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Benzenamine, 4,4'-sulfonylbis-, dihydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24342-67-4

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24342-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24342-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,4 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24342-67:
(7*2)+(6*4)+(5*3)+(4*4)+(3*2)+(2*6)+(1*7)=94
94 % 10 = 4
So 24342-67-4 is a valid CAS Registry Number.

24342-67-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis-(4-amino-phenyl)-sulfone, dihydrochloride

1.2 Other means of identification

Product number -
Other names Bis-(4-amino-phenyl)-sulfon, Dihydrochlorid

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:24342-67-4 SDS

24342-67-4Upstream product

24342-67-4Relevant academic research and scientific papers

Investigating the Solubilities of the Nitrate and Isomorphous Bromide and Chloride Salts of Dapsone

Bitencourt, Monalisa,Corrêa, Charlane C.,De Melo, Cristiane C.,Doriguetto, Antonio C.

, p. 2313 - 2320 (2020)

Dapsone, the major drug for leprosy, has broader application against dermatoses, malaria, and AIDS-related diseases. Besides its antimicrobial/antiprotozoal activity, dapsone has anti-inflammatory properties. However, because of its low aqueous solubility, the high oral doses required and associated side effects limit the tolerability and efficacy of dapsone free base. As a strategy to improve the drug's solubility, new salts of dapsone were prepared. The chloride, bromide, and nitrate salts of dapsone were completely characterized by X-ray diffraction (single and powder), spectroscopic (FT-IR), and thermal (DSC and TGA) techniques. The X-ray results revealed that dapsone chloride and dapsone bromide are isomorphous compounds. Dapsone salts decompose without melting and are thermally less stable than dapsone free base. The equilibrium solubility of dapsone salts was compared to dapsone free base in three aqueous media: HCl buffer pH 1.2, acetate buffer pH 4.5, and phosphate buffer pH 6.8. The highest solubility values were obtained in acid media, and dapsone bromide was found to be slightly more soluble than dapsone free base. The solubility values obtained for the nitrate and chloride salts of dapsone at pH 1.2 cannot be considered real, since the PXRD patterns show their total/partial conversion.

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