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853-35-0

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  • 1,5-Anthracenedisulfonicacid, 9,10-dihydro-9,10-dioxo-, sodium salt (1:2) Manufacturer/High quality/Best price/In stock

    Cas No: 853-35-0

  • USD $ 3.0-3.0 / Kilogram

  • 1 Kilogram

  • 1-100 Metric Ton/Month

  • Dayang Chem (Hangzhou) Co.,Ltd.
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853-35-0 Usage

Chemical Properties

solid

Purification Methods

Separate it from insoluble impurities by continuous extraction with water. Recrystallise it twice from hot water and dry it under vacuum. [Beilstein 11 II 195, 11 III 634.]

Check Digit Verification of cas no

The CAS Registry Mumber 853-35-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 853-35:
(5*8)+(4*5)+(3*3)+(2*3)+(1*5)=80
80 % 10 = 0
So 853-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H8O8S2.2Na/c15-12-7-3-1-2-4-8(7)13(16)11-9(12)5-6-10(23(17,18)19)14(11)24(20,21)22;;/h1-6H,(H,17,18,19)(H,20,21,22);;/q;2*+1/p-2

853-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Anthraquinone-1,5-disulfonic Acid Disodium Salt

1.2 Other means of identification

Product number -
Other names disodium,9,10-dioxoanthracene-1,5-disulfonate

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:853-35-0 SDS

853-35-0Upstream product

853-35-0Relevant articles and documents

Process for the manufacture of anthraquinonesulphonic acid

-

, (2008/06/13)

Process for the manufacture of practically mercury-free anthraquinonesulphonic acids, characterized in that anthraquinone is sulphonated with sulphuric acid containing SO3 in the presence of catalysts containing mercury, at elevated temperature, the sulphonation mixture, if appropriate after dilution with water, is subsequently treated with an inorganic or organic compound of divalent sulphur and thereafter, if appropriate following dilution with water, the mercury compounds present in an insoluble form are separated off and the anthraquinonesulphonic acids are then isolated in a known manner.

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