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sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28434-74-4

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28434-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28434-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,3 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28434-74:
(7*2)+(6*8)+(5*4)+(4*3)+(3*4)+(2*7)+(1*4)=124
124 % 10 = 4
So 28434-74-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H20N2O5S.Na/c1-2-3-9-19-14-10-12(17(20)21)11-15(25(18,22)23)16(14)24-13-7-5-4-6-8-13;/h4-8,10-11,19H,2-3,9H2,1H3,(H,20,21)(H2,18,22,23);/q;+1/p-1

28434-74-4SDS

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 sodium,3-(butylamino)-4-phenoxy-5-sulfamoylbenzoate

1.2 Other means of identification

Product number -
Other names Sodium 3-(aminosulphonyl)-5-(butylamino)-4-phenoxybenzoate

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:28434-74-4 SDS

28434-74-4Upstream product

28434-74-4Downstream Products

28434-74-4Relevant academic research and scientific papers

Sodium and potassium salts of bumetanide trihydrate: Impact of counterion on structure, aqueous solubility and dehydration kinetics

Ong, Winston,Cheung, Eugene Y.,Schultz, Karen A.,Smith, Cartney,Bourassa, James,Hickey, Magali B.

, p. 2428 - 2434 (2012)

A form of bumetanide potassium trihydrate that is structurally similar to bumetanide sodium trihydrate was identified. Structural analysis indicated however that the change from sodium to potassium salt resulted in meaningful changes in the packing arrangement and even greater changes on physicochemical properties. The potassium trihydrate salt was five times more soluble in water relative to the sodium trihydrate salt (27 mg mL-1vs. 5.6 mg mL -1). Both salts underwent complete dehydration to their corresponding anhydrate forms following exposure to low humidity or elevated temperature. Arrhenius plots for the dehydration between 20-30 °C yielded a lower activation barrier for the potassium trihydrate compared to the sodium trihydrate (14.9 kcal mol-1vs. 19.9 kcal mol-1), translating into a 15-20-fold difference in the rate of dehydration. Such a 5.0 kcal mol-1 gap suggests that the H2O molecules are more tightly bound in the sodium trihydrate compared to potassium trihydrate. These differences in solubility and rate of dehydration further illustrate that changes to chemical composition can have a meaningful and unpredictable impact on the physicochemical properties of closely related pharmaceutical salt forms. The Royal Society of Chemistry 2012.

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