N6-Benzoyladenine TCI B3344

Chemical Identity

CAS No.: 4005-49-6
PubChem: CID 97075·SID 87560855
Formula: C12H9N5O
Molecular weight: 239.23 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ChEBI·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: N-(7H-purin-6-yl)benzamide
SMILES: C1=CC=C(C=C1)C(=O)NC2=NC=NC3=C2NC=N3
InChIKey: QQJXZVKXNSFHRI-UHFFFAOYSA-N

Rp 822.150,00

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Berat 5g 25g

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N6-Benzoyladenine is a chemical compound classified under nucleosides and serves as a key reagent in biochemical experiments. It is widely used in research related to organic synthesis, particularly in biochemistry and pharmacology. This compound plays a crucial role in nucleotide modification processes, which are fundamental to the development of new drugs and genetic research. In the laboratory, it functions as a foundational material for chemical reactions requiring specific nucleoside structures. Its chemical structure is complex, enabling it to interact effectively with various reagents.

The compound’s unique chemical properties make it a preferred choice for high-precision reactions. It exhibits stability under certain conditions, which simplifies storage and long-term use. Its ability to participate in diverse chemical reactions makes it indispensable in synthetic pathways. The specificity of its chemical behavior ensures reliable results in experiments that demand accuracy. This reliability is especially important in applications such as organic synthesis and nucleotide modification.

In Indonesian laboratories, N6-Benzoyladenine is commonly used by researchers in universities and research institutions. It is particularly relevant in biomedical research, where it supports the development of new therapeutic agents. Its application in genetic studies and drug discovery highlights its importance in advancing scientific knowledge. The compound is a vital component in many experimental setups, contributing to the success of various research projects.

TCI brochures (PDF)

Nucleosides, Nucleotides, Nucleic Acids and Related Reagents 2026-03-23 · p. 9

Related TCI products

Organic synthesis applications benefit from N6-Benzoyladenine due to its ability to participate in complex chemical reactions and its structural versatility.
Nucleotide modification processes rely on this compound for its role in creating modified nucleosides essential for drug development and genetic research.
Biochemical research utilizes N6-Benzoyladenine for its stability and reactivity, supporting experiments in pharmacology and molecular biology.
Drug development projects incorporate this compound as a key reagent in the synthesis of novel therapeutic agents.
Genetic studies use N6-Benzoyladenine to explore nucleotide structures and their modifications, contributing to advancements in molecular genetics.

Brand	TCI
CAS number	4005-49-6
Molecular formula	—
Purity	—
Category	Life Science > Biochemicals and Reagents > Nucleosides, Nucleotides, Oligonucleotides
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from direct light

N6-Benzoyladenine should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a sealed container to minimize exposure to moisture and air. Suitable storage conditions include a controlled temperature range, typically between 15°C and 25°C. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment to ensure safety. Due to its chemical reactivity, it should be stored away from incompatible substances. Proper labeling and secure storage are essential to prevent accidental exposure and maintain the integrity of the compound during long-term use.

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