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62790-26-5

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62790-26-5 Usage

Description

Sodium Benzoate-d5, also known as sodium benzoate deuterated, is a chemical compound that is isotopically labeled with deuterium. It is commonly used in various applications due to its unique properties and ability to be incorporated into different chemical structures.

Uses

Used in Chemical Synthesis:
Sodium Benzoate-d5 is used as a precursor in the preparation of cobalt/nickel hydroxydiphenylpropanedionate complexes and their benzoate ester derivatives. This application is particularly useful in the field of chemical synthesis, where isotopically labeled compounds can provide valuable insights into the structure and properties of synthesized materials.
Used in Research and Development:
Due to its deuterated nature, Sodium Benzoate-d5 can be employed in research and development for studying the behavior of molecules and reactions under various conditions. Its incorporation into complex structures allows for the investigation of reaction mechanisms, kinetics, and thermodynamics, which can be crucial for optimizing chemical processes and developing new materials.
Used in Analytical Chemistry:
Sodium Benzoate-d5 can also be utilized in analytical chemistry as a reference material or internal standard. Its isotopically labeled nature makes it an ideal candidate for techniques such as nuclear magnetic resonance (NMR) spectroscopy, where it can help in the accurate determination of chemical structures and the quantification of compounds in complex mixtures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Sodium Benzoate-d5 can be used for the development of isotopically labeled drug candidates. These labeled compounds can be valuable for studying the metabolism, pharmacokinetics, and pharmacodynamics of drugs, as well as for assessing the potential for drug-drug interactions and toxicity.
Overall, Sodium Benzoate-d5 is a versatile compound with a wide range of applications across various industries, including chemical synthesis, research and development, analytical chemistry, and the pharmaceutical sector. Its unique properties and ability to be incorporated into complex structures make it an invaluable tool for advancing scientific knowledge and developing innovative materials and products.

Check Digit Verification of cas no

The CAS Registry Mumber 62790-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,9 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62790-26:
(7*6)+(6*2)+(5*7)+(4*9)+(3*0)+(2*2)+(1*6)=135
135 % 10 = 5
So 62790-26-5 is a valid CAS Registry Number.

62790-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,2,3,4,5,6-pentadeuteriobenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid-2,3,4,5,6-d5 sodium salt

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:62790-26-5 SDS

62790-26-5Upstream product

62790-26-5Downstream Products

62790-26-5Relevant articles and documents

H-D Exchange Deuteration of Arenes at Room Temperature

Sawama, Yoshinari,Nakano, Akihiro,Matsuda, Takumi,Kawajiri, Takahiro,Yamada, Tsuyoshi,Sajiki, Hironao

, p. 648 - 653 (2019)

Arene nuclei efficiently underwent the hydrogen (H)-deuterium (D) exchange reaction catalyzed by platinum group metals on carbon in a mixed solvent of 2-propanol and D2O at room temperature to produce deuterium-labeled arenes. Platinum on carbon (Pt/C) and iridium on carbon (Ir/C) were applicable catalysts, and the various arenes bearing a carbonyl group, fluorine, phenolic hydroxy group, amino group, or phosphonic acid on the aromatic nucleus were effectively deuterated. Nonheating conditions are valuable for the scalable industrial preparation.

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