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Key Documents

09651

Sigma-Aldrich

1-Chlorobutane

biotech. grade, for protein sequence analysis, ≥99.8%

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:
NACRES:
NA.22

grade

biotech. grade
for protein sequence analysis

Quality Level

vapor density

3.2 (vs air)

vapor pressure

80.1 mmHg ( 78.4 °C)

Assay

≥99.8%

form

liquid

autoignition temp.

860 °F

expl. lim.

10.1 %

impurities

≤0.01% water (Karl Fischer)

evapn. residue

≤0.0003%

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.)

suitability

corresponds for Infrared spectrum
in accordance for sequence analysis test

storage temp.

2-8°C

SMILES string

CCCCCl

InChI

1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3

InChI key

VFWCMGCRMGJXDK-UHFFFAOYSA-N

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Packaging

Special packaging for direct use in common sequencers; contains 200 ml.

Pictograms

FlameHealth hazard

Signal Word

Danger

Hazard 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

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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.
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

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