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CAS 1460-34-0

3-Methyl-2-oxovaleric Acid TCI K0020

3-Methyl-2-oxovaleric Acid TCI K0020

Chemical Identity

CAS No.
1460-34-0
PubChem
CID 47·SID 87571956
Formula
C6H10O3
Molecular weight
130.14 g/mol
Purity
>95.0%(GC)(T)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
3-methyl-2-oxopentanoic acid
SMILES
CCC(C)C(=O)C(=O)O
InChIKey
JVQYSWDUAOAHFM-UHFFFAOYSA-N
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3-Methyl-2-oxovaleric Acid is a versatile chemical compound widely used in organic synthesis as a building block for creating complex molecular structures. Its reactivity and structural simplicity make it an essential tool in laboratory settings, particularly for those working on organic chemistry research. This compound plays a key role in the development of various organic compounds, including those with heterocyclic or alkyl chain structures. Due to its ability to participate in multiple reaction types, it is a valuable asset in synthetic chemistry workflows.

The compound’s chemical properties, such as its reactivity in substitution, esterification, and redox reactions, make it a preferred choice for researchers. Its stability under controlled conditions ensures safe handling and reliable results during synthesis. The availability of this compound in standard laboratory quantities further enhances its appeal for both academic and industrial applications. Its affordability and widespread use in chemical research contribute to its popularity among scientists and students alike.

In Indonesian laboratories, 3-Methyl-2-oxovaleric Acid is commonly used in organic chemistry research, especially in academic institutions and research centers. It is a staple in synthetic chemistry experiments, supporting the development of new compounds and the modification of existing molecular structures. Its role in educational settings also makes it an important material for training the next generation of chemists.

  • Organic synthesis for creating complex molecular structures due to its reactivity and structural versatility.
  • Esterification reactions as a key intermediate in the formation of ester compounds.
  • Redox reactions where its chemical properties facilitate electron transfer processes.
  • Substitution reactions for modifying functional groups in organic molecules.
  • Structural modification of heterocyclic compounds in synthetic chemistry applications.

Brand TCI
CAS number 1460-34-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent moisture absorption and contamination. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Avoid exposure to heat or direct sunlight to prevent degradation. Proper ventilation is essential when working with this material to ensure safe laboratory practices. Always follow standard chemical handling procedures to minimize risks during use and storage.

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