O-Methylhydroxylamine Hydrochloride TCI M0343

Chemical Identity

CAS No.: 593-56-6
PubChem: CID 521874·SID 87572413
Formula: CH6ClNO
Molecular weight: 83.52 g/mol
Purity: >97.0%(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: O-methylhydroxylamine;hydrochloride
SMILES: CON.Cl
InChIKey: XNXVOSBNFZWHBV-UHFFFAOYSA-N

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O-Methylhydroxylamine Hydrochloride (OMHCl) is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. It serves as a key reagent in organic chemistry, particularly in reactions involving nitrogen-containing compounds. OMHCl is commonly utilized in the preparation of heterocyclic structures and other nitrogen-based molecules, making it an essential building block for chemists. Its versatility allows it to participate in various reaction mechanisms, including substitution and nucleophilic reactions, contributing to the development of new chemical compounds.

The chemical properties of OMHCl make it a preferred choice for researchers. It exhibits stability under certain conditions while remaining highly reactive in others, which is crucial for its application in synthetic processes. Its molecular structure is simple yet effective, enabling it to act as a reactive intermediate in a wide range of chemical transformations. The reactivity of OMHCl allows it to be a valuable reagent in reactions requiring high reactivity, making it a staple in both academic and industrial laboratories.

In Indonesian laboratories, OMHCl is extensively used in chemical research, especially in organic synthesis and analytical chemistry. It is particularly relevant for educational institutions and research centers that focus on the development of new compounds and the study of chemical reactions. Its availability in various packaging options ensures ease of use across different experimental scales, supporting both small-scale research and larger chemical processes.

Related TCI products

Organic synthesis where nitrogen-containing compounds are required due to its role in forming heterocyclic structures.
Nucleophilic substitution reactions where OMHCl acts as a reactive intermediate for the creation of new chemical bonds.
Analytical chemistry applications for the detection and quantification of nitrogen-based compounds in complex mixtures.
Research in medicinal chemistry for the development of pharmaceutical compounds involving nitrogen functionalities.
Teaching and experimental setups in Indonesian universities for demonstrating key chemical reaction mechanisms.

Brand	TCI
CAS number	593-56-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various sizes to suit different experimental needs
Physical form	White crystalline solid
Storage	—

OMHCl should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to keep the material in a tightly sealed container to prevent moisture absorption, which can affect its reactivity. Due to its high reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize exposure. Avoid contact with incompatible substances such as strong oxidizing agents. Always use appropriate personal protective equipment, including gloves and safety goggles, when handling this compound. Proper storage and handling ensure the stability and effectiveness of OMHCl in laboratory applications.

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