Dithiazanine iodide

Dithiazanine iodide
	File:Dithiazanine iodide model.png
Names
	IUPAC name Benzothiazolium, 3-ethyl-2-[5- (3-ethyl-2-benzothiazolinylidene)-1,3-pentadienyl]-, iodide
	Systematic IUPAC name 3-ethyl-2-[(1E,3E,5Z)-5-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)penta-1,3-dien-1-yl]-1,3-benzothiazol-3-ium iodide
Identifiers
CAS Number	514-73-8;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL421701;
ChemSpider	4642986;
ECHA InfoCard	100.007.443
CompTox Dashboard (EPA)	DTXSID8022955 ;
	InChI InChI=1S/C23H23N2S2.HI/c1-3-24-18-12-8-10-14-20(18)26-22(24)16-6-5-7-17-23-25(4-2)19-13-9-11-15-21(19)27-23;/h5-17H,3-4H2,1-2H3;1H/q+1;/p-1 Key: MNQDKWZEUULFPX-UHFFFAOYSA-M;
	SMILES [I-].S\1c4ccccc4N(C/1=C\C=C\C=C\c3sc2ccccc2[n+]3CC)CC;
Properties
Chemical formula	C23H23IN2S2
Molar mass	518.48 g·mol−1
Appearance	Green crystals
Melting point	Decomposes at 478.4 °F (248.0 °C)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Dithiazanine iodide is a chemical compound.^[1] It is used as a veterinary anthelmintic for dogs.^[3] It is a highly toxic chemical, with a lethal dose for humans of about 4–16 mg/kg by oral ingestion. The mechanism of toxicity is not well known but it is believed that this chemical interferes with cells' absorption of glucose, which is essential to obtain energy through cell respiration.

References

^ ^a ^b Cameo Chemicals. "Chemical data". NOAA. Retrieved September 19, 2011.
^ ^a ^b "Chemspider data". Chemspider. Retrieved September 19, 2011.
^ "Law about use". Justia. Retrieved September 19, 2011.

[cameo-1] Cameo Chemicals. "Chemical data". NOAA. Retrieved September 19, 2011.

[chemspider-2] "Chemspider data". Chemspider. Retrieved September 19, 2011.

[uslaw-3] "Law about use". Justia. Retrieved September 19, 2011.

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