60548-60-9 Usage
General Description
1,2-Ethanediol, bissulfamate is an ester compound composed of two molecules of bissulfamic acid and one molecule of ethylene glycol. It is commonly used as a crosslinking agent in the production of thermoset polymers, particularly in the manufacturing of ion exchange resins and coatings. This chemical is known for its ability to improve the heat resistance and chemical stability of these polymers, making them suitable for a wide range of industrial applications. Additionally, 1,2-Ethanediol, bissulfamate is also utilized as a flame retardant in various products, providing enhanced fire safety properties. However, like many chemical compounds, proper handling and storage of this substance is crucial to prevent any potential health or environmental hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 60548-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60548-60:
(7*6)+(6*0)+(5*5)+(4*4)+(3*8)+(2*6)+(1*0)=119
119 % 10 = 9
So 60548-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C2H8N2O6S2/c3-11(5,6)9-1-2-10-12(4,7)8/h1-2H2,(H2,3,5,6)(H2,4,7,8)
60548-60-9Relevant articles and documents
Synthesis and Evaluation of the Male Antifertility Properties of a Series of N-Unsubstituted Sulfamates
Hirsch, Allen F.,Kasulanis, Charles,Kraft, Larry,Mallory, Robert A.,Powell, Gregory,Wong, Benny
, p. 901 - 903 (1981)
A series of six aliphatic and one carbocyclic N-unsubstituted sulfamates have been synthesized and evaluated as potential male antifertility agents.Three of the aliphatic sulfamates 1,2-ethanediyl sulfamate (1), 1,3-propanediyl sulfamate (2), and 1,4-butanediyl sulfamate (3), when administered orally to male rats caused a decrease in the number of pregnant females and/or implantation coupled with increased embryonic and fetal resorption.The compounds were prepared by treating the appropriate glycol salt with sulfamoyl chloride or by the cleavage of a tert-butylsulfamate with trifluoroacetic acid.
