The development of novel compounds often incorporates N-O Dimethylhydroxylamine HCl as a reagent.

N-O Dimethylhydroxylamine Hydrochloride (N-O Dimethylhydroxylamine HCl)

N,O-Dimethylhydroxylamine HCL

1. Chemical Identity

  • Chemical Name: N-O Dimethylhydroxylamine Hydrochloride

  • Other Names: N,N-Dimethylhydroxylamine hydrochloride, DMHA·HCl

  • Molecular Formula: C₂H₇ClNO

  • Molecular Weight: 97.54 g/mol

  • CAS Number: 3283-24-3


2. Molecular Structure

The compound consists of a hydroxylamine (–NHOH) group where the nitrogen atom is substituted with two methyl groups (-CH₃). The compound exists as a hydrochloride salt formed by protonation of the nitrogen and association with a chloride ion.

  • Structural formula:

    H | CH3–N–O·HCl | CH3

  • Description:
    The nitrogen atom carries two methyl groups and is bonded to an oxygen atom (N–O bond). The protonated nitrogen forms the hydrochloride salt with Cl⁻.


3. Physical and Chemical Properties

Property Description
Appearance White to off-white crystalline solid
Melting Point ~120–130 °C (may decompose)
Solubility Highly soluble in water and alcohols
Stability Stable under normal conditions; sensitive to strong oxidizers and acids
Form Hydrochloride salt form increases stability and handling ease

 


4. Synthesis

N-O Dimethylhydroxylamine hydrochloride is generally prepared by:

  • Methylation of hydroxylamine hydrochloride using methylating agents like dimethyl sulfate or methyl iodide under controlled conditions to selectively attach methyl groups to the nitrogen atom.

  • Careful control of reaction conditions is necessary to prevent over-methylation or decomposition.


5. Applications

  • Widely used as a key intermediate in organic synthesis, especially in the preparation of compounds containing N–O functional groups.

  • Utilized for the synthesis of oximes, which are important intermediates in pharmaceuticals and agrochemicals.

  • Used in the manufacture of various fine chemicals where introducing a dimethylhydroxylamine moiety is required.


6. Chemical Reactivity

  • Exhibits nucleophilic properties at the nitrogen and oxygen atoms, allowing it to react with electrophiles.

  • The N–O bond can undergo transformations useful in synthetic pathways, including condensation and oxidation-reduction reactions.


7. Safety and Handling

  • Should be handled with care as it can be an irritant to the skin, eyes, and respiratory system.

  • Use personal protective equipment such as gloves, goggles, and work in a well-ventilated area or fume hood.

  • Store in a cool, dry place, away from strong oxidizers and acids.


8. Summary

N-O Dimethylhydroxylamine Hydrochloride is a stable, water-soluble crystalline compound widely used in organic synthesis to introduce N–O functionality. Its hydrochloride salt form improves stability and ease of handling, making it a valuable reagent and intermediate in pharmaceuticals, agrochemicals, and fine chemical industries.

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