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1,4-Benzenediamine, N-phenyl-N'-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13556-73-5

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13556-73-5 Usage

Appearance

White to light brown crystalline powder

Odor

Slight amine odor

Solubility

Insoluble in water

Primary use

Antioxidant in rubber products and plastics

Function

Inhibits the formation of free radicals, preventing degradation and loss of physical properties in rubber and plastic materials

Additional uses

Stabilizer in adhesive formulations, component in hair dyes and colorants

Safety precautions

Classified as a skin and eye irritant, harmful if swallowed or inhaled

Handling

Handle with caution, use appropriate personal protective equipment (PPE) such as gloves, goggles, and masks.

Check Digit Verification of cas no

The CAS Registry Mumber 13556-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,5 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13556-73:
(7*1)+(6*3)+(5*5)+(4*5)+(3*6)+(2*7)+(1*3)=105
105 % 10 = 5
So 13556-73-5 is a valid CAS Registry Number.

13556-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N-benzyl-4-N-phenylbenzene-1,4-diamine

1.2 Other means of identification

Product number -
Other names Phenyl-<4-benzylamino-phenyl>-amin

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:13556-73-5 SDS

13556-73-5Downstream Products

13556-73-5Relevant academic research and scientific papers

Pt-Sn/γ-Al2O3-catalyzed highly efficient direct synthesis of secondary and tertiary amines and imines

He, Wei,Wang, Liandi,Sun, Chenglin,Wu, Kaikai,He, Songbo,Chen, Jiping,Wu, Ping,Yu, Zhengkun

experimental part, p. 13308 - 13317 (2012/02/02)

Versatile syntheses of secondary and tertiary amines by highly efficient direct N-alkylation of primary and secondary amines with alcohols or by deaminative self-coupling of primary amines have been successfully realized by means of a heterogeneous bimetallic Pt-Sn/γ-Al2O3 catalyst (0.5 wt % Pt, Pt/Sn molar ratio=1:3) through a borrowing-hydrogen strategy. In the presence of oxygen, imines were also efficiently prepared from the tandem reactions of amines with alcohols or between two primary amines. The proposed mechanism reveals that an alcohol or amine substrate is initially dehydrogenated to an aldehyde/ketone or NH-imine with concomitant formation of a [PtSn] hydride. Condensation of the aldehyde/ketone species or deamination of the NH-imine intermediate with another molecule of amine forms an N-substituted imine which is then reduced to a new amine product by the in-situ generated [PtSn] hydride under a nitrogen atmosphere or remains unchanged as the final product under an oxygen atmosphere. The Pt-Sn/γ-Al2O 3 catalyst can be easily recycled without Pt metal leaching and has exhibited very high catalytic activity toward a wide range of amine and alcohol substrates, which suggests potential for application in the direct production of secondary and tertiary amines and N-substituted imines.

Method for the production of vinyl norbornene

-

, (2008/06/13)

A method for producing vinyl norbornene at a high yield preventing the formation of Diels-Alder reaction by-products which is characterized in that cyclopentadiene and butadiene are reacted in the presence of p-phenylenediamine compounds such as N-isopropyl-N'-phenyl-p-phenylenediamine, N,N'-diphenyl-p-phenylenediamine and the like.

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