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Atomfair N4-Acetylcytosine C6H7N3O2

Description N4-Acetylcytosine (CAS No. 14631-20-0) is a high-purity biochemical compound with the molecular formula C6H7N3O2and IUPAC name N-(2-oxo-1H-pyrimidin-6-yl)acetamide . This modified nucleobase derivative is extensively utilized in nucleic acid research, epigenetics, and molecular biology applications. Our product is rigorously tested for purity (??98% by HPLC) and stability, ensuring optimal performance in sensitive experiments. It is supplied as a white to off-white crystalline powder, soluble in DMSO and slightly soluble in water. Ideal for studying cytosine acetylation mechanisms, DNA/RNA modifications, and as a reference standard in analytical workflows. Store at 2-8??C in a dry environment to maintain integrity.

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Description

Description

N4-Acetylcytosine (CAS No. 14631-20-0) is a high-purity biochemical compound with the molecular formula C6H7N3O2 and IUPAC name N-(2-oxo-1H-pyrimidin-6-yl)acetamide. This modified nucleobase derivative is extensively utilized in nucleic acid research, epigenetics, and molecular biology applications. Our product is rigorously tested for purity (??98% by HPLC) and stability, ensuring optimal performance in sensitive experiments. It is supplied as a white to off-white crystalline powder, soluble in DMSO and slightly soluble in water. Ideal for studying cytosine acetylation mechanisms, DNA/RNA modifications, and as a reference standard in analytical workflows. Store at 2-8??C in a dry environment to maintain integrity.

  • CAS No: 14631-20-0
  • Molecular Formula: C6H7N3O2
  • Molecular Weight: 153.14
  • Exact Mass: 153.053826475
  • Monoisotopic Mass: 153.053826475
  • IUPAC Name: N-(2-oxo-1H-pyrimidin-6-yl)acetamide
  • SMILES: CC(=O)NC1=CC=NC(=O)N1
  • Synonyms: N4-Acetylcytosine, 619-683-7, 14631-20-0, N-(2-Oxo-1,2-dihydropyrimidin-4-yl)acetamide, N-Acetylcytosine

Application

N4-Acetylcytosine serves as a critical tool in epigenetic research, particularly for investigating post-transcriptional RNA modifications and their regulatory roles. It is employed as a synthetic precursor for modified oligonucleotides in structural biology studies. Researchers also utilize this compound to explore enzymatic acetylation pathways in nucleic acid metabolism. Its stability under physiological conditions makes it suitable for in vitro modeling of epigenetic markers.

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