Diethyl Oxalate TCI O0078

Chemical Identity

CAS No.: 95-92-1
PubChem: CID 7268·SID 87574090
Formula: C6H10O4
Molecular weight: 146.14 g/mol
Purity: >98.0%(GC)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: diethyl oxalate
SMILES: CCOC(=O)C(=O)OCC
InChIKey: WYACBZDAHNBPPB-UHFFFAOYSA-N

Rp 505.050,00

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Diethyl oxalate is a versatile organic compound widely used in laboratory settings for its reactivity and utility in various chemical reactions. As a key building block in organic synthesis, it plays a crucial role in the formation of complex molecular structures. Its ability to participate in esterification, reduction, and nucleophilic reactions makes it an essential reagent for chemists. This compound is commonly employed in the development of new chemical compounds with specific properties, making it a fundamental tool in both academic and industrial research environments.

The chemical properties of diethyl oxalate, including its stability and moderate reactivity, make it a preferred choice for laboratory applications. It is a liquid with a distinct odor and a relatively high boiling point, which allows for controlled reactions under standard laboratory conditions. Its predictable chemical behavior ensures consistent results, making it a reliable component in synthetic processes. The compound’s compatibility with a wide range of reagents further enhances its utility in diverse chemical experiments.

In Indonesian laboratories, diethyl oxalate is frequently used in organic chemistry research, particularly in higher education institutions and research centers. It is an integral part of the basic chemical supply for routine experiments and specialized studies. Its availability and reliability make it a standard item in the inventory of chemical laboratories across the country.

Related TCI products

Organic synthesis reactions where diethyl oxalate serves as a versatile reagent for forming complex molecular structures.
Esterification processes that require a stable and reactive intermediate for the production of ester compounds.
Nucleophilic substitution reactions where diethyl oxalate acts as a suitable substrate for chemical transformation.
Reduction reactions that benefit from the compound’s moderate reactivity and controlled chemical behavior.
Routine chemical experiments in Indonesian academic and research laboratories for teaching and research purposes.

Brand	TCI
CAS number	95-92-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight

Diethyl oxalate should be stored in a cool, dry location away from direct sunlight to maintain its chemical stability. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and evaporation. Due to its reactivity, it should be handled in a well-ventilated area to avoid inhalation of vapors. Proper personal protective equipment, including gloves and safety goggles, should be worn during handling. The compound should not be stored near incompatible materials such as strong oxidizers or acids. Regular inspection of storage containers is advised to ensure the integrity of the material and prevent any potential hazards.

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