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| Name | D(-)Mannitol (USP, BP, Ph. Eur.) |
| Grade | Pharma |
| Purity | Pure |
| CAS Number | 69-65-8 |
| Molecular Formula | C6H14O6 |
| Molecular Weight | 182.17 g/mol |
| Appearance | White crystalline powder |
| Solubility | Soluble in water |
| Melting Point | 166-170°C |
| Density | 1.52 g/cm3 |
| Storage Conditions | Store in a cool, dry place |
| Shelf Life | Minimum 2 years |
| Usage | Commonly used as an excipient in pharmaceutical formulations |
FAQ
What is D(-) Mannitol (USP, BP, Ph. Eur.) pure, pharma grade?
D(-) Mannitol is a sugar alcohol that is used as a sweetener and a pharmaceutical excipient. It meets the standards set by the United States Pharmacopeia (USP), British Pharmacopoeia (BP), and the European Pharmacopoeia (Ph. Eur.) for purity and quality, making it suitable for use in pharmaceutical applications.
What are the key benefits of using D(-) Mannitol in pharmaceutical products?
D(-) Mannitol offers several key benefits when used in pharmaceutical products. It is non-toxic, non-irritating, and non-allergenic, making it safe for use in a wide range of patients. It also has a mild, pleasant taste, which makes it an ideal choice for oral dosage forms. Additionally, D(-) Mannitol is highly soluble in water, allowing for easy formulation and manufacturing of pharmaceutical products.
How is D(-) Mannitol typically used in pharmaceutical formulations?
D(-) Mannitol is commonly used as a bulking agent, excipient, or filler in pharmaceutical formulations. It can be used in tablets, capsules, powders, or solutions to improve the physical properties of the dosage form. D(-) Mannitol is also often used as a diluent in direct compression and granulation processes to improve flowability and compressibility of the formulation.
What are the quality standards for D(-) Mannitol (USP, BP, Ph. Eur.) pure, pharma grade?
D(-) Mannitol that is labeled as USP, BP, Ph. Eur. pure, pharma grade must meet the strict quality standards set by the respective pharmacopoeias. This includes requirements for purity, identity, appearance, solubility, and other physical and chemical properties. By choosing D(-) Mannitol that meets these standards, pharmaceutical manufacturers can ensure the quality and consistency of their products.
How can I purchase D(-) Mannitol (USP, BP, Ph. Eur.) pure, pharma grade?
D(-) Mannitol that meets the USP, BP, Ph. Eur. standards for purity and quality can be purchased from reputable suppliers and distributors. It is important to ensure that the product comes with the appropriate documentation, such as a Certificate of Analysis (CoA), to verify its compliance with the pharmacopoeial standards. Additionally, working with a trusted supplier can help ensure the quality and reliability of the D(-) Mannitol for use in pharmaceutical formulations.
D(-) Mannitol is a sugar alcohol that is used as a sweetener and a pharmaceutical excipient. It meets the standards set by the United States Pharmacopeia (USP), British Pharmacopoeia (BP), and the European Pharmacopoeia (Ph. Eur.) for purity and quality, making it suitable for use in pharmaceutical applications.
What are the key benefits of using D(-) Mannitol in pharmaceutical products?
D(-) Mannitol offers several key benefits when used in pharmaceutical products. It is non-toxic, non-irritating, and non-allergenic, making it safe for use in a wide range of patients. It also has a mild, pleasant taste, which makes it an ideal choice for oral dosage forms. Additionally, D(-) Mannitol is highly soluble in water, allowing for easy formulation and manufacturing of pharmaceutical products.
How is D(-) Mannitol typically used in pharmaceutical formulations?
D(-) Mannitol is commonly used as a bulking agent, excipient, or filler in pharmaceutical formulations. It can be used in tablets, capsules, powders, or solutions to improve the physical properties of the dosage form. D(-) Mannitol is also often used as a diluent in direct compression and granulation processes to improve flowability and compressibility of the formulation.
What are the quality standards for D(-) Mannitol (USP, BP, Ph. Eur.) pure, pharma grade?
D(-) Mannitol that is labeled as USP, BP, Ph. Eur. pure, pharma grade must meet the strict quality standards set by the respective pharmacopoeias. This includes requirements for purity, identity, appearance, solubility, and other physical and chemical properties. By choosing D(-) Mannitol that meets these standards, pharmaceutical manufacturers can ensure the quality and consistency of their products.
How can I purchase D(-) Mannitol (USP, BP, Ph. Eur.) pure, pharma grade?
D(-) Mannitol that meets the USP, BP, Ph. Eur. standards for purity and quality can be purchased from reputable suppliers and distributors. It is important to ensure that the product comes with the appropriate documentation, such as a Certificate of Analysis (CoA), to verify its compliance with the pharmacopoeial standards. Additionally, working with a trusted supplier can help ensure the quality and reliability of the D(-) Mannitol for use in pharmaceutical formulations.
