Potassium sodium tartrate

Base Information

• Chemical Name: Potassium sodium tartrate
• CAS No.: 147-79-5
• Deprecated CAS: 19598-88-0,1029019-37-1,2089212-74-6
• Molecular Formula: C₄H₄O₆*K*Na
• Molecular Weight: 210.16
• European Community (EC) Number: 206-156-8,205-698-2
• UNII: P49F8NV7ES
• DSSTox Substance ID: DTXSID60932999,DTXSID90889341
• Nikkaji Number: J2.573I
• Wikipedia: Potassium sodium tartrate,Potassium_sodium_tartrate
• NCI Thesaurus Code: C80954
• ChEMBL ID: CHEMBL2219738
• Mol file: 147-79-5.mol

Synonyms:(R*,R*)-(+-)-2,3-dihydroxybutanedioic acid, monoammonium monosodium salt;aluminum tartrate;ammonium tartrate;calcium tartrate;calcium tartrate tetrahydrate;Mn(III) tartrate;potassium tartrate;seignette salt;sodium ammonium tartrate;sodium potassium tartrate;sodium tartrate;stannous tartrate;tartaric acid;tartaric acid, ((R*,R*)-(+-))-isomer;tartaric acid, (R*,S*)-isomer;tartaric acid, (R-(R*,R*))-isomer;tartaric acid, (S-(R*,R*))-isomer;tartaric acid, ammonium sodium salt, (1:1:1) salt, (R*,R*)-(+-)-isomer;tartaric acid, calcium salt, (R-R*,R*)-isomer;tartaric acid, monoammonium salt, (R-(R*,R*))-isomer;tartrate

Chemical Property of Potassium sodium tartrate

Chemical Property:

• Vapor Pressure: 4.93E-08mmHg at 25°C
• Boiling Point: 399.3°Cat760mmHg
• Flash Point: 209.4°C
• Density: g/cm³
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 209.95426361
• Heavy Atom Count: 12
• Complexity: 123

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Chemical Classes: Metals -> Organic Acids, Metal Salts
• Canonical SMILES: C(C(C(=O)[O-])O)(C(=O)[O-])O.[Na+].[K+]
• Isomeric SMILES: [C@@H]([C@H](C(=O)[O-])O)(C(=O)[O-])O.[Na+].[K+]

Technology Process of Potassium sodium tartrate

There total 1 articles about Potassium sodium tartrate 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:

tartar emeric + iodine + sodium hydrogencarbonate (144-55-8) → antimony pentoxide + carbon dioxide (124-38-9,18923-20-1) + water (7732-18-5) + rochelle salt (147-79-5,304-59-6,15490-42-3) + sodium iodide (7681-82-5,24359-64-6,41927-88-2,115813-40-6)

Guidance literature:

In water; oxidn. with iodine;

DOI:10.1007/BF01368977

Reference yield: 92.0%

4-(pyridine-2-yl)benzonitrile (32111-34-5) + rochelle salt (147-79-5,304-59-6,15490-42-3) → 4-(2'-pyridyl)benzaldehyde (127406-56-8)

Guidance literature:

4-(pyridine-2-yl)benzonitrile; With diisobutylaluminium hydride; In dichloromethane; at -70 ℃; for 0.5h; Inert atmosphere;

rochelle salt; In dichloromethane; at -70 - 0 ℃; Temperature; Reagent/catalyst; Inert atmosphere;

DOI:10.2174/1570178616666190514080155

Reference yield: 85.0%

(E)-ethyl 3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)acrylate (1197190-08-1) + rochelle salt (147-79-5,304-59-6,15490-42-3) → (E)-3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)prop-2-en-1-ol (1197190-18-3)

Guidance literature:

(E)-ethyl 3-((S)-2-((R)-3-(4-methoxybenzyloxy)-1-(methoxymethoxy)propyl)oxiran-2-yl)acrylate; With diisobutylaluminium hydride; In tetrahydrofuran; hexane; at -78 ℃; for 1h;

rochelle salt; In tetrahydrofuran; hexane; ethyl acetate; at -78 - 20 ℃; for 1h; regioselective reaction;

DOI:10.1039/b912267b

upstream raw materials:

sodium hydrogencarbonate

Downstream raw materials:

LACTIC ACID

tartronic acid

gluconic acid

D-Glucuronic acid