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L(+)-Potassium hydrogen tartrate

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Name

L(+)-Potassium hydrogen tartrate

EINECS 212-769-1
CAS No. 868-14-4 Density 1.954 g/cm3
PSA 117.89000 LogP -3.45730
Solubility Soluble in water and dilute mineral acid. Insoluble in alcohol. Melting Point 267 °C (dec.)
Formula KC4H5O6 Boiling Point 318℃[at 101 325 Pa]
Molecular Weight 188.178 Flash Point 210℃
Transport Information N/A Appearance white crystalline powder
Safety 24/25 Risk Codes N/A
Molecular Structure Molecular Structure of 868-14-4 (L(+)-Potassium hydrogen tartrate) Hazard Symbols N/A
Synonyms

Butanedioicacid, 2,3-dihydroxy- (2R,3R)-, monopotassium salt (9CI);Butanedioic acid,2,3-dihydroxy-[R-(R*,R*)]-, monopotassium salt;Tartaric acid, monopotassiumsalt (8CI);Acid potassium tartrate;Cream of tartar;Cremor tartari;Faccla;Faccula;Faecla;Faecula;Monopotassium tartrate;NSC 155080;Potassium acidtartrate;Potassium bitartrate;Potassium hydrogen L(+)-tartrate;Potassiumhydrogen tartrate;Potassium hydrotartrate;Potassium tartrate (KHC4H4O6);Tartar;Tartar cream;

 

L(+)-Potassium hydrogen tartrate Synthetic route

crude wine-stone (tartarus crudus)

crude wine-stone (tartarus crudus)

868-14-4

potassium bitartrate

Conditions
ConditionsYield
With water
With water
crude wine-stone

crude wine-stone

868-14-4

potassium bitartrate

87-69-4

tartaric acid

neutral potassium tartrate

neutral potassium tartrate

868-14-4

potassium bitartrate

Conditions
ConditionsYield
With water

L(+)-Potassium hydrogen tartrate Specification

The Potassium bitartrate, with the CAS registry number 868-14-4, is also known as Butanedioic acid, 2,3-dihydroxy- (2R,3R)-, potassium salt (1:1). Its EINECS registry number is 212-769-1. This chemical's molecular formula is KC4H5O6 and molecular weight is 188.177. Its IUPAC name is called potassium (2R,3R)-2,3,4-trihydroxy-4-oxobutanoate. When you are using this chemical, please be cautious about it. You must avoid contact with skin and eyes. 

Physical properties of Potassium bitartrate: (1)H-Bond Donor: 3; (2)H-Bond Acceptor: 6; (3)Rotatable Bond Count: 3; (4)Exact Mass: 187.97232; (5)MonoIsotopic Mass: 187.97232; (6)Topological Polar Surface Area: 118; (7)Heavy Atom Count: 11; (8)Formal Charge: 0; (9)Complexity: 157; (10)Isotope Atom Count: 0; (11)Defined Atom StereoCenter Count: 2; (12)Undefined Atom StereoCenter Count: 0; (13)Defined Bond StereoCenter Count: 0; (14)Undefined Bond StereoCenter Count: 0; (15)Covalently-Bonded Unit Count: 2.

Preparation of Potassium bitartrate: this chemical can be prepared by tartaric acid and K2CO3. This reaction will need PH value 2. At last, it will gain Potassium bitartrate via cooling and crystallization.

2 H2C4H4O6+K2CO3→2 KHC4H4O6+CO2↑+H2O

Uses of Potassium bitartrate: In food, potassium bitartrate is used for: stabilising egg whites, increasing their heat tolerance and volume; Preventing sugar syrups from crystallising; Reducing discolouration of boiled vegetables; Frequent combination with baking soda, which requires an acid ingredient to activate it, in formulations of baking powder; Commonly used in combination with potassium chloride in sodium-free salt substitutes; Gingerbread house icing; Stabilising whipped cream stiffness, added after whipping. Potassium bitartrate can be used with white vinegar to make a paste-like cleaning agent.[citation needed] This mixture is sometimes mistakenly made with vinegar and sodium bicarbonate (baking soda), which actually react to neutralise each other, creating carbon dioxide and a sodium acetate solution. Potassium acid tartrate, also known as potassium hydrogen tartrate, is, according to NIST, used as a primary reference standard for a pH buffer.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: C(C(C(=O)[O-])O)(C(=O)O)O.[K+]
(2)Isomeric SMILES: [C@@H]([C@H](C(=O)[O-])O)(C(=O)O)O.[K+]
(3)InChI: InChI=1S/C4H6O6.K/c5-1(3(7)8)2(6)4(9)10;/h1-2,5-6H,(H,7,8)(H,9,10);/q;+1/p-1/t1-,2-;/m1./s1
(4)InChIKey: KYKNRZGSIGMXFH-ZVGUSBNCSA-M

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
rat LDLo oral 22gm/kg (22000mg/kg)   Toxicology and Applied Pharmacology. Vol. 3, Pg. 689, 1961.

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