추천 제품
Quality Level
분석
98%
양식
liquid
refractive index
n20/D 1.523 (lit.)
bp
98-100 °C/17 mmHg (lit.)
density
1.02 g/mL at 25 °C (lit.)
SMILES string
C1OC1Cc2ccccc2
InChI
1S/C9H10O/c1-2-4-8(5-3-1)6-9-7-10-9/h1-5,9H,6-7H2
InChI key
JFDMLXYWGLECEY-UHFFFAOYSA-N
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
179.6 °F - closed cup
Flash Point (°C)
82 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
T M Guenthner et al.
Toxicology, 160(1-3), 47-58 (2001-03-14)
The genotoxic potential of naturally occurring allylbenzene analogs, including safrole, eugenol, estragole, and others, has been examined in many studies over the past 30 years. It has been established that these compounds are subject to biotransformation in the liver, which
G Luo et al.
Drug metabolism and disposition: the biological fate of chemicals, 22(5), 731-737 (1994-09-01)
The enzymatic detoxication in vitro of the 2',3'-epoxide derivatives of allylbenzene and estragole was examined, and the relative rates of enzymatic glutathione conjugation and epoxide hydrolysis were compared with those for styrene 1',2'-oxide. HPLC was used to determine the amounts
G Luo et al.
Drug metabolism and disposition: the biological fate of chemicals, 24(9), 1020-1027 (1996-09-01)
Epoxidation at the allylic side chain is a major metabolic pathway for allylbenzene and its naturally occurring analogs safrole, estragole, and eugenol. We demonstrate herein that the epoxide metabolites of allylbenzene, estragole, and safrole can form covalent adducts with DNA
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