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293229

Supelco

1-Chlorobutane

HPLC grade, ≥99.5%

Synonym(s):

Butyl chloride

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About This Item

Linear Formula:
CH3(CH2)3Cl
CAS Number:
109-69-3
Molecular Weight:
92.57
Beilstein/REAXYS Number:
1730909
EC Number:
203-696-6
MDL number:
MFCD00001009
UNSPSC Code:
12190000
PubChem Substance ID:
329753225

grade

HPLC grade

Quality Level

100

vapor density

3.2 (vs air)

vapor pressure

80.1 mmHg ( 78.4 °C)

assay

≥99.5%

autoignition temp.

860 °F

purified by

glass distillation

expl. lim.

10.1 %

impurities

<0.020% water

evapn. residue

<0.0003%

refractive index

n20/D 1.402 (lit.)

bp

77-78 °C (lit.)
77-78 °C

mp

−123 °C (lit.)

density

0.886 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 220 nm Amax: 1.00
λ: 225 nm Amax: 0.35
λ: 250 nm Amax: 0.05
λ: 300-400 nm Amax: 0.01

SMILES string

CCCCCl

InChI

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

InChI key

VFWCMGCRMGJXDK-UHFFFAOYSA-N

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pictograms

FlameHealth hazard
GHS02,GHS08

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

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

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Certificates of Analysis (COA)

Lot/Batch Number
01218AX
00514BW
04723AX
U14977
06861HC

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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).
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
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
Javier Catalán et al.
Physical chemistry chemical physics : PCCP, 13(33), 15022-15030 (2011-07-16)
In this work, we substantiate the change in the emitting state of indole caused by the dipolarity increase in the solvent 1-chlorobutane, observed on lowering the temperature from 293 to 133 K, accompanied by no significant changes in the corresponding
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