Skip to Content
Merck
All Photos(2)

Key Documents

B82251

Sigma-Aldrich

Bromotrichloromethane

99%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BrCCl3
CAS Number:
Molecular Weight:
198.27
Beilstein:
1732543
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

vapor density

6.85 (vs air)

Quality Level

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service