
|ImageSize=121
|ImageName=Skeletal formula of sec-butyllithium
|ImageFile1=Sec-butyllithium-2D-skeletal.png
|ImageFile1_Ref={{chemboximage|correct|??}}
|ImageSize1=121
|ImageName1=Skeletal formula of tetrameric sec-butyllithium
|IUPACName=''sec''-Butyllithium
|SystematicName=Butan-2-yllithium{{Reference necessary|date=March 2010}}
|Section1={{Chembox Identifiers
|CASNo=598-30-1
|CASNo_Ref={{cascite|correct|CAS}}
|PubChem=102446
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=10254345
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|EINECS=209-927-7
|Beilstein=3587206
|SMILES=[Li]C(C)CC
|SMILES1=CC([Li])CC
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C4H9.Li/c1-3-4-2;/h3H,4H2,1-2H3;
|InChI=1/C4H9.Li/c1-3-4-2;/h3H,4H2,1-2H3;/rC4H9Li/c1-3-4(2)5/h4H,3H2,1-2H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=VATDYQWILMGLEW-UHFFFAOYSA-N
|InChIKey=VATDYQWILMGLEW-MHILWDCKAX
}}
|Section2={{Chembox Properties
|C=4
|H=9
|Li=1
|ExactMass=64.086429337 g mol<sup>-1</sup>
}}
|Section3={{Chembox Hazards
|ExternalMSDS=[https://fscimage.fishersci.com/msds/00217.htm Fisher MSDS]
}}
}}

@@@

@@@

Vernolic acid[edit]

{{chembox
|Watchedfields=changed
|verifiedrevid=391138095
|Name=Vernolic acid
|ImageFile=Vernolic Acid.png
|ImageSize=200px
|IUPACName=(+)-(12S,13R)-Epoxy-cis-9-octadecenoic acid
|OtherNames=Linoleic acid 12:13-oxide
|Section1={{Chembox Identifiers
|SMILES=
|CASNo=503-07-1
|CASNo_Ref={{cascite|correct|CAS}}
|RTECS=
  }}
|Section2={{Chembox Properties
|C=18|H=32|O=3
|Appearance=Colorless oil
|Density=
|Solubility=Insoluble
|Solvent=other solvents
|SolubleOther=organic solvents
|MeltingPt=23-25 °C
|BoilingPt=
|pKa=
|Viscosity=
  }}
|Section3={{Chembox Structure
|MolShape=
|Dipole=
  }}
|Section7={{Chembox Hazards
|MainHazards=flammable
|RPhrases=
|SPhrases=
  }}
|Section8={{Chembox Related
|Function=compounds
|OtherFunctn=
  }}
}}

@@@

@@@

Vasotocin[edit]

{{Chembox
|verifiedrevid=441829086
|ImageFile=vasotocin.png
|ImageSize=200px
|IUPACName=1-[(1''R'',4''S'',7''S'',13''S'',16''R'')-16-amino-4-(2-amino-2-oxoethyl)-7-(3-amino-3-oxopropyl)-10-[(2''S'')-butan-2-yl]-13-[(4-hydroxyphenyl)methyl]-3,6,9,12,15-pentaoxo-18,19-dithia-2,5,8,11,14-pentazacycloicosane-1-carbonyl]-''N''-[(2''S'')-1-[(2-amino-2-oxoethyl)amino]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]pyrrolidine-2-carboxamide
|OtherNames=Argiprestocin; Arg-vasotocin; 8-Arg-vasotocin; Arginine vasotocin
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite|correct|??}}
|CASNo=113-80-4
|PubChem=68649
|SMILES=CC[C@H](C)C1C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CSSC[C@@H](C(=O)N[C@H](C(=O)N1)CC2=CC=C(C=C2)O)N)C(=O)N3CCCC3C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(=O)N)CC(=O)N)CCC(=O)N}}
|Section2={{Chembox Properties
|C=43|H=67|N=15|O=12|S=2
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=}}
}}

@@@

@@@

Tebufenpyrad[edit]

{{chembox
|verifiedrevid=401442534
|Reference=<ref name=epa>[http://www.epa.gov/opprd001/factsheets/tebufenpyrad.pdf Tebufenpyrad Pesticide Fact Sheet], [[آژانس حفاظت محیط زیست ایالات متحده آمریکا]]</ref>
|Name=Tebufenpyrad
|ImageFile=Tebufenpyrad.svg
|ImageSize=200px
|ImageName=Tebufenpyrad
|IUPACName=''N''-(4-''tert''-Butylbenzyl)-4-chloro-3-ethyl-1-methylpyrazole-5-carboxamide
|OtherNames=4-Chloro-''N''-[[4-(1,1-dimethylethyl)phenyl]]methyl]-3-ethyl-1-methyl-1''H''-pyrazole-5-carboxamide
|Section1={{Chembox Identifiers
|CASNo=119168-77-3
|KEGG_Ref={{keggcite|correct|kegg}}={{keggcite|correct|kegg}}
|KEGG=C11126
  }}
|Section2={{Chembox Properties
|Appearance=White crystalline solid
|C=18|H=24|Cl=1|N=3|O=1
|MeltingPt=64-66 °C
|Density=0.5 g/mL at 24.1 °C
|Solubility=2.61 ppm at pH 5.9<br>3.21 ppm at pH 4<br>2.39 ppm at pH 7<br>2.32 ppm at pH 10
|pKa=5.9 in water
  }}
}}

@@@

@@@

Steviol[edit]

{{Chembox
|Verifiedfields=changed
|verifiedrevid=470470860
|ImageFile=steviol structure.svg
|ImageSize=200px
|IUPACName=(5β,8α,9β,10α,13α)-13-Hydroxykaur-16-en-18-oic acid
|OtherNames=Hydroxydehydrostevic acid; 13-Hydroxykaurenoic acid; ''ent''-13-Hydroxy-kauran-16-en-19-oic acid
|Section1={{Chembox Identifiers
|CASNo=471-80-7
|CASNo_Ref={{cascite|changed|??}}
|PubChem=452967
|ChemSpiderID=398979
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChEMBL=444122      
|ChEMBL_Ref={{ebicite|changed|EBI}}
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=4741LYX6RT
|SMILES=O=C(O)[C@]4([C@H]3CC[C@@]21C[C@](O)(\C(=C)C1)CC[C@H]2[C@]3(C)CCC4)C
|InChI=1/C20H30O3/c1-13-11-19-9-5-14-17(2,7-4-8-18(14,3)16(21)22)15(19)6-10-20(13,23)12-19/h14-15,23H,1,4-12H2,2-3H3,(H,21,22)/t14-,15-,17+,18+,19+,20-/m0/s1
|InChIKey=QFVOYBUQQBFCRH-VQSWZGCSBR
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C20H30O3/c1-13-11-19-9-5-14-17(2,7-4-8-18(14,3)16(21)22)15(19)6-10-20(13,23)12-19/h14-15,23H,1,4-12H2,2-3H3,(H,21,22)/t14-,15-,17+,18+,19+,20-/m0/s1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=QFVOYBUQQBFCRH-VQSWZGCSSA-N
  }}
|Section2={{Chembox Properties
|C=20|H=30|O=3
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Undecylenic acid[edit]

{{chembox
|verifiedrevid=444239527
|ImageFile=Undecylenic acid.png
|ImageSize=200px
|IUPACName=undec-10-enoic acid
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=10771160
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=K3D86KJ24N
|InChI=1/C11H20O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2,(H,12,13)
|InChIKey=FRPZMMHWLSIFAZ-UHFFFAOYAJ
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C11H20O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2,(H,12,13)
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=FRPZMMHWLSIFAZ-UHFFFAOYSA-N
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=112-38-9
|PubChem=5634
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=35045
|SMILES=C=CCCCCCCCCC(=O)O
|MeSHName=Undecylenic+acid
|ATCCode_prefix=D01
|ATCCode_suffix=AE04
  }}
|Section2={{Chembox Properties
|C=11
|H=20
|O=2
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Ursolic acid[edit]

{{chembox
|verifiedrevid=476993789
|Name=Ursolic acid
|ImageFile=Ursolic acid.svg
|ImageSize=250px
|ImageName=
|IUPACName=(1''S'',2''R'',4a''S'',6a''R'',6a''S'',6b''R'',8a''R'',10''S'',12a''R'',14b''S'')-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1''H''-picene-4a-carboxylic acid<ref name="pubchem">{{PubChem|64945}}</ref>  
|OtherNames=Prunol, Malol, ''beta''-Ursolic acid, NSC4060, CCRIS 7123, TOS-BB-0966, 3-''beta''-hydroxyurs-12-en-28-oic acid<ref name="pubchem"/>
|Section1={{Chembox Identifiers
|PubChem=64945 
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=169
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=9908
|SMILES=O=C(O)[C@@]54[C@H](/C3=C/C[C@H]1[C@](CC[C@@H]2[C@]1(C)CC[C@H](O)C2(C)C)(C)[C@]3(C)CC4)[C@@H](C)[C@H](C)CC5
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=58472
|InChI=1/C30H48O3/c1-18-10-15-30(25(32)33)17-16-28(6)20(24(30)19(18)2)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h8,18-19,21-24,31H,9-17H2,1-7H3,(H,32,33)/t18-,19+,21+,22-,23+,24+,27+,28-,29-,30+/m1/s1
|InChIKey=WCGUUGGRBIKTOS-GPOJBZKABB
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C30H48O3/c1-18-10-15-30(25(32)33)17-16-28(6)20(24(30)19(18)2)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h8,18-19,21-24,31H,9-17H2,1-7H3,(H,32,33)/t18-,19+,21+,22-,23+,24+,27+,28-,29-,30+/m1/s1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=WCGUUGGRBIKTOS-GPOJBZKASA-N
|CASNo=77-52-1
|CASNo_Ref={{cascite|correct|CAS}}
|RTECS=
  }}
|Section2={{Chembox Properties
|C=30|H=48|O=3
|Appearance=
|Density=
|Solubility=
|MeltingPt=
|BoilingPt=
|pKa=
|pKb=
|Viscosity=
  }}
|Section3={{Chembox Structure
|MolShape=
|Coordination=
|CrystalStruct=
|Dipole=
  }}
|Section7={{Chembox Hazards
|ExternalMSDS=
|MainHazards=
|FlashPt=
|RPhrases=
|SPhrases=
  }}
|Section8={{Chembox Related
|OtherAnions=
|OtherCations=
|OtherCpds=
  }}
}}

@@@

@@@

Sterigmatocystin[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=470470810
|ImageFile=Sterigmatocystin.png
|ImageSize=200
|IUPACName=(3a''R'',12c''S'')-8-hydroxy-6-methoxy-3a,12c-dihydro-7''H''-furo[3',2':4,5]furo[2,3-''c'']xanthen-7-one
|OtherNames=Sterigmatocystin
|Section1={{Chembox Identifiers
|Abbreviations=
|CASNo_Ref={{cascite|changed|??}}
|CASNo=10048-13-2
|EINECS=
|PubChem=
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=4447522
|StdInChI_Ref={{stdinchicite|changed|chemspider}}
|StdInChI=1S/C18H12O6/c1-21-11-7-12-13(8-5-6-22-18(8)24-12)17-15(11)16(20)14-9(19)3-2-4-10(14)23-17/h2-8,18-19H,1H3/t8-,18+/m0/s1
|StdInChIKey_Ref={{stdinchicite|changed|chemspider}}
|StdInChIKey=UTSVPXMQSFGQTM-DCXZOGHSSA-N
|SMILES=COC1=C2C(=C3[C@@H]4C=CO[C@@H]4OC3=C1)OC5=C(C2=O)C(=CC=C5)O
|InChI=
|RTECS=
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=
|ChEMBL_Ref={{ebicite|changed|EBI}}
|ChEMBL=524291
|KEGG_Ref={{keggcite|changed|kegg}}
|KEGG=C00961 }}
|Section2={{Chembox Properties
|C=18|H=12|O=6
|MolarMass=324.28 g/mol
|ExactMass=324.063388 u
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
|SolubleOther=
|Solvent=
|pKa=
|pKb=
|IsoelectricPt=
|SpecRotation=
|RefractIndex=
|Viscosity=
|Dipole=}}
|Section5={{Chembox Pharmacology
|ATCCode=
|Bioavail=
|Metabolism=
|HalfLife=
|Excretion=
|PregCat=
|AdminRoutes=}}
|Section7={{Chembox Hazards
|EUClass=
|MainHazards=
|NFPA-H=
|NFPA-F=
|NFPA-R=
|NFPA-O=
|RPhrases=
|SPhrases=
|RSPhrases=
|FlashPt=
|Autoignition=
|ExploLimits=
|PEL=}}
|Section9={{Chembox Related
|OtherAnions=
|OtherCations=
|OtherFunctn=
|Function=
|OtherCpds=}}
}}

@@@

@@@

Syn-Propanethial-S-oxide[edit]

{{chembox
|verifiedrevid=450632630
|Name=''syn''-Propanethial ''S''-oxide
|ImageFile=propanethial-S-oxide.png
|ImageSize=150px
|ImageFile1=Syn-propanethial-S-oxide-3D-balls.png
|ImageSize1=150px
|IUPACName=1-Sulfinylpropane
|OtherNames=Thiopropanal S-oxide
|Section1={{Chembox Identifiers
|CASNo=32157-29-2
|PubChem=441491
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=390214
|SMILES=O=S=C/CC
|InChI=1/C3H6OS/c1-2-3-5-4/h3H,2H2,1H3
|InChIKey=BAZSXBOAXJLRNH-UHFFFAOYAF
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C3H6OS/c1-2-3-5-4/h3H,2H2,1H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=BAZSXBOAXJLRNH-UHFFFAOYSA-N
  }}
|Section2={{Chembox Properties
|C=3|H=6|O=1|S=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

TCEP[edit]

{{chembox
|Verifiedfields=changed
|Watchedfields=changed
|verifiedrevid=423494642
|ImageFile=TCEP.png
|ImageSize=200px
|IUPACName=3,3',3"-Phosphanetriyltripropanoic acid  
|OtherNames=TCEP<br>Tris(2-carboxyethyl)phosphine
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite|changed|??}}
|CASNo=5961-85-3
|PubChem=119411
|SMILES=OC(CCP(CCC(O)=O)CCC(O)=O)=O
|InChI=1S/C9H15O6P/c10-7(11)1-4-16(5-2-8(12)13)6-3-9(14)15/h1-6H2,(H,10,11)(H,12,13)(H,14,15)
|InChIKey1=PZBFGYYEXUXCOF-UHFFFAOYSA-N
|InChI1=1S/C9H15O6P/c10-7(11)1-4-16(5-2-8(12)13)6-3-9(14)15/h1-6H2,(H,10,11)(H,12,13)(H,14,15)
  }}
|Section2={{Chembox Properties
|C=9|H=15|O=6|P=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

@@@

@@@

Radicicol[edit]

{{chembox
|verifiedrevid=401038937
|ImageFile=Radicicol Winssinger et al.svg
|ImageSize=250
|IUPACName=(1a''R'',​2''E'',​4''E'',​14''R'',​15a''R'')-​8-​chloro-​9,​11-​dihydroxy-​14-​methyl-​1a,​14,​15,​15a-​tetrahydro-​6''H''-​oxireno​[''e'']​[2]​benzoxacyclotetradecine-​6,​12(7''H'')-​dione
|OtherNames=
|Section1={{Chembox Identifiers
|Abbreviations=
|InChI=1S/C18H17ClO6/c1-9-6-15-14(25-15)5-3-2-4-10(20)7-11-16(18(23)24-9)12(21)8-13(22)17(11)19/h2-5,8-9,14-15,21-22H,6-7H2,1H3/b4-2+,5-3-
|InChIKey=WYZWZEOGROVVHK-HZDAAVBUBT
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C18H17ClO6/c1-9-6-15-14(25-15)5-3-2-4-10(20)7-11-16(18(23)24-9)12(21)8-13(22)17(11)19/h2-5,8-9,14-15,21-22H,6-7H2,1H3/b4-2+,5-3-
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=WYZWZEOGROVVHK-HZDAAVBUSA-N
|InChIKey1=WYZWZEOGROVVHK-HZDAAVBUSA-N
|CASNo=12772-57-5
|CASNo_Ref={{cascite|??|??}}
|EINECS=
|PubChem=6323491
|ChEMBL=453386
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=16735913   
|SMILES=O=C1\C=C\C=C/C3OC3CC(C)OC(=O)c2c(O)cc(O)c(Cl)c2C1
|RTECS=
|MeSHName=
|ChEBI=
|KEGG=
|ATCCode=}}
|Section2={{Chembox Properties
|MolarMass=
|C=18|H=17|Cl=1|O=6
|Appearance=
|Density=
|MeltingPt=
|Melting_notes=
|BoilingPt=
|Boiling_notes=
|Solubility=
|SolubleOther=
|Solvent=
|pKa=
|pKb=
|IsoelectricPt=
|SpecRotation=
|RefractIndex=
|Viscosity=
|Dipole=}}
|Section3={{Chembox Structure
|CrystalStruct=
|Coordination=
|MolShape=
|Dipole=}}
|Section4={{Chembox Thermochemistry
|DeltaHf=
|DeltaHc=
|Entropy=
|HeatCapacity=}}
|Section5={{Chembox Pharmacology
|AdminRoutes=
|Bioavail=
|Metabolism=
|HalfLife=
|ProteinBound
|Excretion=
|Legal_status=
|Legal_US=
|Legal_UK=
|Legal_AU=
|Legal_CA=
|PregCat=
|PregCat_AU=
|PregCat_US=}}
|Section6={{Chembox Explosive
|ShockSens=
|FrictionSens=
|ExplosiveV=
|REFactor=}}
|Section7={{Chembox Hazards
|ExternalMSDS=
|EUClass=
|EUIndex=
|MainHazards=
|NFPA-H=
|NFPA-F=
|NFPA-R=
|NFPA-O=
|RPhrases=
|SPhrases=
|RSPhrases=
|FlashPt=
|Autoignition=
|ExploLimits=
|PEL=}}
|Section8={{Chembox Related
|OtherAnions=
|OtherCations=
|OtherFunctn=
|Function=
|OtherCpds=}}
}}

@@@

@@@

Sulfolene[edit]

{{chembox
|Reference=<ref>[http://www.sigmaaldrich.com/catalog/search/ProductDetail/ALDRICH/B84505 Sulfolene] at [[Sigma-Aldrich]]</ref>
|ImageFile=Sulfolene.png
|ImageSize=100px
|IUPACName=2,5-Dihydrothiophene 1,1-dioxide
|OtherNames=Butadiene sulfone<br>3-Sulfolene
|Section1={{Chembox Identifiers
|Abbreviations=
|CASNo=77-79-2
|EINECS=
|PubChem=6498
|SMILES=C1C=CCS1(=O)=O
|ChemSpiderID=6253
|InChI=
|RTECS=
|MeSHName=
|ChEBI=
|KEGG=
|ATCCode_prefix=
|ATCCode_suffix=
|ATC_Supplemental=}}
|Section2={{Chembox Properties
|C=4 |H=6 |S=1 |O=2
|Appearance=
|Density=
|MeltingPt=65-66 °C
|Melting_notes=
|BoilingPt=
|Boiling_notes=
|Solubility=
|SolubleOther=
|Solvent=
|pKa=
|pKb=}}
|Section7={{Chembox Hazards
|EUClass=
|EUIndex=
|MainHazards=
|NFPA-H=
|NFPA-F=
|NFPA-R=
|NFPA-O=
|RPhrases=
|SPhrases=
|RSPhrases=
|FlashPt=
|Autoignition=
|ExploLimits=
|PEL=}}
}}

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Sodium nonanoyloxybenzenesulfonate[edit]

{{Chembox
|verifiedrevid=401060155
|ImageFile=Sodium nonanoyloxybenzenesulfonate.png
|ImageSize=200px
|IUPACName=Sodium 4-nonanoyloxybenzenesulfonate
|OtherNames=4-Sulfophenyl nonanoate sodium salt; Sodium ''p''-nonanoyloxybenzenesulfonate; ''p''-(Nonanoyloxy)benzenesulfonic acid sodium salt; ''p''-Sodiosulfophenyl nonanoate
|Section1={{Chembox Identifiers
|Abbreviations=NOBS
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=152449
|InChI=1/C15H22O5S.Na/c1-2-3-4-5-6-7-12-15(16)20-13-10-8-9-11-14(13)21(17,18)19;/h8-11H,2-7,12H2,1H3,(H,17,18,19);/q;+1/p-1
|InChIKey=QSKQNALVHFTOQX-REWHXWOFAO
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C15H22O5S.Na/c1-2-3-4-5-6-7-12-15(16)20-13-10-8-9-11-14(13)21(17,18)19;/h8-11H,2-7,12H2,1H3,(H,17,18,19);/q;+1/p-1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=QSKQNALVHFTOQX-UHFFFAOYSA-M
|CASNo=89740-11-4
|PubChem=174822
|SMILES=[Na+].O=C(Oc1ccccc1S([O-])(=O)=O)CCCCCCCC
}}
|Section2={{Chembox Properties
|C=15|H=21|Na=1|O=5|S=1
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=}}
}}

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Stercobilinogen[edit]

{{chembox
|verifiedrevid=409106787
|ImageFile=stercobilinogen.png
|ImageSize=200px
|IUPACName=3-[2-[[3-(2-carboxyethyl)-5-[[(2''S'',3''R'',4''R'')-4-ethyl-3-methyl-5-oxopyrrolidin-2-yl]methyl]-4-methyl-1''H''-pyrrol-2-yl]methyl]-5-[[(2''S'',3''R'',4''R'')-3-ethyl-4-methyl-5-oxopyrrolidin-2-yl]methyl]-4-methyl-1''H''-pyrrol-3-yl]propanoic acid
|OtherNames=Fecal urobilinogen
|Section1={{Chembox Identifiers
|CASNo=17095-63-5
|PubChem=9548718
|SMILES=CC[C@@H]1[C@H](C(=O)N[C@H]1CC2=C(C(=C(N2)CC3=C(C(=C(N3)C[C@H]4[C@@H]([C@H](C(=O)N4)CC)C)C)CCC(=O)O)CCC(=O)O)C)C
|MeSHName=Stercobilinogen
  }}
|Section2={{Chembox Properties
|C=33|H=48|N=4|O=6
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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Sucrose acetate isobutyrate[edit]

{{chembox
|Watchedfields=changed
|verifiedrevid=428736494
|ImageFile1=Sucrose acetate isobutyrate.svg
|IUPACName=[(2''S'',3''S'',4''R'',5''R'')-2-(acetyloxymethyl)-2-[(2''R'',3''R'',4''S'',5''R'',6''R'')-6-(acetyloxymethyl)-3,4,5-tris(2-methylpropanoyloxy)oxan-2-yl]oxy-4-(2-methylpropanoyloxy)-5-(2-methylpropanoyloxymethyl)oxolan-3-yl] 2-methylpropanoate
|IUPACName_hidden=yes
|OtherNames=Sucrose acetoisobutyrate; Sucrose diacetate hexaisobutyrate;  HSDB 5657; AI3-25354;  E444
|Section1={{Chembox Identifiers
|Abbreviations=SAIB
|EINECS=204-771-6
|CASNo_Ref={{cascite|correct|??}}
|CASNo=27216-37-1
|PubChem=31339 
|SMILES=CC(C)C(=O)OC[C@@H]1[C@H]([C@@H]([C@](O1)(COC(=O)C)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)COC(=O)C)OC(=O)C(C)C)OC(=O)C(C)C)OC(=O)C(C)C)OC(=O)C(C)C)OC(=O)C(C)C
  }}
|Section2={{Chembox Properties
|C=40|H=62|O=19
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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SA-4503[edit]

{{chembox
|verifiedrevid=400821242
|ImageFile=SA 4503.png
|ImageSize=200px
|IUPACName=1-[2-(3,4-Dimethoxyphenyl)ethyl]-4-(3-phenylpropyl)piperazine
|OtherNames=
|Section1={{Chembox Identifiers
|CASNo=165377-43-5
|CASOther=<br>[165377-44-6] (dihydrochloride)
|PubChem=9954941
|SMILES=COC1=C(OC)C=C(CCN2CCN(CCCC3=CC=CC=C3)CC2)C=C1
|MeSHName=
  }}
|Section2={{Chembox Properties
|C=23|H=32|N=2|O=2
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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Ractopamine[edit]

{{chembox
|Verifiedfields=changed
|Watchedfields=changed
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=57370OZ3P1
|verifiedrevid=458436321
|ImageFile=Ractopamine.png
|ImageSize=200px
|IUPACName=4-[3-[[2-Hydroxy-2-(4-hydroxyphenyl)ethyl]amino]butyl]phenol
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=50604
|InChI=1/C18H23NO3/c1-13(2-3-14-4-8-16(20)9-5-14)19-12-18(22)15-6-10-17(21)11-7-15/h4-11,13,18-22H,2-3,12H2,1H3
|InChIKey=YJQZYXCXBBCEAQ-UHFFFAOYAP
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=509336
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C18H23NO3/c1-13(2-3-14-4-8-16(20)9-5-14)19-12-18(22)15-6-10-17(21)11-7-15/h4-11,13,18-22H,2-3,12H2,1H3
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=YJQZYXCXBBCEAQ-UHFFFAOYSA-N
|CASNo_Ref={{cascite|changed|??}}
|CASNo=97825-25-7
|PubChem=56052
|SMILES=OC(c1ccc(O)cc1)CNC(C)CCc2ccc(O)cc2
|MeSHName=Ractopamine
  }}
|Section2={{Chembox Properties
|C=18|H=23|N=1|O=3
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=4100 mg/L
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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Scyllo-Inositol[edit]

{{Chembox
|Watchedfields=changed
|verifiedrevid=439020881
|ImageFile=Scyllo-inositol.svg
|ImageSize=200px
|Name=''scyllo''-Inositol
|IUPACName=(1''R'',2''R'',3''R'',4''R'',5''R'',6''R'')-Cyclohexane-1,2,3,4,5,6-hexaol
|OtherNames=Scyllitol; Cocositol; Quercinitol; AZD 103; 1,3,5/2,4,6-Hexahydroxycyclohexane; ''scyllo''-Cyclohexanehexol
|Section1={{Chembox Identifiers
|CASNo_Ref={{cascite|correct|??}}
|CASNo=488-59-5
|PubChem=
|SMILES=O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O
}}
|Section2={{Chembox Properties
|C=6|H=12|O=6
|Appearance=White crystalline solid
|Density=
|MeltingPt=348.5–350 °C
|BoilingPt=
|Solubility=}}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=}}
}}

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Triclocarban[edit]

{{chembox
|verifiedrevid=444232279
|ImageFile_Ref={{chemboximage|correct|??}}
|ImageFile=Triclocarban.png
|ImageSize=200px
|IUPACName=3-(4-Chlorophenyl)-1-(3,4-dichlorophenyl)urea
|OtherNames=
|Section1={{Chembox Identifiers
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=7266
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=BGG1Y1ED0Y
|InChI=1/C13H9Cl3N2O/c14-8-1-3-9(4-2-8)17-13(19)18-10-5-6-11(15)12(16)7-10/h1-7H,(H2,17,18,19)
|InChIKey=ICUTUKXCWQYESQ-UHFFFAOYAL
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=1076347
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C13H9Cl3N2O/c14-8-1-3-9(4-2-8)17-13(19)18-10-5-6-11(15)12(16)7-10/h1-7H,(H2,17,18,19)
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=ICUTUKXCWQYESQ-UHFFFAOYSA-N
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=101-20-2
|PubChem=7547
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=48347
|SMILES=Clc2ccc(NC(=O)Nc1ccc(Cl)cc1)cc2Cl
}}
|Section2={{Chembox Properties
|C=13|H=9|Cl=3|N=2|O=1
|Appearance=
|Density=1.53
|MeltingPt=254-256 °C
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=>150 °C
|Autoignition=
  }}
}}

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Strontium peroxide[edit]

{{chembox
|verifiedrevid=429190694
|ImageFile=BaO2structure.jpg
|ImageSize=
|IUPACName=
|OtherNames=
|Section1={{Chembox Identifiers
|CASNo=1314-18-7
|PubChem=
|SMILES=
}}
|Section2={{Chembox Properties
|Formula=
|MolarMass=119.619 g/mol 
|Appearance=white powder 
|Density=4.56 g/cm<sup>3</sup>
|MeltingPt=215°C
|Melting_notes=decomposes
|BoilingPt=
|Solubility=
}}
|Section3={{Chembox Structure
|CrystalStruct=Tetragonal <ref>{{cite journal|doi=10.1023/A:1015105922260|year=2002|author=Massalimov, I. A.|journal=Inorganic Materials|volume=38|issue=4|pages=363|last2=Kireeva|first2=M. S.|last3=Sangalov|first3=Yu. A.}}</ref>
|SpaceGroup=D<sup>17</sup><sub>4h</sub>, I4/mmm, [[Pearson symbol|tI6]]
|Coordination=6
  }}
|Section7={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
}}
}}

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Ranirestat[edit]

{{chembox
|UNII_Ref={{fdacite|correct|FDA}}
|UNII=Z26P56GFTV
|verifiedrevid=437206457
|ImageFile=Ranirestat_stereo.png
|ImageSize=
|IUPACName=(3''R'')-2'-(4-bromo-2-fluorobenzyl)-1'''H'',2''H'',5''H''-spiro[pyrrolidine-3,4'-pyrrolo[1,2-''a'']pyrazine]-1',2,3',5(2'''H'')-tetrone
|OtherNames=
|Section1={{Chembox Identifiers
|CASNo=147254-64-6
|PubChem=153948

|SMILES=C1C(=O)NC(=O)C12C(=O)N(C(=O)C3=CC=CN23) CC4=C(C=C(C=C4)Br)F
  }}
|Section2={{Chembox Properties
|C=17|H=11|Br=1|F=1|N=3|O=4
|MolarMass=420.189
|Appearance=
|Density=
|MeltingPt=
|BoilingPt=
|Solubility=
  }}
|Section3={{Chembox Hazards
|MainHazards=
|FlashPt=
|Autoignition=
  }}
}}

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Trichloro(chloromethyl)silane[edit]

{{Chembox
|ImageFileL1=Trichloro(chloromethyl)silane.svg
|ImageSizeL1=120
|ImageAltL1=Structural formula
|ImageFileR1=Trichloro(chloromethyl)silane-3D-balls.png
|ImageSizeR1=120
|ImageAltR1=Ball-and-stick model
|IUPACName=Trichloro(chloromethyl)silane
|OtherNames=(Chloromethyl)trichlorosilane
|Section1={{Chembox Identifiers
|CASNo=1558-25-4
|CASNo_Ref={{cascite|correct|??}}
|PubChem=15258
|PubChem_Ref={{Pubchemcite|correct|PubChem}}
|ChemSpiderID=14523
|ChemSpiderID_Ref={{Chemspidercite|correct|ChemSpider}}
|EINECS=216-316-9
|UNNumber=3389
|RTECS=VV2200000
|SMILES=ClC[Si](Cl)(Cl)Cl
|StdInChI=1S/CH2Cl4Si/c2-1-6(3,4)5/h1H2
|StdInChIKey=FYTPGBJPTDQJCG-UHFFFAOYSA-N
|Beilstein=1811640}}
|Section2={{Chembox Properties
|C=1
|H=2
|Cl=4
|Si=1
|ExactMass=181.867987425 g mol<sup>-1</sup>}}
}}

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Vomitoxin[edit]

{{chembox
|Verifiedfields=changed
|verifiedrevid=470631708
|ImageFile=Deoxynivalenol.png|200px|Deoxynivalenol
|ImageSize=
|IUPACName=(3α,​7α)-​3,​7,​15-​trihydroxy-​12,​13-​epoxytrichothec-​9-​en-​8-​one
|OtherNames=<br/>Deoxynivalenol (DON)<br/>Vomitoxin
|C=15|H=20|O=6
|Section1={{Chembox Identifiers
|Abbreviations=
|ChemSpiderID_Ref={{chemspidercite|correct|chemspider}}
|ChemSpiderID=36584
|ChEMBL_Ref={{ebicite|correct|EBI}}
|ChEMBL=513300
|InChIKey=LINOMUASTDIRTM-QGRHZQQGBF
|StdInChI_Ref={{stdinchicite|correct|chemspider}}
|StdInChI=1S/C15H20O6/c1-7-3-9-14(5-16,11(19)10(7)18)13(2)4-8(17)12(21-9)15(13)6-20-15/h3,8-9,11-12,16-17,19H,4-6H2,1-2H3/t8-,9-,11-,12-,13-,14-,15+/m1/s1
|StdInChIKey_Ref={{stdinchicite|correct|chemspider}}
|StdInChIKey=LINOMUASTDIRTM-QGRHZQQGSA-N
|CASNo_Ref={{cascite|correct|CAS}}
|CASNo=51481-10-8
|EINECS=
|PubChem=40024
|KEGG_Ref={{keggcite|changed|kegg}}
|KEGG=C09747
|SMILES=O=C4\C(=C/[C@H]3O[C@H]2[C@]1(OC1)[C@](C[C@H]2O)([C@@]3(CO)[C@@H]4O)C)C
|InChI=1/C15H20O6/c1-7-3-9-14(5-16,11(19)10(7)18)13(2)4-8(17)12(21-9)15(13)6-20-15/h3,8-9,11-12,16-17,19H,4-6H2,1-2H3/t8-,9-,11-,12-,13-,14-,15+/m1/s1
|RTECS=
|MeSHName=
|ChEBI_Ref={{ebicite|correct|EBI}}
|ChEBI=
|ATCCode=}}
|Section2={{Chembox Properties
|C=15 |H=20 |O=6
|Appearance=
|Density=
|MeltingPt=
|Melting_notes=
|BoilingPt=
|Boiling_notes=
|Solubility=
|SolubleOther=
|Solvent=
|pKa=
|pKb=
|IsoelectricPt=
|SpecRotation=
|RefractIndex=
|Viscosity=
|Dipole=}}
|Section3={{Chembox Structure
|CrystalStruct=
|Coordination=
|MolShape=
|Dipole=}}
|Section4={{Chembox Thermochemistry
|DeltaHf=
|DeltaHc=
|Entropy=
|HeatCapacity=}}
|Section5={{Chembox Pharmacology
|AdminRoutes=
|Bioavail=
|Metabolism=
|HalfLife=
|ProteinBound
|Excretion=
|Legal_status=
|Legal_US=
|Legal_UK=
|Legal_AU=
|Legal_CA=
|PregCat=
|PregCat_AU=
|PregCat_US=}}
|Section7={{Chembox Hazards
|ExternalMSDS=[http://www.fermentek.co.il/MSDS/Deoxynivalenol-MSDS.htm External MSDS]
|EUClass=
|EUIndex=
|MainHazards=
|NFPA-H=
|NFPA-F=
|NFPA-R=
|NFPA-O=
|RPhrases=
|SPhrases=
|RSPhrases=
|FlashPt=
|Autoignition=
|ExploLimits=
|PEL=}}
|Section8={{Chembox Related
|OtherAnions=
|OtherCations=
|OtherFunctn=
|Function=
|OtherCpds=}}
}}

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