Hydrochloric Acid → Sulfadiazine

HRID 365062

Reaction equation

HRID 365062 reaction equation
[CH:1]1[CH:6]=[N:5][C:4]([N-:7][S:8]([C:11]2[CH:16]=[CH:15][C:14]([NH2:17])=[CH:13][CH:12]=2)(=[O:10])=[O:9])=[N:3][CH:2]=1.[Na+].S([O-])([O-])(=O)=O.[Na+].[Na+].Cl>C(O)C>[CH:1]1[CH:2]=[N:3][C:4]([NH:7][S:8]([C:11]2[CH:12]=[CH:13][C:14]([NH2:17])=[CH:15][CH:16]=2)(=[O:10])=[O:9])=[N:5][CH:6]=1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 24436Sodium SulfateHCID 15899898Sulfadiazine Sodium

Product 1

HCID 5215Sulfadiazine

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

An aqueous solution consisting of 0.5 g sodium sulfadiazine, 0.5 ml ethyl alcohol, 13 ml of 20% sodium sulfate and 20 ml of 5% gelatin (type B: acid processed) was titrated, while under constant agitation with a magnetic stirrer, with 18.4 ml of 0.1N hydrochloric acid solution. This procedure resulted in a white suspension of microencapsulated sulfadiazine particles. The suspension was then stirred for an additional 15 minutes, following which it was poured into 200 ml of cold (5° C.) 7% sodium sulfate solution, and stirred for 30 minutes at ice-bath temperature. This procedure caused gelling of the liquid gelatin shell of the microcapsules. The entire process was monitored by observation of samples in the optical microscope. The microcapsules were of assymetric appearance and of a size less than 10 μm.

Sources & evidence

ORD record
ord-bf57c3b2dabf41d1825b6a2669e8256b
Source dataset
uspto-grants-1986_08
Patent number
US04608278

Linked notes

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