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CAS 6638-79-5

N,O-Dimethylhydroxylamine Hydrochloride TCI D1899

N,O-Dimethylhydroxylamine Hydrochloride TCI D1899

Chemical Identity

Other names
N-Methoxy-N-methylamine Hydrochloride
CAS No.
6638-79-5
PubChem
CID 81138·SID 87568359
Formula
C2H7NO.HCl
Molecular weight
97.54 g/mol
Purity
>98.0%(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
N-methoxymethanamine;hydrochloride
SMILES
CNOC.Cl
InChIKey
USZLCYNVCCDPLQ-UHFFFAOYSA-N
MDL
MDL00012485
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N,O-Dimethylhydroxylamine Hydrochloride is a chemical compound widely used in laboratory settings for organic synthesis reactions. It serves as a versatile building block in the creation of complex organic molecules and heterocyclic compounds. This reagent plays a crucial role in substitution and oxidation reactions, making it an essential component in synthetic chemistry workflows. Its ability to participate in various reaction mechanisms allows chemists to design and execute a wide range of chemical transformations with high efficiency and selectivity.

The compound is known for its stability in solid form and its solubility in organic solvents such as ethyl acetate and acetone. These properties make it particularly suitable for reactions that require the use of organic solvents. Its reactivity and solubility characteristics ensure that it can be effectively integrated into diverse experimental setups. Additionally, its relatively safe handling profile under normal conditions contributes to its popularity among laboratory professionals.

In Indonesian laboratories, N,O-Dimethylhydroxylamine Hydrochloride is commonly used in both fundamental and applied chemical research. Educational and research institutions rely on this compound for specific chemical reactions that are critical to their experimental protocols. Its availability in the local market makes it a practical choice for laboratory needs, supporting both academic and industrial chemical studies.

TCI brochures (PDF)

  • Heterocyclic Compound Synthesis: This compound is ideal for creating heterocyclic structures due to its reactivity and ability to participate in various reaction mechanisms.
  • Organic Reaction Optimization: Its solubility in organic solvents makes it suitable for reactions requiring efficient mixing and dissolution of reactants.
  • Oxidation Reactions: The compound’s reactivity supports oxidation processes, enabling the synthesis of complex organic molecules with high yield.
  • Substitution Reactions: Its role in substitution reactions allows for the selective modification of organic molecules, enhancing the versatility of synthetic pathways.
  • Educational Research Experiments: It is frequently used in academic settings to teach and demonstrate key chemical reaction principles and synthetic techniques.

Brand TCI
CAS number 6638-79-5
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply formats
Physical form Solid
Storage Store in a cool, dry place away from direct sunlight and moisture

Data from the TCI brochure

Kemasan25g / 100g / 500g

Source: TCI brochure RR113 (2025-04-18)

This compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to use airtight containers to prevent moisture absorption and contamination. Proper labeling of storage containers is essential to ensure safe handling and easy identification. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to minimize exposure. Regular inspection of storage conditions and containers is advised to maintain the integrity of the compound. Always ensure that the compound is kept away from incompatible materials to prevent any potential chemical interactions.

References cited in the TCI brochure

  1. Hisao Nemoto. Direct One-Pot Synthesis of α-Siloxy-Weinreb Amides from Aldehydes The Journal of Organic Chemistry, 2007. doi:10.1021/jo701859a