239887
1-Bromobutane
ReagentPlus®, ≥99%
Sinónimos:
Butyl bromide
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About This Item
Fórmula lineal:
CH3(CH2)3Br
Número de CAS:
Peso molecular:
137.02
Beilstein/REAXYS Number:
1098260
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Productos recomendados
vapor density
4.7 (vs air)
vapor pressure
150 mmHg ( 50 °C)
40 mmHg ( 25 °C)
product line
ReagentPlus®
assay
≥99%
autoignition temp.
509 °F
expl. lim.
2.8-6.6 %, 100 °F
refractive index
n20/D 1.439 (lit.)
bp
100-104 °C (lit.)
mp
−112 °C (lit.)
density
1.276 g/mL at 25 °C (lit.)
SMILES string
CCCCBr
InChI
1S/C4H9Br/c1-2-3-4-5/h2-4H2,1H3
InChI key
MPPPKRYCTPRNTB-UHFFFAOYSA-N
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Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
replaced by
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W C E Schofield et al.
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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
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.
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
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