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CAS 57822-06-7

5-Oxoazelaic Acid TCI O0258

5-Oxoazelaic Acid TCI O0258

Chemical Identity

CAS No.
57822-06-7
PubChem
CID 269945·SID 87574248
Formula
C9H14O5
Molecular weight
202.20 g/mol
Purity
>96.0%(GC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
5-oxononanedioic acid
SMILES
C(CC(=O)CCCC(=O)O)CC(=O)O
InChIKey
GTCHZEFRDKAINX-UHFFFAOYSA-N
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5-Oxoazelaic Acid is a chemical compound widely utilized in laboratory settings for the synthesis of complex molecules. As a building block in organic chemistry, it plays a crucial role in various synthetic pathways, particularly in the development of heterocyclic compounds. Its unique molecular structure, featuring two carboxylic acid groups and one carbonyl group, makes it a versatile reagent for chemical reactions. This compound is commonly employed in research involving high reactivity and structural modification of organic molecules.

The compound's stability under normal conditions, combined with its ability to participate in specific reactions, makes it a preferred choice for synthetic chemists. It exhibits good solubility in organic solvents, which enhances its usability in a wide range of chemical processes. Its reactivity in substitution, esterification, and redox reactions further solidifies its importance in laboratory applications. These properties ensure that it remains a reliable and efficient reagent for synthetic chemists.

In Indonesian laboratories, 5-Oxoazelaic Acid is frequently used in organic chemistry research, especially in the synthesis of new compounds or the modification of existing ones. Its availability in small pack sizes, such as 1g and 5g, makes it practical for both small-scale and intermediate experiments. This accessibility supports ongoing research and development in chemical synthesis within the Indonesian scientific community.

  • Synthesis of heterocyclic compounds for drug development due to its reactivity and structural versatility.
  • Esterification reactions where its carboxylic acid groups can participate in forming ester linkages.
  • Redox reactions where its carbonyl group can act as an electron acceptor or donor.
  • Organic synthesis of complex molecules requiring high reactivity and functional group manipulation.
  • Modification of existing organic compounds to create new derivatives with enhanced properties.

Brand TCI
CAS number 57822-06-7
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes 1g, 5g
Physical form Solid
Storage Store in a cool, dry place away from moisture and direct sunlight

5-Oxoazelaic Acid should be stored in a cool, dry place, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. As a solid, it is typically handled in a fume hood to ensure proper ventilation, especially when working with small quantities. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, to minimize direct contact. Due to its reactivity in certain conditions, it should be stored separately from strong bases or reducing agents to avoid unintended chemical interactions. Proper storage and handling protocols ensure the safety and effectiveness of this compound in laboratory settings.

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