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132942

Sigma-Aldrich

Bromoform

contains 1-3% ethanol as stabilizer, 96%

Sinónimos:

Tribromomethane

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About This Item

Fórmula empírica (notación de Hill):
CHBr3
Número de CAS:
75-25-2
Peso molecular:
252.73
Beilstein/REAXYS Number:
1731048
EC Number:
200-854-6
MDL number:
MFCD00000128
UNSPSC Code:
12352100
PubChem Substance ID:
24848085
NACRES:
NA.22

vapor density

8.7 (vs air)

vapor pressure

5 mmHg ( 20 °C)

assay

96%

form

liquid

contains

1-3% ethanol as stabilizer

refractive index

n20/D 1.595 (lit.)

bp

146-150 °C (lit.)

mp

5-8 °C (lit.)

solubility

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

density

2.89 g/mL at 25 °C (lit.)

SMILES string

BrC(Br)Br

InChI

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

InChI key

DIKBFYAXUHHXCS-UHFFFAOYSA-N

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General description

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.

Application

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

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

106.3 °F - closed cup - (own results)

flash_point_c

41.3 °C - closed cup - (own results)

ppe

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

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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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