238368
1-Chlorooctadecane
96%
Synonym(s):
Octadecyl chloride, Stearyl chloride
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About This Item
Linear Formula:
CH3(CH2)16CH2Cl
CAS Number:
Molecular Weight:
288.94
Beilstein:
1703350
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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.)
functional group
alkyl halide
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 4 - Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
230.0 °F - closed cup
Flash Point(C)
110 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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