Merck
CN
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文件

139564

Sigma-Aldrich

1,2,7,8-二环氧辛烷

97%

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别名:
1,7-Octadiene bisoxide, 1,7-Octadiene diepoxide, 2,2′-(1,4-Butanediyl)bis[oxirane]
经验公式（希尔记法）:
C8H14O2
CAS号:
2426-07-5
分子量:
142.20
EC 号:
219-375-9
MDL编号:
MFCD00005155
PubChem化学物质编号:
24848422
NACRES:
NA.23

质量水平

200

检测方案

97%

形式

liquid

折射率

n20/D 1.445 (lit.)

bp

240 °C (lit.)

密度

0.997 g/mL at 25 °C (lit.)

SMILES string

C(CCC1CO1)CC2CO2

InChI

1S/C8H14O2/c1(3-7-5-9-7)2-4-8-6-10-8/h7-8H,1-6H2

InChI key

LFKLPJRVSHJZPL-UHFFFAOYSA-N

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相关类别

象形图

Skull and crossbonesHealth hazard
GHS06,GHS08

警示用语：

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Carc. 1B - Muta. 2

储存分类代码

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

208.4 °F - closed cup

闪点(°C)

98 °C - closed cup

个人防护装备

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

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E H Vock et al.
Mutation research, 441(1), 85-93 (1999-05-04)
The time-dependent dose-response relationships for the induction of DNA double-strand breaks (DSB) assessed by pulsed-field gel electrophoresis (PFGE) and for viability (evaluated by the MTT cytotoxicity test) were investigated in order to discriminate between genotoxic and cytotoxic mechanisms of DNA
Cristina Pungartnik et al.
Genetics and molecular research : GMR, 1(1), 79-89 (2004-02-14)
The sensitivity responses of seven pso mutants of Saccharomyces cerevisiae towards the mutagens N-nitrosodiethylamine (NDEA), 1,2:7,8-diepoxyoctane (DEO), and 8-hydroxyquinoline (8HQ) further substantiated their allocation into two distinct groups: genes PSO1 (allelic to REV3), PSO2 (SNM1), PSO4 (PRP19), and PSO5 (RAD16)
D J Eide et al.
Molecular and cellular biology, 5(1), 1-6 (1985-01-01)
The mutation e1662 is an allele of the Caenorhabditis elegans unc-54 gene induced with the difunctional alkylating agent 1,2,7,8-diepoxyoctane. unc-54 encodes the major myosin heavy chain isozyme of body wall muscle cells. Filter-transfer hybridization and DNA sequence analysis show that
J T Millard et al.
Biochemistry, 40(35), 10677-10685 (2001-08-29)
Diepoxyalkanes form interstrand cross-links in DNA oligomers preferentially at 5'-GNC sites. We have examined cross-linking by 1,2,3,4-diepoxybutane (DEB) and 1,2,7,8-diepoxyoctane (DEO) within a fragment of the 5S RNA gene of Xenopus borealis in both the free and nucleosomal states. Sites
M J Yunes et al.
Chemical research in toxicology, 9(6), 994-1000 (1996-09-01)
The carcinogenicity of epoxide compounds has been attributed to covalent binding to DNA. Whereas monoepoxides form only monoadducts, diepoxides can form both monoadducts and interstrand cross-links. The latter are believed to be the more significant cytotoxic lesions as diepoxides are
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