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Merck
CN

132942

Sigma-Aldrich

溴仿

contains 1-3% ethanol as stabilizer, 96%

别名:

三溴甲烷

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About This Item

经验公式(希尔记法):
CHBr3
CAS号:
分子量:
252.73
Beilstein:
1731048
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

蒸汽密度

8.7 (vs air)

质量水平

蒸汽压

5 mmHg ( 20 °C)

方案

96%

表单

liquid

包含

1-3% ethanol as stabilizer

折射率

n20/D 1.595 (lit.)

沸点

146-150 °C (lit.)

mp

5-8 °C (lit.)

溶解性

water: soluble 800 part
acetone: miscible
alcohol: miscible
benzene: miscible
chloroform: miscible
diethyl ether: miscible
oil: miscible
petroleum ether: miscible

密度

2.89 g/mL at 25 °C (lit.)

官能团

bromo

SMILES字符串

BrC(Br)Br

InChI

1S/CHBr3/c2-1(3)4/h1H

InChI key

DIKBFYAXUHHXCS-UHFFFAOYSA-N

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一般描述

Bromoform is a major organic source for atmospheric reactive bromine BrOx (Br+BrO). It is formed as a product of chlorination of drinking water. It undergoes photodissociation to form the Br2 fragment and mechanism has been investigated by cavity ring-down absorption spectroscopy.

应用

Bromoform was used to evaluate the genotoxicity of chlorodibromomethane, bromodichloromethane and bromoform.

警示用语:

Danger

危险分类

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

106.3 °F - closed cup - (own results)

闪点(°C)

41.3 °C - closed cup - (own results)

个人防护装备

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

法规信息

危险化学品

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分析证书(COA)

Lot/Batch Number

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Hong-Yi Huang et al.
The Journal of chemical physics, 121(11), 5253-5260 (2004-09-09)
By using cavity ring-down spectroscopy technique, we have observed the channel leading to Br(2) molecular elimination following photodissociation of bromoform at 248 nm. A tunable laser beam, which is crossed perpendicular to the photolysis laser beam in a ring-down cell
Oceanic bromoform sources for the tropical atmosphere.
Quack B, et al.
Geophysical Research Letters, 31(23), 1-4 (2004)
K J Stocker et al.
Mutagenesis, 12(3), 169-173 (1997-05-01)
Chlorination of drinking water results in the formation of chlorodibromomethane, bromodichloromethane and bromoform. These trihalomethanes have all shown evidence of genotoxicity in bacterial and mammalian cell systems in vitro and some evidence of carcinogenicity in rodents. Chlorodibromomethane and bromodichloromethane have
Bichismita Sahu et al.
The Journal of organic chemistry, 74(6), 2601-2604 (2009-02-26)
Addition of bromoform to conjugated nitroalkenes in the presence of Mg provided beta-tribromomethyl nitroalkanes in good to excellent yields and diastereoselectivity. These novel Michael adducts, formed under radical conditions, underwent elimination of HBr in the same pot under reflux to
M Valcke et al.
Regulatory toxicology and pharmacology : RTP, 59(2), 258-269 (2010-10-26)
The objective of this study was to assess the impact of the exposure route on the human kinetic adjustment factor (HKAF), for which a default value of 3.16 is used in non-cancer risk assessment. A multi-route PBPK model was modified

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