284474-73-3 Usage
Description
N-HEXADECYL-D33 ALCOHOL, with the CAS# 284474-73-3, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a derivative of n-hexadecyl alcohol, which has been enriched with deuterium (D33), a stable isotope of hydrogen. This enrichment allows for enhanced detection and tracing capabilities in research settings.
Uses
Used in Research and Development:
N-HEXADECYL-D33 ALCOHOL is used as a research compound for [application reason] in the field of [application industry]. The deuterium labeling provides a unique signature that can be easily distinguished from its non-deuterated counterpart, making it valuable for studying metabolic pathways, reaction mechanisms, and other biochemical processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-HEXADECYL-D33 ALCOHOL is used as a labeled compound for [application reason], such as in the development of new drugs or the study of drug metabolism. The isotopically labeled compound can help researchers understand the behavior of the drug in the body and its interactions with biological systems.
Used in Analytical Chemistry:
N-HEXADECYL-D33 ALCOHOL is used as a labeled standard for [application reason] in analytical chemistry. N-HEXADECYL-D33 ALCOHOL can be employed to calibrate instruments, validate analytical methods, and ensure the accuracy of measurements in various chemical analyses.
Used in Biomedical Research:
In biomedical research, N-HEXADECYL-D33 ALCOHOL is used as a tracer molecule for [application reason], such as studying the transport and distribution of lipids in cells or investigating the effects of drugs on cellular lipid metabolism.
Used in Environmental Science:
N-HEXADECYL-D33 ALCOHOL is used as an isotopically labeled tracer for [application reason] in environmental science. It can be employed to track the fate and transport of pollutants in the environment or to study the bioaccumulation of contaminants in organisms.
Used in Material Science:
In material science, N-HEXADECYL-D33 ALCOHOL is used as a labeled additive for [application reason], such as in the development of new materials with enhanced properties or the study of the interaction between materials and biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 284474-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,4,4,7 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 284474-73:
(8*2)+(7*8)+(6*4)+(5*4)+(4*7)+(3*4)+(2*7)+(1*3)=173
173 % 10 = 3
So 284474-73-3 is a valid CAS Registry Number.
284474-73-3Relevant articles and documents
Inter- and intramolecular temperature-dependent vibrational perturbations of alkanethiol self-assembled monolayers
Garand, Eì?tienne,Picard, Jean-Francì§ois,Rowntree, Paul
, p. 8182 - 8189 (2007/10/03)
The infrared spectra of octanethiol, dodecanethiol, and hexadecanethiol (C8, C12, and C16, respectively) monolayers adsorbed on Au(111) textured surfaces have been explored in the 25-300 K regime. The C-H stretching modes typically shift by several wavenumbers to lower frequencies and the intensities increase by as much as 75% as the temperature is decreased, providing evidence of, among other effects, the coupling of these stretching modes with lower energy vibrational modes. In contrast, for all temperatures below 300 K, the positions of the C-H bands of fully hydrogenated C16, shift by several wavenumbers to higher frequencies as the hydrogenated adsorbates are increasingly diluted in a matrix of fully deuterated C16, showing that all bands are subject to intermolecular couplings. The analysis of the behavior of the C-H stretching bands suggests that the temperature dependence of the vibrational frequencies associated with the methylene stretching modes is principally due to intermolecular couplings, whereas the temperature dependence of the vibrations associated with the methyl terminations is largely due to intramolecular couplings. It is suggested that the highly constrained geometry of the isotopically diluted monolayer may provide an environment that is less sensitive to intramolecular couplings with low-frequency modes than that of urea-clathrate-isolated species.
