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Alanine, 3-oxo-, also known as 3-oxoalanine or pyruvate amino acid, is an important organic compound that plays a crucial role in various biological processes. It is an intermediate in the metabolism of amino acids, particularly alanine, and is involved in the transamination reactions that convert alanine to pyruvate. Alanine, 3-oxo- is also a key player in the citric acid cycle, also known as the Krebs cycle or the tricarboxylic acid (TCA) cycle, where it is converted to acetyl-CoA, a central molecule in cellular respiration. The molecular formula for 3-oxoalanine is C3H5NO3, and it has a molecular weight of 101.08 g/mol. Its significance in biochemistry lies in its ability to link amino acid metabolism with energy production pathways, making it an essential component in the maintenance of cellular homeostasis and energy balance.

5735-66-0

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5735-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5735-66-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,3 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5735-66:
(6*5)+(5*7)+(4*3)+(3*5)+(2*6)+(1*6)=110
110 % 10 = 0
So 5735-66-0 is a valid CAS Registry Number.

5735-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-3-oxopropanoic acid

1.2 Other means of identification

Product number -
Other names 2-Ammoniomalonate semialdehyde

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:5735-66-0 SDS

5735-66-0Downstream Products

5735-66-0Relevant academic research and scientific papers

Oxidation of amoxicillin by hexacyanoferrate(III) in aqueous alkaline medium-A kinetic and mechanistic approach

Durgannavar, Amar K.,Patgar, Manjanath B.,Chimatadar, Shivamurti A.

, p. 1085 - 1091 (2015/09/28)

The kinetics and mechanism of oxidation of amoxicillin by hexacyanoferrate(III) in aqueous alkaline medium at constant ionic strength of 0.10 mol dm-3 is studied spectrophotometrically at 25 °C. The reaction exhibits 2:1 ([Fe(CN)6]3-: amoxicillin) stoichiometry. The reaction products have been identified with the help of TLC and characterized by FT-IR, GCMS and LCMS. The reaction is first order in hexacyanoferrate(III) concentration but fractional order in both amoxicillin and alkali concentrations. The effects of ionic strength and dielectric constant have been investigated. In a composite equilibrium step, amoxicillin binds to hexacyanoferrate(III) to form a complex that subsequently decomposes to the products. Based on investigation of the reaction at different temperatures, computation of the activation parameters with respect to the slow step of the proposed mechanism was evaluated.

Under-flame oxidation of amines and amino acids in an aqueous solution

Nomoto, Shinya,Shimoyama, Akira,Shiraishi, Susumu,Sahara, Denzo

, p. 1851 - 1855 (2007/10/03)

Flames from town gas-oxygen, hydrogen-oxygen, and ethylene-oxygen mixtures, when blown against the surface of an aqueous solution of amines and amino acids, induced an oxidation reaction in the aqueous phase, while an acetylene-oxygen flame failed to oxidize the compounds in solution. The hydrogen flame caused direct hydroxylation of the aromatic rings of phenylglycine homologs. The isomeric ratio of o-, m-, and p-hydroxyphenyl- amino acids produced was in accordance with that obtained by using the reaction systems of Fe2+-H2O2-EDTA and Fe2+-ascorbic acid-H2O2-EDTA, which are known to involve a hydroxyl radical as the agent for hydroxylating the aromatic rings. These results strongly suggest that the active species of flame-induced oxidation in an aqueous solution was the hydroxyl radical which was produced in the flames and extracted into the aqueous phase.

Fixation of Molecular Nitrogen Using Aliphatic Carboxylic Acid by Nitrogen Arc Plasma. Formation of Amino Acids

Takasaki, Michiaki,Harada, Kaoru

, p. 365 - 368 (2007/10/02)

When argon-nitrogen plasma was blown into an aqueous solution containing aliphatic carboxylic acids, formation of several amino acids and amines was identified.

OXIDATION REACTION OF AMINO ACIDS IN AQUEOUS SOLUTION INDUCED BY ARGON ARC PLASMA

Harada, Kaoru,Takasaki, Michiaki

, p. 4839 - 4842 (2007/10/02)

It was found that Argon arc plasma induced a powerful and clean stepwise oxidation reaction in aqueous solution containing various amino acids without using any oxidizing agent.

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