Paclitaxel BP-USP API

Paclitaxel BP-USP API Specification

Melting Point
213 C

Shelf Life
3 Years

Molecular Weight
853.92

Molecular Formula
C47H51NO14

Storage
Dry Place

Medicine Name
Paclitaxel

Chemical Name
N-benzyl-beta-enylisoserine; paclitaxel,

CAS No
33069-62-4

Type
Antibiotic and Antimicrobial Agents

Grade
Medicine Grade

Usage
Pharmaceutical

Purity(%)
99%

Appearance
White crystalline powder

Physical Form
Powder

Paclitaxel BP-USP API Trade Information

Minimum Order Quantity
1000 Kilograms

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

About Paclitaxel BP-USP API

Paclitaxel injection is used to treatadvanced cancer of the ovaries, breast, non-small cell lung cancer, and Kaposisarcoma. Kaposi sarcoma is a cancer of the skin and mucous membranes that iscommonly found in patients with acquired immunodeficiency syndrome (AIDS). Paclitaxelbelongs to the group of medicines called antineoplastics. It interferes withthe growth of cancer cells, which are eventually destroyed. Since the growth ofnormal body cells may also be affected, other unwanted effects will also occur.Some of these may be serious and must be reported to your doctor. Other effectsmay not be serious but may cause concern. Some effects may not occur untilmonths or years after the medicine is used.Before you begin treatment withpaclitaxel, you and your doctor should talk about the good this medicine willdo as well as the risks of using it.

Reliable Pharmaceutical Ingredient for Advanced Therapies

Paclitaxel BP-USP API is a cornerstone in various medical formulations, recognized for its efficacy and purity. With a chemical structure tailored for pharmaceutical use, it provides consistent results in antibiotic and antimicrobial therapies. Its stability and longevity make it a preferred choice among manufacturers and healthcare providers.

Stringent Quality Control for Patient Safety

Each batch of Paclitaxel undergoes rigorous testing as per BP and USP standards, ensuring unmatched quality and purity. With a long shelf life of 3 years and easy-to-handle physical form, it supports efficient pharmaceutical manufacturing and storage solutions.

FAQs of Paclitaxel BP-USP API:

Q: How is Paclitaxel BP-USP API used in pharmaceutical formulations?

A: Paclitaxel BP-USP API is primarily used as an active ingredient in the formulation of medicines for treating various conditions, including cancer and infections, due to its antibiotic and antimicrobial properties.

Q: What are the main benefits of using Paclitaxel BP-USP API?

A: The chief benefits include its high purity level (99%), reliable shelf life of 3 years, and consistent pharmaceutical efficacy, making it a trusted option for producing stable and effective medicines.

Q: When should Paclitaxel BP-USP API be stored and handled?

A: It should always be stored in a dry place at room temperature to maintain its chemical stability and effectiveness throughout its 3-year shelf life.

Q: Where does the supplied Paclitaxel BP-USP API originate?

A: This Paclitaxel API is manufactured, exported, and supplied from India, meeting international BP and USP quality standards for pharmaceutical use.

Q: What is the standard process for ensuring Paclitaxel BP-USP API quality?

A: Quality is maintained by following strict BP and USP guidelines, including comprehensive testing for purity, physical characteristics, and stability before distribution.

Q: How can pharmaceutical manufacturers benefit from choosing this Paclitaxel API?

A: Manufacturers benefit from its versatility, high purity, and ease of integration into pharmaceutical preparations, ensuring therapeutic reliability for end users.

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