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TCI

CAS 73-40-5

Guanine TCI G0169

Guanine TCI G0169

Chemical Identity

Other names
2-Amino-6-hydroxypurine · 2-Aminohypoxanthine
CAS No.
73-40-5
PubChem
CID 135398634·SID 87570363
Formula
C5H5N5O
Molecular weight
151.13 g/mol
Purity
>98.0%(T)(HPLC)
Reference databases
ChEBI·ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-amino-1,7-dihydropurin-6-one
SMILES
C1=NC2=C(N1)C(=O)NC(=N2)N
InChIKey
UYTPUPDQBNUYGX-UHFFFAOYSA-N
MDL
MDL00071533
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Guanine (73-40-5) is a chemical compound classified under the heterocyclic category and is one of the four nitrogenous bases found in DNA and RNA. As a fundamental building block, Guanine plays a crucial role in various chemical reactions aimed at synthesizing complex compounds, including pharmaceuticals, pesticides, and industrial chemicals. In the laboratory, it is widely used as a key reagent in organic synthesis reactions, particularly in the production of heterocyclic compounds with intricate molecular structures. Its presence in nucleic acids makes it essential for biochemical research and molecular studies.

Guanine is known for its stable molecular structure and aromatic properties, which contribute to its reactivity under diverse chemical conditions. It exhibits good solubility in organic solvents such as ethylamine and acetone, making it a preferred choice for precise and stable chemical reactions. These characteristics ensure its reliability in laboratory settings where accuracy and consistency are paramount. Its chemical stability and solubility properties make it a versatile reagent for a wide range of applications in both organic and biochemical research.

In Indonesian laboratories, Guanine is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and the development of pharmaceutical materials. It is also utilized in biochemical studies to investigate the structure and function of biological molecules. Its presence in DNA and RNA makes it a valuable tool for molecular biology research, contributing to advancements in both academic and industrial scientific fields.

  • Organic synthesis of heterocyclic compounds due to its stable molecular structure and aromatic nature.
  • Pharmaceutical development for the synthesis of nucleoside derivatives and other bioactive molecules.
  • Biochemical research to study the structural and functional properties of nucleic acids.
  • Industrial chemical production for the creation of pesticides and specialty chemicals.
  • Molecular biology experiments involving DNA and RNA analysis and modification.

Brand TCI
CAS number 73-40-5
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory requirements
Physical form Crystalline solid
Storage Store in a cool, dry place away from light and moisture

Guanine 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 air, which could affect its solubility and reactivity. In laboratory settings, proper ventilation is essential to avoid inhalation of any vapors, although Guanine is generally considered to have low volatility. Handling should be done with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety during preparation and use. The compound is non-toxic in small quantities but should be treated with care to prevent any unnecessary exposure. Its stable nature makes it safe for routine laboratory use when stored and handled correctly.

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