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| Product Name | Di-Sodium Hydrogen Phosphate anhydrous |
| Grade | Pharma Grade |
| Standards | USP, BP, Ph. Eur. |
| Physical Form | Powder |
| Color | White |
| Odor | Odorless |
| Solubility | Soluble in water |
| Purity | Min. 98% |
| Molecular Formula | Na2HPO4 |
| Molecular Weight | 141.96 g/mol |
| CAS Number | 7558-79-4 |
FAQ
What is di-Sodium Hydrogen Phosphate anhydrous (USP, BP, Ph. Eur.) pure, pharma
grade?
di-Sodium Hydrogen Phosphate is a white, crystalline powder used in various pharmaceutical applications. It meets the standards set by the United States Pharmacopeia (USP), British Pharmacopoeia (BP), and the European Pharmacopoeia (Ph. Eur.), ensuring its purity and quality for pharmaceutical use.
What are the main benefits of using di-Sodium Hydrogen Phosphate in pharmaceutical manufacturing?
di-Sodium Hydrogen Phosphate is commonly used as a buffering agent, emulsifier, and pH regulator in pharmaceutical formulations. It helps maintain the stability and effectiveness of various medications and ensures consistent quality in manufacturing processes.
How is di-Sodium Hydrogen Phosphate anhydrous (USP, BP, Ph. Eur.) pure, pharma grade different from other grades of the compound?
The pharma grade di-Sodium Hydrogen Phosphate complies with strict quality standards set by regulatory agencies, ensuring its suitability for use in pharmaceutical applications. Other grades may not meet these standards and could contain impurities that are not safe for human consumption.
What are some common pharmaceutical applications of di-Sodium Hydrogen Phosphate?
di-Sodium Hydrogen Phosphate is used in the production of tablets, capsules, liquid medications, and topical ointments. It is also used in the manufacturing of intravenous solutions and other parenteral products. Its versatile properties make it an essential ingredient in various pharmaceutical formulations.
How can I ensure the purity and quality of di-Sodium Hydrogen Phosphate anhydrous (USP, BP, Ph. Eur.) pure, pharma grade for my pharmaceutical manufacturing needs?
When purchasing di-Sodium Hydrogen Phosphate, make sure to source it from reputable suppliers who provide documentation of its compliance with USP, BP, and Ph. Eur. standards. Conducting regular quality control tests on the material received will also help ensure its purity and consistency for use in pharmaceutical manufacturing.
di-Sodium Hydrogen Phosphate is a white, crystalline powder used in various pharmaceutical applications. It meets the standards set by the United States Pharmacopeia (USP), British Pharmacopoeia (BP), and the European Pharmacopoeia (Ph. Eur.), ensuring its purity and quality for pharmaceutical use.
What are the main benefits of using di-Sodium Hydrogen Phosphate in pharmaceutical manufacturing?
di-Sodium Hydrogen Phosphate is commonly used as a buffering agent, emulsifier, and pH regulator in pharmaceutical formulations. It helps maintain the stability and effectiveness of various medications and ensures consistent quality in manufacturing processes.
How is di-Sodium Hydrogen Phosphate anhydrous (USP, BP, Ph. Eur.) pure, pharma grade different from other grades of the compound?
The pharma grade di-Sodium Hydrogen Phosphate complies with strict quality standards set by regulatory agencies, ensuring its suitability for use in pharmaceutical applications. Other grades may not meet these standards and could contain impurities that are not safe for human consumption.
What are some common pharmaceutical applications of di-Sodium Hydrogen Phosphate?
di-Sodium Hydrogen Phosphate is used in the production of tablets, capsules, liquid medications, and topical ointments. It is also used in the manufacturing of intravenous solutions and other parenteral products. Its versatile properties make it an essential ingredient in various pharmaceutical formulations.
How can I ensure the purity and quality of di-Sodium Hydrogen Phosphate anhydrous (USP, BP, Ph. Eur.) pure, pharma grade for my pharmaceutical manufacturing needs?
When purchasing di-Sodium Hydrogen Phosphate, make sure to source it from reputable suppliers who provide documentation of its compliance with USP, BP, and Ph. Eur. standards. Conducting regular quality control tests on the material received will also help ensure its purity and consistency for use in pharmaceutical manufacturing.
