241157-06-2 Usage
Uses
Used in Research and Development:
GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as an isotopically labeled compound for various research purposes. The expression is: GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as a research compound for [application reason].
Used in Pharmaceutical Industry:
In the pharmaceutical industry, GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as a research compound for studying the effects of deuterium labeling on the pharmacokinetics, pharmacodynamics, and metabolic pathways of related drug molecules. The expression is: Used in Pharmaceutical Industry, GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as a research compound for investigating the impact of deuterium labeling on drug behavior and metabolism.
Used in Chemical Industry:
In the chemical industry, GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as a research compound for understanding the synthesis, properties, and applications of isotopically labeled triglycerides. The expression is: Used in Chemical Industry, GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as a research compound for exploring the synthesis and characteristics of isotopically labeled triglycerides.
Used in Material Science:
In material science, GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as a research compound for examining the structural and mechanical properties of isotopically labeled materials, which can be useful in the development of new materials with enhanced properties. The expression is: Used in Material Science, GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as a research compound for studying the structural and mechanical properties of isotopically labeled materials.
Used in Analytical Chemistry:
In analytical chemistry, GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as a research compound for developing and validating analytical methods, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy, which can provide insights into the molecular structure and interactions of isotopically labeled compounds. The expression is: Used in Analytical Chemistry, GLYCERYL TRI(HEXADECANOATE-2,2-D2) is used as a research compound for method development and validation in mass spectrometry and NMR spectroscopy.
Check Digit Verification of cas no
The CAS Registry Mumber 241157-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,1,1,5 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 241157-06:
(8*2)+(7*4)+(6*1)+(5*1)+(4*5)+(3*7)+(2*0)+(1*6)=102
102 % 10 = 2
So 241157-06-2 is a valid CAS Registry Number.
241157-06-2Relevant academic research and scientific papers
Neutron diffraction of deuterated tripalmitin and the influence of shear on its crystallisation
Stuart,Maynard-Casely,Booth,Leung,Thomas
, p. 108 - 113 (2019/04/08)
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.
