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Merck

132942

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:
Molecular Weight:
252.73
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-854-6
Beilstein/REAXYS Number:
1731048
MDL number:
Assay:
96%
Form:
liquid
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vapor density

8.7 (vs air)

Quality Level

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

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.


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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

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


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

75-25-2

CAS No.


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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