Diacetyl Monoxime TCI B0683

Chemical Identity

CAS No.: 57-71-6
PubChem: CID 6398969·SID 87563685
Formula: C4H7NO2
Molecular weight: 101.10 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-hydroxyiminobutan-2-one
SMILES: CC(=NO)C(=O)C
InChIKey: FSEUPUDHEBLWJY-UHFFFAOYSA-N

Rp 1.829.100,00

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Diacetyl Monoxime (DM), with CAS number 57-71-6, is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. As a building block in chemistry, it plays a crucial role in the development of complex organic molecules. Its simple molecular structure allows for various chemical modifications, making it an essential reagent in synthetic pathways. This compound is particularly valuable in the formation of heterocyclic compounds and other complex structures, which are fundamental in pharmaceutical and industrial chemistry.

DM is favored for its reactivity and compatibility with a wide range of functional groups. It exhibits stability under specific conditions, yet remains highly reactive towards acids, bases, and alkali metals, enabling the formation of new compounds with diverse structures and functions. Its ability to participate in substitution, oxidation, and coupling reactions makes it a preferred choice for researchers aiming to modify organic molecules. The compound’s adaptability to different reaction conditions enhances its utility in both academic and industrial research environments.

In Indonesian laboratories, Diacetyl Monoxime is commonly used in organic chemistry research, particularly in higher education institutions and research centers. It is a key component in the synthesis of compounds needed for drug development and industrial chemical production. Its availability and effectiveness make it a staple in chemical laboratories across Indonesia, supporting ongoing scientific advancements and innovation.

Related TCI products

Organic synthesis reactions where DM is used to form heterocyclic compounds due to its reactivity and structural versatility.
Substitution reactions in which DM acts as a nucleophile, facilitating the replacement of functional groups in organic molecules.
Oxidation processes where DM serves as an intermediate, enabling the transformation of aldehydes into carboxylic acids.
Coupling reactions that require a reactive intermediate, making DM suitable for forming complex organic structures.
Industrial chemical production where DM is employed to create derivatives used in pharmaceutical and polymer applications.

Brand	TCI
CAS number	57-71-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight and incompatible materials

Diacetyl Monoxime should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent exposure to air and moisture, which could affect its stability. Suitable containers for storage include glass or high-density polyethylene (HDPE) bottles, which are resistant to chemical degradation. Due to its reactivity with acids, bases, and alkali metals, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances and ensure proper ventilation in the laboratory to minimize exposure risks. Always follow standard safety protocols when working with reactive chemicals to maintain a safe laboratory environment.

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