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| Product Name | Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade |
| Chemical Formula | Na2SeO3 |
| Molecular Weight | 172.9 g/mol |
| Appearance | White to off-white crystalline powder |
| Solubility | Soluble in water |
| Purity | ≥98% |
| Melting Point | 653°C |
| Storage Conditions | Store in a cool, dry place away from light |
| Usage | Used as a dietary supplement or in the production of pharmaceuticals |
| Shelf Life | At least 2 years |
| CAS Number | 10102-18-8 |
FAQ
What is Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade and how is it used in the
pharmaceutical industry?
Sodium Selenite anhydrous is a pharmaceutical-grade form of the mineral selenium, which is an essential micronutrient with antioxidant properties. It is commonly used in pharmaceutical formulations as a source of selenium, which plays a crucial role in various biological processes in the body. Sodium Selenite anhydrous is utilized in the pharmaceutical industry for its therapeutic benefits and as a dietary supplement to address selenium deficiencies in patients.
How does Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade differ from other forms of selenium supplements?
Sodium Selenite anhydrous is a highly pure and stable form of selenium supplement that meets the stringent quality standards set by the European Pharmacopoeia (Ph. Eur.) and British Pharmacopoeia (BP). This pharmaceutical-grade form of selenium is manufactured to ensure consistency in potency and efficacy, making it a preferred choice for pharmaceutical formulations. Unlike other forms of selenium supplements, Sodium Selenite anhydrous is specifically designed for use in pharmaceutical applications where quality and purity are of utmost importance.
What are the key benefits of using Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade in pharmaceutical formulations?
Sodium Selenite anhydrous offers several benefits when used in pharmaceutical formulations. As a potent source of selenium, it helps support the body's antioxidant defense mechanisms and plays a critical role in cellular function and overall health. By incorporating Sodium Selenite anhydrous into pharmaceutical products, manufacturers can ensure that patients receive a reliable and effective source of selenium to address deficiencies or therapeutic needs. Additionally, the pharmaceutical-grade quality of Sodium Selenite anhydrous ensures that it meets the highest standards of purity and safety for pharmaceutical use.
How is Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade produced and what quality control measures are in place to ensure its purity and efficacy?
Sodium Selenite anhydrous is produced through a controlled manufacturing process that involves the synthesis of sodium selenite under strict quality control conditions. The raw materials used in the production of Sodium Selenite anhydrous are carefully selected to ensure purity and potency. Throughout the manufacturing process, rigorous quality control measures are in place to monitor the product's purity, stability, and efficacy. The final product is tested for compliance with the standards set by the European Pharmacopoeia (Ph. Eur.) and British Pharmacopoeia (BP) to ensure that it meets the required specifications for pharmaceutical use.
In what pharmaceutical applications is Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade commonly used and what dosage forms are available?
Sodium Selenite anhydrous is used in a variety of pharmaceutical applications where selenium supplementation is indicated, such as in the treatment of selenium deficiencies and certain medical conditions. It is commonly included in formulations for oral administration, such as tablets, capsules, and liquid suspensions, to provide a consistent and reliable source of selenium. Sodium Selenite anhydrous can also be used in topical formulations for dermal applications where selenium therapy is needed. The availability of different dosage forms allows pharmaceutical manufacturers to tailor their products to meet the specific needs of patients requiring selenium supplementation.
Sodium Selenite anhydrous is a pharmaceutical-grade form of the mineral selenium, which is an essential micronutrient with antioxidant properties. It is commonly used in pharmaceutical formulations as a source of selenium, which plays a crucial role in various biological processes in the body. Sodium Selenite anhydrous is utilized in the pharmaceutical industry for its therapeutic benefits and as a dietary supplement to address selenium deficiencies in patients.
How does Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade differ from other forms of selenium supplements?
Sodium Selenite anhydrous is a highly pure and stable form of selenium supplement that meets the stringent quality standards set by the European Pharmacopoeia (Ph. Eur.) and British Pharmacopoeia (BP). This pharmaceutical-grade form of selenium is manufactured to ensure consistency in potency and efficacy, making it a preferred choice for pharmaceutical formulations. Unlike other forms of selenium supplements, Sodium Selenite anhydrous is specifically designed for use in pharmaceutical applications where quality and purity are of utmost importance.
What are the key benefits of using Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade in pharmaceutical formulations?
Sodium Selenite anhydrous offers several benefits when used in pharmaceutical formulations. As a potent source of selenium, it helps support the body's antioxidant defense mechanisms and plays a critical role in cellular function and overall health. By incorporating Sodium Selenite anhydrous into pharmaceutical products, manufacturers can ensure that patients receive a reliable and effective source of selenium to address deficiencies or therapeutic needs. Additionally, the pharmaceutical-grade quality of Sodium Selenite anhydrous ensures that it meets the highest standards of purity and safety for pharmaceutical use.
How is Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade produced and what quality control measures are in place to ensure its purity and efficacy?
Sodium Selenite anhydrous is produced through a controlled manufacturing process that involves the synthesis of sodium selenite under strict quality control conditions. The raw materials used in the production of Sodium Selenite anhydrous are carefully selected to ensure purity and potency. Throughout the manufacturing process, rigorous quality control measures are in place to monitor the product's purity, stability, and efficacy. The final product is tested for compliance with the standards set by the European Pharmacopoeia (Ph. Eur.) and British Pharmacopoeia (BP) to ensure that it meets the required specifications for pharmaceutical use.
In what pharmaceutical applications is Sodium Selenite anhydrous (Ph. Eur., BP) pharma grade commonly used and what dosage forms are available?
Sodium Selenite anhydrous is used in a variety of pharmaceutical applications where selenium supplementation is indicated, such as in the treatment of selenium deficiencies and certain medical conditions. It is commonly included in formulations for oral administration, such as tablets, capsules, and liquid suspensions, to provide a consistent and reliable source of selenium. Sodium Selenite anhydrous can also be used in topical formulations for dermal applications where selenium therapy is needed. The availability of different dosage forms allows pharmaceutical manufacturers to tailor their products to meet the specific needs of patients requiring selenium supplementation.
