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N-(3-AMINOPROPYL)-N-ETHYL-N-PHENYLAMINE, also known as N-(γ-Aminopropyl)-N-ethylaniline, is an organic compound with amine functional groups. It is characterized by its molecular structure that includes a propyl chain with an amino group attached to the third carbon, an ethyl group, and a phenyl group. N-(3-AMINOPROPYL)-N-ETHYL-N-PHENYLAMINE is known for its potential applications in various fields due to its chemical properties.

53606-48-7

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53606-48-7 Usage

Uses

Used in Dye Compositions:
N-(3-AMINOPROPYL)-N-ETHYL-N-PHENYLAMINE is used as a component in dye compositions for its ability to contribute to the formation of colored compounds. Its amine groups can participate in chemical reactions that lead to the creation of dyes with specific color characteristics, making it a valuable ingredient in the development of new dyes for various applications.
Used in Hydrogen Peroxide Detection:
N-(3-AMINOPROPYL)-N-ETHYL-N-PHENYLAMINE is utilized as a reagent for detecting hydrogen peroxide. Its amine groups can react with hydrogen peroxide in a redox reaction, which can be monitored to determine the presence and concentration of hydrogen peroxide in a sample. This makes it a useful tool in analytical chemistry and various industries where hydrogen peroxide detection is required.

Check Digit Verification of cas no

The CAS Registry Mumber 53606-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53606-48:
(7*5)+(6*3)+(5*6)+(4*0)+(3*6)+(2*4)+(1*8)=117
117 % 10 = 7
So 53606-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N2/c1-2-13(10-6-9-12)11-7-4-3-5-8-11/h3-5,7-8H,2,6,9-10,12H2,1H3/p+1

53606-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(N-ethylanilino)propylazanium

1.2 Other means of identification

Product number -
Other names 3-(ethyl-phenyl-amino)propylazanium

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:53606-48-7 SDS

53606-48-7Relevant academic research and scientific papers

Cobalt-based nanoparticles prepared from MOF-carbon templates as efficient hydrogenation catalysts

Murugesan, Kathiravan,Senthamarai, Thirusangumurugan,Sohail, Manzar,Alshammari, Ahmad S.,Pohl, Marga-Martina,Beller, Matthias,Jagadeesh, Rajenahally V.

, p. 8553 - 8560 (2018/11/30)

The development of efficient and selective nanostructured catalysts for industrially relevant hydrogenation reactions continues to be an actual goal of chemical research. In particular, the hydrogenation of nitriles and nitroarenes is of importance for the production of primary amines, which constitute essential feedstocks and key intermediates for advanced chemicals, life science molecules and materials. Herein, we report the preparation of graphene shell encapsulated Co3O4- and Co-nanoparticles supported on carbon by the template synthesis of cobalt-terephthalic acid MOF on carbon and subsequent pyrolysis. The resulting nanoparticles create stable and reusable catalysts for selective hydrogenation of functionalized and structurally diverse aromatic, heterocyclic and aliphatic nitriles, and as well as nitro compounds to primary amines (>65 examples). The synthetic and practical utility of this novel non-noble metal-based hydrogenation protocol is demonstrated by upscaling several reactions to multigram-scale and recycling of the catalyst.

Salts of 2- or 3-haloalkylamines in the synthesis of N-aminoalkyl derivatives of heterocyclic and aromatic amines

Vasilyeva,Vorobyeva,Osipov

, p. 2211 - 2215 (2017/05/12)

Reactions of 2-haloethyl- or 3-halopropylamine salts with NH-substrates (indoline, 1,2,3,4-tetrahydroquinoline, aniline, and N-ethylaniline) in the presence of NaHCO3 in water furnished various N-aminoalkyl derivatives of heterocyclic and aromatic amines.

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