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128-94-9

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128-94-9 Usage

Uses

1,8-Diaminochrysazine is an intermediate in the synthesis of compounds used to disperse dye for synthetic polyester fibers.

Check Digit Verification of cas no

The CAS Registry Mumber 128-94-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128-94:
(5*1)+(4*2)+(3*8)+(2*9)+(1*4)=59
59 % 10 = 9
So 128-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O4/c15-5-1-3-7(17)11-9(5)13(19)10-6(16)2-4-8(18)12(10)14(11)20/h1-4,17-18H,15-16H2

128-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,8-diamino-4,5-dihydroxyanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 9,10-Anthracenedione, 1,8-diamino-4,5-dihydroxy-

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:128-94-9 SDS

128-94-9Relevant articles and documents

An improved practical synthesis of leuco-1,4,5,8-tetrahydroxyanthraquinone

Chang,Cheng

, p. 1893 - 1900 (1995)

Leuco-1,4,5,8-tetrahydroxyanthraquinone was prepared from chrysazin by nitration and reduction with iron powder, followed by treatment with sodium hydrosulfite in alkaline solution. This method is suitable for scaling, and is significant and improved over literature methods.

Process for the manufacture of aminohydroxyanthraquinones

-

, (2008/06/13)

The invention relates to a process for the manufacture of an aminohydroxyanthraquinone of the formula STR1 wherein both of X are hydrogen or one X is --NH2 and the other is --OH and Z is hydrogen, C1 -C4 alkyl or carboxyl, with the proviso that, if Z is C1 -C4 alkyl or carboxyl, both of X must be hydrogen, which process comprises reacting a nitroanthraquinone of the formula STR2 wherein both of Y are hydrogen or one Y is --NO2 and the other is hydrogen and Z is as defined for formula (1), with the proviso that, if Z is C1 -C4 alkyl or carboxyl, both of Y must be hydrogen, in an aprotic dipolar solvent, with an alkali metal azide or alkaline earth metal azide, in the temperature range between 0° and 30° C. The reaction products are disperse dyes or intermediates for obtaining vat dyes and disperse dyes.

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