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Diisononyl phthalate

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This is an old revision of this page, as edited by Emeldir (talk | contribs) at 00:35, 9 September 2016 (preferred IUPAC name (PIN) according to ''Nomenclature of Organic Chemistry – IUPAC Recommendations and Preferred Names 2013 (Blue Book)''). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Diisononyl phthalate[1]
Names
Preferred IUPAC name
Bis(7-methyloctyl) benzene-1,2-dicarboxylate
Other names
Bis(7-methyloctyl) phthalate
Identifiers
3D model (JSmol)
Abbreviations DINP
ChEBI
ChemSpider
ECHA InfoCard 100.044.602 Edit this at Wikidata
UNII
  • InChI=1S/C26H42O4/c1-21(2)15-9-5-7-13-19-29-25(27)23-17-11-12-18-24(23)26(28)30-20-14-8-6-10-16-22(3)4/h11-12,17-18,21-22H,5-10,13-16,19-20H2,1-4H3 checkY
    Key: HBGGXOJOCNVPFY-UHFFFAOYSA-N checkY
  • InChI=1/C26H42O4/c1-21(2)15-9-5-7-13-19-29-25(27)23-17-11-12-18-24(23)26(28)30-20-14-8-6-10-16-22(3)4/h11-12,17-18,21-22H,5-10,13-16,19-20H2,1-4H3
    Key: HBGGXOJOCNVPFY-UHFFFAOYAX
  • O=C(OCCCCCCC(C)C)c1ccccc1C(=O)OCCCCCCC(C)C
Properties
C26H42O4
Molar mass 418.609 g/mol
Appearance Oily viscous liquid
Density 0.98 g/cm3
Melting point −43 °C (−45 °F; 230 K)
Boiling point 244 to 252 °C (471 to 486 °F; 517 to 525 K) at 0.7 kPa
<0.01 g/mL at 20 °C
Viscosity 64 to 265 mPa·s
Hazards
Flash point 221 °C (430 °F; 494 K) (c.c.)
380 °C (716 °F; 653 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Diisononyl phthalate (DINP) is a phthalate used as a plasticizer. DINP is typically a mixture of chemical compounds consisting of various isononyl esters of phthalic acid.

The European Union has set a maximum specific migration limit from food contact materials of 9 mg/kg food for the sum of diisononyl phthalates and diisodecyl phthalates.[2]

DINP was listed as a substance "known to the State of California to cause cancer" under Proposition 65 legislation on 2013-12-20.[3]

Yet not only for cause of cancer is this substance known. Generally phtalate esters of higher alkanes (or cykloalkanes) (like dipentyl/hexyl/nonyl phthalate etc.) are harmful to organism, because destruction of their esteric bond puts these higher alkane/cykloalcane..etc. into organism, though these molecules are heavily degradable and remain to circulate in veins and cause - for example - reproduction issues.[4] source (in Czech)

See also

References

  1. ^ Diisononyl phthalate at Inchem.org
  2. ^ "EU legislative list for food contact materials".
  3. ^ "State of California, Chemicals known to the state to cause cancer or reproductive toxicity, January 3, 2014" (PDF).
  4. ^ Lenka Pohlodková.Estery kyseliny ftalové a jejich vliv na živý organismus: bachelor work. prof. Ing. Alžbeta Jarošová, Ph. D. Brno, Czech republic :2012. http://is.mendelu.cz/zp/portal_zp.pl?prehled=vyhledavani;podrobnosti=44501;download_prace=1