285979-78-4 Usage
Description
GLYCERYL TRI(HEXADECANOATE-16,16,16-D3), with the CAS number 285979-78-4, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a derivative of glyceryl trihexadecanoate, also known as glyceryl tristearate, which is a triglyceride consisting of three stearic acid chains attached to a glycerol molecule. The presence of deuterium (D3) in the hexadecanoate groups makes it a valuable tool for researchers to investigate the properties and behavior of this compound in different conditions.
Uses
Used in Research and Development:
GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as an isotopically labeled compound for various research purposes. The expression is: GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a research compound for [application reason].
Used in Pharmaceutical Industry:
In the pharmaceutical industry, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a research compound for the development of new drugs and therapies. The expression is: Used in Pharmaceutical Industry, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a research compound for the development of new drugs and therapies.
Used in Chemical Industry:
In the chemical industry, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a research compound for the synthesis of various chemical products and the investigation of reaction mechanisms. The expression is: Used in Chemical Industry, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a research compound for the synthesis of various chemical products and the investigation of reaction mechanisms.
Used in Material Science:
In material science, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a research compound for the development of new materials with specific properties, such as improved stability or enhanced performance. The expression is: Used in Material Science, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a research compound for the development of new materials with specific properties.
Used in Analytical Chemistry:
In analytical chemistry, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a reference compound for the calibration of analytical instruments and the validation of analytical methods. The expression is: Used in Analytical Chemistry, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a reference compound for the calibration of analytical instruments and the validation of analytical methods.
Used in Environmental Science:
In environmental science, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a tracer compound for the study of environmental processes and the monitoring of pollutants. The expression is: Used in Environmental Science, GLYCERYL TRI(HEXADECANOATE-16,16,16-D3) is used as a tracer compound for the study of environmental processes and the monitoring of pollutants.
Check Digit Verification of cas no
The CAS Registry Mumber 285979-78-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,5,9,7 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 285979-78:
(8*2)+(7*8)+(6*5)+(5*9)+(4*7)+(3*9)+(2*7)+(1*8)=224
224 % 10 = 4
So 285979-78-4 is a valid CAS Registry Number.
285979-78-4Relevant articles and documents
Neutron diffraction of deuterated tripalmitin and the influence of shear on its crystallisation
Stuart,Maynard-Casely,Booth,Leung,Thomas
, p. 108 - 113 (2019)
This neutron diffraction study of deuterated tripalmitin has provided further insight into a forensic observation of the crystallisation of lipids under high-shear conditions. To achieve this, an experimental set up was designed to enable simultaneous rheological data from a Couette cell to be recorded with neutron powder diffraction, enabling the influence of shear on the polymorph transformation on cooling to be monitored in real time. Tripalmitin was observed to directly transform from a liquid phase to a β polymorph under the influence of shear. Although the liquid to β transition was not observed to be influenced by shear rate, the degree of crystallinity, qualitatively denoted by an increase in the sharpness of the diffraction peaks, was observed at higher shear rates. Evidence is also presented that the rate of cooling influences the ordering in the β-polymorph produced in zero shear conditions.
