65753-93-7

Basic information

• Product Name: N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID
• Synonyms: 2-DIMETHYLAMINO-N-HYDROXY-N-METHYLACETAMIDE;N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID;Methyldimethylaminoacetohydroxamicacid;Acetamide, 2-(dimethylamino)-N-hydroxy-N-methyl- (9CI);N-Methyl-2-dimethylaminoacetohydroxamic Acid
• CAS NO: 65753-93-7
• Molecular Formula: C₅H₁₂N₂O₂
• Molecular Weight: 132.16
• Product Categories: AMINETERTIARY;Hydroxylamines;Hydroxylamines (N-Substituted)
• Mol File: 65753-93-7.mol
• Article Data: 2

Chemical Properties

• Melting Point: 100°C
• Boiling Point: 193.2±42.0 °C(Predicted)
• Appearance: /
• Density: 1.099±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 7.27±0.50(Predicted)
• CAS DataBase Reference: N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID(65753-93-7)
• EPA Substance Registry System: N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID(65753-93-7)

Safety Data

• Hazardous Substances Data: 65753-93-7(Hazardous Substances Data)

Usage

Description

N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID, with the molecular formula C5H12N2O3, is a hydroxamic acid derivative characterized by its chelating properties. This functional group is adept at forming stable complexes with metal ions, making it a versatile compound in various scientific and industrial applications.

Uses

Used in Metal Ion Extraction and Separation Processes:
N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID is used as a chelating agent for the extraction and separation of metal ions. Its ability to form stable complexes with these ions makes it a valuable tool in processes that require the selective removal or concentration of specific metal ions.
Used in Analytical Chemistry:
In the field of analytical chemistry, N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID is used as a chelating agent for various metal ions. It aids in the accurate determination and analysis of metal ion concentrations, contributing to the advancement of chemical research and quality control in various industries.
Used in Research for Biological Activities:
N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID is also utilized in research for exploring its potential biological activities. Studies have investigated its anticancer and antimicrobial properties, indicating that this compound could have significant implications in the development of new therapeutic agents and treatments.
Used in Pharmaceutical Development:
In the pharmaceutical industry, N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID is used as a starting material or intermediate in the synthesis of drugs with potential therapeutic benefits. Its unique properties make it a promising candidate for the development of new medications, particularly those targeting cancer and infectious diseases.
Overall, N-METHYL-2-DIMETHYLAMINOACETOHYDROXAMIC ACID's diverse applications in chemistry, engineering, and biology underscore its importance as a versatile and valuable compound in scientific research and industrial processes.

Upstream product

• 7148-06-3 N,N-dimethylglycine methyl ester 
• 4229-44-1 N-methylhydroxyamine hydrochloride 
• 593-77-1 N-Methylhydroxylamine 
• 1954-58-1 Dimethylamino-acetic acid methyl ester; hydrochloride 

Downstream Products

• 111130-85-9 1-Hydroxy-5-(2,2,2-trifluoro-acetylamino)-naphthalene-2-carboxylic acid phenyl ester 
• 86-93-1 1-Phenyl-1H-tetrazole-5-thiol 
• 122913-69-3 Acetic acid 3-chloro-4-hydroxy-2,6-dimethyl-phenyl ester 
• 67184-41-2 2,5‐dimethoxybenzaldoxime 
• 17696-62-7 Phenyl 4-hydroxybenzoate 
• 103-90-2 4-acetaminophenol 
• 80767-12-0 4-hydroxybenzyl acetate 
• 6045-67-6 Acetic acid (8R,9S,13S,14S)-3-hydroxy-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-yl ester 
• 141-97-9 ethyl acetoacetate 

Relevant articles and documents

Method for producing an n-alkyl-alpha-dialkyl-aminoacethohydroxamic acid compound

There is disclosed a method for producing an N-alkyl-α-dialkylaminoacetohydroxamic acid compound represented by formula (2), which comprises reacting an α-dialkylaminoacetic acid ester compound represented by formula (1) with an N-alkylhydroxylamine, wherein the reaction is carried out in water and an ether-series organic solvent, STR1 wherein R1, R2, R3 and R4, which are the same or different, each represents an alkyl group. According to the method, it is possible to obtain the objective compound in a high yield with a short reaction time, with restrained formation of a by-product.