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245623

Sigma-Aldrich

1-Chlorohexadecane

95%

Synonym(s):

Cetyl chloride, Hexadecyl chloride

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About This Item

Linear Formula:
CH3(CH2)15Cl
CAS Number:
4860-03-1
Molecular Weight:
260.89
Beilstein:
1748498
EC Number:
225-461-7
MDL number:
MFCD00000959
UNSPSC Code:
12352100
PubChem Substance ID:
24854746
NACRES:
NA.22

vapor pressure

129 mmHg ( 21 °C)

Quality Level

200

Assay

95%

form

liquid

refractive index

n20/D 1.449 (lit.)

bp

149 °C/1 mmHg (lit.)

mp

8-14 °C (lit.)

density

0.865 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCCCl

InChI

1S/C16H33Cl/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h2-16H2,1H3

InChI key

CLWAXFZCVYJLLM-UHFFFAOYSA-N

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General description

The electron impact mass spectra of 1-chlorohexadecane was studied by sampling with supersonic molecular beams.

WGK

WGK 3

Flash Point(F)

276.8 °F

Flash Point(C)

136 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

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S Dagan et al.
Journal of the American Society for Mass Spectrometry, 6(2), 120-131 (1995-02-01)
The electron impact mass spectrometry of straight chain alkanes C8H18-C40H82, squalane, methylstearate, 1-chlorohexadecane, 1-bromohexadecane, and dioctylphthalate was studied by sampling them with supersonic molecular beams. A fly-through Brink-type electron impact ion source was used, utilizing a vacuum background ion filtration
G L Murphy et al.
Applied and environmental microbiology, 53(1), 10-13 (1987-01-01)
The composition of phospholipids from Mycobacterium convolutum R22 was determined after growth at two temperatures (20 and 30 degrees C) with 1-chlorohexadecane as the substrate. Comparisons were made with the phospholipids of cells grown on n-hexadecane. Phosphatidylinositolmannosides and phosphatidylethanolamine (PE)
K Koike et al.
Applied and environmental microbiology, 65(12), 5636-5638 (1999-12-03)
A mutant Rhodococcus strain lacking the ability to utilize 1-chlorohexadecane was found to cis-desaturate aliphatic compounds, such as 1-chlorohexadecane, n-hexadecane, and heptadecanonitrile, yielding corresponding products with a double bond mainly at the ninth carbon from the terminal methyl groups. A
Nicolas Goujon et al.
Physical chemistry chemical physics : PCCP, 17(35), 23059-23068 (2015-08-15)
The development of new polymerizable lyotropic liquid crystals (LLCs) utilizing charged amphiphilic molecules such as those based on long chain imidazolium compounds, is a relatively new design direction for producing robust membranes with controllable nano-structures. Here we have developed a
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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