Skip to Content
Merck
All Photos(3)

Key Documents

View All Documentation

367850

Sigma-Aldrich

Oleoyl chloride

≥89%

Synonym(s):

(9Z)-9-Octadecenoyl chloride, (Z)-9-Octadecenoyl chloride, 9-(Z)-Octadecen-1-oyl chloride, Oleic acid chloride, Oleic chloride, Oleyl chloride, cis-9-Octadecenoyl chloride

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
CH3(CH2)7CH=CH(CH2)7COCl
CAS Number:
112-77-6
Molecular Weight:
300.91
Beilstein:
1211748
EC Number:
204-005-0
MDL number:
MFCD00134332
UNSPSC Code:
12352100
PubChem Substance ID:
24862853
NACRES:
NA.22

Assay

≥89%

form

liquid

refractive index

n20/D 1.463 (lit.)

bp

193 °C/4 mmHg (lit.)

density

0.91 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCC\C=C/CCCCCCCC(Cl)=O

InChI

1S/C18H33ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h9-10H,2-8,11-17H2,1H3/b10-9-

InChI key

MLQBTMWHIOYKKC-KTKRTIGZSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Oleoyl chloride is a fatty acid derivative.

Application

Oleoyl chloride may be used:
  • in the chemical modification of the jute fibbers to confer hydrophobicity and resistance to biofibers
  • in the synthesis of Oleoyl-S-lipoate, via reaction with dihydrolipoate
  • in the preparation of symmetrical triglyceride, 2-oleoyl distearin
  • in the preparation of ergosteryl oleate

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

339.8 °F - closed cup

Flash Point(C)

171 °C - closed cup

Personal Protective Equipment

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

The specificity of pancreatic lipase for the primary hydroxyl groups of glycerides.
F H MATTSON et al.
The Journal of biological chemistry, 219(2), 735-740 (1956-04-01)
K Ohta et al.
Applied and environmental microbiology, 46(4), 821-825 (1983-10-01)
An exogenous ternary complex composed of Tween 80, ergosterol, and albumin increased the final ethanol concentration of fermentation by sake yeasts from 17.2 to 19.0% (vol/vol) and reduced the fermentation time from 30 to 25 days. Likewise, a complex of
D E Griffiths
The Biochemical journal, 160(3), 809-812 (1976-12-15)
ATP synthase preparations [complex V, proton-translocatin ATPase (adenosine triphosphatase) and oligomycin-sensitive ATPase ] contain stoicheiometric amounts of lipoic acid residues (up to 6mol of lipoic acid/mol of ATPase complex) and catalyse net ATP synthesis in an uncoupler-and oligomycin-sensitive reaction utilizing
F Corrales et al.
Journal of hazardous materials, 144(3), 730-735 (2007-02-27)
Natural fiber reinforced composites is an emerging area in polymer science. Fibers derived from annual plants are considered a potential substitute for non-renewable synthetic fibers like glass and carbon fibers. The hydrophilic nature of natural fibers affects negatively its adhesion
Noemi Jiménez-Rojo et al.
Current biology : CB, 30(19), 3775-3787 (2020-08-29)
Sphingolipids play important roles in physiology and cell biology, but a systematic examination of their functions is lacking. We performed a genome-wide CRISPRi screen in sphingolipid-depleted human cells and identified hypersensitive mutants in genes of membrane trafficking and lipid biosynthesis
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service