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3,4-Diamino-4-oxobutyric acid, also known as diaminomalonate, is a chemical compound with the molecular formula C4H8N2O3. It is an amino acid derivative and serves as a key intermediate in the biosynthesis of the amino acid threonine. 3,4-Diamino-4-oxobutyric acid plays a significant role in the research and development of biochemistry, as it is crucial for studying metabolic pathways, protein structure, and function.

498-25-9

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498-25-9 Usage

Uses

Used in Pharmaceutical Production:
3,4-Diamino-4-oxobutyric acid is used as a building block in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs, contributing to the advancement of medicine.
Used in Biochemistry Research:
3,4-Diamino-4-oxobutyric acid is utilized as a key intermediate in the study of metabolic pathways, providing valuable insights into the processes that occur within living organisms. This understanding can lead to the discovery of new therapeutic targets and the development of novel treatments for various diseases.
Used in Organic Synthesis:
As a versatile building block, 3,4-Diamino-4-oxobutyric acid is employed in organic synthesis for the creation of a wide range of chemical compounds. Its ability to be modified and combined with other molecules makes it a valuable tool in the synthesis of complex organic structures.
Used in Protein Structure and Function Studies:
3,4-Diamino-4-oxobutyric acid is used as a component in the investigation of protein structure and function. By studying its interactions with other molecules and its role in protein formation, researchers can gain a deeper understanding of the mechanisms that govern protein behavior and potentially develop new strategies for manipulating protein function in therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 498-25-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 498-25:
(5*4)+(4*9)+(3*8)+(2*2)+(1*5)=89
89 % 10 = 9
So 498-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O3/c5-2(4(6)9)1-3(7)8/h2H,1,5H2,(H2,6,9)(H,7,8)

498-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name aspartic 1-amide

1.2 Other means of identification

Product number -
Other names Inakt. l-Amino-aethan-dicarbonsaeure-(1.2)-monoamid

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:498-25-9 SDS

498-25-9Downstream Products

498-25-9Relevant academic research and scientific papers

Chemical evolution of simple amino acids to asparagine under discharge onto the primitive hydrosphere: Simulation experiments using contact glow discharge

Munegumi, Toratane

, p. 1208 - 1215 (2015/02/19)

Asparagine is an important amino acid for abiotic polypeptide synthesis. In simulation experiments, it was obtained in 3.0% yield (based on the amount of consumed alanine) from alanine (100 mM) and formamide (200 mM) by contact glow discharge (Harada discharge) onto aqueous solutions. The present results suggest that asparagine could be abiotically synthesized from simple amino acids under possible primitive earth conditions.

Abiotic asparagine formation from simple amino acids by contact glow discharge electrolysis

Munegumi, Toratane,Shimoyama, Akira,Harada, Kaoru

, p. 393 - 394 (2007/10/03)

Asparagine, one of the most important amino acids for prebiotic peptide formation in aqueous media, was formed using Contact Glow Discharge Electrolysis (CGDE) against aqueous solutions containing simple amino acids and carboxylic acid amides.

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