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24069-55-4

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24069-55-4 Usage

Functional groups

Amino, hydroxy, and nitro

Chemical class

Anthraquinone derivative

Color

Yellowish-red

Applications

a. Dye intermediate
b. Production of dyes and pigments
c. Pharmaceutical industry (antibacterial and antifungal properties)

Potential hazard

Mutagenic under certain conditions

Safety precautions

Handle with caution due to mutagenicity

Check Digit Verification of cas no

The CAS Registry Mumber 24069-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,6 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24069-55:
(7*2)+(6*4)+(5*0)+(4*6)+(3*9)+(2*5)+(1*5)=104
104 % 10 = 4
So 24069-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H8N2O6/c15-5-1-3-7(17)11-9(5)13(19)10-6(16(21)22)2-4-8(18)12(10)14(11)20/h1-4,17-18H,15H2

24069-55-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-4,5-dihydroxy-8-nitroanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,8-Dihydroxy-4-amino-5-nitroanthraquinone

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:24069-55-4 SDS

24069-55-4Downstream Products

24069-55-4Relevant articles and documents

Production of aminonitrodihydroxyanthraquinones by partial reduction dinitrodihydroxyanthraquinones

-

, (2008/06/13)

The production of aminonitrodihydroxyanthraquinones of the formula: STR1 in which one X is OH and the other X is NO2 by partial reduction of the corresponding dinitrodihydroxyanthraquinone or mixtures thereof by heating at 80°-250° C in the presence of 1/2 to 5 times the weight thereof of an unsubstituted or substituted phenol. The reduction is accelerated by being carried out in the presence of a small amount such as 0.5-20 mol percent of an alkaline-reacting agent. Pure aminonitrohydroxyanthraquinones are obtained which are free from diaminodihydroxyanthraquinones.

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