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Merck
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241032

Sigma-Aldrich

Bromoform

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

Sinónimos:

Tribromomethane

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About This Item

Fórmula empírica (notación de Hill):
CHBr3
Número de CAS:
75-25-2
Peso molecular:
252.73
Beilstein/REAXYS Number:
1731048
EC Number:
200-854-6
MDL number:
MFCD00000128
UNSPSC Code:
12352100
PubChem Substance ID:
24854456
NACRES:
NA.22

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.)

SMILES string

BrC(Br)Br

InChI

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

InChI key

DIKBFYAXUHHXCS-UHFFFAOYSA-N

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Categorías relacionadas

Application

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

signalword

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

wgk_germany

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
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
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
Carolina Lourencetti et al.
Environment international, 45, 59-67 (2012-05-11)
This first study of trihalomethanes (THMs) in swimming pools using bromine agents for water disinfection under real conditions shows that the mixtures of these compounds are largely dominated by bromoform in a similar process as chloroform becomes the dominant THM
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