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Catalog Number:
21836
CAS Number:
931-86-2
5-Azacitosina
Purity:
≥ 98 % (HPLC)
Synonym(s):
2-Amino-4-hidroxi-S-triazina, 4-Amino-1,3,5-triazina-2[1 H ]-ona
Documents
$22.83 /5G
Tamaño
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Product Information

Se utilizan como los imitadores de citosina más eficaces para la
Diseño de nuevos fármacos candidatos antivirales y antitumorales.

Synonyms
2-Amino-4-hidroxi-S-triazina, 4-Amino-1,3,5-triazina-2[1 H ]-ona
CAS Number
931-86-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C3H4N4O
Molecular Weight
112.09
MDL Number
MFCD00006033
PubChem ID
19956
Melting Point
> 300 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
2-Amino-4-hidroxi-S-triazina, 4-Amino-1,3,5-triazina-2[1 H ]-ona
CAS Number
931-86-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C3H4N4O
Molecular Weight
112.09
MDL Number
MFCD00006033
PubChem ID
19956
Melting Point
> 300 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Azacytosine is widely utilized in research focused on:

  • Epigenetics Research: It serves as a powerful tool for studying DNA methylation patterns, helping researchers understand gene regulation and expression.
  • Antiviral Agents: The compound has shown potential in developing antiviral therapies, particularly against certain viruses by interfering with their replication processes.
  • Pharmaceutical Development: It is used in the synthesis of various pharmaceuticals, particularly in creating compounds that target specific biological pathways.
  • Genetic Studies: 5-Azacytosine is applied in genetic engineering and modification, aiding in the development of transgenic organisms for agricultural and medical research.
  • Biotechnology Applications: Its role in biotechnological innovations includes enhancing the efficiency of gene editing techniques, making it valuable for researchers in synthetic biology.

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