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Merck
CN

19750

1-Chlorobutane

puriss. p.a., ≥99.5% (GC)

Synonym(s):

Butyl chloride

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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:
12190000
PubChem Substance ID:
Beilstein/REAXYS Number:
1730909
MDL number:
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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

puriss. p.a.

assay

≥99.5% (GC)

autoignition temp.

860 °F

expl. lim.

10.1 %

impurities

≤0.5% benzene (UV)

evapn. residue

≤0.001%

mp

−123 °C (lit.)

density

0.886 g/mL at 25 °C (lit.)

cation traces

Al: ≤0.5 mg/kg, Ba: ≤0.1 mg/kg, Bi: ≤0.1 mg/kg, Ca: ≤0.5 mg/kg, Cd: ≤0.05 mg/kg, Co: ≤0.02 mg/kg, Cr: ≤0.02 mg/kg, Cu: ≤0.02 mg/kg, Fe: ≤0.1 mg/kg, K: ≤0.5 mg/kg, Li: ≤0.1 mg/kg, Mg: ≤0.1 mg/kg, Mn: ≤0.02 mg/kg, Mo: ≤0.1 mg/kg, Na: ≤0.5 mg/kg, Ni: ≤0.02 mg/kg, Pb: ≤0.1 mg/kg, Sr: ≤0.1 mg/kg, Zn: ≤0.1 mg/kg

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pictograms

FlameHealth hazard

signalword

Danger

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
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).
Boaz Shapira et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 182(1), 12-21 (2006-06-30)
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
Hazel M Rivera et al.
European journal of mass spectrometry (Chichester, England), 9(6), 599-607 (2004-04-22)
A sensitive and selective high-performance liquid chromatography/atmospheric pressure chemical ionisation tandem mass spectrometry (HPLC/APCI-MS/MS) method for the simultaneous detection of 18 benzodiazepines and metabolites in human blood is described. The procedure utilises butyl chloride extraction at alkaline pH followed by

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