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Merck
CN

B65586

Sigma-Aldrich

2-溴乙醇

95%

别名:

乙烯溴醇

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About This Item

线性分子式:
BrCH2CH2OH
CAS号:
分子量:
124.96
Beilstein:
878140
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

蒸汽密度

4.3 (vs air)

质量水平

蒸汽压

2.4 mmHg ( 20 °C)

方案

95%

表单

liquid

折射率

n20/D 1.492 (lit.)

沸点

56-57 °C/20 mmHg (lit.)

密度

1.763 g/mL at 25 °C (lit.)

储存温度

2-8°C

SMILES字符串

OCCBr

InChI

1S/C2H5BrO/c3-1-2-4/h4H,1-2H2

InChI key

LDLCZOVUSADOIV-UHFFFAOYSA-N

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应用

2-溴乙醇可用于由乙酰化糖制备 2-溴乙基糖苷。它也可以用作合成 2-溴乙基甲氧基甲基醚的原料。
2-溴乙醇用于选择性还原硝基芳烃(PcFe(II)/NaBH4/2-溴乙醇催化剂体系)。

象形图

Skull and crossbonesCorrosion

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

230.0 °F - closed cup

闪点(°C)

110 °C - closed cup

个人防护装备

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

法规信息

危险化学品

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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访问文档库

Regio?and Stereoselective Intramolecular Hydrosilylation of α?Hydroxy Enol Ethers: 2, 3?syn?2?Methoxymethoxy?1, 3?Nonanediol: 1, 3?Nonanediol, 2?(methoxymethoxy)?,(R, R)?(?)?.
Tamao K, et al.
Organic Syntheses, 73, 94-94 (2003)
2-Bromoethyl glycosides: synthesis and characterisation.
Dahmen J, et al.
Carbohydrate Research, 116(2), 303-307 (1983)
A R Jones et al.
Xenobiotica; the fate of foreign compounds in biological systems, 11(11), 763-770 (1981-11-01)
1. The metabolism of 2-bromo[U-14C]ethanol an [U-14C]ethylene oxide has been studied in the rat. 2. As both compounds give rise to similar amounts of two urinary metabolites, identified as S-(2-hydroxyethyl)cysteine and N-acetyl-S-(2-hydroxyethyl)cysteine, it is proposed that 2-bromoethanol is converted into
B L Van Duuren et al.
Teratogenesis, carcinogenesis, and mutagenesis, 5(6), 393-403 (1985-01-01)
1,2-Dibromoethane (DBE) and two of its potential metabolites, bromoethanol (BE) and bromoacetaldehyde (BA), were tested for carcinogenicity in male and female B6C3F1 mice using 30 animals of each sex per group. The carcinogen DBE was included in this assay as
S Khan et al.
Biochemical pharmacology, 45(2), 439-447 (1993-01-26)
The cytotoxicity of dibromoalkanes to isolated hepatocytes was proportional to the dibromoalkane concentration and increasing chain length of the dibromoalkane (C2-C6). The rapid hepatocyte glutathione (GSH) depletion which occurred upon addition of the dibromoalkanes was also dependent on the concentration

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