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85730

Sigma-Aldrich

Stearoyl chloride

technical, ≥90% (GC), strongly brown

Synonym(s):

Octadecanoyl chloride

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About This Item

Linear Formula:
CH3(CH2)16COCl
CAS Number:
112-76-5
Molecular Weight:
302.92
Beilstein:
639784
EC Number:
204-004-5
MDL number:
MFCD00000744
UNSPSC Code:
12352100
PubChem Substance ID:
57653069
NACRES:
NA.22

grade

technical

Assay

≥90% (GC)

form

liquid

color

strongly brown

refractive index

n20/D 1.454 (lit.)

bp

174-178 °C/2 mmHg (lit.)

mp

21-22 °C (lit.)

density

0.897 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCCCC(Cl)=O

InChI

1S/C18H35ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h2-17H2,1H3

InChI key

WTBAHSZERDXKKZ-UHFFFAOYSA-N

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Application

Stearoyl chloride can modify cellulose diacetate (CDA) by replacing residual free hydroxyl groups in synthesizing materials that are used to produce surgical masks, smocks and other industrial products to absorb dust and haze-fog. It can be used in the synthesis of ultrastable coaxial cable-like superhydrophobic mesh. It is also used in the synthesis of stearoyl modified chitosan as drug vehicles for paclitaxel delivery.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Supplementary Hazards

EUH014

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

329.0 °F - closed cup

Flash Point(C)

165 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Ultrastable coaxial cable-like superhydrophobic mesh with self-adaption effect: facile synthesis and oil/water separation application.
Xiao C, et al.
Journal of Material Chemistry A, 4(21), 8080-8090 (2016)
Amphiphilic nanoparticles based on poly (vinyl pyrrolidone) and stearoyl modified chitosan as drug vehicles for paclitaxel delivery.
Liu Z, et al.
Materials Letters, 185, 226-229 (2016)
Çağla Koşak Söz et al.
ACS applied materials & interfaces, 10(43), 37478-37488 (2018-10-27)
We introduce the design of Janus-type paper sheets where one side of the paper exhibits superhydrophobic properties, whereas the other side of the sheet remains hydrophilic and therefore can take up aqueous solutions by capillary wicking. Such papers are being
Acylation of Cellulose Diacetate by Stearoyl Chloride and Characterization for the Acylated Product.
Wang Q, et al.
J. Polym. Mater., 32(4) (2015)
A V Kabanov et al.
Biomedical science, 1(1), 63-67 (1990-01-01)
A method is proposed for the inhibition of viral reproduction in cells by means of fatty-acylated antiviral antibodies which, in contrast to the unmodified antibodies, have the ability to enter the cells. The potential of this technique is demonstrated in
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