N6-Benzoyladenosine TCI B3093

Chemical Identity

CAS No.: 4546-55-8
PubChem: CID 44629869·SID 87559972
Formula: C17H17N5O5
Molecular weight: 371.3 g/mol
Purity: >96.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: N-[9-[(2R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide
SMILES: C1=CC=C(C=C1)C(=O)NC2=C3C(=NC=N2)N(C=N3)[C@H]4C([C@@H]([C@H](O4)CO)O)O
InChIKey: NZDWTKFDAUOODA-WKZGZVLGSA-N

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N6-Benzoyladenosine is a chemical compound widely utilized in chemical and biochemical experiments, particularly in the study of nucleic acids and nucleotide-related reactions. This compound is derived from adenine, with a benzoil group attached at the N6 position, making it a key molecule in nucleic acid chemistry. Its structural complexity and functional versatility make it an essential tool for researchers working in molecular biology and chemical synthesis. In laboratory settings, it serves as both a building block for synthesizing other compounds and a substrate in enzymatic reactions, contributing to the advancement of scientific research.

The compound is chemically stable under specific conditions, though it is highly sensitive to moisture and light exposure. These properties require careful handling and storage to maintain its integrity and effectiveness. Its solubility in organic solvents such as ethyl acetate and acetone further enhances its usability in various experimental procedures. This solubility profile allows for efficient processing and application in a wide range of laboratory techniques, making it a preferred choice for researchers seeking reliable and consistent results.

In Indonesian laboratories, N6-Benzoyladenosine is commonly used in research across chemistry, biochemistry, and pharmacology. It plays a crucial role in studies involving reaction mechanisms, drug development, and molecular structure analysis. Its availability supports the work of research institutions and universities, enabling them to conduct advanced experiments and contribute to scientific innovation in the region.

TCI brochures (PDF)

Oligonucleotide Synthesis Reagents 2025-07-24 · p. 2
Nucleosides, Nucleotides, Nucleic Acids and Related Reagents 2026-03-23 · p. 5

Related TCI products

Chemical synthesis of nucleotide derivatives where precise structural modification is required.
Enzymatic reaction studies to investigate the activity and specificity of nucleotide-binding enzymes.
Drug development research to explore the interaction of nucleotide analogs with biological targets.
Molecular structure analysis to understand the behavior of nucleic acid components in different environments.
Biochemical assays to assess the stability and reactivity of modified nucleotides under various experimental conditions.

Brand	TCI
CAS number	4546-55-8
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Nucleic Acid Chemistry
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Solid powder
Storage	Store in a cool, dry place away from light and moisture

N6-Benzoyladenosine should be stored in a cool, dry environment, away from direct light and moisture to prevent degradation. It is recommended to use airtight containers made of glass or high-density polyethylene to maintain its chemical integrity. Due to its sensitivity to humidity, it is important to ensure that the storage area has controlled environmental conditions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment to avoid exposure. Proper labeling and storage practices are essential to ensure the safety and effectiveness of this compound in research applications.

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