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| Product | L-Valine (Ph. Eur., USP) pure, pharma grade |
| Appearance | White crystalline powder |
| Purity | ≥ 98.5% |
| Melting Point | 295-300°C |
| Solubility | Soluble in water |
| Identification | IR spectrum matches with Ph. Eur. standard |
| Loss On Drying | ≤ 0.3% |
| Heavy Metals | ≤ 10 ppm |
| Residue On Ignition | ≤ 0.1% |
| Specific Rotation | +26.6° to +28.8° |
| Microbial Limits | Complies with Ph. Eur. requirements |
FAQ
What is L-Valine and how is it used in the pharmaceutical industry?
L-Valine is an essential amino acid that is necessary for protein synthesis in the body. It is one of the three branched-chain amino acids (BCAAs) along with L-leucine and L-isoleucine. In the pharmaceutical industry, L-Valine is commonly used in the formulation of parenteral nutrition products, as well as in the production of certain drugs and supplements.
What are the key benefits of using L-Valine in pharmaceutical applications?
L-Valine plays a critical role in promoting muscle growth and repair, making it essential for athletes and individuals looking to improve their physical performance. It also helps to regulate blood sugar levels and support cognitive function. In pharmaceutical applications, L-Valine is valued for its ability to enhance the stability and solubility of formulations, as well as its role in ensuring the proper delivery of active ingredients to the body.
What sets Pharma Grade L-Valine apart from other sources of this amino acid?
Pharma Grade L-Valine meets the strictest purity and quality standards set forth by the European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP). This ensures that the product is free from impurities and contaminants that could compromise its safety and efficacy. With Pharma Grade L-Valine, pharmaceutical manufacturers can have confidence in the consistency and reliability of their formulations.
How can pharmaceutical manufacturers incorporate Pharma Grade L-Valine into their products?
Pharma Grade L-Valine can be easily incorporated into a wide range of pharmaceutical formulations, including injectable solutions, tablets, and capsules. The powder form of L-Valine allows for precise dosing and blending with other ingredients. Manufacturers can work closely with their suppliers to determine the optimal concentration of L-Valine in their products to achieve the desired therapeutic effects.
What quality control measures are in place to ensure the purity and potency of Pharma Grade L-Valine?
Pharma Grade L-Valine undergoes rigorous testing throughout the manufacturing process to guarantee its purity and potency. This includes analysis for heavy metals, microbiological contaminants, and other impurities that could compromise the quality of the product. By adhering to these stringent quality control measures, manufacturers can trust that Pharma Grade L-Valine will consistently meet their specifications and regulatory requirements.
L-Valine is an essential amino acid that is necessary for protein synthesis in the body. It is one of the three branched-chain amino acids (BCAAs) along with L-leucine and L-isoleucine. In the pharmaceutical industry, L-Valine is commonly used in the formulation of parenteral nutrition products, as well as in the production of certain drugs and supplements.
What are the key benefits of using L-Valine in pharmaceutical applications?
L-Valine plays a critical role in promoting muscle growth and repair, making it essential for athletes and individuals looking to improve their physical performance. It also helps to regulate blood sugar levels and support cognitive function. In pharmaceutical applications, L-Valine is valued for its ability to enhance the stability and solubility of formulations, as well as its role in ensuring the proper delivery of active ingredients to the body.
What sets Pharma Grade L-Valine apart from other sources of this amino acid?
Pharma Grade L-Valine meets the strictest purity and quality standards set forth by the European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP). This ensures that the product is free from impurities and contaminants that could compromise its safety and efficacy. With Pharma Grade L-Valine, pharmaceutical manufacturers can have confidence in the consistency and reliability of their formulations.
How can pharmaceutical manufacturers incorporate Pharma Grade L-Valine into their products?
Pharma Grade L-Valine can be easily incorporated into a wide range of pharmaceutical formulations, including injectable solutions, tablets, and capsules. The powder form of L-Valine allows for precise dosing and blending with other ingredients. Manufacturers can work closely with their suppliers to determine the optimal concentration of L-Valine in their products to achieve the desired therapeutic effects.
What quality control measures are in place to ensure the purity and potency of Pharma Grade L-Valine?
Pharma Grade L-Valine undergoes rigorous testing throughout the manufacturing process to guarantee its purity and potency. This includes analysis for heavy metals, microbiological contaminants, and other impurities that could compromise the quality of the product. By adhering to these stringent quality control measures, manufacturers can trust that Pharma Grade L-Valine will consistently meet their specifications and regulatory requirements.
