64118-19-0 Usage
Description
N-Pentyl-5,5,5-d3 Alcohol, with the CAS number 64118-19-0, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. Its unique isotopic labeling allows for the tracking and analysis of specific chemical reactions and processes, making it a valuable tool in the field of research.
Uses
Used in Research and Development:
N-Pentyl-5,5,5-d3 Alcohol is used as a research compound for the study of chemical reactions and processes. Its isotopic labeling enables scientists to track and analyze specific pathways and mechanisms, providing valuable insights into the behavior of molecules and their interactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-Pentyl-5,5,5-d3 Alcohol is used as a labeled compound for the development and testing of new drugs. Its unique properties allow researchers to study the effects of these drugs on biological systems, helping to identify potential therapeutic applications and optimize drug design.
Used in Chemical Synthesis:
N-Pentyl-5,5,5-d3 Alcohol is also used as a labeled building block in the synthesis of various chemical compounds. Its isotopic labeling can help researchers identify and isolate specific products, facilitating the development of new materials and chemicals with tailored properties.
Used in Analytical Chemistry:
In analytical chemistry, N-Pentyl-5,5,5-d3 Alcohol serves as a labeled reference material for the calibration and validation of analytical instruments and methods. Its unique isotopic signature allows for accurate quantification and identification of target compounds, improving the reliability and accuracy of analytical results.
Used in Environmental Studies:
N-Pentyl-5,5,5-d3 Alcohol can be employed in environmental studies as a labeled tracer to track the fate and transport of pollutants or contaminants in various ecosystems. Its isotopic labeling enables researchers to monitor the behavior of these substances in the environment, providing valuable information for the development of effective remediation strategies.
Used in Biomedical Research:
In biomedical research, N-Pentyl-5,5,5-d3 Alcohol is used as a labeled compound for studying cellular processes and mechanisms. Its isotopic labeling allows researchers to investigate the interactions of biological molecules and their role in various physiological and pathological processes, contributing to a better understanding of human health and disease.
Check Digit Verification of cas no
The CAS Registry Mumber 64118-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,1 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64118-19:
(7*6)+(6*4)+(5*1)+(4*1)+(3*8)+(2*1)+(1*9)=110
110 % 10 = 0
So 64118-19-0 is a valid CAS Registry Number.
64118-19-0Relevant articles and documents
Raman spectroscopy of n-pentyl methyl ether and deuterium labelledanalogues
Bowen, Richard D.,Edwards, Howell G. M.,Farwell, Dennis W.,Morgan, Sara E
experimental part, p. 1725 - 1734 (2012/04/04)
The Raman spectra of n-pentyl methyl ether, C5H 11OCH3, and six selectively deuteriated analogues arereported and discussed. Correlations between the observed ν(sp 3CH)stretching and bending bands and the position of the deuterium atoms in thealkyl chain are developed and refined. Similar progress is possible inassociating specific skeletal vibrations with bands in the Raman spectra. Therelevance of this study to improving the assignment of bands in the Ramanspectra of larger systems of biological interest is highlighted. Copyright
H-D Exchange Reaction of 2-Thiophenecarboxylic Acids and Convenient Synthesis of Valeric Acid with Ni-Al Alloy in Alkaline Deuterium Oxide
Tsuzuki, Hirohisa,Mukumoto, Mamoru,Mataka, Shuntaro,Yonemitsu, Tadashi,Tashiro, Masashi
, p. 1046 - 1058 (2007/10/02)
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Studies on the the metabolism of unsaturated fatty acids. VI. Stereochemical studies of the reaction catalyzed by cis-2-enoyl-coenzyme A reductase of escherichia coli.
Mizugaki,Unuma,Nishimaki,Shiraishi,Kawaguchi,Saito,Okuda,Yamanaka
, p. 2155 - 2160 (2007/10/02)
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