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132942

Sigma-Aldrich

Bromoform

contains 1-3% ethanol as stabilizer, 96%

Synonym(s):

Tribromomethane

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About This Item

Empirical Formula (Hill Notation):
CHBr3
CAS Number:
75-25-2
Molecular Weight:
252.73
Beilstein:
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.)

functional group

bromo

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.

Signal Word

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 Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

106.3 °F - closed cup - (own results)

Flash Point(C)

41.3 °C - closed cup - (own results)

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Oceanic bromoform sources for the tropical atmosphere.
Quack B, et al.
Geophysical Research Letters, 31(23), 1-4 (2004)
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
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
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
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
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