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5102-83-0

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  • Pigment Dispersion Waterborne Golden Yellow Pigment Yellow 13

    Cas No: 5102-83-0

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  • Butanamide,2,2'-[(3,3'-dichloro[1,1'-biphenyl]-4,4'-diyl)bis(2,1-diazenediyl)]bis[N-(2,4-dimethylphenyl)-3-oxo- 5102-83-0

    Cas No: 5102-83-0

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5102-83-0 Usage

Description

Pigment Yellow 12 is a yellow powder with a greenish shade, characterized by its heat resistance of a minimum of 180°C, light fastness of 5, and resistance to both acids and alkalis with a rating of 5. It has a fastness to bleeding rating of 5, an oil absorption of 45-50%, a specific surface area of 27 m2/g, a density of 1.50 g/cm3, a residue on 80 mesh of 5.0% max, a water solubility of 1.0% max, and a volatilite at 105°C of 1.0% max. It is used as a color stabilizer for wood flour/polypropylene composites and has a tinging strength of 100-105%.

Uses

Used in Plastic Industry:
Pigment Yellow 12 is used as a color stabilizer for wood flour/polypropylene composites to enhance their appearance and provide color consistency. Its heat resistance, light fastness, and resistance to acids and alkalis make it a suitable choice for this application.

TEST ITEMS

SPECIFICATION

HEAT RESISTANCE

180 °C min

LIGHT FASTNESS

5

ACID RESISTANCE

5

ALKALI RESISTANCE

5

FASTNESS TO BLEEDING

5

OIL ABSORPTION

45-50%

SPECIFIC SURFACE

27 m 2 /g

DENSITY

1.50 g/cm 3

RESIDUE ON 80 MESH

5.0% max

VOLATITE 105 °C

1.0% max

Check Digit Verification of cas no

The CAS Registry Mumber 5102-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,0 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5102-83:
(6*5)+(5*1)+(4*0)+(3*2)+(2*8)+(1*3)=60
60 % 10 = 0
So 5102-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C36H34Cl2N6O4/c1-19-7-11-29(21(3)15-19)39-35(47)33(23(5)45)43-41-31-13-9-25(17-27(31)37)26-10-14-32(28(38)18-26)42-44-34(24(6)46)36(48)40-30-12-8-20(2)16-22(30)4/h7-18,41-42H,1-6H3,(H,39,47)(H,40,48)/b43-33+,44-34+

5102-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[2-chloro-4-[3-chloro-4-[[1-(2,4-dimethylanilino)-1,3-dioxobutan-2-yl]diazenyl]phenyl]phenyl]diazenyl]-N-(2,4-dimethylphenyl)-3-oxobutanamide

1.2 Other means of identification

Product number -
Other names Tertropigment PGR

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Pigments
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:5102-83-0 SDS

5102-83-0Downstream Products

5102-83-0Relevant articles and documents

A quantitative one-pot synthesis method for industrial azo pigments with recyclable wastewater

Feng, Guangyuan,Zhu, Meiling,Liu, Lei,Li, Chunbao

supporting information, p. 1769 - 1776 (2019/04/08)

Most industrial azo pigments are synthesized by diazotization in one pot and then coupling in another. This two-pot process has been transformed into a one-pot method by adding granular PTFE (polytetrafluoroethylene) to a mechanically agitated aqueous mixture of NaNO2, HCl, a diazo component and a coupling component. This method avoids the step of using a base or a surfactant to dissolve the coupling component. The reactions were fast and quantitative. The granular PTFE, wastewater and excess HCl were then reused 11 times without deteriorating the reaction rate and product purity. Altogether, 22 industrial pigments and 3 azo compounds were synthesized and the reaction can produce up to 22.7 g of product in the laboratory. Some reactions require less than 2 equiv. of HCl and a mechanism explaining this is proposed. In addition, an o-nitro group effect is advanced to explain the differences in coupling reaction rates for o-, m- and p-nitroaniline.

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