Piperazine hydrate

The thermodynamic parameters for protonation of 1,4- bis (3-aminopropyl)-piperazine (BAPP) were studied in aqueous solution using a potentiometric technique . Application 1,4- Bis (3-aminopropyl)piperazine was used to functionalize natural

The thermodynamic parameters for protonation of 1,4-bis(3-aminopropyl)-piperazine (BAPP) were studied in aqueous solution using a potentiometric technique.1,4-Bis(3-aminopropyl)piperazine was used to functionalize natural montmorillonite (M) and

The thermodynamic parameters for protonation of 1,4-bis(3-aminopropyl)-piperazine (BAPP) were studied in aqueous solution using a potentiometric technique.1,4-Bis(3-aminopropyl)piperazine was used to functionalize natural montmorillonite (M) and

The thermodynamic parameters for protonation of 1,4-bis(3-aminopropyl)-piperazine (BAPP) were studied in aqueous solution using a potentiometric technique.1,4-Bis(3-aminopropyl)piperazine was used to functionalize natural montmorillonite (M) and

The thermodynamic parameters for protonation of 1,4-bis(3-aminopropyl)-piperazine (BAPP) were studied in aqueous solution using a potentiometric technique.1,4-Bis(3-aminopropyl)piperazine was used to functionalize natural montmorillonite (M) and

2 3-PIPERAZINEDIONE MONOHYDRATE-

3-Nitrobenzenesulfonic Acid Hydrate.

Application 4-Methoxybenzhydrazide may be used to synthesize: N &#8242-[( E )-5-bromo-2-hydroxy-3-methoxybenzylidene]-4-methoxybenzohydrazide monohydrate 2,5-bis(4-methoxyphenyl)-1,3,4-oxadiazole hydrazone ligands, which readily forms

4-Nitrobenzenesulfonic Acid Hydrate.

4-Nitrobenzenesulfonic Acid Hydrate.

4，4’-dipyridyl hydrate.

4，4’-dipyridyl hydrate.