Urea crystalline (USP, BP, Ph. Eur.) pharma grade

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Product Name Urea crystalline
Grade Pharma grade
Standards USP, BP, Ph. Eur.
Appearance White crystalline powder
CAS Number 57-13-6
Molecular Formula CH4N2O
Molecular Weight 60.06 g/mol
Solubility Soluble in water
Melting Point 132-135°C
Storage Conditions Store in a cool, dry place
Application Used in the pharmaceutical industry as a diuretic and in skincare products
FAQ
What is Urea crystalline (USP, BP, Ph. Eur.) pharma grade?
Urea is a naturally occurring compound found in the human body. It is also produced synthetically for various pharmaceutical and industrial purposes. Urea crystalline (USP, BP, Ph. Eur.) pharma grade refers to urea that meets the standards set by the United States Pharmacopeia (USP), British Pharmacopoeia (BP), and European Pharmacopoeia (Ph. Eur.) for pharmaceutical use. This ensures high levels of purity and quality, making it suitable for use in pharmaceutical formulations.

What are the applications of Urea crystalline (USP, BP, Ph. Eur.) pharma grade?
Urea crystalline (USP, BP, Ph. Eur.) pharma grade has several pharmaceutical applications. It is commonly used in topical formulations such as creams and lotions for its moisturizing properties. Urea is also used in certain medications to treat conditions like psoriasis and eczema. In addition, urea is utilized in the manufacture of slow-release drug delivery systems and as a protein denaturant in protein extraction and analysis.

What are the benefits of using Urea crystalline (USP, BP, Ph. Eur.) pharma grade?
One of the main benefits of using Urea crystalline (USP, BP, Ph. Eur.) pharma grade is its high purity and quality, which ensures the safety and efficacy of pharmaceutical products. Urea's moisturizing properties make it a valuable ingredient in skincare products, helping to hydrate and soften the skin. Additionally, the versatile nature of urea allows for its application in various pharmaceutical formulations, providing flexibility for formulators to create effective medications.

How is Urea crystalline (USP, BP, Ph. Eur.) pharma grade manufactured?
Urea crystalline (USP, BP, Ph. Eur.) pharma grade is typically manufactured through a controlled synthesis process to ensure high purity and quality. The synthesis involves reacting ammonia and carbon dioxide under specific conditions to produce urea crystals. The resulting product is then carefully processed and tested to meet the stringent standards set by the USP, BP, and Ph. Eur. pharmacopoeias for pharmaceutical use.

Is Urea crystalline (USP, BP, Ph. Eur.) pharma grade safe for use in pharmaceutical formulations?
Yes, Urea crystalline (USP, BP, Ph. Eur.) pharma grade is considered safe for use in pharmaceutical formulations when used according to established guidelines and dosages. The high purity and quality of urea crystals ensure that they meet the necessary standards for pharmaceutical use, reducing the risk of impurities or contaminants in the final product. However, it is important for formulators to follow proper handling and storage procedures to maintain the integrity of the urea crystals.
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