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1-HEXADECANOYL-3-OCTADECANOYL-RAC-GLYCEROL, also known as 1-Palmitoyl-3-stearoylglycerol, is a type of glycerol molecule that is composed of a glycerol backbone with one palmitic acid and one stearic acid chain attached to it. This molecule is a component of various lipids and has specific applications in different industries due to its unique structure and properties.

17708-08-6

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17708-08-6 Usage

Uses

Used in Pharmaceutical Industry:
1-HEXADECANOYL-3-OCTADECANOYL-RAC-GLYCEROL is used as an ingredient in the formulation of orally disintegrating tablets for telmisartan (T017000). The molecule plays a crucial role in enhancing the stability, solubility, and bioavailability of the drug, allowing for faster and more efficient absorption in the body.

Check Digit Verification of cas no

The CAS Registry Mumber 17708-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,0 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17708-08:
(7*1)+(6*7)+(5*7)+(4*0)+(3*8)+(2*0)+(1*8)=116
116 % 10 = 6
So 17708-08-6 is a valid CAS Registry Number.

17708-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-HEXADECANOYL-3-OCTADECANOYL-RAC-GLYCEROL

1.2 Other means of identification

Product number -
Other names 1-pelmitoyl 3-stearoyl glycerol

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:17708-08-6 SDS

17708-08-6Relevant 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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