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About This Item
Linear Formula:
CH3CH2CHBrCH3
CAS Number:
Molecular Weight:
137.02
Beilstein:
505949
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
98%
form
liquid
refractive index
n20/D 1.437 (lit.)
bp
91 °C (lit.)
density
1.255 g/mL at 25 °C (lit.)
SMILES string
CCC(C)Br
InChI
1S/C4H9Br/c1-3-4(2)5/h4H,3H2,1-2H3
InChI key
UPSXAPQYNGXVBF-UHFFFAOYSA-N
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General description
2-Bromobutane is an alkyl halide. Degradation of 2-bromobutane by reductive dehalogenation in the presence of nickel-aluminum alloy in potassium hydroxide solution has been reported. Gas chromatographic determination of 2-bromobutane in mixture of alkyl bromides has been reported. Stereochemistry of dehydrobromination of 2-bromobutane over KOH-silica has been investigated.
Viscosities of binary mixtures of 2-bromobutane and the isomeric forms of butanol have been evaluated at 298.15 and 313.15K. 2,2-dibromobutane, meso-2,3-dibromobutane and dl-2,3-dibromobutane are formed as major photobromination reaction products, during its reaction with molecular bromine. Smaller yields of 1,2-dibromobutane and 2,2,3-tribromobutane are also obtained in this reaction.
Application
2-Bromobutane may be used in the synthesis of series of non-nucleosides.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Flam. Liq. 2
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
Certificates of Analysis (COA)
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Selective Reactivity in Gas-Liqiud Chromatography. Determination of 2-Bromobutane and 1-Bromo-2-methylpropane.
Harris WE and McFadden WH.
Analytical Chemistry, 31(1), 114-117 (1959)
Viscosities of binary mixtures of 2-bromobutane and 2-bromo-2-methylpropane with isomeric butanols at 298.15 and 313.15 K.
Artigas H, et al.
International Journal of Thermophysics, 23(6), 1455-1468 (2002)
Photobromination of (-)-(2R)-2-bromobutane with bromine-81.
Tanner DD, et al.
Journal of the American Chemical Society, 99(8), 2714-2723 (1977)
G T Sperl et al.
Antonie van Leeuwenhoek, 46(4), 331-341 (1980-01-01)
A member of the genus Arthrobacter was isolated which grew at the expense of 2-bromobutane as sole source of carbon and energy. Evidence is presented which suggests that the initial conversion of 2-bromobutane to 2-butanol is a spontaneous chemical hydrolysis
D M Rampulla et al.
The journal of physical chemistry. B, 110(21), 10411-10420 (2006-05-26)
The enantioselective surface chemistry of chiral R-2-bromobutane was studied on the naturally chiral Cu(643)R&S and Cu(531)R&S surfaces by comparing relative product yields during temperature-programmed reaction spectroscopy. Molecularly adsorbed R-2-bromobutane can desorb molecularly or debrominate to form R-2-butyl groups on the
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