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| Product | D-Mannitol low endotoxin (Ph. Eur., BP, USP, JP) pure, pharma grade |
| Chemical Formula | C6H14O6 |
| Molecular Weight | 182.17 g/mol |
| Appearance | White crystalline powder |
| Solubility | Freely soluble in water |
| Melting Point | 165-170°C |
| Assay | ≥ 98% |
| Endotoxin Level | ≤ 0.5 EU/mg |
| Residue On Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 10 ppm |
| Loss On Drying | ≤ 0.5% |
| Purity | Pharma grade |
FAQ
What is D-Mannitol?
D-Mannitol is a naturally occurring sugar alcohol that is commonly used in pharmaceuticals, foods, and personal care products. It is known for its ability to act as an osmotic diuretic, helping to increase urine production and reduce swelling in the body.
Why is low endotoxin D-Mannitol important?
Low endotoxin D-Mannitol is crucial in pharmaceutical applications where endotoxin contamination must be kept to a minimum. Endotoxins are toxic components found in the cell walls of certain bacteria, and can cause harmful effects if present in pharmaceutical products. By using low endotoxin D-Mannitol, the risk of endotoxin contamination is significantly reduced.
What are the different pharmacopoeial standards for D-Mannitol?
D-Mannitol is regulated by various pharmacopoeial standards, including Ph. Eur. (European Pharmacopoeia), BP (British Pharmacopoeia), USP (United States Pharmacopeia), and JP (Japanese Pharmacopoeia). These standards ensure the quality, purity, and safety of D-Mannitol for use in pharmaceutical products.
What is the purity level of pharma grade D-Mannitol?
Pharma grade D-Mannitol is highly pure, meeting the strict requirements set forth by pharmacopoeial standards. This ensures that the D-Mannitol is free from impurities and contaminants, making it suitable for use in pharmaceutical formulations.
Why choose limited to 2000 words or 5 Q&A questions pure, pharma grade D-Mannitol?
Limited to 2000 words or 5 Q&A questions pure, pharma grade D-Mannitol is the ideal choice for pharmaceutical manufacturers seeking a high-quality ingredient for their products. With its low endotoxin levels, adherence to pharmacopoeial standards, and high purity, limited to 2000 words or 5 Q&A questions D-Mannitol is a reliable and safe option for pharmaceutical formulations.
D-Mannitol is a naturally occurring sugar alcohol that is commonly used in pharmaceuticals, foods, and personal care products. It is known for its ability to act as an osmotic diuretic, helping to increase urine production and reduce swelling in the body.
Why is low endotoxin D-Mannitol important?
Low endotoxin D-Mannitol is crucial in pharmaceutical applications where endotoxin contamination must be kept to a minimum. Endotoxins are toxic components found in the cell walls of certain bacteria, and can cause harmful effects if present in pharmaceutical products. By using low endotoxin D-Mannitol, the risk of endotoxin contamination is significantly reduced.
What are the different pharmacopoeial standards for D-Mannitol?
D-Mannitol is regulated by various pharmacopoeial standards, including Ph. Eur. (European Pharmacopoeia), BP (British Pharmacopoeia), USP (United States Pharmacopeia), and JP (Japanese Pharmacopoeia). These standards ensure the quality, purity, and safety of D-Mannitol for use in pharmaceutical products.
What is the purity level of pharma grade D-Mannitol?
Pharma grade D-Mannitol is highly pure, meeting the strict requirements set forth by pharmacopoeial standards. This ensures that the D-Mannitol is free from impurities and contaminants, making it suitable for use in pharmaceutical formulations.
Why choose limited to 2000 words or 5 Q&A questions pure, pharma grade D-Mannitol?
Limited to 2000 words or 5 Q&A questions pure, pharma grade D-Mannitol is the ideal choice for pharmaceutical manufacturers seeking a high-quality ingredient for their products. With its low endotoxin levels, adherence to pharmacopoeial standards, and high purity, limited to 2000 words or 5 Q&A questions D-Mannitol is a reliable and safe option for pharmaceutical formulations.
