62163-39-7 Usage
Description
Octadecanoic-18,18,18-D3 Acid, with the CAS number 62163-39-7, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. OCTADECANOIC-18,18,18-D3 ACID is characterized by its stable isotope labeling, which allows for enhanced tracking and analysis of its behavior in biological systems.
Uses
Used in Research Applications:
Octadecanoic-18,18,18-D3 Acid is used as a research compound for its isotopically labeled properties, which enable scientists to study metabolic pathways, enzymatic reactions, and other biological processes with greater precision and accuracy. The stable isotope labeling aids in distinguishing this compound from its naturally occurring counterparts, thus facilitating detailed investigations into its interactions within complex biological systems.
Used in Analytical Chemistry:
In the field of analytical chemistry, Octadecanoic-18,18,18-D3 Acid serves as a valuable tool for the development and validation of analytical methods. Its isotopically labeled nature allows for the accurate quantification of the compound in samples, even in the presence of other similar molecules. This is particularly useful in environmental monitoring, food analysis, and pharmaceutical research, where precise measurement and identification are crucial.
Used in Pharmaceutical Development:
Octadecanoic-18,18,18-D3 Acid is employed in the pharmaceutical industry as a labeled analog of octadecanoic acid (stearic acid), which can be used to study drug metabolism, distribution, and excretion. OCTADECANOIC-18,18,18-D3 ACID can also be incorporated into drug formulations as a tracer to monitor the effectiveness of drug delivery systems and to optimize their design for improved therapeutic outcomes.
Used in Metabolic Studies:
In metabolic research, Octadecanoic-18,18,18-D3 Acid is utilized to investigate the metabolism of fatty acids and their role in various physiological and pathological conditions. The isotopically labeled compound provides a means to track its metabolic fate within organisms, offering insights into the regulation of lipid metabolism and its implications for health and disease.
Used in Nutritional Science:
In nutritional science, Octadecanoic-18,18,18-D3 Acid is used to study the消化吸收, utilization, and metabolic effects of fatty acids in the human body. The stable isotope labeling allows researchers to monitor the compound's impact on lipid profiles, energy metabolism, and overall health, contributing to a better understanding of dietary fat intake and its implications for wellness and disease prevention.
Check Digit Verification of cas no
The CAS Registry Mumber 62163-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,6 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62163-39:
(7*6)+(6*2)+(5*1)+(4*6)+(3*3)+(2*3)+(1*9)=107
107 % 10 = 7
So 62163-39-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h2-17H2,1H3,(H,19,20)/i1D3
62163-39-7Relevant articles and documents
Synthesis of ceramides NS and NP with perdeuterated and specifically ω deuterated N-acyl residues
Sonnenberger, Stefan,Lange, Stefan,Langner, Andreas,Neubert, Reinhard H.H.,Dobner, Bodo
, p. 531 - 542 (2016/11/06)
The synthesis of 12 deuterated ceramides with either a deuteration at the last carbon atom of the amide bound fatty acid or a perdeuterated fatty acid chain is described. The ceramides were prepared starting from sphingosine or phytosphingosine and ω deuterated or perdeuterated fatty acids with PyBOP as activating agent in high yields. For the synthesis of the specifically deuterated fatty acids, dicarboxylic acids were transformed into ω deuterated alkyl bromide, which was chain elongated with blocked ω bromo alcohols by copper catalyzed Grignard coupling. Oxidation of regenerated alcohol function yields the ω deuterated fatty acids.
