5710-54-3 Usage
Description
1,2-Benzenedisulfonic Acid, Dipotassium Salt, also known as Potassium Benzene-1,2-Disulfonate, is a white to off-white or light-grey powder. It is a chemical compound derived from benzene with two hydrophilic sulfonic acid groups attached to the first and second carbon atoms, and two potassium ions as its counterions. This structure endows it with unique chemical properties that make it suitable for various applications.
Uses
Used in Chemical Synthesis:
1,2-Benzenedisulfonic Acid, Dipotassium Salt is used as a chemical intermediate for the synthesis of other compounds, such as potassium 1-phenolate-4-disulfonate, by reacting with potassium hydroxide. This application takes advantage of its reactivity and ability to form new chemical bonds with other molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,2-Benzenedisulfonic Acid, Dipotassium Salt may be utilized as a building block for the development of new drugs or drug candidates. Its unique chemical structure can be exploited to create molecules with specific biological activities, potentially leading to the discovery of novel therapeutic agents.
Used in Dye Manufacturing:
1,2-Benzenedisulfonic Acid, Dipotassium Salt can be used in the manufacturing of dyes due to its chemical properties. The sulfonic acid groups can form complexes with various metal ions, which can result in the production of dyes with different colors and properties.
Used in Water Treatment:
In the water treatment industry, 1,2-Benzenedisulfonic Acid, Dipotassium Salt may be employed as a coagulant or flocculant to remove impurities from water. Its ability to form complexes with metal ions can help in the aggregation of suspended particles, making it easier to separate them from the water.
Used in Electrochemistry:
1,2-Benzenedisulfonic Acid, Dipotassium Salt can be used in electrochemical applications, such as in the development of sensors or batteries. Its ability to form complexes with metal ions and its electroactive properties make it a promising candidate for these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5710-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5710-54:
(6*5)+(5*7)+(4*1)+(3*0)+(2*5)+(1*4)=83
83 % 10 = 3
So 5710-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O6S2.K.H/c7-13(8,9)5-3-1-2-4-6(5)14(10,11)12;;/h1-4H,(H,7,8,9)(H,10,11,12);;/q;+1;-1
5710-54-3Relevant articles and documents
STUDIEN ZUM VORGANG DER WASSERSTOFFUEBERTRAGUNG 62. HERSTELLUNG UND ELEKTROREDUKTIVE SPALTUNG EINIGER ARYLDISULFONSAEUREDERIVATE
Horner, Leopold,Schmitt, Rolf-Elhard
, p. 169 - 178 (2007/10/02)
Benzene-disulfonylchlorides were converted to the corresponding dialkyl- and diphenylesters, N-alkyl- and N-aryl disulfonamides.The half-wave-potentials E11/2 and E21/2 were measured and the products obtained on potentiostatic fission at E11/2 were isolated and characterized.The electroreduction of benzene-1,4-disulfonic acid-diphenylester in methanol yields phenol in quantity approximately corresponding to the current passed, but no corresponding quantity of sulfinic acid.In dry acetonitrile, benzene-1,4-disulfonic acid diesters and diamides undergo potentiostatic fission (at E11/2) in good chemical and current yields, giving the corresponding monosulfonate-sulfinic acid or monosulfonamide-sulfinic acid and alcohol or amine.The passage of further electrical current reduces the sulfinic acids to other, as yet undetermined, products.
