576-42-1 Usage
Description
Potassium bisaccharate, also known as D-Saccharic acid potassium salt, is a naturally occurring compound found in plants and animals. It is produced by the chemical oxidation of glucose with nitric acid and is characterized by its light, off-white powder form with a pH of 3.5. Potassium bisaccharate exhibits chemotherapeutic properties, lowers cholesterol, and has antimutagenic activity. It is slightly soluble in cold water but becomes soluble in hot water, acid, or alkaline solutions and is combustible.
Uses
Used in Pharmaceutical Industry:
Potassium bisaccharate is used as an intermediate in the synthesis of D-Glucaro-1,4-lactone Monohydrate (G415600), which is an anticancer agent. This application takes advantage of its chemotherapeutic properties to contribute to the development of cancer treatments.
Used in Chelating Applications:
Potassium bisaccharate serves as a chelating agent, which is essential in various industrial processes. Its ability to form complexes with metal ions makes it useful in applications where metal ion sequestration is required.
Used in Rubber Formulations:
In the rubber industry, potassium bisaccharate is used to enhance the properties of rubber formulations. Its chelating properties can improve the stability and performance of rubber products.
Used in Metal Plating:
Potassium bisaccharate is utilized in metal plating processes due to its chelating capabilities. It helps in the efficient deposition of metals on various surfaces, improving the quality and durability of the plated products.
Used in Soap and Detergent Industry:
In the soap and detergent industry, potassium bisaccharate is used to improve the cleaning properties of these products. Its chelating action helps to remove dirt and stains more effectively, providing better cleaning results.
Check Digit Verification of cas no
The CAS Registry Mumber 576-42-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 576-42:
(5*5)+(4*7)+(3*6)+(2*4)+(1*2)=81
81 % 10 = 1
So 576-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O8.K/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;+1/p-1
576-42-1Relevant articles and documents
Modifications in the nitric acid oxidation of d-glucose
Smith, Tyler N.,Hash, Kirk,Davey, Cara-Lee,Mills, Heidi,Williams, Holly,Kiely, Donald E.
, p. 6 - 13 (2012)
The nitric acid oxidation of d-glucose was reinvestigated in an effort to better understand and improve the oxidation and subsequent work up steps. The oxidation was carried out using a computer controlled reactor employing a closed reaction flask under an atmosphere of oxygen which allowed for a catalytic oxidation process with oxygen as the terminal oxidant. Removal of nitric acid from product included the use of both diffusion dialysis and nanofiltration methodologies. Product analysis protocols were developed using ion chromatography.
METHOD FOR PRODUCING ADIPAMIDE AS INTERMEDIATE FOR PRODUCTION OF RAW MATERIAL FOR BIO-BASED NYLON
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Paragraph 0044-0053, (2020/03/17)
Disclosed is a method for producing adipamide, which may include the steps of: (a) reacting glucose, nitric acid (HNO3), sodium nitrite (NaNO2) and potassium hydroxide (KOH) to produce a glucaric acidpotassium salt, (b) producing glucamide by reacting the glutaric acid potassium salt, with an acidic solution and removing a potassium ion from the glucaric acid potassium salt, (c) preparing an reaction admixture by adding the glucamide and a catalyst to hydrogen halide and acetic acid, and (d) treating the reaction admixture with hydrogen gas in a reactor thereby producing the adipamide.
METHOD OF PREPARING ADIPIC ACID
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Paragraph 0072-0074, (2020/03/23)
Disclosed is a method of preparing adipic acid from d-glucaro-1,4:6,3-dilactone, particularly using a rhenium catalyst and a noble metal catalyst. Further the method may include using an environmentally friendly solvent such as water. Thus, the obtained adipic acid may have high purity as a final product and economic efficiency of the preparation process may be improved.