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03-3360

Sigma-Aldrich

Bromine

JIS special grade, ≥99.0%

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About This Item

Empirical Formula (Hill Notation):
Br2
CAS Number:
7726-95-6
Molecular Weight:
159.81
EC Number:
231-778-1
MDL number:
MFCD00010896
UNSPSC Code:
41116105
PubChem Substance ID:
329747591

grade

JIS special grade

vapor density

7.14 (vs air)

vapor pressure

175 mmHg ( 20 °C)
671 mmHg ( 55 °C)

assay

≥99.0%

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.)

SMILES string

BrBr

InChI

1S/Br2/c1-2

InChI key

GDTBXPJZTBHREO-UHFFFAOYSA-N

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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_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles

Certificates of Analysis (COA)

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Bromine-77 and iodine-123 radiopharmaceuticals.
G Stöcklin
The International journal of applied radiation and isotopes, 28(1-2), 131-147 (1977-01-01)
Teresa M Bisson et al.
Environmental science & technology, 46(21), 12186-12193 (2012-10-02)
Recent laboratory and field-scale experiments demonstrated the potential for brominated industrial solid waste from biomass combustion (Br-Ash) to be an efficient, cost-effective alternative to activated carbon for capturing mercury from coal-fired power plants. To develop this attractive alternative technology to
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)
Erin J Sheridan et al.
Journal of synchrotron radiation, 20(Pt 2), 226-233 (2013-02-16)
The first example of synchrotron X-ray fluorescence imaging of cultured mammalian cells in cyclic peptide research is reported. The study reports the first quantitative analysis of the incorporation of a bromine-labelled cyclic RGD peptide and its effects on the biodistribution
Takashi Kippo et al.
Journal of the American Chemical Society, 135(2), 632-635 (2012-12-28)
Bromine radical-mediated cyclopropylcarbinyl-homoallyl rearrangement of alkylidenecyclopropanes was effectively accomplished by C-C bond formation with allylic bromides, which led to the syntheses of 2-bromo-1,6-dienes. A three-component coupling reaction comprising alkylidenecyclopropanes, allylic bromides, and carbon monoxide also proceeded well to give 2-bromo-1,7-dien-5-ones
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