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238368

Sigma-Aldrich

1-Chlorooctadecane

96%

Synonym(s):

Octadecyl chloride, Stearyl chloride

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About This Item

Linear Formula:
CH3(CH2)16CH2Cl
CAS Number:
3386-33-2
Molecular Weight:
288.94
Beilstein/REAXYS Number:
1703350
EC Number:
222-207-7
MDL number:
MFCD00000960
UNSPSC Code:
12352100
PubChem Substance ID:
24854298
NACRES:
NA.22

Quality Level

100

assay

96%

form

liquid

refractive index

n20/D 1.451 (lit.)

bp

157-158 °C/1.5 mmHg (lit.)

density

0.849 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCCCCCl

InChI

1S/C18H37Cl/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h2-18H2,1H3

InChI key

VUQPJRPDRDVQMN-UHFFFAOYSA-N

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General description

Kinetic and thermodynamic analysis of catalytic hydrodechlorination of 1-chlorooctadecane in supercritical carbon dioxide using 5% Pd supported on γ-Al2O3 has been reported. Incorporation of 1-chlorooctadecane into a host monolayer of stearic acid has been reported.

Application

1-Chlorooctadecane has been used as internal standard for the determination of endocrine disrupters in water samples by stir bar sorptive extraction method.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H413

Hazard Classifications

Aquatic Chronic 4 - Skin Irrit. 2

wgk_germany

WGK 1

flash_point_f

230.0 °F

flash_point_c

110 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Catalytic hydrodechlorination of 1-chlorooctadecane, 9, 10-dichlorostearic acid, and 12, 14-dichlorodehydroabietic acid in supercritical carbon dioxide.
Aikawa B, et al.
Applied Catalysis. B, Environmental, 43(4), 371-387 (2003)
A Peñalver et al.
Journal of chromatography. A, 1007(1-2), 1-9 (2003-08-20)
Stir bar sorptive extraction (SBSE) combined with gas chromatography (GC) with mass spectrometric detection (MS) has been applied to determine a group of suspected endocrine disrupters in water samples. One centimeter stir bars coated with PDMS were used to extract
The production of stable monolayers from nonamphiphilic 1-chlorooctadecane.
Peters A and Rogers K.
Journal of Colloid and Interface Science, 157(2), 511-512 (1993)
Elisabeth Aubert et al.
Lipids, 39(1), 75-79 (2004-04-02)
The lipids of the gram-negative marine bacterium Marinobacter hydrocarbonoclasticus, cultivated in synthetic seawater supplemented with 1-chlorooctadecane as sole source of carbon, were isolated, purified, and their structures determined. Three pools of lipids were isolated according to the sequential procedure used:
G L Murphy et al.
Journal of bacteriology, 156(3), 1158-1164 (1983-12-01)
The cellular fatty acid composition of Mycobacterium vaccae JOB5 and Mycobacterium convolutum R22 was examined after growth on n-alkanes and compared with the fatty acids of the organisms after growth on 1-chlorohexadecane and 1-chlorooctadecane. Growth on n-alkanes resulted in normal
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