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Safety Information

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)

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

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.

JAN Code

B82251-500G:
B82251-BULK:
B82251-100G:
B82251-VAR:
B82251-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBK3745
SHBH8013
SHBG1833V
SHBD9363V
34796MKV

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Tetrahedron, 50, 31-31 (1994)
Macromolecules, 27, 5863-5863 (1994)
C K Moon et al.
Drug and chemical toxicology, 15(1), 81-91 (1992-01-01)
Brazilin, the main constituent of Caesalpinia sappan, is an antioxidative substance that has catechol moiety in its chemical structure. Considering the antioxidant-activity of brazilin, it was expected to have protective effects on the toxicities of radical generating chemicals. The incubation
G D Castro et al.
Free radical research, 23(5), 431-442 (1995-11-01)
Free radicals generated by benzoyl peroxide-mediated catalytic decomposition of bromotrichloromethane (eg. trichloromethyl) were allowed to react under nitrogen or under air with uracil. Under nitrogen two reaction products were formed, one was identified as 5-chlorouracil and the other as a
Journal of the Chemical Society. Chemical Communications, 747-747 (1994)
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