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Merck

03-3370

Bromine

SAJ first grade, ≥97.0%

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About This Item

Empirical Formula (Hill Notation):
Br2
CAS Number:
Molecular Weight:
159.81
UNSPSC Code:
41116105
PubChem Substance ID:
EC Number:
231-778-1
MDL number:
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InChI key

GDTBXPJZTBHREO-UHFFFAOYSA-N

InChI

1S/Br2/c1-2

SMILES string

BrBr

grade

SAJ first grade

vapor density

7.14 (vs air)

vapor pressure

175 mmHg ( 20 °C), 671 mmHg ( 55 °C)

assay

≥97.0%

form

liquid

availability

available only in Japan

resistivity

7.8E18 μΩ-cm, 20°C

bp

58.8 °C (lit.)

mp

−7.2 °C (lit.)

density

3.119 g/mL at 25 °C (lit.)

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signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1A

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles


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Jenny Rattfelt Nyholm et al.
The Science of the total environment, 443, 307-314 (2012-12-04)
The environmental occurrence of potentially emerging brominated flame retardants (BFRs) was investigated near suspected source zones in Norway, within seepage water, sewage waste water, sewage sludges, and sediments. Analyzed emerging BFRs included 1,2-dibromo-4-(1,2-dibromoethyl) cyclohexane (TBECH), 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE), decabromodiphenylethane (DBDPE)
John D Sivey et al.
Environmental science & technology, 47(3), 1330-1338 (2013-01-18)
HOBr, formed via oxidation of bromide by free available chlorine (FAC), is frequently assumed to be the sole species responsible for generating brominated disinfection byproducts (DBPs). Our studies reveal that BrCl, Br(2), BrOCl, and Br(2)O can also serve as brominating
Nickel-butadiene catalytic system for the cross-coupling of bromoalkanoic acids with alkyl Grignard reagents: a practical and versatile method for preparing fatty acids.
Takanori Iwasaki et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(9), 2956-2960 (2013-02-02)
Bromine-77 and iodine-123 radiopharmaceuticals.
G Stöcklin
The International journal of applied radiation and isotopes, 28(1-2), 131-147 (1977-01-01)
Vitalij V Levin et al.
Organic letters, 15(4), 917-919 (2013-02-02)
Reactions of difluorocarbene with benzyl and alkylzinc halides leading to fluorinated organozinc species have been described. The generated α-difluorinated organozinc reagents are reasonably stable in solution and can be quenched with external electrophiles (iodine, bromine, proton), affording compounds containing the

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