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| Product Name | Diethanolamine (USP-NF) Pharma Grade |
| Type | Chemical compound |
| Grade | USP-NF (United States Pharmacopeia-National Formulary) |
| Appearance | Clear, colorless liquid |
| Odor | Slight amine odor |
| Solubility | Soluble in water, alcohol, and ether |
| Boiling Point | 269°C |
| Melting Point | 28-31°C |
| Density | 1.095 g/cm3 |
| Usage | Commonly used in cosmetics, pharmaceuticals, and personal care products |
| Storage | Store in a cool, dry, and well-ventilated area |
| Handling | Avoid contact with skin and eyes, use in a well-ventilated area |
| Packaging | Available in drums, IBC totes, and tank trucks |
| Shelf Life | Minimum 2 years if stored properly |
| Regulatory Compliance | Complies with USP-NF standards |
| Manufacturer | Various pharmaceutical companies produce Diethanolamine pharma grade |
| Applications | Emulsifier, wetting agent, solubilizer, pH adjuster in various industries |
FAQ
What is Diethanolamine (USP-NF) pharma grade used for?
Diethanolamine (USP-NF) pharma grade is commonly used in the pharmaceutical industry as an organic compound that acts as a buffering agent. It helps to regulate and maintain the pH of various medications, making it a crucial component in the formulation of pharmaceutical products.
Is Diethanolamine (USP-NF) pharma grade safe for use in pharmaceutical products?
Yes, Diethanolamine (USP-NF) pharma grade is considered safe for use in pharmaceutical products when used in accordance with regulations and guidelines set by regulatory bodies such as the United States Pharmacopeia (USP) and the National Formulary (NF).
What are the benefits of using Diethanolamine (USP-NF) pharma grade in pharmaceutical formulations?
Diethanolamine (USP-NF) pharma grade offers several benefits in pharmaceutical formulations. It serves as an effective buffering agent, helping to stabilize the pH of medications and ensuring their efficacy. Additionally, it can enhance the solubility of certain active ingredients, allowing for improved bioavailability and therapeutic effects.
How is Diethanolamine (USP-NF) pharma grade typically incorporated into pharmaceutical formulations?
Diethanolamine (USP-NF) pharma grade is typically added to pharmaceutical formulations during the manufacturing process. It can be dissolved in water or other solvents to create a solution that is then mixed with other ingredients to form the final product.
Are there any considerations or precautions to be aware of when using Diethanolamine (USP-NF) pharma grade in pharmaceutical formulations?
While Diethanolamine (USP-NF) pharma grade is generally safe for use in pharmaceutical formulations, it is important to follow recommended guidelines for handling and storage to ensure product quality and safety. Additionally, it is essential to conduct thorough testing and analysis to ensure compatibility with other ingredients and to verify the stability of the final product.
Diethanolamine (USP-NF) pharma grade is commonly used in the pharmaceutical industry as an organic compound that acts as a buffering agent. It helps to regulate and maintain the pH of various medications, making it a crucial component in the formulation of pharmaceutical products.
Is Diethanolamine (USP-NF) pharma grade safe for use in pharmaceutical products?
Yes, Diethanolamine (USP-NF) pharma grade is considered safe for use in pharmaceutical products when used in accordance with regulations and guidelines set by regulatory bodies such as the United States Pharmacopeia (USP) and the National Formulary (NF).
What are the benefits of using Diethanolamine (USP-NF) pharma grade in pharmaceutical formulations?
Diethanolamine (USP-NF) pharma grade offers several benefits in pharmaceutical formulations. It serves as an effective buffering agent, helping to stabilize the pH of medications and ensuring their efficacy. Additionally, it can enhance the solubility of certain active ingredients, allowing for improved bioavailability and therapeutic effects.
How is Diethanolamine (USP-NF) pharma grade typically incorporated into pharmaceutical formulations?
Diethanolamine (USP-NF) pharma grade is typically added to pharmaceutical formulations during the manufacturing process. It can be dissolved in water or other solvents to create a solution that is then mixed with other ingredients to form the final product.
Are there any considerations or precautions to be aware of when using Diethanolamine (USP-NF) pharma grade in pharmaceutical formulations?
While Diethanolamine (USP-NF) pharma grade is generally safe for use in pharmaceutical formulations, it is important to follow recommended guidelines for handling and storage to ensure product quality and safety. Additionally, it is essential to conduct thorough testing and analysis to ensure compatibility with other ingredients and to verify the stability of the final product.
