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Ethyl(methyl)phenylamine oxide, also known as N-ethyl-N-methylphenylamine oxide, is an organic compound with the chemical formula C9H13NO. It is a derivative of phenylamine, where one hydrogen atom is replaced by an ethyl group and another by a methyl group, and the resulting amine is oxidized to form an oxide. ethyl(methyl)phenylamine oxide is a colorless liquid with a strong, pungent odor and is soluble in organic solvents. Ethyl(methyl)phenylamine oxide is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential applications in the field of materials science, particularly in the development of new polymers and other advanced materials. Due to its reactivity and potential health risks, it is important to handle this chemical with proper safety precautions.

825-19-4

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825-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 825-19-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 825-19:
(5*8)+(4*2)+(3*5)+(2*1)+(1*9)=74
74 % 10 = 4
So 825-19-4 is a valid CAS Registry Number.

825-19-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-methylbenzeneamine oxide

1.2 Other means of identification

Product number -
Other names (+-)-Aethyl-methyl-anilin-oxid,inaktives Methylaethylanilinoxyd

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:825-19-4 SDS

825-19-4Upstream product

825-19-4Relevant academic research and scientific papers

Deoxygenation of tertiary amine N-oxides under metal free condition using phenylboronic acid

Gupta, Surabhi,Sureshbabu, Popuri,Singh, Adesh Kumar,Sabiah, Shahulhameed,Kandasamy, Jeyakumar

supporting information, p. 909 - 913 (2017/02/15)

A simple and efficient method for the deoxygenation of amine N-oxides to corresponding amines is reported using the green and economical reagent phenylboronic acid. Deoxygenation of N,N-dialkylaniline N-oxides, trialkylamine N-oxides and pyridine N-oxides were achieved in good to excellent yields. The reduction susceptible functional groups such as ketone, amide, ester and nitro groups are well tolerated with phenylboronic acid during the deoxygenation process even at high temperature. In addition, an indirect method for identification and quantification of tert-amine N-oxide is demonstrated using UV–Vis spectrometry which may be useful for drug metabolism studies.

Rhenium-catalyzed highly efficient oxidations of tertiary nitrogen compounds to N-oxides using sodium percarbonate as oxygen source

Jain, Suman L.,Joseph, Jomy K.,Sain, Bir

, p. 2661 - 2663 (2008/09/16)

Sodium percarbonate was found to be an ideal and efficient oxygen source for the oxidation of tertiary nitrogen compounds to N-oxides in excellent yields in presence of various rhenium-based catalysts under mild reaction conditions. Georg Thieme Verlag Stuttgart.

OPTICAL RESOLUTION OF AMINE N-OXIDE BY DIASTEREOISOMERIC COMPLEX FORMATION WITH OPTICALLY ACTIVE HOST COMPOUND

Toda, Fumio,Mori, Koji

, p. 1841 - 1844 (2007/10/02)

Optical stereoisomers of various amine N-oxides with one or two chiral centers can effectively be resolved by selective crystalline complexation with an optically active host.Intermolecular interaction schemes and absolute configurations of the N-oxide guests are revealed by crystallographic analyses of the diastereoisomeric complexes.

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