19760
1-Chlorobutane
purum, ≥99.0% (GC)
Synonym(s):
Butyl chloride
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About This Item
Linear Formula:
CH3(CH2)3Cl
CAS Number:
Molecular Weight:
92.57
Beilstein:
1730909
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
vapor density
3.2 (vs air)
vapor pressure
80.1 mmHg ( 78.4 °C)
grade
purum
Assay
≥99.0% (GC)
autoignition temp.
860 °F
expl. lim.
10.1 %
impurities
≤1% benzene
refractive index
n20/D 1.402 (lit.)
n20/D 1.402
bp
77-78 °C (lit.)
mp
−123 °C (lit.)
density
0.886 g/mL at 25 °C (lit.)
SMILES string
CCCCCl
InChI
1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3
InChI key
VFWCMGCRMGJXDK-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
10.4 °F - closed cup
Flash Point(C)
-12 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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M E Alburges et al.
Journal of analytical toxicology, 19(6), 381-386 (1995-10-01)
Ibogaine, an indolamine derivative, is currently being investigated as a potential agent in the treatment of stimulant and opiate addiction. We developed a rapid, sensitive, and specific method for the analysis of ibogaine and its putative active metabolite, 12-hydroxy-ibogamine (12-OH-ibogamine).
Benjamin Erable et al.
Chemosphere, 65(7), 1146-1152 (2006-05-26)
Five bacterial strains were compared for halogenated compounds conversion in aqueous media. Depending on the strain, the optimal temperature for dehalogenase activity of resting cells varied from 30 to 45 degrees C, while optimal pH raised from 8.4 to 9.0.
D B Janssen et al.
Applied and environmental microbiology, 53(3), 561-566 (1987-03-01)
A 1,6-dichlorohexane-degrading strain of Acinetobacter sp. was isolated from activated sludge. The organism could grow with and quantitatively release halide from 1,6-dichlorohexane, 1,9-dichlorononane, 1-chloropentane, 1-chlorobutane, 1-bromopentane, ethylbromide, and 1-iodopropane. Crude extracts contained an inducible novel dehalogenase that liberated halide from
T Yokota et al.
Journal of bacteriology, 169(9), 4049-4054 (1987-09-01)
A haloalkane dehalogenase was purified to electrophoretic homogeneity from cell extracts of a 1-chlorobutane-utilizing strain, m15-3, which was identified as a Corynebacterium sp. The enzyme hydrolyzed C2 to C12 mono- and dihalogenated alkanes, some haloalcohols, and haloacids. The Km value
C Chebli et al.
Pharmaceutical research, 16(9), 1436-1440 (1999-09-25)
Amylose derivatives form an important group of polymers, and many of them can be used as drug sustained-release systems. Substituted amylose can be prepared in a 1-step reaction with substituent(s) in a basic medium. The substituents can be represented as
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