241157-04-0 Usage
Description
GLYCERYL TRI(HEXADECANOATE-D31), also known as Glyceryl Tri(hexadecanoate-d31), is an isotopically labeled research compound with the CAS number 241157-04-0. It is a derivative of glyceryl tristearate, where the hydrogen atoms in the stearate chains are replaced with deuterium atoms. GLYCERYL TRI(HEXADECANOATE-D31) is primarily used in scientific research and development for various applications due to its unique isotopic properties.
Uses
Used in Research and Development:
GLYCERYL TRI(HEXADECANOATE-D31) is used as a research compound for studying the properties and behavior of isotopically labeled molecules in various chemical and biological processes. The presence of deuterium atoms in the molecule allows for better understanding of the effects of isotopic substitution on molecular interactions, stability, and reactivity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, GLYCERYL TRI(HEXADECANOATE-D31) is used as a labeled compound for the development and optimization of drug delivery systems. The isotopically labeled nature of the compound can help researchers investigate the pharmacokinetics, biodistribution, and metabolic fate of similar drug molecules, ultimately leading to the design of more effective and safer therapeutics.
Used in Cosmetics Industry:
GLYCERYL TRI(HEXADECANOATE-D31) can be used as a labeled compound in the cosmetics industry for studying the absorption, distribution, and effectiveness of skincare products. The isotopic labeling allows for better tracking and understanding of the compound's behavior when applied to the skin, which can help in the development of more effective and targeted cosmetic formulations.
Used in Analytical Chemistry:
In analytical chemistry, GLYCERYL TRI(HEXADECANOATE-D31) serves as a valuable tool for the development and validation of analytical methods, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. The isotopically labeled compound can be used as an internal standard or a reference material to improve the accuracy and precision of these analytical techniques, particularly in the study of complex biological samples.
Used in Environmental Science:
GLYCERYL TRI(HEXADECANOATE-D31) can be employed in environmental science as a labeled compound for tracing the fate and transport of similar organic compounds in the environment. The isotopic labeling allows for the differentiation between naturally occurring and anthropogenic sources of these compounds, providing valuable insights into their environmental impact and potential risks to ecosystems and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 241157-04-0 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 241157-04:
(8*2)+(7*4)+(6*1)+(5*1)+(4*5)+(3*7)+(2*0)+(1*4)=100
100 % 10 = 0
So 241157-04-0 is a valid CAS Registry Number.
241157-04-0Relevant 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 (2019/04/08)
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.
