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08953

Supelco

1-Bromobutane

analytical standard

Synonym(s):

Butyl bromide

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About This Item

Linear Formula:
CH3(CH2)3Br
CAS Number:
109-65-9
Molecular Weight:
137.02
Beilstein:
1098260
EC Number:
203-691-9
MDL number:
MFCD00000260
UNSPSC Code:
41116107
PubChem Substance ID:
329748647
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor density

4.7 (vs air)

vapor pressure

150 mmHg ( 50 °C)
40 mmHg ( 25 °C)

Assay

≥99.5% (GC)

autoignition temp.

509 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

2.8-6.6 %, 100 °F

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.439 (lit.)
n20/D 1.440

bp

100-104 °C (lit.)

mp

−112 °C (lit.)

density

1.276 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

CCCCBr

InChI

1S/C4H9Br/c1-2-3-4-5/h2-4H2,1H3

InChI key

MPPPKRYCTPRNTB-UHFFFAOYSA-N

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General description

1-Bromobutane, an organobromine compound, is a commonly used industrial solvent for cleaning, extraction and chemical synthesis.

Application

1-Bromobutane may be used as a derivatization reagent for multiple functional groups (amino, carboxyl, and phenolic hydroxyl groups) of amino acids to improve hydrophobicities and basicities of the amino acids. It may also be used as an internal standard for the quantification of 1- and 2-bromopropane in human urine by headspace gas chromatography.

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 2 - Carc. 2 - Flam. Liq. 2 - Repr. 1B - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

Target Organs

Liver, Respiratory system

WGK

WGK 2

Flash Point(F)

50.0 °F

Flash Point(C)

10 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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Sang Kyu Lee et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48(10), 2707-2711 (2010-07-06)
Halogenated organic compounds, such as 1-bromobutane (1-BB), have been used as cleaning agents, agents for chemical syntheses, or extraction solvents. In the present study, hepatotoxic effects of 1-BB and its conjugation with glutathione (GSH) were investigated in female BALB/c mice.
W C E Schofield et al.
ACS applied materials & interfaces, 1(12), 2763-2767 (2010-04-02)
Existing methods for imparting antibacterial performance to solid surfaces tend to either be substrate-specific or rely upon leaching modes of action that cause ecological damage. An alternative approach is outlined comprising plasmachemical functionalization of solid surfaces with poly(4-vinyl pyridine) moieties
Congbo Cai et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 211(2), 162-169 (2011-06-15)
Recently, a method based on intermolecular multiple quantum coherences (iMQCs) has been proposed to obtain high-resolution 2D COSY spectra in inhomogeneous fields via 3D acquisitions. However, the very long acquisition time prevents its practical application. To overcome this shortage, the
Christina Lederle et al.
The Journal of chemical physics, 134(6), 064512-064512 (2011-02-17)
Mixtures of the monohydroxy alcohol n-butanol with n-bromobutane are investigated via dielectric and nuclear magnetic resonance (NMR) techniques. Static- and pulsed-field gradient proton NMR yielded self-diffusion coefficients as a function of concentration and temperature. To monitor reorientational motions, broadband dielectric
Martin Hesseler et al.
Applied microbiology and biotechnology, 91(4), 1049-1060 (2011-05-24)
A haloalkane dehalogenase (DppA) from Plesiocystis pacifica SIR-1 was identified by sequence comparison in the NCBI database, cloned, functionally expressed in Escherichia coli, purified, and biochemically characterized. The three-dimensional (3D) structure was determined by X-ray crystallography and has been refined
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