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34227-83-3

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34227-83-3 Usage

Definition

ChEBI: A dihydroceramide in which the ceramide N-acyl group is specified as (9Z)-octadecenoyl (oleoyl).

Check Digit Verification of cas no

The CAS Registry Mumber 34227-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,2 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34227-83:
(7*3)+(6*4)+(5*2)+(4*2)+(3*7)+(2*8)+(1*3)=103
103 % 10 = 3
So 34227-83-3 is a valid CAS Registry Number.
InChI:InChI=1/C36H71NO3/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-36(40)37-34(33-38)35(39)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h17-18,34-35,38-39H,3-16,19-33H2,1-2H3,(H,37,40)/b18-17-/t34-,35+/m0/s1

34227-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-N-[(2S,3R)-1,3-dihydroxyoctadecan-2-yl]octadec-9-enamide

1.2 Other means of identification

Product number -
Other names C18:1 Sphinganine

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:34227-83-3 SDS

34227-83-3Downstream Products

34227-83-3Relevant articles and documents

PROCESS FOR PREPARING SPHINGOLIPIDS

-

Paragraph 0108; 0112, (2019/10/23)

The invention provides a process for preparing sphingolipids, compositions comprising sphingolipids and further components, and for the use of the compositions.

Method of making primary amide derivative

-

, (2008/06/13)

A method of selective N-acylation of an aminodiol having a primary alcoholic hydroxyl group and a secondary alcoholic hydroxyl group, in which the objective product can be prepared in high yield and without troublesome extraction and purification operations. More particularly, a method of making a primary amide derivative represented by the following general formula (3) is disclosed: STR1 wherein R1 represents a linear saturated aliphatic hydrocarbon group having 11 to 19 carbon atoms, R2 represents a linear saturated or unsaturated aliphatic hydrocarbon group having 9 to 19 carbon atoms which may have a hydroxyl group at the 1-position, which includes the steps of reacting an aminodiol represented by the following general formula (1): STR2 wherein R1 is the same as R1 in general formula (3) with a fatty acid alkyl ester represented by the following general formula (2): wherein R2 is the same as R2 in general formula (3) and R3 represents a lower alkyl group, in a reaction system comprising an alcoholic solvent and in the presence of a basic catalyst, said reacting step forming a lower alcohol as a by-product; and removing the lower alcohol formed during the reaction from the reaction system.

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