Capecitabine BP-EP-USP

Capecitabine BP-EP-USP Specification

Molecular Formula
C15H22FN3O6

Melting Point
110-121 C

Boiling point
437.874 C

Storage
Dry Place

Molecular Weight
359.35

Medicine Name
Capecitabine

Chemical Name
Pentyl [1-(3,4-dihydroxy-5-methyl-oxolan-2-yl)-5-fluoro-2-oxo-pyrimidin-4-yl]aminoformate;

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical

Purity(%)
99%

Appearance
white to off-white crystalline powder

Physical Form
Powder

Capecitabine BP-EP-USP Trade Information

Minimum Order Quantity
10 Kilograms

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

About Capecitabine BP-EP-USP

It is used alone or incombination with other cancer treatments in patients with colon cancer that hasspread (Stage III) to help prevent colon cancer from coming back after surgery.It is also used together with other cancer treatments and radiation treatment,around the time of surgery, to treat rectal cancer that has spread. Thismedicine is also used alone or in combination with other cancer treatments totreat colorectal cancer that has spread or cannot be removed by surgery. Capecitabineis also used together with docetaxel to treat breast cancer that has spreadthroughout the body in patients who have received other medicines (eg,anthracycline medicine) that did not worked well. This medicine is also usedalone to treat breast cancer in patients who are not able to receiveanthracycline medicine or taxane medicine.

Key Features and Quality

Capecitabine BP-EP-USP stands out due to its exceptional purity and compliance with international standards (BP, EP, USP). As an industrial-grade compound, it is carefully refined to meet stringent pharmaceutical criteria. Its physical form as a stable powder simplifies handling, transportation, and storage requirements, making it a dependable component in pharmaceutical manufacturing.

Applications in Pharmaceuticals

Widely used as a pharmaceutical intermediate, Capecitabine is crucial in the synthesis of active pharmaceutical ingredients. Its chemical stability and purity ensure consistent results in drug production processes. As a result, manufacturers rely on this compound to maintain integrity and efficacy in the medicines they create.

Storage and Handling Guidelines

To retain its high purity, Capecitabine BP-EP-USP should be stored in a dry environment, protected from moisture and contamination. Thanks to its moderate melting and boiling points, it remains stable under standard industrial conditions, reducing the risk of degradation during storage or processing.

FAQs of Capecitabine BP-EP-USP:

Q: How should Capecitabine BP-EP-USP be stored to maintain its quality?

A: Capecitabine BP-EP-USP should be stored in a dry place, away from moisture and direct sunlight. Keeping it in its original packaging and sealed tightly helps preserve its purity and crystalline form.

Q: What are the primary uses of Capecitabine BP-EP-USP in the pharmaceutical industry?

A: This compound is utilized as a pharmaceutical intermediate, mainly in the synthesis of active ingredients for various medications. Its high purity and stability make it indispensable in pharmaceutical research and manufacturing.

Q: When is Capecitabine BP-EP-USP typically used in the medicine manufacturing process?

A: Capecitabine is employed at the intermediate stage of pharmaceutical production, where it acts as a building block for creating active ingredients in finished drugs.

Q: Where can Capecitabine BP-EP-USP be sourced from?

A: This high-purity intermediate is available from exporters, manufacturers, and suppliers in India, which is a prominent hub for pharmaceutical chemicals meeting BP, EP, and USP standards.

Q: What process ensures the high purity of Capecitabine BP-EP-USP?

A: The compound undergoes rigorous purification and quality control processes aligned with BP-EP-USP specifications, ensuring that it consistently achieves a purity level of 99%.

Q: How does the quality of Capecitabine benefit pharmaceutical manufacturers?

A: The exceptional purity and compliance with international standards reduce contamination risks and enhance the reliability of drug synthesis, ultimately improving product safety and efficacy.

Q: What is the recommended physical handling form of Capecitabine BP-EP-USP?

A: It is recommended to handle Capecitabine BP-EP-USP in its powdered crystalline form, which allows for straightforward measurement, transport, and incorporation into manufacturing processes.

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