42548-78-7

Usage

Uses

Used in Organic Synthesis:
N-Ethylhydroxylamine hydrochloride is used as a reducing agent for the synthesis of various chemicals, including pharmaceuticals and pesticides. Its stability and efficiency make it a valuable component in the production of these compounds.
Used in Chemical Production:
N-Ethylhydroxylamine hydrochloride is used as a key intermediate in the production of other chemicals, contributing to the development of new materials and products in the chemical industry.
Used in Research and Development:
In the field of research and development, N-Ethylhydroxylamine hydrochloride is used as a reagent to explore new chemical reactions and pathways, potentially leading to the discovery of novel compounds and applications.

InChI:InChI=1/C2H7NO.ClH/c1-2-3-4;/h3-4H,2H2,1H3;1H

Upstream product

• 79-24-3 Nitroethane 
• 109-89-7 diethylamine 

Downstream Products

• 3585-94-2 4-nitro-benzaldehyd-(N-ethyl oxime ) 
• 15796-52-8 N,N'-diethyl-N,N'-dihydroxymethanediamine 
• 40934-32-5 N-Cyclohexyl-2-(1-cyclohexylcarbamoyl-ethylamino)-propionamide 
• 40934-34-7 2-(1-Cyclohexylcarbamoyl-ethylamino)-pentanoic acid cyclohexylamide 
• 10514-12-2 2,4,4-triethyl-isoxazolidine-3,5-dione 
• 106577-14-4 adamantalydene ethyl nitron 
• 52271-40-6 N-idrossifenfluramina 
• 83490-54-4 N-Ethyl-2-hydroxy-3-methylbutyrohydroxamsaeure 
• 82820-53-9 N-tert-butoxycarbonyl-N-ethylhydroxylamine 
• 88051-42-7 N-Ethyl-2-hydroxy-2,3-diphenylpropiohydroxamsaeure 
• 88051-43-8 N-Ethyl-2-hydroxy-2-phenylpropiohydroxamsaeure 
• 83490-58-8 N-Ethyl-2-hydroxy-3-phenylpropiohydroxamsaeure 
• 110842-41-6 N-ethyl-N-hydroxy-6-(6-methoxy-2-naphthyl)-6-oxohexanamide 
• 83490-56-6 N-Ethyl-2-hydroxy-2-phenylacetohydroxamsaeure 

Relevant academic research and scientific papers

PROCESS FOR THE PURIFICATION OF A MIXTURE COMPRISING N-ALKYL-HYDROXYLAMMONIUM SALTS

The present invention relates to a process for purification of a mixture comprising water, N-alkyl-hydroxylammonium salts and some byproducts wherein from the mixture water and byproducts are distilled off until the purity of N-alkyl-hydroxylammonium salts in the residue is 95% or higher and additionally keeping the water content during and after the distillation ≥ 40 wt.-% according to the residue.

NITRONE COMPOUNDS AND USE THEREOF

The present invention relates to novel nitrone compounds of formula (I), wherein, A, A1, R1, R2, R3, R4 and n are as defined in the description. The present invention further relates to their preparation and use to protect crops against undesired phytopathogenic microorganisms, phytopathogenic fungi and pests such as nematodes.

Molybdenum(VI) complexes with N-substituted hydroxylamines

New molybdenum(VI) complexes with N-monoalkylsubstituted hydroxylamines have been synthesized and studied. The structure of [MoO2(C 2H5NHO)2] and [MoO2(i-C 3H7NHO)2], whose distinguishing feature is the bidentate chelate coordination of the ligand to molybdenum with the formation of the three-membered NMoO chelate ring, has been determined by X-ray diffraction.

Process for obtaining N-monosubstituted hydroxylamine

The subject of the present invention is a new process for obtaining nitrones. It more particularly relates to a process for obtaining N-monosubstituted hydroxylamine comprising a stage in which a nitrone is formed from a secondary amine in the presence of an oxidizing agent and of at least one C=O containing species chosen from the group consisting of carbon dioxide, hydrogencarbonates and carbonates.