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Diisononyl phthalate

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Diisononyl phthalate Basic information

Product Name:
Diisononyl phthalate
Synonyms:
  • 1,2-benzenedicarboxylicacid,di-c8-c10-branchedalkylester,c9-rich
  • 1,2-Benzenedicarboxylic acid di-C8-10-branched alkyl esters C9-rich
  • BIS(3,5,5-TRIMETHYLHEXYL) PHTHALATE
  • PHTHALIC ACID BIS(3,5,5-TRIMETHYLHEXYL) ESTER
  • DIISONONYL PHTHALATE, TECH.
  • DI(ISONONYL)PHTHALATE1
  • 1,2-BENZENEDICARBOXYLICACID,DI-C8-C10BRANCHEDALKYLESTERS,C9-RICH
  • DINP-1
CAS:
68515-48-0
MF:
C26H42O4
MW:
418.61
EINECS:
271-090-9
Product Categories:
  • Plasticizers
  • Polymer Additives
  • Polymer Science
Mol File:
68515-48-0.mol
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Diisononyl phthalate Chemical Properties

Boiling point:
279-287 °C
Density 
0.972 g/mL at 25 °C(lit.)
vapor pressure 
1 mm Hg ( 200 °C)
refractive index 
n20/D 1.485(lit.)
Flash point:
>230 °F
storage temp. 
Refrigerator
solubility 
Chloroform, Methanol
form 
Oil
color 
Colourless to Pale Yellow
Merck 
13,3319
EPA Substance Registry System
Di(C8-10, C9 rich) branched alkyl phthalates (68515-48-0)
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Safety Information

Risk Statements 
62-63
Safety Statements 
23-36/37
WGK Germany 
-
RTECS 
CZ3395000
HS Code 
29173490

MSDS

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Diisononyl phthalate Usage And Synthesis

Chemical Properties

The empirical formula of diisononyl phthalate (DINP) is C26H42O4. The structural formula of DINP varies because the iso-alcohols used in the manufacture contain several isomers. DINP is a clear, colorless to light yellow liquid. DINP is insoluble in water, but it is soluble in organic solvents.

Uses

Its major use is as a plasticizer.

Uses

Diisononyl Phthalate is a general-purpose plasticizer for polyvinyl chloride.

Production Methods

DINP is manufactured by the reaction of phthalic anhydride with isononanol in the presence of an acid catalyst.

Flammability and Explosibility

Non flammable

Carcinogenicity

As stated, there have been two carcinogenesis studies in F344 rats and one in B6C3F1 mice. An increased incidence of hepatocellular neoplasms (i.e., adenomas and carcinomas) is observed in both rats and mice. An increased incidence of renal cell carcinomas and mononuclear cell leukemia has also been described. These studies establish that at dose levels of approximately 600 mg/kg/day, DINP can induce hepatocellular carcinoma in rats and mice. As there was evidence of peroxisomal proliferation at the carcinogenic doses in both species, it seems most likely that this was the mechanism for hepatocellular carcinoma induction. The renal cell carcinomas observed in the male rats were associated with the induction of α 2u-globulin, indicating that it was a sex- and species-specific effect. Kidney tumors that are the consequence of α 2u-globulin induction are not considered to be clinically relevant to humans.MNCL is a tumor type that occurs spontaneously at a high and variable frequency in F344 rats. Because there is no human equivalent, MNCL is not considered to be relevant to humans.

Diisononyl phthalate Preparation Products And Raw materials

Raw materials

Diisononyl phthalateSupplier

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