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Merck
CN

B65586

Sigma-Aldrich

2-溴乙醇

95%

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别名:
乙烯溴醇
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)

检测方案

95%

形式

liquid

折射率

n20/D 1.492 (lit.)

bp

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

WGK

WGK 3

闪点(°F)

230.0 °F

闪点(°C)

110 °C

个人防护装备

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

法规信息

危险化学品

分析证书(COA)

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2-Bromoethyl glycosides: synthesis and characterisation.
Dahmen J, et al.
Carbohydrate Research, 116(2), 303-307 (1983)
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)
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
W Van Rillaer et al.
Zeitschrift fur Lebensmittel-Untersuchung und -Forschung, 189(1), 21-25 (1989-07-01)
This study describes a headspace gas-chromatographic method for the quantitative determination of inorganic bromide in vegetables. Different parameters influencing the reaction of the bromide ion into 2-bromoethanol have been investigated. The analysis of 2-bromoethanol is performed by the headspace--electron capture--gas
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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