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Octadecanoic acid, 3-hydroxy-2-[(1-oxohexadecyl)oxy]propyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14015-55-5

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14015-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14015-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,1 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14015-55:
(7*1)+(6*4)+(5*0)+(4*1)+(3*5)+(2*5)+(1*5)=65
65 % 10 = 5
So 14015-55-5 is a valid CAS Registry Number.

14015-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-hexadecanoyloxy-3-hydroxypropyl) octadecanoate

1.2 Other means of identification

Product number -
Other names 1,2,3-Propanetriol hexadecanoate octadecanoate

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:14015-55-5 SDS

14015-55-5Downstream Products

14015-55-5Relevant academic research and scientific papers

Interesterification Kinetics of Triglycerides and Fatty Acids with Modified Lipase in n-Hexane

Basheer, Sobhi,Mogi, Ken-ichi,Nakajima, Mitsutoshi

, p. 511 - 518 (2007/10/02)

The kinetics of lipase-catalyzed interesterification of triglycerides and fatty acids in organic media was studied.First, the lipase Saiken 100, Rhizopus japonicus, was modified by surfactant to form an enzyme precipitate in aqueous solution, which was well dispersed in organic solvents.This modified lipase catalyzed the interesterification of tripalmitin and stearic acid.The enzyme has 1,3-positional specificity and does not distinguish between stearic and palmitic acids.The kinetic model developed to describe the interesterification reaction system is based on mass balance of two consecutive second-order reversible reactions.The reaction rate constant, k, was determined by solving the differential rate equations of the reaction system and by expressing the value of k as a function of concentrations of the substrates with time.The model gave satisfactory results.The best value of the specific reaction rate constant k* that fits all experimental data was 1.2*10-5 2/(mmol*mg biocatalyst*h)> under the reaction conditions in this study. Key words: Acidolysis, biocatalyst, fatty acids, interesterification kinetics, modified lipase, palmitic acid, reaction rate constant, stearic acid, triglycerides.

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