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3-(Octadecylsulfanyl)propane-1,2-diol is a complex organic compound with the chemical formula C21H44O2S. It is a derivative of propane-1,2-diol, where one of the hydroxyl groups is replaced by an octadecylsulfanyl group. 3-(octadecylsulfanyl)propane-1,2-diol is characterized by a long aliphatic chain (octadecyl) attached to the propane-1,2-diol backbone through a sulfur atom. It is known for its surfactant properties, which means it can lower the surface tension between two liquids, a property that makes it useful in various industrial applications such as detergents, emulsifiers, and stabilizers. The compound's amphiphilic nature, with a hydrophilic head (the diol part) and a hydrophobic tail (the octadecyl chain), allows it to interact with both water and oils, facilitating the mixing of otherwise immiscible substances.

7400-44-4

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7400-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7400-44-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7400-44:
(6*7)+(5*4)+(4*0)+(3*0)+(2*4)+(1*4)=74
74 % 10 = 4
So 7400-44-4 is a valid CAS Registry Number.

7400-44-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-octadecylsulfanylpropane-1,2-diol

1.2 Other means of identification

Product number -
Other names 1-S-octadecyl-rac-thioglycerol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7400-44-4 SDS

7400-44-4Relevant academic research and scientific papers

Nucleoside Conjugates. 13. Synthesis and Antitumor Activity of 1-β-D-Arabinofuranosylcytosine Conjugates of Thioether Lipids with Improved Water Solubility

Hong, Chung Il,Nechaev, Alexander,Kirisits, Alan J.,Vig, Rakesh,West, Charles R.

, p. 1785 - 1790 (2007/10/02)

A series of ara-CDP-rac-1-S-alkyl-2-O-acyl-1-thioglycerols (3-12), analogues of highly active Cytoros (1), was prepared, and solubility, lipophilicity, and structure-activity relationships of these conjugates were investigated.The conjugates with sn-1 alk

Nucleoside conjugates. 11. Synthesis and antitumor activity of 1-β-D-arabinofuranosylcytosine and cytidine conjugates of thioether lipids

Il Hong,Kirisits,Nechaev,Buchheit,West

, p. 1380 - 1386 (2007/10/02)

Five 1-β-D-arabinofuranosylcytosine conjugates and two cytidine conjugates of thioether lipids (1-S-alkylthioglycerols) linked by a pyrophosphate diester bond have been prepared and their antitumor activity against an ara-C2 sensitive (L1210/0)

SYNTHESE DE LA d,l-(ACETOXY-2 OCTADECYLTHIO-1) PROPYL-3 PHOSPHORYLCHOLINE OU THIA-PAF

Garrigues, Bernard,Bertrand, Guy,Frehel, Daniel,Maffrand, Jean-Pierre

, p. 171 - 176 (2007/10/02)

d,l-thia-PAF 2 was synthesised using a selective method of protection (ClSiMe2t-Bu) and deprotection (BF3-Et2O) of the primary alcohol function.This method could be used with advantage in the syn

SYNTHESIS OF ALKYLTHIOGLYCEROLS AND THEIR DIACYL DERIVATIVES

Malina, E.V.,Serebrennikova, G.A.,Evstigneeva, R.P.

, p. 840 - 841 (2007/10/02)

1-Hexadecylthio-rac-glycerol and 1-octadecylthio-rac-glycerol were synthesized by the reaction of 1-bromo-1-deoxy-2,3-isopropylidene-rac-glycerol and higher alkanethiols with subsequent removal of the isopropylidene protection. 1-Hexadecylthio-2,3-dipalmitoyl-rac-glycerol and 1-hexadecylthio-2,3-distearoyl-rac-glycerol were also obtained directly from 1-hexadecylthio-2,3-isopropylidene-rac-glycerol and palmitoyl and stearoyl chlorides.

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