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γ-苯基-γ-丁内酯

γ-苯基-γ-丁内酯名称

[ CAS 号 ]:
1008-76-0

[ 中文名 ]:
γ-苯基-γ-丁内酯

[ 英文名 ]:
2(3H)-Furanone,dihydro-5-phenyl-

[中文别名 ]:

[英文别名 ]:

MFCD00005398
γ-PHENYL-γ-BUTYROLACTONE
EINECS 213-761-0

γ-苯基-γ-丁内酯物理化学性质

[ 密度 ]:
1.155 g/mL at 25 °C(lit.)

[ 沸点 ]:
306 °C(lit.)

[ 熔点 ]:
36-37 °C(lit.)

[ 分子式 ]:
C₁₀H₁₀O₂

[ 分子量 ]:
162.18500

[ 闪点 ]:
>230 °F

[ 精确质量 ]:
162.06800

[ PSA ]:
26.30000

[ LogP ]:
2.06470

[ 外观性状 ]:
固体;White to Almost white powder to crystal

[ 蒸汽压 ]:
0.000793mmHg at 25°C

[ 折射率 ]:
1.5415-1.5435

[ 储存条件 ]:
室温，密封，干燥

[ 水溶解性 ]:
可溶于：甲醇

γ-苯基-γ-丁内酯MSDS

详细MSDS(安全技术说明书)

γ-苯基-γ-丁内酯毒性和生态

CHEMICAL IDENTIFICATION

RTECS NUMBER :: LU3690000

CHEMICAL NAME :: 2(3H)-Furanone, 4,5-dihydro-5-phenyl-

CAS REGISTRY NUMBER :: 1008-76-0

BEILSTEIN REFERENCE NO. :: 0125169

LAST UPDATED :: 199612

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C10-H10-O2

MOLECULAR WEIGHT :: 162.20

WISWESSER LINE NOTATION :: T5OVTJ ER

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LDLo - Lowest published lethal dose

ROUTE OF EXPOSURE :: Intraperitoneal

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 2 gm/kg

TOXIC EFFECTS :: Behavioral - altered sleep time (including change in righting reflex) Behavioral - ataxia Lungs, Thorax, or Respiration - respiratory depression

REFERENCE :: RCOCB8 Research Communications in Chemical Pathology and Pharmacology. (PJD Pub. Ltd., P.O. Box 966, Westbury, NY 11590) V.1- 1970- Volume(issue)/page/year: 18,439,1977

γ-苯基-γ-丁内酯安全信息

[ 个人防护装备 ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ 危害码 (欧洲) ]:
Xi

[ 安全声明 (欧洲) ]:
S24/25

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ RTECS号 ]:
LU3690000

[ 海关编码 ]:
2932209090

γ-苯基-γ-丁内酯海关

[ 海关编码 ]: 2932209090

[ 中文概述 ]:
2932209090. 其他内酯. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

γ-苯基-γ-丁内酯文献

Pronounced differences in inhibition potency of lactone and non-lactone compounds for mouse and human coumarin 7-hydroxylases (CYP2A5 and CYP2A6).

Xenobiotica 30(1) , 81-92, (2000)

1. The structural requirements for a compound to be a potent inhibitor for mouse CYP2A5 and human CYP2A6 enzymes catalysing coumarin 7-hydroxylase activity have been studied. 2. The IC50 of 28 compoun...

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