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Merck

241032

Bromoform

contains 60-120 ppm 2-methyl-2-butene as stabilizer, 99%

Synonyme(s) :

Tribromomethane

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About This Item

Formule empirique (notation de Hill) :
CHBr3
Numéro CAS:
Poids moléculaire :
252.73
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-854-6
Beilstein/REAXYS Number:
1731048
MDL number:

Nom du produit

Bromoform, contains 60-120 ppm 2-methyl-2-butene as stabilizer, 99%

InChI key

DIKBFYAXUHHXCS-UHFFFAOYSA-N

InChI

1S/CHBr3/c2-1(3)4/h1H

SMILES string

BrC(Br)Br

vapor density

8.7 (vs air)

vapor pressure

5 mmHg ( 20 °C)

assay

99%

form

liquid

contains

60-120 ppm 2-methyl-2-butene as stabilizer

refractive index

n20/D 1.595 (lit.)

bp

146-150 °C (lit.)

mp

5-8 °C (lit.)

solubility

water: soluble 800 part(lit.)
acetone: miscible(lit.)
alcohol: miscible(lit.)
benzene: miscible(lit.)
chloroform: miscible(lit.)
diethyl ether: miscible(lit.)
oil: miscible(lit.)
petroleum ether: miscible(lit.)

density

2.89 g/mL at 25 °C (lit.)

functional group

bromo

Quality Level

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Application

Bromoform (Tribromomethane) was used in the synthesis of α-tribromomethylated N-sulfonylamines.

General description

Bromoform (CHBr3), also known as Tribromomethane, is a very short-lived substance (VSLS) and an important precursor of reactive bromine species (BrOx). It is widely used as a laboratory reagent and as an industrial extraction solvent. It can also be used as a sedative and to create block copolymers.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Classe de stockage

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)

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Elumalai Gopi et al.
Organic & biomolecular chemistry, 12(17), 2769-2777 (2014-03-29)
Mg-mediated addition of bromoform to electron deficient imines such as N-sulfonylimines affords α-tribromomethylated N-sulfonylamines in good to excellent yields. The procedure could be further simplified by transforming the imine precursors, α-sulfonyl-N-tosyl- and Boc-amines, in one pot to the corresponding α-tribromomethyl
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
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
Lisa George et al.
The Journal of chemical physics, 135(12), 124503-124503 (2011-10-07)
Iso-polyhalomethanes are known reactive intermediates that play a pivotal role in the photochemistry of halomethanes in condensed phases. In this work, iso-bromoform (iso-CHBr(3)) and its deuterated isotopomer were characterized by matrix isolation infrared and UV/visible spectroscopy, supported by ab initio
David R Geter et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 43(9), 1405-1412 (2005-06-01)
Folate and folic acid are forms of the B vitamin that are involved in the synthesis, repair, and functioning of DNA and are required for the production and maintenance of cells. Low levels of folate have been associated with several

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