5793-88-4 Usage
General Description
D-Saccharic Acid Calcium Salt is a chemical compound widely used in various industries for multiple applications. It is chemically stable, non-hazardous, and non-toxic. It's most known function is its role as an acidity regulator, emulsifying agent, and a buffering agent in different food items. Besides this, it also has pharmaceutical benefits and is used in some medicines due to its calcium content and non-toxic nature. It is soluble in water and its purity level is high, making it suitable for several uses. Despite its wide use, it is essential to use it as per guided safety guidelines.
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.
