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Merck
CN

341274

单氧化异戊二烯

95%

别名:

一氧化异戊二烯

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关于此项目

经验公式(希尔记法):
C5H8O
化学文摘社编号:
分子量:
84.12
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
MDL number:
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InChI

1S/C5H8O/c1-3-5(2)4-6-5/h3H,1,4H2,2H3

SMILES string

CC1(CO1)C=C

InChI key

FVCDMHWSPLRYAB-UHFFFAOYSA-N

assay

95%

form

liquid

refractive index

n20/D 1.416 (lit.)

bp

80-81 °C (lit.)

density

0.857 g/mL at 25 °C (lit.)

storage temp.

2-8°C

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

17.6 °F - closed cup

flash_point_c

-8 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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J J Bogaards et al.
Chemico-biological interactions, 138(3), 247-265 (2001-11-21)
The present study was designed to explain the differences in isoprene toxicity between mouse and rat based on the liver concentrations of the assumed toxic metabolite isoprene diepoxide. In addition, extrapolation to the human situation was attempted. For this purpose
J J Bogaards et al.
Chemico-biological interactions, 102(3), 169-182 (1996-12-20)
The metabolism of isoprene was investigated with microsomes derived from cell lines expressing human CYP1A1, CYP1A2, CYP2A6, CYP2B6, CYP2C9, CYP2D6, CYP2E1, or CYP3A4. The formation of epoxide metabolites was determined by gas chromatographic analysis. CYP2E1 showed the highest rates of
J J Bogaards et al.
Chemico-biological interactions, 117(1), 1-14 (1999-04-06)
In the present study, the enzymatic conjugation of the isoprene monoepoxides 3,4 epoxy-3-methyl-1-butene (EPOX-I) and 3,4-epoxy-2-methyl-1-butene (EPOX-II) with glutathione was investigated, using purified glutathione S-transferases (GSTs) of the alpha, mu, pi and theta-class of rat and man. HPLC analysis of
Roberto Fabiani et al.
Mutation research, 629(1), 7-13 (2007-02-24)
Isoprene is produced in combustion processes and is widely used as an industrial chemical. It is a natural product emitted by plants and endogenously produced by humans and other mammals. Therefore, exposure to isoprene from both endogenous and exogenous sources

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