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Catalog Number:
29968
CAS Number:
5417-13-0
Oxyma-B anhydrous
Purity:
≥ 99% (HPLC)
Synonym(s):
DMVA, 5-(Hydroxyimino)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione anhydrous
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$29.34 /1G
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Product Information

Oxyma-B anhydrous is a versatile and innovative compound widely recognized for its applications in organic synthesis and pharmaceutical development. This compound, also known as 6-hydroxy-1,3-dimethyl-5-nitrosopyrimidine-2,4-dione, serves as an efficient reagent for the formation of oxime derivatives, which are crucial intermediates in the synthesis of various bioactive molecules. Its unique structure allows for enhanced reactivity and selectivity, making it a preferred choice among researchers aiming to streamline their synthetic pathways.

In addition to its role in organic synthesis, Oxyma-B anhydrous has shown promise in the field of medicinal chemistry, particularly in the development of novel therapeutics. Its ability to facilitate the formation of stable oximes can lead to the discovery of new drug candidates with improved efficacy and safety profiles. The compound's stability and ease of handling further enhance its appeal in laboratory settings, ensuring that it meets the rigorous demands of both academic and industrial research.

Synonyms
DMVA, 5-(Hydroxyimino)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione anhydrous
CAS Number
5417-13-0
Purity
≥ 99% (HPLC)
Molecular Formula
C6H7N3O4
Molecular Weight
185.14
MDL Number
MFCD02685596
PubChem ID
222079
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
DMVA, 5-(Hydroxyimino)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione anhydrous
CAS Number
5417-13-0
Purity
≥ 99% (HPLC)
Molecular Formula
C6H7N3O4
Molecular Weight
185.14
MDL Number
MFCD02685596
PubChem ID
222079
Appearance
White powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Oxyma-B anhydrous is widely utilized in research focused on:

  • Peptide Synthesis: It serves as a coupling reagent in peptide synthesis, enhancing the efficiency of amide bond formation while minimizing side reactions, which is crucial for producing high-purity peptides.
  • Drug Development: In pharmaceutical research, it is used to optimize the synthesis of complex molecules, allowing for the rapid development of new drug candidates with improved efficacy and safety profiles.
  • Organic Synthesis: Oxyma-B is employed in various organic reactions, particularly in the formation of carbon-nitrogen bonds, making it valuable for chemists working on diverse synthetic pathways.
  • Bioconjugation: It is utilized in bioconjugation processes, aiding in the attachment of biomolecules to surfaces or other molecules, which is essential in developing targeted therapies and diagnostics.
  • Research on Nitrosation: The compound is also studied for its role in nitrosation reactions, providing insights into nitrogen chemistry and its applications in environmental and biological systems.

Citations