Stearoyl chloride

Stearoyl chloride Structure
Stearoyl chloride structure
Common Name Stearoyl chloride
CAS Number 112-76-5 Molecular Weight 302.923
Density 0.9±0.1 g/cm3 Boiling Point 347.8±5.0 °C at 760 mmHg
Molecular Formula C18H35ClO Melting Point 21-22 °C(lit.)
MSDS Chinese USA Flash Point 169.8±8.0 °C
Symbol GHS05
GHS05
Signal Word Danger

Incorporation of chemically modified proteins into liposomes.

Acta Biol. Med. Ger. 40(3) , 331-5, (1981)

Enzymes, not anchored into bilayers of membranes like trypsin, alpha-chymotrypsin, and carboxypeptidase A are chemically modified by acylation with fatty acids chlorides. This treatment renders these proteins hydrophobic so that they can combine with the phos...

Encapsulation of fish oil with N-stearoyl O-butylglyceryl chitosan using membrane and ultrasonic emulsification processes.

Carbohydr. Polym. 123 , 432-42, (2015)

Fish oil-loaded microcapsules were prepared from oil-in-water emulsions using N-stearoyl O-butylglyceryl chitosan as shell material. The emulsions were prepared by both membrane and ultrasonic emulsification processes under variable conditions to examine the ...

A new and efficient strategy for the synthesis of shimofuridin analogs: 2'-O-(4-O-stearoyl-alpha-L-fucopyranosyl)thymidine and -uridine.

Carbohydr. Res. 338(1) , 55-60, (2003)

Two shimofuridin analogs: 2'-O-(4-O-stearoyl-alpha-L-fucopyranosyl)thymidine (2) and -uridine (3) have been synthesized using D-arabinose, L-fucose, thymine, uracil, and stearoyl chloride as the starting materials. The synthetic procedures involve the facile ...

Stereoselective synthesis of (2S,3S,4Z)-4-fluoro-1,3-dihydroxy-2-(octadecanoylamino)octadec-4-ene, [(Z)-4-fluoroceramide], and its phase behavior at the air/water interface.

Beilstein J. Org. Chem. 4 , 12, (2008)

Sphingolipids belong to the most important constituents of the membranes of eukaryotic cells. As intermediates in sphingolipid metabolism, sphingosine and its N-octadecanoyl-derivative, ceramide, exhibit a variety of biological functions. These compounds play...

Effective inhibition of viral reproduction by hydrophobised antiviral antibodies.

Biomed. Sci. 1(1) , 63-7, (1990)

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 exp...

[Chemical modification of proteins (enzymes) by water-insoluble reagents].

Dokl. Akad. Nauk. SSSR 278(1) , 246-8, (1984)

Incorporation of chemically modified (hydrophobized) ferritin in liposomal membranes: electron microscopic studies.

Biomed. Biochim. Acta 43(7) , 963-9, (1984)

The assembly of electron dense ferritin modified by acylation with steaorylchloride into small and large egg lecithin vesicles is reported. From electron micrographs conclusions are drawn: on the mode of ferritin incorporation in the lipid bilayer: Small lipo...