5793-88-4 Usage
Description
D-SACCHARIC ACID CALCIUM SALT is a chemical compound that is chemically stable, non-hazardous, and non-toxic. It is widely used in various industries for multiple applications, including its role as an acidity regulator, emulsifying agent, and a buffering agent in different food items. Additionally, it has pharmaceutical benefits and is used in some medicines due to its calcium content and non-toxic nature. It is soluble in water and has a high purity level, making it suitable for several uses.
Uses
Used in Food Industry:
D-SACCHARIC ACID CALCIUM SALT is used as an acidity regulator, emulsifying agent, and a buffering agent for maintaining the quality and taste of various food items.
Used in Pharmaceutical Industry:
D-SACCHARIC ACID CALCIUM SALT is used as a pharmaceutical ingredient for its calcium content and non-toxic nature, contributing to the development of medicines that require these properties.
It is essential to use D-SACCHARIC ACID CALCIUM SALT as per guided safety guidelines to ensure its safe and effective application in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5793-88-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,9 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5793-88:
(6*5)+(5*7)+(4*9)+(3*3)+(2*8)+(1*8)=134
134 % 10 = 4
So 5793-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O8.Ca/c7-1(3(9)5(11)12)2(8)4(10)6(13)14;/h1-4,7-10H,(H,11,12)(H,13,14);/q;+2/p-2/t1-,2-,3-,4+;/m0./s1
5793-88-4Relevant articles and documents
SYNTHESIS OF L-IDARO-1,4-LACTONE, AN INHIBITOR OF α-L-IDOSID-URONASE
Herd, J. Kenneth,Mayberry, William R.,Snell, Robert L.
, p. 33 - 40 (2007/10/02)
L-Idaro-1,4-lactone was synthesized by two different, published methods: (1) epimerization of monopotassium D-glucarate by refluxing in aqueous barium hydroxide, and (2) oxidation of L-iditol by heating in dilute nitric acid.The lactone, formed by heat dehydration from aqueous solution at low pH, was purified by paper chromatography, and quantitated by gas-liquid chromatography using inositol as the internal standard.The monolactone inhibited human, seminal-fluid α-L-idosiduronase activity, with either phenyl or 4-methylumbelliferyl α-L-idosiduronic acid as the substrate, to the same degree as D-glucaro-1,4-lactone inhibits α-D-glucosiduranose.
