N4-Benzoyl-2'-deoxycytidine TCI B3102

Chemical Identity

CAS No.: 4836-13-9
PubChem: CID 9797617·SID 87559864
Formula: C16H17N3O5
Molecular weight: 331.32 g/mol
Purity: >98.0%(N)(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: N-[1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]benzamide
SMILES: C1[C@@H]([C@H](O[C@H]1N2C=CC(=NC2=O)NC(=O)C3=CC=CC=C3)CO)O
InChIKey: MPSJHJFNKMUKCN-OUCADQQQSA-N

Rp 505.050,00

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Berat 100mg 1g

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N4-Benzoyl-2'-deoxycytidine is a chemical compound widely used in chemical biology, particularly in the study of nucleic acids. It functions as an analog of cytidine, a key component of DNA and RNA. In laboratory settings, this compound plays a crucial role in research related to nucleotide modification, drug development, and enzymatic studies involved in DNA synthesis. Its unique chemical properties make it a valuable tool for biochemical and genetic experiments.

The compound is known for its stable chemical structure and controlled reactivity, which allows it to be used in a variety of chemical and biochemical reactions. Its high purity and availability in solid form make it convenient for laboratory procedures. Additionally, its good solubility in organic solvents simplifies its handling and application in experimental workflows. These characteristics ensure its reliability and effectiveness in various research applications.

In Indonesian laboratories, N4-Benzoyl-2'-deoxycytidine is commonly used in academic and industrial research settings. It is applied in studies related to DNA replication mechanisms, enzymatic activity, and the development of nucleotide-based pharmaceuticals. Its presence in research institutions and laboratories supports advancements in molecular biology and related fields.

TCI brochures (PDF)

Oligonucleotide Synthesis Reagents 2025-07-24 · p. 2
Nucleosides, Nucleotides, Nucleic Acids and Related Reagents 2026-03-23 · p. 4

Related TCI products

DNA replication mechanism studies: This compound is used to investigate how DNA is synthesized and replicated in cells, offering insights into genetic processes.
Enzymatic activity research: It serves as a substrate or inhibitor in enzyme assays, helping to understand the function of DNA-modifying enzymes.
Nucleotide analog development: Its structure makes it ideal for designing and testing new nucleotide-based drugs and therapeutic agents.
Genetic mutation analysis: It is employed in experiments that study how nucleotide modifications affect genetic expression and stability.
Biochemical reaction optimization: Its controlled reactivity allows researchers to fine-tune reaction conditions in biochemical experiments.

Brand	TCI
CAS number	4836-13-9
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Nucleic Acid Chemistry
Pack sizes	Available in various quantities as per standard laboratory requirements
Physical form	Solid
Storage	Store in a cool, dry place away from light

N4-Benzoyl-2'-deoxycytidine should be stored in a cool, dry environment, away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper labeling of containers is essential for safe handling and to prevent accidental exposure. The compound is non-hazardous under normal conditions but should be stored separately from incompatible substances. Regular inspection of storage conditions is advised to ensure the integrity of the material throughout its shelf life.

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