Potassium gluconate

Base Information

• Chemical Name: Potassium gluconate
• CAS No.: 299-27-4
• Deprecated CAS: 8059-85-6
• Molecular Formula: C6H11O7K
• Molecular Weight: 234.247
• Hs Code.: 2918.16 Oral rat LD50: 6060 mg/kg
• European Community (EC) Number: 206-074-2,252-355-8
• UNII: 12H3K5QKN9
• ChEMBL ID: CHEMBL2106978
• DSSTox Substance ID: DTXSID7029617
• NCI Thesaurus Code: C81070
• Nikkaji Number: J5.466F
• RXCUI: 89903
• Wikidata: Q1122870
• Wikipedia: Potassium_gluconate
• Mol file: 299-27-4.mol

Synonyms:D-Gluconicacid, monopotassium salt (9CI);Gluconic acid, monopotassium salt, D- (8CI);Gluconic acid potassium salt;Gluconsan K;Helshas K;K-IAO;Kalimozan;Kalium-Beta;Kaon;Katorin;Katrin;Potalium;Potasoral;Potassium D-gluconate;Potassuril;Sirokal;Tumil K;

Chemical Property of Potassium gluconate

Chemical Property:

• Appearance/Colour: white to off-white crystalline or granular powder
• Melting Point: 183 °C (dec.)(lit.)
• Boiling Point: 673.6 °C at 760 mmHg
• Flash Point: 375.2 °C
• PSA: 141.28000
• Density: 1.73 g/cm3
• LogP: -4.82780
• Storage Temp.: room temp
• Solubility.: H2O: soluble50mg/mL
• Water Solubility.: Soluble in water. (50 mg/ml).
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 5
• Exact Mass: 234.01418417
• Heavy Atom Count: 14
• Complexity: 176

Purity/Quality:

99% ^*data from raw suppliers

D-Gluconic acid potassium salt ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C(C(C(C(C(C(=O)[O-])O)O)O)O)O.[K+]
• Isomeric SMILES: C([C@H]([C@H]([C@@H]([C@H](C(=O)[O-])O)O)O)O)O.[K+]
• Recent ClinicalTrials: Single-dose Potassium Supplementation in Patients With ADHD for Whom the Anesthetic Lidocaine is Ineffective
• Uses: Replenisher (electrolyte). Potassium Gluconate is a nutritional source of potassium used in fortification. it has solubility in water at 20°c of greater than 900 g/l, and a ph of approximately 7.0 at 1% solution. it can be used as a partial replacement for sodium chloride to reduce the level of sodium, such as in cheese and bakery goods. Potassium D-gluconate widely used as sequestering compounds for metal ions in alkaline systems. It is used in a newly developed process entitled ARS for the prevention of shrinkage in dyed wool fabric. Potassium gluconate has been shown to elevate lactate production, and ATP content, as well as induce the Hemoglobin (methemoglobin) reduction rate in rat erythrocytes. It is used in cell culture and in large scale applications such as the cleaning of metal surfaces.

Technology Process of Potassium gluconate

There total 3 articles about Potassium gluconate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

2,3-Anhydro-6-bromo-6-deoxy-D-mannono-1,4-lactone (143539-05-3) → potassium gluconate (299-27-4)

Guidance literature:

With hydrogenchloride; potassium carbonate; In water; 4-methyl-2-pentanone; for 48h; pH=2 - 7;

Reference yield:

D-glucose (50-99-7) → potassium gluconate (299-27-4)

Guidance literature:

With potassium carbonate; potassium bromide; Electrolysis_.durch elektrolytische Oxydation;

Reference yield:

D-Glucono-1,5-lactone (90-80-2,1335-57-5,4253-68-3) → potassium gluconate (299-27-4)

Guidance literature:

With potassium hydroxide; In water; for 2h; Thermodynamic data; Heating;

DOI:10.1007/s10973-017-6657-x

upstream raw materials:

D-glucose

2,3-Anhydro-6-bromo-6-deoxy-D-mannono-1,4-lactone

D-Glucono-1,5-lactone

Downstream raw materials:

L-glucono-1,5-lactone

γ lactone of/the/ l-gluconic acid

furan-2,5-dicarboxylic acid