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| Name | Sodium Sulfite anhydrous (BP, Ph. Eur.) |
| Type | Pharma grade |
| Form | Powder |
| Color | White to slightly yellow |
| Odor | Sulfurous |
| Solubility | Soluble in water |
| PH | Neutral to slightly alkaline |
| Purity | Min. 96% |
| Storage | Store in a cool, dry place |
| Shelf Life | Minimum 2 years |
| Packaging | In drums or bags |
| Usage | Antioxidant, preservative, reducing agent |
| Applications | Pharmaceuticals, food industry, photographic industry |
FAQ
What is Sodium Sulfite anhydrous (BP, Ph. Eur.) pharma grade?
Sodium Sulfite anhydrous is a white crystalline powder that is commonly used in the pharmaceutical industry as a reducing agent and antioxidant. It conforms to the British Pharmacopoeia (BP) and European Pharmacopoeia (Ph. Eur.) standards for pharmaceutical grade sodium sulfite.
What are the main applications of Sodium Sulfite anhydrous (BP, Ph. Eur.) pharma grade?
Sodium Sulfite anhydrous is primarily used in the pharmaceutical industry as a reagent for various processes such as the manufacturing of parenteral and oral dosage forms, as well as in the preparation of injectable solutions and intravenous infusions. It is also utilized in the production of active pharmaceutical ingredients (APIs) and in the stabilization of certain medications.
What are the benefits of using Sodium Sulfite anhydrous (BP, Ph. Eur.) pharma grade?
The pharmaceutical grade of Sodium Sulfite anhydrous ensures a high level of purity and quality, meeting the stringent requirements of the BP and Ph. Eur. It provides reliable and consistent performance as a reducing agent and antioxidant, helping to maintain the stability of pharmaceutical formulations and ensure the efficacy of medications.
How should Sodium Sulfite anhydrous (BP, Ph. Eur.) pharma grade be stored and handled?
Sodium Sulfite anhydrous should be stored in a cool, dry place away from sources of heat and light. It should be kept tightly sealed in its original container to prevent moisture absorption and contamination. Proper handling practices should be followed to avoid skin contact and inhalation of dust particles.
What is the regulatory compliance status of Sodium Sulfite anhydrous (BP, Ph. Eur.) pharma grade?
Sodium Sulfite anhydrous complies with the regulations and standards set forth by the British Pharmacopoeia (BP) and European Pharmacopoeia (Ph. Eur.) for pharmaceutical grade substances. It undergoes rigorous testing and analysis to ensure its purity, identity, and potency, making it suitable for use in pharmaceutical applications.
Sodium Sulfite anhydrous is a white crystalline powder that is commonly used in the pharmaceutical industry as a reducing agent and antioxidant. It conforms to the British Pharmacopoeia (BP) and European Pharmacopoeia (Ph. Eur.) standards for pharmaceutical grade sodium sulfite.
What are the main applications of Sodium Sulfite anhydrous (BP, Ph. Eur.) pharma grade?
Sodium Sulfite anhydrous is primarily used in the pharmaceutical industry as a reagent for various processes such as the manufacturing of parenteral and oral dosage forms, as well as in the preparation of injectable solutions and intravenous infusions. It is also utilized in the production of active pharmaceutical ingredients (APIs) and in the stabilization of certain medications.
What are the benefits of using Sodium Sulfite anhydrous (BP, Ph. Eur.) pharma grade?
The pharmaceutical grade of Sodium Sulfite anhydrous ensures a high level of purity and quality, meeting the stringent requirements of the BP and Ph. Eur. It provides reliable and consistent performance as a reducing agent and antioxidant, helping to maintain the stability of pharmaceutical formulations and ensure the efficacy of medications.
How should Sodium Sulfite anhydrous (BP, Ph. Eur.) pharma grade be stored and handled?
Sodium Sulfite anhydrous should be stored in a cool, dry place away from sources of heat and light. It should be kept tightly sealed in its original container to prevent moisture absorption and contamination. Proper handling practices should be followed to avoid skin contact and inhalation of dust particles.
What is the regulatory compliance status of Sodium Sulfite anhydrous (BP, Ph. Eur.) pharma grade?
Sodium Sulfite anhydrous complies with the regulations and standards set forth by the British Pharmacopoeia (BP) and European Pharmacopoeia (Ph. Eur.) for pharmaceutical grade substances. It undergoes rigorous testing and analysis to ensure its purity, identity, and potency, making it suitable for use in pharmaceutical applications.
