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TCI

CAS 22059-22-9

Acetamidoxime TCI A2646

Acetamidoxime TCI A2646

Chemical Identity

CAS No.
22059-22-9
PubChem
CID 30926·SID 253660036
Formula
C2H6N2O
Molecular weight
74.08 g/mol
Purity
>97.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
N'-hydroxyethanimidamide
SMILES
CC(=NO)N
InChIKey
AEXITZJSLGALNH-UHFFFAOYSA-N
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Acetamidoxime (TCI A2646), with CAS number 22059-22-9, is a chemical compound widely used in organic synthesis as a fundamental building block. It plays a crucial role in laboratory settings by serving as a versatile reagent in various chemical reactions. Its molecular structure enables it to participate in substitution and coupling reactions, facilitating the formation of complex organic molecules from simpler precursors. This compound is essential for researchers working on the development of new pharmaceuticals, polymers, and other advanced chemical products.

Acetamidoxime is valued for its chemical stability under controlled conditions and its reactivity toward environmental factors such as temperature and humidity. It exhibits good solubility in organic solvents like ethylamine and methanol, which makes it highly suitable for purification and reaction processes. These properties allow it to be a preferred choice for chemists seeking reliable and efficient reagents for their experiments. Its compatibility with a wide range of solvents and reagents further enhances its utility in diverse chemical applications.

In Indonesian laboratories, acetamidoxime is commonly used by researchers and students in higher education institutions and research organizations. It is an integral part of organic chemistry courses and practical experiments, where it is employed to demonstrate key synthetic techniques. Its availability and effectiveness make it a staple in both academic and industrial research environments, supporting the advancement of chemical knowledge and innovation.

  • Organic synthesis reactions where acetamidoxime acts as a key intermediate in the formation of heterocyclic compounds.
  • Substitution reactions that require a reactive functional group for the creation of complex molecular structures.
  • Coupling reactions that benefit from acetamidoxime’s ability to form stable intermediates during bond formation.
  • Purification processes due to its solubility in organic solvents, allowing for efficient separation of target compounds.
  • Teaching laboratories where it is used to demonstrate fundamental chemical reactions and synthetic methodologies.

Brand TCI
CAS number 22059-22-9
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

Acetamidoxime should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to minimize exposure to moisture and air, which can affect its reactivity. Due to its potential reactivity with certain environmental conditions, it should be handled in a well-ventilated area. Proper labeling of containers is essential for safety and identification. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Regular monitoring of storage conditions ensures the integrity of the material and supports safe laboratory practices.

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