N4-Acetylcytosine TCI A2089

Chemical Identity

CAS No.: 14631-20-0
PubChem: CID 99309·SID 87560444
Formula: C6H7N3O2
Molecular weight: 153.14 g/mol
Purity: >98.0%(T)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: N-(2-oxo-1H-pyrimidin-6-yl)acetamide
SMILES: CC(=O)NC1=CC=NC(=O)N1
InChIKey: IJCKBIINTQEGLY-UHFFFAOYSA-N

Rp 637.350,00

~~Rp 460.950,00~~ Rp 637.350,00

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Berat 5g 25g

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N4-Acetylcytosine is a chemical compound classified under the category of heterocyclic building blocks, commonly used in organic chemistry and biochemical research. As a derivative of cytosine, it plays a crucial role in the synthesis of complex organic compounds, particularly those related to nucleotide structures. In laboratory settings, this compound serves as a foundational element for the development of various molecules, including pharmaceuticals, biochemical reagents, and synthetic compounds. Its structural versatility makes it an essential tool for researchers aiming to explore molecular modifications and functional group transformations.

N4-Acetylcytosine is valued for its chemical stability and reactivity, which allow it to participate effectively in substitution, coupling, and modification reactions. Its solubility in organic solvents such as ethyl acetate and acetone enhances its usability in diverse experimental conditions. These properties make it a preferred choice for synthetic chemists and biochemists who require reliable and consistent performance in their experiments. The compound’s predictable behavior under various reaction conditions ensures reproducibility and accuracy in laboratory procedures.

In Indonesian laboratories, N4-Acetylcytosine is frequently utilized in organic chemistry research, especially in projects involving the synthesis of biomedically relevant compounds or the development of new chemical materials. It supports studies focused on nucleotide-related structures and their applications in drug discovery and biochemical analysis. Its availability and performance make it a key component in both academic and industrial research environments.

TCI brochures (PDF)

Nucleosides, Nucleotides, Nucleic Acids and Related Reagents 2026-03-23 · p. 8

Related TCI products

Organic synthesis of nucleotide derivatives due to its structural similarity to cytosine and its reactivity in functional group modifications.
Development of pharmaceutical compounds as a building block for nucleoside analogs used in drug design and therapeutic research.
Biochemical research involving nucleic acid analogs for studying DNA and RNA interactions and modifications.
Synthesis of synthetic polymers and biocompatible materials through controlled chemical reactions and molecular assembly.
Analytical chemistry applications for standardization and calibration in nucleotide-related assays and spectroscopic studies.

Brand	TCI
CAS number	14631-20-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid (as per standard chemical product form)
Storage	Store in a cool, dry place away from light and moisture

N4-Acetylcytosine should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Proper labeling of storage containers is essential for safe handling and identification. In laboratory settings, it is important to follow standard chemical safety protocols, including the use of personal protective equipment such as gloves and goggles. The compound is generally non-hazardous under normal conditions but should be handled with care to avoid any potential chemical interactions. Regular monitoring of storage conditions ensures the integrity of the material for research applications.

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