1219799-18-4 Usage
Description
n-Hexadecyl--d5 Alcohol, also known as n-Hexadecyl-2,2,16,16,16-d5 Alcohol (CAS# 1219799-18-4), is an isotopically labeled research compound. It is a deuterated version of n-Hexadecyl alcohol, which means it contains deuterium atoms instead of regular hydrogen atoms. This characteristic makes it valuable for various research applications, particularly in the field of chemistry and biochemistry.
Uses
Used in Research Applications:
n-Hexadecyl--d5 Alcohol is used as a research compound for various scientific investigations. The expression is: n-Hexadecyl--d5 Alcohol is used as a research compound for [application reason].
Used in Chemical Reactions:
In the field of chemistry, n-Hexadecyl--d5 Alcohol is used as a reactant or a starting material in specific chemical reactions. The deuterium labeling allows researchers to track the behavior of the molecule and study the reaction mechanisms in greater detail. The expression is: n-Hexadecyl--d5 Alcohol is used as a reactant in [specific chemical reaction] for [application reason].
Used in Biochemical Studies:
In biochemistry, n-Hexadecyl--d5 Alcohol can be employed as a labeled substrate or a probe to study enzyme kinetics, metabolic pathways, and protein-ligand interactions. The deuterium labeling provides a unique tool for investigating these biological processes without interference from endogenous compounds. The expression is: n-Hexadecyl--d5 Alcohol is used as a labeled substrate/probe in biochemical studies for [application reason].
Used in Analytical Techniques:
n-Hexadecyl--d5 Alcohol can also be utilized in various analytical techniques, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. The deuterium labeling enhances the detection and differentiation of the compound from other similar molecules, providing more accurate and reliable results. The expression is: n-Hexadecyl--d5 Alcohol is used in [analytical technique] for [application reason].
Used in Pharmaceutical Research:
In the pharmaceutical industry, n-Hexadecyl--d5 Alcohol may be used as a reference compound or a building block for the synthesis of new drug candidates. The isotopically labeled nature of the compound can help in understanding the pharmacokinetics, pharmacodynamics, and potential side effects of the drug under development. The expression is: n-Hexadecyl--d5 Alcohol is used as a reference compound/building block in pharmaceutical research for [application reason].
Used in Material Science:
n-Hexadecyl--d5 Alcohol can be employed in the field of material science for studying the properties of deuterated materials and their potential applications in various industries. The deuterium labeling can provide insights into the structural and mechanical properties of these materials, leading to the development of new materials with improved performance. The expression is: n-Hexadecyl--d5 Alcohol is used in material science research for [application reason].
Check Digit Verification of cas no
The CAS Registry Mumber 1219799-18-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,7,9 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1219799-18:
(9*1)+(8*2)+(7*1)+(6*9)+(5*7)+(4*9)+(3*9)+(2*1)+(1*8)=194
194 % 10 = 4
So 1219799-18-4 is a valid CAS Registry Number.
1219799-18-4Relevant 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.
