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13057-50-6

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13057-50-6 Usage

Purification Methods

Crystallise the laurate from Me2CO, Et2O or pet ether. [Breusch & Oguzer Chem Ber 88 1511 1955.]

Check Digit Verification of cas no

The CAS Registry Mumber 13057-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,5 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13057-50:
(7*1)+(6*3)+(5*0)+(4*5)+(3*7)+(2*5)+(1*0)=76
76 % 10 = 6
So 13057-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C53H100O8/c1-5-9-13-17-21-25-29-33-37-41-49(54)58-45-53(46-59-50(55)42-38-34-30-26-22-18-14-10-6-2,47-60-51(56)43-39-35-31-27-23-19-15-11-7-3)48-61-52(57)44-40-36-32-28-24-20-16-12-8-4/h5-48H2,1-4H3

13057-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-dodecanoyloxy-2,2-bis(dodecanoyloxymethyl)propyl] dodecanoate

1.2 Other means of identification

Product number -
Other names Dodecanoic acid,1,1'-(2,2-bis(((1-oxododecyl)oxy)methyl)-1,3-propanediyl) ester

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:13057-50-6 SDS

13057-50-6Downstream Products

13057-50-6Relevant articles and documents

A simple and convenient one-pot synthesis of fatty acid esters from hindered alcohols using N,N-dimethylchloro-sulfitemethaniminium chloride as dehydrating agent

Kaul, Savita,Kumar, Ajay,Sain, Bir,Gupta

, p. 2885 - 2891 (2007/10/03)

N,N-Dimethylchlorosulfitemethaniminium chloride (SOCl2-DMF) has been found to be an efficient reagent for one-pot synthesis of esters from equimolar amounts of fatty acids and hindered alcohols under mild conditions.

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