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TCI

CAS 30516-87-1

3'-Azido-3'-deoxythymidine TCI A2052

3'-Azido-3'-deoxythymidine TCI A2052

Chemical Identity

CAS No.
30516-87-1
PubChem
CID 35370·SID 87559740
Formula
C10H13N5O4
Molecular weight
267.24 g/mol
Purity
>98.0%(T)
Reference databases
ChEBI·ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-[(2R,4S,5S)-4-azido-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione
SMILES
CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)CO)N=[N+]=[N-]
InChIKey
HBOMLICNUCNMMY-XLPZGREQSA-N
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3'-Azido-3'-deoxythymidine (AZT) is a chemical compound widely used in biochemical and pharmacological research. It plays a crucial role in laboratory settings where molecular interactions and drug development are studied. AZT is particularly valuable for its ability to participate in specific chemical reactions, making it a key component in conjugation chemistry and click chemistry applications. Its versatility allows researchers to modify molecular structures with precision, supporting the creation of compounds with targeted biological activities.

The properties of AZT that make it a preferred choice include its stable yet reactive chemical structure, as well as its ease of solubilization in various solvents. These characteristics enable efficient use in a wide range of experimental protocols. Additionally, its availability in solid form simplifies handling and storage, making it a practical option for laboratory use. The compound’s reactivity and specificity are essential for applications requiring high precision and controlled chemical transformations.

In Indonesian laboratories, AZT is commonly used in research related to infectious diseases, especially in the development of vaccines and therapeutic agents. Its role in biochemical studies that require precise chemical reactions underscores its importance in both academic and industrial research settings. The compound’s utility in molecular modification and its relevance to drug discovery make it a staple in modern laboratory practices.

Advantages (TCI brochure)

  • Discovered by Mitsuya et al. in 1985; used for treatment of HIV infection

  • Drug development research benefits from AZT’s ability to participate in specific chemical reactions, enabling the synthesis of compounds with targeted biological activities.
  • Infectious disease studies utilize AZT for investigating molecular interactions and developing therapeutic agents against viral infections.
  • Conjugation chemistry applications rely on AZT’s reactivity and stability, allowing for the creation of complex molecular structures with high precision.
  • Click chemistry experiments use AZT as a building block due to its compatibility with click reaction mechanisms, facilitating rapid and efficient molecular modifications.
  • Biochemical assays incorporate AZT to study molecular interactions and evaluate the effects of chemical modifications on biological activity.

From the TCI brochure

  • HIV infection treatment

Brand TCI
CAS number 30516-87-1
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Conjugation Chemistry/Click Chemistry
Pack sizes —
Physical form Solid
Storage Store in a cool, dry place away from light

AZT 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 reactivity, it should be handled with care in a well-ventilated laboratory setting. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. The compound is not flammable but may react with strong oxidizing agents, so compatibility with other chemicals should be considered. Storage conditions should be consistent to ensure the integrity of the material for extended use in research applications.

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