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Merck
CN

238368

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854298
EC Number:
222-207-7
Beilstein/REAXYS Number:
1703350
MDL number:
MFCD00000960
Assay:
96%
Form:
liquid

Key Documents

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InChI key

VUQPJRPDRDVQMN-UHFFFAOYSA-N

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

SMILES string

CCCCCCCCCCCCCCCCCCCl

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, chloro

Quality Level

100

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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

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR4800
MKCQ9386
MKCQ6033
MKCQ0592
MKCM3280

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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)
Abid Hussain et al.
Molecules (Basel, Switzerland), 25(8) (2020-04-25)
Date palm dust mites are important pests severely infesting valuable nutritious fruits (dates) of date palm. In search of an alternative to acaricides, joint action of Metarhizium anisopliae EBCL 02049 spores and 1-Chlorooctadecane was evaluated as a potential candidate for
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:
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