Shaanxi Kaishi Biotechnology Co., Ltd

English

Phone:
15537834455

Select Language
English
Products> Enzyme Preparation> Pharmaceutical Enzymes> Paclitaxel 98% Pharmaceutical API Powder
Paclitaxel 98% Pharmaceutical API Powder

Paclitaxel 98% Pharmaceutical API Powder

  • $40

    1-199 Others

  • $30

    200-499 Others

  • $20

    ≥500 Others

Share:
Product Attributes

Product Description

Product Overview

Paclitaxel 98% is a high-purity pharmaceutical active pharmaceutical ingredient (API) widely used in oncology drug development and sterile injectable chemotherapy formulations. It is a naturally derived diterpenoid compound originally extracted from Taxus species and remains one of the most important anticancer agents in modern pharmaceutical manufacturing.

In global pharmaceutical supply chains, Paclitaxel plays a key role in GMP-certified production, Supplement Contract Manufacturing, and CDMO operations. It is widely applied in injectable drug formulation, oncology R&D, and clinical trial material supply.

Content Note: Prepared by our technical team based on peer-reviewed scientific literature. This content is intended for industrial and research use only and complies with FDA/EFSA communication guidelines. Last reviewed: June 2026
According to a study in Journal of Clinical Oncology (1998), paclitaxel demonstrated significant therapeutic efficacy in patients with ovarian and breast cancer as part of combination chemotherapy regimens.
According to a study in The New England Journal of Medicine (1994), paclitaxel showed clinically meaningful anti-tumor activity in previously treated ovarian cancer patients, establishing its importance in chemotherapy protocols.

Key Ingredients & Specifications

Paclitaxel 98% is manufactured under strict GMP-controlled environments to ensure high purity, stability, and pharmaceutical-grade compliance for global distribution.

Parameter Specification
Active Ingredient Paclitaxel
Purity ≥ 98%
Appearance White to off-white crystalline powder
Test Method HPLC
Form API powder / injectable intermediate
Storage Condition 2–8°C, protected from light and moisture

Differentiation Content – Extraction & Quality Control

The quality of Paclitaxel 98% depends on extraction source, purification technology, and GMP-certified manufacturing systems. Advanced processing ensures high bioactivity and low impurity levels.

Process Stage Quality Impact
Natural extraction from Taxus species Maintains molecular integrity and therapeutic activity
Advanced chromatographic purification Reduces impurities and improves safety profile
Sterile crystallization process Enhances stability for injectable applications

Comparison with Key Oncology APIs

API Mechanism Clinical Application
Paclitaxel Microtubule stabilization Breast, ovarian, lung cancers
Docetaxel Microtubule stabilization Solid tumor chemotherapy
Doxorubicin DNA intercalation Broad-spectrum oncology treatment

Applications & Benefits

Paclitaxel 98% is widely used in pharmaceutical oncology manufacturing and clinical drug development programs.

  • Injectable chemotherapy drug production
  • Oncology formulation R&D
  • Combination cancer therapy development
  • Clinical trial active pharmaceutical ingredient supply
  • GMP contract manufacturing (CMO/CDMO)

It is also applied in research involving Plant Extracts , Standardized Extracts, Herbal Extracts , Nutritional Ingredients, and Antioxidants for pharmaceutical innovation and formulation science.

Core Keyword Integration

Why Choose Us – Quality & OEM Capability

We supply Paclitaxel 98% under strict GMP-certified systems with full regulatory support for global pharmaceutical markets.

  • Certifications: GMP, ISO, HACCP
  • OEM Services: Private label, formulation support, CDMO collaboration
  • Dosage Forms: API powder and injectable intermediates
  • MOQ: Flexible for R&D and bulk procurement
  • Quality Control: HPLC, NMR, microbial testing

Frequently Asked Questions

What is Paclitaxel 98% used for?

It is used as an active pharmaceutical ingredient in chemotherapy drug production for cancer treatment.

Is Paclitaxel suitable for injectable formulations?

Yes, it is commonly processed into sterile injectable dosage forms under GMP conditions.

What is the purity standard of Paclitaxel API?

The standard purity is ≥98%, confirmed by HPLC testing methods.

How should Paclitaxel 98% be stored?

It should be stored at 2–8°C in a sealed, light-protected environment.

Do you support OEM or CDMO services?

Yes, we provide OEM, private label, and contract manufacturing services for global pharmaceutical clients.

44
Packaging & Delivery

Packaging & Delivery

The file is encrypted. Please fill in the following information to continue accessing it

GET IN TOUCH
If you have any questions our products or services,feel free to reach out to us.Provide unique experiences for everyone involved with a brand.we've got preferential price and best-quality products for you.
Please fill in the information
* Please fill in your e-mail
* Please fill in the content
Products> Enzyme Preparation> Pharmaceutical Enzymes> Paclitaxel 98% Pharmaceutical API Powder
  • Contact Us

  • Mobile Phone: 15537834455
  • Email: sales01@kaishibio.com
  • Address: No. 11206, 12th Floor, Unit 1, Building 15, Zhongmao Plaza, West of Nanguanzheng Street, Beilin District, Xian, Shaanxi China
  • Website: https://www.kaishibio.com
  • Send Inquiry

Copyright © 2026 Shaanxi Kaishi Biotechnology Co., Ltd All rights reserved. Privacy Policy

Send Inquiry
*
*

We will contact you immediately

Fill in more information so that we can get in touch with you faster

Privacy statement: Your privacy is very important to Us. Our company promises not to disclose your personal information to any external company with out your explicit permission.

Send