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99762-80-8

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99762-80-8 Usage

Description

N,N'-Dibutylquinacridone is a red-violet colored quinacridone pigment with two butyl groups attached to the nitrogen atoms, enhancing its solubility and dispersion in various mediums. Known for its high resistance to heat, light, and chemicals, it is a popular choice for various applications due to its high color strength and durability.

Uses

Used in Inks, Dyes, and Coatings Industry:
N,N'-Dibutylquinacridone is used as a pigment for its high color strength and durability, making it suitable for the production of inks, dyes, and coatings.
Used in Automotive Industry:
N,N'-Dibutylquinacridone is used as a pigment in automotive coatings for its high resistance to heat, light, and chemicals, ensuring long-lasting color and protection.
Used in Plastic Industry:
N,N'-Dibutylquinacridone is used as a pigment in the manufacturing of colored plastics, providing high color strength and resistance to environmental factors.
Used in Textile Industry:
N,N'-Dibutylquinacridone is used as a pigment in textile dyeing and printing, offering vibrant colors and excellent resistance to fading and washing.
Used in Toner and Digital Printing Industry:
N,N'-Dibutylquinacridone is used in the production of toners and digital printing inks, providing high-quality color reproduction and durability on various substrates.
Used in High-Performance Paints Industry:
N,N'-Dibutylquinacridone is used as a pigment in high-performance paints, offering exceptional color strength, resistance to environmental factors, and long-lasting protection.

Check Digit Verification of cas no

The CAS Registry Mumber 99762-80-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,7,6 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99762-80:
(7*9)+(6*9)+(5*7)+(4*6)+(3*2)+(2*8)+(1*0)=198
198 % 10 = 8
So 99762-80-8 is a valid CAS Registry Number.

99762-80-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'- Dibutylquinacridone

1.2 Other means of identification

Product number -
Other names 5,12-Dimethylbenz<a>anthracen

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:99762-80-8 SDS

99762-80-8Relevant articles and documents

Quinacridone-pyridine dicarboxylic acid based donor-acceptor supramolecular nanobelts for significantly enhanced photocatalytic hydrogen production

Xu, Mengyu,Kong, Kangyi,Ding, Haoran,Chu, Yanmeng,Zhang, Shicong,Yu, Fengtao,Ye, Haonan,Hu, Yue,Hua, Jianli

, p. 930 - 934 (2020)

The self-assembled nanobelt photocatalysts (SQAP-C4 and SQAP-C8) with quinacridone containing butyl and octyl side chains as electron donors and pyridine dicarboxylic acid as an acceptor were firstly developed for efficient hydrogen evolution. SQAP-C4 without the loading of cocatalyst Pt exhibited a superior H2 evolution reaction rate of 656 μmol h-1 g-1 and excellent stability.

SYNTHESIS OF N,N'-DIALKYLQUINACRIDONES UNDER THE CONDITIONS OF HETEROGENEOUS CATALYSIS

Pushkina, L. L.,Shelyapin, O. P.,Shein, S. M.

, p. 792 - 795 (2007/10/02)

Alkylation of quinacridone in a heterogeneous medium in the presence of catalytic amounts of quaternary ammonium salts was used to synthesize N,N'-dialkyl derivatives with yields of 80-92percent.Performance of the reaction with phase transfer catalysts allows the use of alkylsulfates and alkylsulfonates besides alkyl halides.The use of a branched alkylating agent (isopropyl iodide) increases, due to steric factors, the reaction time, and reduces the yield of the product of alkylation.

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