Sodium benzoate
The company strictly follows the "GMP for Pharmaceutical Excipients" in production. It currently has approvals for 30 pharmaceutical excipients, including Potassium Chloride, Potassium Dihydrogen Phosphate, Anhydrous Disodium Hydrogen Phosphate, Anhydrous Sodium Carbonate, Disodium Hydrogen Phosphate, Magnesium Chloride, Potassium Sorbate, Mannitol, Urea, Sodium Citrate, Calcium Chloride, Span 40, Glycerol, Cross-linked Polyvinylpyrrolidone, Chitosan, PEG400, Hydroxypropyl Methylcellulose, Microcrystalline Cellulose, Low-substituted Hydroxypropyl Cellulose, Sucrose (Sucrose Powder), Citric Acid, Sodium Benzoate, Anhydrous Citric Acid, Calcium Carbonate, Light Magnesium Oxide, Tween 80, Fructose, Taurine, Dipotassium Hydrogen Phosphate, and Sodium Glutamate.
Category: Product Center
Keyword: Pharmaceutical
Product Parameters
Packaging Specifications: 25kg/bag Storage: Store in a sealed container
Also known as sodium benzoate, chemical name: sodium benzoate. It is a white granular, powder, or crystalline powder; odorless or slightly odorous, with a slightly sweet and salty taste. It is easily soluble in water and slightly soluble in ethanol.
In pharmaceutical preparations, sodium benzoate is mainly used as an antibacterial preservative. Sodium benzoate can be used as a lubricant for tablets, and it was once used to determine liver function by oral or injection of sodium benzoate.
Incompatibility: It is incompatible with quaternary compounds, gelatin, iron salts, calcium salts and heavy metal salts (including silver, lead and mercury), and its preservative activity is reduced when used with kaolin or non-ionic surfactants.
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