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352431-38-0

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352431-38-0 Usage

Description

2-ETHYLHEXANOIC-D15 ACID, with the CAS number 352431-38-0, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a deuterated version of 2-ethylhexanoic acid, which means it contains deuterium atoms instead of regular hydrogen atoms. This characteristic makes it a valuable tool for researchers to investigate the behavior and properties of molecules in different environments.

Uses

Used in Research and Development:
2-ETHYLHEXANOIC-D15 ACID is used as a research compound for studying the effects of isotopic labeling on the chemical and physical properties of molecules. The application reason is to enhance the understanding of molecular interactions, reaction mechanisms, and the behavior of compounds in various conditions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-ETHYLHEXANOIC-D15 ACID is used as a labeled compound for the development and testing of new drugs. The application reason is to facilitate the study of drug metabolism, pharmacokinetics, and pharmacodynamics, which are crucial for the design and optimization of drug candidates.
Used in Chemical Industry:
2-ETHYLHEXANOIC-D15 ACID is employed in the chemical industry as a labeled reference material for the calibration and validation of analytical instruments. The application reason is to ensure the accuracy and reliability of measurements in various chemical processes and quality control procedures.
Used in Environmental Science:
In environmental science, 2-ETHYLHEXANOIC-D15 ACID is used as a tracer compound for tracking the fate and transport of pollutants in the environment. The application reason is to provide insights into the behavior of contaminants and their potential impact on ecosystems and human health.
Used in Material Science:
2-ETHYLHEXANOIC-D15 ACID is utilized in material science as a labeled additive for studying the properties and performance of materials at the molecular level. The application reason is to improve the design and development of advanced materials with specific characteristics and functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 352431-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,4,3 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 352431-38:
(8*3)+(7*5)+(6*2)+(5*4)+(4*3)+(3*1)+(2*3)+(1*8)=120
120 % 10 = 0
So 352431-38-0 is a valid CAS Registry Number.

352431-38-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,3,4,4,5,5,6,6,6-decadeuterio-2-(1,1,2,2,2-pentadeuterioethyl)hexanoic acid

1.2 Other means of identification

Product number -
Other names 2-Ethylhexanoic-d15 acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:352431-38-0 SDS

352431-38-0Upstream product

352431-38-0Downstream Products

352431-38-0Relevant articles and documents

2D-NMR strategy dedicated to the analysis of weakly ordered, fully deuterated enantiomers in chiral liquid crystals

Lesot, Philippe,Sarfati, Muriel,Merlet, Denis,Ancian, Bernard,Emsley, James W.,Timimi, Bakir A.

, p. 7689 - 7695 (2007/10/03)

Methods for the assignment of the quadrupolar doublets in the deuterium NMR spectra of weakly ordered, perdeuterated or partially deuterated enantiomers dissolved in chiral liquid crystals are described which use robust 2D correlation NMR experiments. To overcome a lack of resolution in deuterium tilted Q-COSY 2D spectra in such materials, we propose and explore a correlation 2D sequence which is based on deuterium-carbon 2D correlation spectroscopy. The technique results in a 13C-2H contour plot and allows the full resonance assignment of overcrowded deuterium 1D spectra using carbon-deuterium correlations. The 2H autocorrelation and 13C-2H correlation experiments are applied in the case of a racemic mixture of 2-ethylhexanoic acid-d15 dissolved in a polypeptidic chiral oriented solvent. The performance and the limits of both techniques are presented and discussed. For the last step of the assignment procedure, we propose a simple method for obtaining two coherent sets of quadrupolar splittings, one for each enantiomer.

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