20295-82-3

Basic information

• Product Name: Aminooxyacetic Acid, Hydrochloride Salt Discontinued See: C178730
• Synonyms: Aminooxyacetic Acid, Hydrochloride Salt Discontinued See: C178730;AMinoxyacetic Acid Hydrochloride;CarboxyMethoxyaMine Hydrochloride;O-(CarboxyMethyl)hydroxylaMine Hydrochloride;Aminooxyacetic Acid,Hydrochloride Salt (AOA HCL (1:1))
• CAS NO: 20295-82-3
• Molecular Formula: C₂H₅NO₃*ClH
• Molecular Weight: 127.52694
• Product Categories: Aliphatics;Amines;Aliphatics, Amines
• Mol File: 20295-82-3.mol
• Article Data: 4

Chemical Properties

• Melting Point: 180-188.5 °C
• Appearance: /
• CAS DataBase Reference: Aminooxyacetic Acid, Hydrochloride Salt Discontinued See: C178730(CAS DataBase Reference)
• NIST Chemistry Reference: Aminooxyacetic Acid, Hydrochloride Salt Discontinued See: C178730(20295-82-3)
• EPA Substance Registry System: Aminooxyacetic Acid, Hydrochloride Salt Discontinued See: C178730(20295-82-3)

Safety Data

• Hazardous Substances Data: 20295-82-3(Hazardous Substances Data)

Usage

General Description

Aminooxyacetic Acid, Hydrochloride Salt is a chemical compound that has been discontinued and is now identified as a different product with the code C178730. Aminooxyacetic acid is a compound that is used in the synthesis of pharmaceuticals and is also known for its ability to inhibit the enzymatic activity of pyridoxal phosphate-dependent enzymes. Aminooxyacetic Acid, Hydrochloride Salt Discontinued See: C178730, when in its hydrochloride salt form, is generally used in research and laboratory settings for its unique chemical properties. However, due to its discontinuation, it is no longer commercially available but can still be obtained under the new product code C178730.

Upstream product

• 5382-89-8 [(propan-2-ylideneamino)oxy]acetic acid 
• 5251-93-4 N-benzoylaminooxyacetic acid 
• 93-58-3 benzoic acid methyl ester 
• 495-18-1 Benzohydroxamic acid 

Downstream Products

• 161579-74-4 (19E,20R)-3β,20-dihydroxypregn-5-en-19-al 3-benzoate 20-formate 19-(O-carboxymethyl)oxime 
• 50909-89-2 Progesteron-3-(O-carboxymethyl)-oxim 
• 660452-21-1 [({(1E)-[3-{[(tert-butoxycarbonyl)amino]methyl}-2-isobutyl-4-(4-methylphenyl)quinolin-6-yl]methylene}amino)oxy]acetic acid 
• 131971-15-8 3,3-diphenyl-4-oxo-hexanal-1-(O-carboxymethyl)oxime 
• 162473-89-4 O-(carboxymethyl)-p-azidotetrafluorobenzaldoxime 
• 14417-89-1 2-[(cyclohexylideneamino)oxy]ethanoic acid 
• 53260-10-9 17α-hydroxyprogesterone-3-carboxymethyloxime 
• 43188-86-9 hydrocortisone 3-(O-carboxymethyl)oxime 
• 65132-67-4 Benzoic acid (8R,9S,13S,14S,17S)-6-[(E)-carboxymethoxyimino]-17-hydroxy-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3-yl ester 
• 35048-47-6 6-keto-1,3,5(10)estratriene-3,17β-diol 6-carboxymethyloxime 

Relevant articles and documents

PROCESS FOR PRODUCTION OF O-SUBSTITUTED HYDROXYLAMINES

[Purpose] The purpose of the present invention is to provide a method for the production of O-substituted hydroxylamine compounds at a high yield by using industrially available starting material. [Solution method] Method for the production of O-substituted hydroxylamine compounds comprising a process of obtaining O-substituted hydroxylamine disulfonic acid alkali metal salts by reacting hydroxylamine disulfonic acid alkali metal salts with halides exemplified by alkylating agents (RX), and a process of hydrogenating the obtained O-substituted hydroxylamine disulfonic acid alkali metal salt.

Process for producing aminooxyacetic acid salts

A process for producing an aminooxyacetic acid salt comprises reacting benzhydroxamic acid of formula: STR1 (where R1 is a hydrogen atom, an alkyl group, an alkoxy group or a halogen atom) with a halogenoacetic acid of formula: (where X is an iodine, bromine or chlorine atom) in the presence of a metal hydroxide or a metal carbonate to form benzamidooxyacetic acid of formula (IV): STR2 and thereafter hydrolyzing the benzamidooxyacetic acid in the presence of a mineral acid to obtain an aminooxyacetic acid salt of formula: