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B82251

Sigma-Aldrich

Bromotrichloromethane

99%

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About This Item

Linear Formula:
BrCCl3
CAS Number:
75-62-7
Molecular Weight:
198.27
Beilstein:
1732543
EC Number:
200-886-0
MDL number:
MFCD00000783
UNSPSC Code:
12162002
PubChem Substance ID:
24892061
NACRES:
NA.23

vapor density

6.85 (vs air)

Quality Level

200

vapor pressure

38.4 mmHg ( 25 °C)

Assay

99%

form

liquid

refractive index

n20/D 1.5065 (lit.)

bp

105 °C (lit.)

mp

−6 °C (lit.)

density

2.012 g/mL at 25 °C (lit.)

SMILES string

ClC(Cl)(Cl)Br

InChI

1S/CBrCl3/c2-1(3,4)5

InChI key

XNNQFQFUQLJSQT-UHFFFAOYSA-N

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Related Categories

Application

Chain transfer agent for radical polymerization of methacrylates. Brominating reagent.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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Journal of the Chemical Society. Chemical Communications, 747-747 (1994)
Tetrahedron, 50, 31-31 (1994)
Macromolecules, 27, 5863-5863 (1994)
C Jochmann et al.
Pharmacology & toxicology, 75(1), 7-16 (1994-07-01)
The role of glutathione (GSH) and protein thiols in the pathobiochemical process of CBrCl3 cytotoxicity was investigated in isolated hepatocytes. Administration of 0.5, 1.0 and 1.5 mmol/l CBrCl3 affected cellular viability as assessed by trypan blue exclusion, release of lactate
O Danni et al.
Research communications in chemical pathology and pharmacology, 76(3), 355-366 (1992-06-01)
The liver toxicity of several halogen compound mixtures have been tested. The compounds were selected on the basis of their metabolic pathways: carbon tetrachloride (CT) and trichlorobromomethane (TCBM) undergo a dehalogenation via P450-dependent enzyme system, 1,2-dichloroethane (DCE) and 1,2-dibromoethane (DBE)
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