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Merck
CN

310387

2,3-Dibromobutane, mixture of (±) and meso

99%

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About This Item

Linear Formula:
CH3CH(Br)CH(Br)CH3
CAS Number:
Molecular Weight:
215.91
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-476-1
MDL number:
Assay:
99%
Form:
liquid
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form

liquid

InChI key

BXXWFOGWXLJPPA-UHFFFAOYSA-N

InChI

1S/C4H8Br2/c1-3(5)4(2)6/h3-4H,1-2H3

SMILES string

CC(Br)C(C)Br

assay

99%

refractive index

n20/D 1.5126 (lit.)

bp

103-108 °C/160 mmHg (lit.)

density

1.756 g/mL at 25 °C (lit.)

functional group

bromo

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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


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J C Livesey et al.
Drug metabolism and disposition: the biological fate of chemicals, 10(3), 201-204 (1982-05-01)
The stereochemistry of the metabolism of vic-dihaloalkanes to alkenes has been studied. This glutathione-dependent biotransformation may occur by two mechanism. The first mechanism involves the nucleophilic attack of glutathione on the substrate resulting in S-(beta-haloalkyl)glutathione formation; subsequent attack of a

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