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10050-89-2

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10050-89-2 Usage

Description

1,4-Benzenediamine,N4-[[4-(dimethylamino)phenyl]methylene]-N1,N1-dimethyl-, also known as N4-[[4-(dimethylamino)phenyl]methylene]-N1,N1-dimethyl-1,4-benzenediamine, is a chemical compound belonging to the aromatic amine family. It is characterized by its potential toxicity and has been associated with skin and eye irritation, respiratory and immune system effects, as well as potential carcinogenic and mutagenic effects. Due to these concerns, it is crucial to handle and use this chemical with caution and in accordance with safety guidelines.

Uses

Used in Dye Production:
1,4-Benzenediamine,N4-[[4-(dimethylamino)phenyl]methylene]-N1,N1-dimethylis used as a key intermediate in the production of dyes. Its unique chemical structure allows for the creation of a wide range of colors, making it a valuable component in the dye industry.
Used in Hair Coloring Products:
This chemical compound is also commonly used in the formulation of hair coloring products. Its ability to bind with hair proteins enables it to provide long-lasting color results. However, due to its potential toxicity, it is essential to ensure that the final hair coloring products are safe for consumer use and comply with regulatory standards.
Used in Pharmaceutical Industry:
1,4-Benzenediamine,N4-[[4-(dimethylamino)phenyl]methylene]-N1,N1-dimethylmay also find applications in the pharmaceutical industry, where it can be used as a building block for the synthesis of various drugs. Its chemical properties make it a versatile component in the development of new medications.
Used in Research and Development:
Due to its unique chemical structure and potential applications, 1,4-Benzenediamine,N4-[[4-(dimethylamino)phenyl]methylene]-N1,N1-dimethylis also used in research and development settings. Scientists and researchers can explore its properties and potential uses in various fields, such as material science, chemistry, and biology.

Check Digit Verification of cas no

The CAS Registry Mumber 10050-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10050-89:
(7*1)+(6*0)+(5*0)+(4*5)+(3*0)+(2*8)+(1*9)=52
52 % 10 = 2
So 10050-89-2 is a valid CAS Registry Number.

10050-89-2SDS

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-(dimethylamino)phenyl]iminomethyl]-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names N.N-Dimethyl-N'-(4-dimethylamino-benzyliden)-p-phenylendiamin

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:10050-89-2 SDS

10050-89-2Relevant articles and documents

Pathway Dependence in Redox-Driven Metal–Organic Gels

Panja, Santanu,Adams, Dave J.

, p. 6130 - 6135 (2020)

Pathway dependence is common in self-assembly. Herein, the importance of pathway dependence for redox-driven gels is shown by constructing a FeII/FeIII redox-based metal–organic gel system is shown. In situ oxidation of the FeII

Substituent cross-interaction effects on the electronic character of the C=N bridging group in substituted benzylidene anilines - Models for molecular cores of mesogenic compounds. A 13C NMR study and comparison with theoretical results

Neuvonen, Helmi,Neuvonen, Kari,Fueloep, Ferenc

, p. 3141 - 3148 (2007/10/03)

13C NMR chemical shifts δc(C=N) were measured in CDCl 3 for a wide set of mesogenic molecule model compounds, viz. the substituted benzylidene anilines P-X-C6H4CH=NC 6H4-p-Y (X = NO2, CN, CF3, F, Cl, H, Me, MeO, or NMe2; Y = NO2, CN, F, Cl, H, Me, MeO, or NMe2). The substituent dependence of δc(C=N) was used as a tool to study electronic substituent effects on the azomethine unit. The benzylidene substituents X have a reverse effect on δc(C=N): electron-withdrawing substituents cause shielding, while electron-donating ones behave oppositely, the inductive effects clearly predominating over the resonance effects. In contrast, the aniline substituents Y exert normal effects: electron-withdrawing substituents cause deshielding, while electron-donating ones cause shielding of the C=N carbon, the strengths of the inductive and resonance effects being closely similar. Additionally, the presence of a specific cross-interaction between X and Y could be verified. The electronic effects of the neighboring aromatic ring substituents systematically modify the sensitivity of the C=N group to the electronic effects of the benzylidene or aniline ring substituents. Electron-withdrawing substituents on the aniline ring decrease the sensitivity of δc(C=N) to the substitution on the benzylidine ring, while electron-donating substituents have the opposite effect. In contrast, electron-withdrawing substituents on the benzylidene ring increase the sensitivity of δc(C=N) to the substituent on the aniline ring, while electron-donating substituents act in the opposite way. These results can be rationalized in terms of the substituent-sensitive balance of the electron delocalization (mesomeric effects). The present NMR characteristics are discussed as regards the computational literature data. Valuable information has been obtained on the effects of the substituents on the molecular core of the mesogenic model compounds.

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