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TCI

CAS 4229-44-1

N-Methylhydroxylamine Hydrochloride TCI M0804

N-Methylhydroxylamine Hydrochloride TCI M0804

Chemical Identity

CAS No.
4229-44-1
PubChem
CID 77906·SID 87572803
Formula
CH6ClNO
Molecular weight
83.52 g/mol
Purity
>97.0%(T)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
N-methylhydroxylamine;hydrochloride
SMILES
CNO.Cl
InChIKey
RGZRSLKIOCHTSI-UHFFFAOYSA-N
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N-Methylhydroxylamine Hydrochloride is a chemical compound widely used as a building block in various chemical reactions, particularly in the synthesis of organic compounds. It serves as an electron donor and plays a crucial role in facilitating reduction or oxidation reactions. This compound is essential for the formation of heterocyclic structures and complex molecules that require intermediate reaction steps. Its versatility makes it a valuable tool in both academic and industrial research settings.

One of the key properties that make N-Methylhydroxylamine Hydrochloride a preferred choice is its chemical stability and solubility in organic solvents such as ethyl acetate and acetone. These characteristics ensure that it remains effective during chemical processes without significant degradation. Additionally, its high consistency and low volatility make it easy to store and handle, enhancing its practicality in laboratory environments.

In Indonesian laboratories, N-Methylhydroxylamine Hydrochloride is commonly used in pure and applied chemical research, especially in the fields of pharmacy and organic chemistry. Researchers and students at universities and research institutions rely on this compound for experiments requiring high reactivity and chemical stability. Its reliability and effectiveness have made it a staple in both teaching and research laboratories across Indonesia.

  • Organic Synthesis: This compound is ideal for synthesizing complex organic molecules due to its ability to act as an electron donor in various reaction mechanisms.
  • Heterocyclic Compound Formation: It facilitates the creation of heterocyclic structures, which are essential in pharmaceutical and medicinal chemistry.
  • Redox Reactions: Its role in both reduction and oxidation processes makes it suitable for a wide range of chemical transformations.
  • Intermediate Reactions: It is frequently used as an intermediate in multi-step synthetic pathways, providing stability and reactivity.
  • Analytical Chemistry: Its chemical stability and solubility make it useful in analytical procedures requiring precise chemical behavior.

Brand TCI
CAS number 4229-44-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form White crystalline solid
Storage Store in a cool, dry place away from moisture and direct sunlight

N-Methylhydroxylamine Hydrochloride should be stored in a cool, dry place, away from moisture and direct sunlight to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its integrity. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible materials, and ensure that storage conditions are consistent with standard laboratory safety practices. Proper handling and storage are essential to preserve its effectiveness and ensure safe usage in laboratory settings.

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