1,2,3-Propanetricarboxylic acid, 2-hydroxy-, calcium salt → Tricalcium Citrate

HRID 2234722Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2234722
[C:1]([OH:13])(=[O:12])[CH2:2][C:3]([CH2:8][C:9]([OH:11])=[O:10])([C:5]([OH:7])=[O:6])[OH:4].[Ca:14]>O>[C:1]([O-:13])(=[O:12])[CH2:2][C:3]([CH2:8][C:9]([O-:11])=[O:10])([C:5]([O-:7])=[O:6])[OH:4].[Ca+2:14].[C:1]([O-:13])(=[O:12])[CH2:2][C:3]([CH2:8][C:9]([O-:11])=[O:10])([C:5]([O-:7])=[O:6])[OH:4].[Ca+2:14].[Ca+2:14].[Ca:14].[C:1]([O-:13])(=[O:12])[CH2:2][C:3]([CH2:8][C:9]([O-:11])=[O:10])([C:5]([O-:7])=[O:6])[OH:4]

Komponenten

5

Edukt 1

HCID 866002201,2,3-Propanetricarboxylic acid, 2-hydroxy-, calcium salt

Produkt 3

HCID 13136Tricalcium CitrateHCID 31348CitrateHCID 5460341Calcium

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

The amorphous water-soluble calcium citrate salts of this invention are prepared by reacting a calcium compound with citric acid in an aqueous medium to produce calcium citrate having a calcium to citrate mole ratio of less than 2.5:2. The resulting reaction mixture is then quickly dried (or quickly frozen for drying at a later time) in order to separate and isolate amorphous calcium citrate as a dry powder. It is important that the amorphous water-soluble calcium citrate reaction salt is recovered from the aqueous reaction mixture as a dry amorphous material before it can be transformed into insoluble crystalline tricalcium citrate (TCC) or other water-insoluble calcium citrate salts. As shown in the examples below, both the condition of providing a calcium:citrate mole ratio of less than 2.5:2, and the condition of drying the reaction mixture soon enough after the salt-producing reaction, as detailed herein, to avoid reaction product transformation into water-insoluble calcium citrate salts, are important to ensure that the solid calcium citrate reaction product is recovered in an amorphous state. Preferably rapid drying techniques are also used to minimize the opportunity for crystallization of the reaction product during the drying operation. Suitable rapid drying techniques include, for example, freeze drying and spray drying.

Quellen und Nachweise

ORD-Eintrag
ord-ca7e8426b2914e4fab3f8511ce4fb280
Quelldatensatz
uspto-grants-2010_05
Patentnummer
US07713559B2

Notizen zur Reaktion

Wird geladen…