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About This Item
Linear Formula:
CH3(CH2)3Cl
CAS Number:
Molecular Weight:
92.57
EC Number:
203-696-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1730909
MDL number:
InChI key
VFWCMGCRMGJXDK-UHFFFAOYSA-N
InChI
1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3
SMILES string
CCCCCl
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
mp
−123 °C (lit.)
density
0.886 g/mL at 25 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
10.4 °F - closed cup
flash_point_c
-12 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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A Lewandowicz et al.
Journal of the American Chemical Society, 123(19), 4550-4555 (2001-07-18)
We have found chlorine kinetic isotope effects on the dehalogenation catalyzed by haloalkane dehalogenase from Xanthobacter autotrophicus GJ10 to be 1.0045 +/- 0.0004 for 1,2-dichloroethane and 1.0066 +/- 0.0004 for 1-chlorobutane. The latter isotope effect approaches the intrinsic chlorine kinetic
J M Czuczwa et al.
Journal - Association of Official Analytical Chemists, 72(5), 752-759 (1989-09-01)
A gel permeation chromatographic (GPC) method, used by the U.S. Environmental Protection Agency (USEPA), was modified for cleanup of soil, sediments, wastes, and oily wastes before determination of semivolatile organic pollutants. The modifications included new calibration procedures and control of
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.
M E Alburges et al.
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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).
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We have recently proposed a protocol for retrieving nuclear magnetic resonance (NMR) spectra based on a spatially-dependent encoding of the MR interactions. It has also been shown that the spatial selectivity with which spins are manipulated during such encoding opens
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