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63302-40-9

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63302-40-9 Usage

Common Uses

Production of dyes, foams, and rubber products

Chemical Class

Aromatic amine derivative

Physical State

Solid (typically)

Appearance

Yellow to brown crystalline solid

Solubility

Soluble in organic solvents like ethanol and acetone

Melting Point

Varies depending on the specific compound

Boiling Point

Varies depending on the specific compound

Density

Varies depending on the specific compound

Hazardous Nature

Strong skin and eye irritant

Allergic Reactions

Can cause severe allergic reactions in some individuals

Carcinogenic Potential

Classified as a potential human carcinogen

Health Concerns

Linked to respiratory issues and other health problems

Handling Precautions

Careful handling and safety measures necessary when working with this chemical

Storage

Store in a cool, dry, and well-ventilated area, away from incompatible substances

Disposal

Dispose of according to local, national, and international regulations for hazardous materials

Regulatory Status

Subject to various regulations and restrictions depending on the country or region

Safety Measures

Use personal protective equipment (PPE) such as gloves, goggles, and masks when handling

First Aid

In case of skin or eye contact, immediately flush with water and seek medical attention

Environmental Impact

Potentially harmful to the environment if not disposed of properly

Check Digit Verification of cas no

The CAS Registry Mumber 63302-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,0 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63302-40:
(7*6)+(6*3)+(5*3)+(4*0)+(3*2)+(2*4)+(1*0)=89
89 % 10 = 9
So 63302-40-9 is a valid CAS Registry Number.

63302-40-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methylpentan-2-ylideneamino)-N-phenylaniline

1.2 Other means of identification

Product number -
Other names 1,4-Benzenediamine,N-(1,3-dimethylbutylidene)-N'-phenyl

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:63302-40-9 SDS

63302-40-9Relevant articles and documents

Tailoring supported palladium sulfide catalysts through H 2-assisted sulfidation with H2S

Xu, Wei,Ni, Jun,Zhang, Qunfeng,Feng, Feng,Xiang, Yizhi,Li, Xiaonian

, p. 12811 - 12817 (2013)

Supported palladium sulfide catalysts are of great interest in selective hydrogenation reactions. In this work, "Pd4S", "Pd3S", "Pd16S7" and "PdS" supported on activated carbon were selectively synthesized by tailoring the H2-assisted sulfidation of Pd/C with H2S at 150-750°C, and were characterized by means of XRD, XPS, TEM, HRTEM, EDS, BET and H2-TPR techniques. The results indicated that the sulfidation atmosphere, the sulfidation temperature and the metal-support interaction all played important roles in determining the crystal structure and composition of the PdxSy/C catalysts, which in turn gave different catalytic performances in the synthesis of N-(1,3-dimethylbutyl)-N′- phenyl-p-phenylenediamine (6PPD) by the reductive N-alkylation of aromatic amines. PdS/C showed the highest selectivity (>97%) and stability among all the PdxSy/C catalysts.

Preparation, structural characterization of a novel egg-shell palladium sulfide catalyst and its application in selective reductive alkylation reaction

Zhang, Qun Feng,Wu, Jia Chun,Su, Chang,Feng, Feng,Ding, Qiao Ling,Yuan, Zhao Lian,Wang, Hong,Ma, Lei,Lu, Chun Shan,Li, Xiao Nian

, p. 1111 - 1114,4 (2020/08/20)

A novel egg-shell Pd-S catalyst with palladium metal as the core and a membrane of palladium sulfide as the surface has been prepared by sulphidizing Pd/C with H2S. This catalyst is effective for the reductive alkylation of p-amino diphenylamine (PADPA) and methylisobutyl ketone (MIBK) to afford N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenedianine (DBPPD) with conversion up to 99.42% and selectivity to 97.46%. Comparing with the other common palladium sulfide catalysts, the membrane of palladium sulfide on the surface and the core of palladium metal cause the Pd on the surface of the new catalyst in a lower sulfur coordination, which improves its activity. Our result indicates that this new egg-shell Pd-S/C is an efficient hydrogenation catalyst.

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