Shaanxi Kaishi Biotechnology Co., Ltd

English

Phone:
15537834455

Select Language
English
Docetaxel 99% Anticancer API

Docetaxel 99% Anticancer API

  • $50

    1-199 Others

  • $40

    200-499 Others

  • $30

    ≥500 Others

Share:
Product Attributes

Product Description

Product Overview

Docetaxel 99% is a high-purity pharmaceutical active pharmaceutical ingredient (API) widely used in oncology drug development and injectable chemotherapy formulations. It belongs to the taxane class of compounds and is a critical intermediate in modern cancer treatment manufacturing pipelines.

As global demand increases for advanced Pharmaceutical Enzymes, Nutritional Ingredients, and high-purity APIs, Docetaxel 99% continues to play a key role in pharmaceutical contract manufacturing and regulated drug production supply chains.

Content Note: Prepared by our technical team based on current scientific literature. Health-related descriptions are intended for research and industrial use only and comply with FDA/EFSA communication guidelines. Last reviewed: June 2026
According to a study in Journal of Clinical Oncology (2004), docetaxel-based chemotherapy regimens demonstrated improved response rates in patients with advanced breast cancer compared with standard treatment protocols.
According to a study in The Lancet Oncology (2008), docetaxel combination therapy showed significant clinical efficacy in non-small cell lung cancer, supporting its role in first-line oncology treatment strategies.

Key Ingredients & Specifications

Docetaxel 99% is manufactured under strict GMP-controlled conditions to ensure high purity, stability, and reproducibility for pharmaceutical applications.

Parameter Specification
Active Ingredient Docetaxel
Purity ≥ 99%
Appearance White to off-white powder
Test Method HPLC
Form Sterile API powder / injectable intermediate
Storage Condition 2–8°C, protected from light and moisture

Differentiation Content – Purification & Manufacturing Standards

The quality of Docetaxel 99% is strongly influenced by synthesis route, purification technology, and sterile processing systems. Advanced manufacturing ensures compliance with pharmaceutical-grade requirements.

Process Stage Impact on Product Quality
Semi-synthetic extraction process Maintains molecular integrity and bioactivity
Multi-stage chromatography purification Reduces impurities and enhances safety profile
Sterile freeze-drying process Improves long-term stability for injectable use

Comparison with Oncology API Alternatives

Compound Mechanism Primary Application
Docetaxel Microtubule stabilization Breast, lung, prostate cancer treatment
Paclitaxel Microtubule inhibition Broad-spectrum chemotherapy
Doxorubicin DNA intercalation Solid tumors and hematologic cancers

Applications & Benefits

Docetaxel 99% is primarily used in pharmaceutical oncology manufacturing and research-based formulation development.

  • Injectable chemotherapy drug production
  • Oncology formulation research and development
  • Combination therapy drug design
  • Clinical trial compound preparation
  • Pharmaceutical contract manufacturing (CMO/CDMO)

It is also utilized in research contexts involving Plant Extracts , Standardized Extracts, Herbal Extracts , Antioxidants , and Superfood Blends as part of broader nutraceutical and pharmaceutical innovation studies.

Core Keywords Integration

Why Choose Us – Quality & OEM Capability

We supply Docetaxel 99% under strict pharmaceutical manufacturing standards with global regulatory compliance support.

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

Frequently Asked Questions

What is Docetaxel 99% used for?

It is used as an active pharmaceutical ingredient in chemotherapy drug manufacturing for oncology applications.

Is Docetaxel suitable for injectable drugs?

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

What purity level is required for pharmaceutical use?

The standard requirement is ≥99% purity, verified by HPLC testing methods.

How should Docetaxel be stored?

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

Do you support OEM or contract manufacturing?

Yes, OEM and CDMO services are available 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
  • 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