프탈산디이소노닐에스테르

프탈산디이소노닐에스테르
프탈산디이소노닐에스테르 구조식 이미지
카스 번호:
68515-48-0
한글명:
프탈산디이소노닐에스테르
동의어(한글):
다이아이소노닐프탈산;디이소노닐프탈산;프탈산디이소노닐에스테르;다이아이소노닐프탈산(DIISONONYLPHTHALATE);1,2-벤젠다이카복실산, 다이(C=8-10) 가지친 알킬 에스터, (C=9)-풍부;1,2-벤젠다이카복실산, 다이-C8-10 가지친 알킬 에스터, C9-풍부;1,2-벤젠다이카복실산, 다이-C8-10-가지친 알킬 에스터, C9-풍부
상품명:
Diisononyl phthalate
동의어(영문):
BIS(3,5,5-TRIMETHYLHEXYL) PHTHALATE;1,2-benzenedicarboxylicacid,di-c8-c10-branchedalkylester,c9-rich;DINP-1;Diisononyl phthalate;DI(ISONONYL)PHTHALATE1;Dialkyl-(C8-C10)phthalate;Diisononyl Phthalate Bis(3,5,5-trimethylhexyl);DIISONONYL PHTHALATE, TECH.;DI-ISONONYLPHTHALATE,BRANCHED
CBNumber:
CB5452848
분자식:
C26H42O4
포뮬러 무게:
418.61
MOL 파일:
68515-48-0.mol
MSDS 파일:
SDS

프탈산디이소노닐에스테르 속성

끓는 점
279-287 °C
밀도
0.972 g/mL at 25 °C(lit.)
Pour Point 
-54
증기압
1 mm Hg ( 200 °C)
굴절률
n20/D 1.485(lit.)
인화점
>230 °F
저장 조건
Refrigerator
용해도
클로로포름, 메탄올에 용해됨
물리적 상태
기름
색상
무색~담황색
Merck
13,3319
EPA
Di(C8-10, C9 rich) branched alkyl phthalates (68515-48-0)

안전

위험 카페고리 넘버 62-63
안전지침서 23-36/37
WGK 독일 -
RTECS 번호 CZ3395000
TSCA TSCA listed
HS 번호 29173490
기존화학 물질 KE-02208

프탈산디이소노닐에스테르 C화학적 특성, 용도, 생산

화학적 성질

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.

용도

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

생산 방법

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

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.

프탈산디이소노닐에스테르 준비 용품 및 원자재

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