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Pyrrolo3,4-cpyrrole-1,4-dione, 3,6-bis4-(1,1-dimethylethyl)phenyl-2,5-dihydrois an organic compound with a complex structure. It is characterized by its orange powder appearance and yellowish shade. Pyrrolo3,4-cpyrrole-1,4-dione, 3,6-bis4-(1,1-dimethylethyl)phenyl-2,5-dihydroexhibits heat resistance of at least 300°C, light fastness of 8, and moderate acid and alkali resistance levels of 5. It also has a specific surface area of 24 m2/g and a density of 1.20 g/cm3. The oil absorption rate is between 40-50%, and it has a maximum residue on 80 mesh of 5.0%. Additionally, it has a water solubility of 1.0% max and a volatile content at 105 °C of 1.0% max. Pyrrolo3,4-cpyrrole-1,4-dione, 3,6-bis4-(1,1-dimethylethyl)phenyl-2,5-dihydrohas a tinting strength of 100-105%.

84632-59-7

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84632-59-7 Usage

Uses

Used in Dye and Pigment Industry:
Pyrrolo3,4-cpyrrole-1,4-dione, 3,6-bis4-(1,1-dimethylethyl)phenyl-2,5-dihydrois used as a dye or pigment due to its color properties and tinting strength of 100-105%. Its heat resistance, light fastness, and acid and alkali resistance make it suitable for various applications in the dye and pigment industry.
Used in Heat Resistant Applications:
Pyrrolo3,4-cpyrrole-1,4-dione, 3,6-bis4-(1,1-dimethylethyl)phenyl-2,5-dihydro-'s heat resistance of at least 300°C makes it suitable for use in applications that require high temperature stability, such as in the manufacturing of plastics, coatings, and other materials that need to withstand high temperatures.
Used in Oil Absorption Applications:
With an oil absorption rate of 40-50%, Pyrrolo3,4-cpyrrole-1,4-dione, 3,6-bis4-(1,1-dimethylethyl)phenyl-2,5-dihydrocan be used in applications that require oil absorption, such as in the formulation of lubricants or in the development of materials with specific oil absorption properties.
Used in Chemical Analysis and Research:
Due to its unique chemical structure and properties, Pyrrolo3,4-cpyrrole-1,4-dione, 3,6-bis4-(1,1-dimethylethyl)phenyl-2,5-dihydrocan be used in chemical analysis and research for studying its properties and potential applications in various fields.

TEST ITEMS

SPECIFICATION

HEAT RESISTANCE

300 °C min

LIGHT FASTNESS

8

ACID RESISTANCE

5

ALKALI RESISTANCE

5

FASTNESS TO BLEEDING

5

OIL ABSORPTION

40-50%

RESIDUE ON 80 MESH

5.0% max

VOLATITE 105 °C

1.0% max

Check Digit Verification of cas no

The CAS Registry Mumber 84632-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,3 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84632-59:
(7*8)+(6*4)+(5*6)+(4*3)+(3*2)+(2*5)+(1*9)=147
147 % 10 = 7
So 84632-59-7 is a valid CAS Registry Number.

84632-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Pyrrolo3,4-cpyrrole-1,4-dione, 3,6-bis4-(1,1-dimethylethyl)phenyl-2,5-dihydro-

1.2 Other means of identification

Product number -
Other names C.I. Pigment Orange 73

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:84632-59-7 SDS

84632-59-7Relevant academic research and scientific papers

SOLVENT-FREE PROCESS FOR THE PREPARATION OF DIKETOPYRROLOPYRROLE DERIVATIVES

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Page 17, (2010/02/08)

The present application relates to compounds of formula A(D)X(E)y, (I), compounds of formula (III), compounds of formula (X), as well as processes for the preparation thereof, processes where the compounds (I) are converted to pigments of formula (II) and the use of the compounds (I).

Fluorescent Dyes with Large Stokes Shifts - Soluble Dihydropyrrolopyrrolediones

Potrawa, Thomas,Langhals, Heinz

, p. 1075 - 1078 (2007/10/02)

The synthesis of 3,6-Diaryl-2,5-dihydropyrrolopyrrole-1,4-diones 1a-d and 3,6-Diaryl-2,5-dihydro-2,5-dimethylpyrrolopyrrole-1,4-diones e-h is described.By substitution of the aryl groups with tert-butyl groups, photostable fluorescent dyes w

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