Reaktionsgleichung
[C:1]([OH:9])(=[O:8])[CH:2]([CH2:4][C:5]([OH:7])=[O:6])[OH:3].[O-2:10].[Mg+2:11]>O>[C:1]([OH:9])(=[O:8])[CH:2]([CH2:4][C:5]([OH:7])=[O:6])[OH:3].[C:1]([O:9][OH:10])(=[O:8])[CH:2]([CH2:4][C:5]([O-:7])=[O:6])[OH:3].[Mg+2:11].[Mg+2:11].[OH:10][O:8][C:1](=[O:9])[CH:2]([CH2:4][C:5]([O-:7])=[O:6])[OH:3].[OH:10][O:8][C:1](=[O:9])[CH:2]([CH2:4][C:5]([O-:7])=[O:6])[OH:3].[OH:10][O:8][C:1](=[O:9])[CH:2]([CH2:4][C:5]([O-:7])=[O:6])[OH:3]Komponenten
5
Edukt 2
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
An aqueous solution of malic acid was prepared by mixing 5.859 kg of malic acid with 18.18 L of water until the solution was clear. An aqueous solution of magnesium oxide was also prepared in a separate container by thoroughly mixing 3.515 kg of magnesium oxide in 18.18 L of water. The magnesium oxide solution was then slowly added to the malic acid solution. The resulting solution was cooled, and then spray dried to produce a powdered dimagnesiumhydroxy malate.
Aufarbeitung
- temperatureThe resulting solution was cooled
- customspray dried
Quellen und Nachweise
- ORD-Eintrag
- ord-77c4bba85a22402b9eccb03159ac0ade
- Quelldatensatz
- uspto-grants-2004_03
- Patentnummer
- US06706904B1
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