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N,N-diethyl-N,N-diphenyl-methanediamine, also known as 1,1-diphenyl-N,N-diethyl-methylendiamin, is an organic compound with the chemical formula C18H22N2. It is a colorless to pale yellow liquid with a molecular weight of 270.38 g/mol. N,N-diethyl-N,N-diphenyl-methanediamine is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is characterized by its amine functional groups, which contribute to its reactivity and ability to form complexes with metal ions. The compound is also known for its potential applications in the production of dyes and pigments, as well as in the rubber and plastics industry. Due to its chemical structure, it is important to handle this substance with care, as it may have certain health and environmental impacts.

5419-13-6

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5419-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5419-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5419-13:
(6*5)+(5*4)+(4*1)+(3*9)+(2*1)+(1*3)=86
86 % 10 = 6
So 5419-13-6 is a valid CAS Registry Number.

5419-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-diethyl-N,N'-diphenylmethanediamine

1.2 Other means of identification

Product number -
Other names N,N'-diethyl-N,N'-diphenyl-methanediyldiamine

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:5419-13-6 SDS

5419-13-6Relevant academic research and scientific papers

Bridging amines with CO2: Organocatalyzed reduction of CO2 to aminals

Frogneux, Xavier,Blondiaux, Enguerrand,Thuéry, Pierre,Cantat, Thibault

, p. 3983 - 3987 (2015/11/11)

The four-electron reduction of CO2 in the presence of secondary aromatic amines is described for the first time to access aminals. Under metal-free hydrosilylation conditions, the four C-O bonds of CO2 are cleaved, and the organocatalysts are able to balance the reactivity of CO2 to promote the selective formation of two C-N and two C-H bonds. The methodology enables the formation of various symmetrical and unsymmetrical aminals.

A Novel Synthesis of Diaminomethanes

Melis, Stefana,Monni, Francesca,Piras, Pier Paolo,Sotgiu, Francesca

, p. 463 (2007/10/02)

Diaminomethanes have been synthesized by reaction of 1,3-benzodioxole and 1,3-benzoxathiole with a double amount of sodium dialkyl and alkyl aryl amides.

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