Diisononyl phthalate

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
Diisononyl phthalate Structure
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.)
Fp >230 °F
storage temp. Refrigerator
solubility Chloroform, Methanol
form Oil
color Colourless to Pale Yellow
Merck 13,3319
EPA Substance Registry SystemDi(C8-10, C9 rich) branched alkyl phthalates (68515-48-0)
Safety Information
Risk Statements 62-63
Safety Statements 23-36/37
WGK Germany -
RTECS CZ3395000
HS Code 29173490
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
Diisononyl phthalate Usage And Synthesis
Chemical PropertiesThe 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.
UsesIts major use is as a plasticizer.
UsesDiisononyl Phthalate is a general-purpose plasticizer for polyvinyl chloride.
Production MethodsDINP is manufactured by the reaction of phthalic anhydride with isononanol in the presence of an acid catalyst.
Flammability and ExplosibilityNonflammable
CarcinogenicityAs 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 materialsPhthalic anhydride-->7-METHYL-1-OCTANOL
DI-N-HEXYL PHTHALATE Benzyl butyl phthalate DI-N-PENTYL PHTHALATE-D4 Dinonyl phthalate Dicyclohexyl phthalate Dibutyl phthalate Bis(2-ethylhexyl) phthalate Didecyl phthalate 1,2-Benzenedicarboxylic acid di-C9-11-branched alkyl esters C10-rich Ethyl 2-(Chlorosulfonyl)acetate BIS(3,5,5-TRIMETHYLHEXYL) PHTHALATE Ascoric Acid Folic acid Diisononyl phthalate Tetradecyldimethylbenzylammonium chloride Di-iso-amyl phthalate Benzyl benzoate Dimethyl phthalate

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