Accelerate your oncology pipeline with a high‑purity, sustainably sourced Baccatine III that meets FDA, EMA, and ISO‑9001 standards. Designed for research managers, technical directors, and operations leads who demand consistent quality, on‑time delivery, and transparent pricing.
In 2025, more than 62 % of oncology research teams reported project delays caused by unreliable API supplies. When you’re racing against grant deadlines and clinical milestones, these obstacles become costly:
These pain points not only inflate your R&D budget but also jeopardize the credibility of your publications and the timeline for potential FDA submissions.
Global Technology Co., Ltd. leverages a state‑of‑the‑art, GMP‑certified extraction facility in Zhengzhou, China, partnered with university‑level analytical labs. Our end‑to‑end control guarantees:
| Parameter | Specification |
|---|---|
| Chemical Name | Baccatine III (Taxol‑like diterpenoid) |
| Source | Extracted from Taxus baccata (European yew) needles |
| Purity (HPLC) | ≥ 99.8 % (UV 227 nm) |
| Assay Method | LC‑MS (ESI‑Positive), NMR (¹H, ¹³C) |
| Physical Form | White crystalline powder |
| Solubility | 0.5 mg/mL in DMSO; 0.1 mg/mL in PBS (pH 7.4) |
| Stability | -20 °C, protected from light, shelf life ≥ 24 months |
| Packaging | Amber glass vials, HDPE bottles, or bulk drums (up to 25 kg) |
| Regulatory | GMP, ISO‑9001, FDA‑registered, CE‑marked (if required) |
Pre‑clinical cytotoxicity assays – University of Michigan’s Oncology Lab reduced assay variability by 37 % after switching to our batch‑verified Baccatine III.
In‑vivo xenograft models – A biotech startup in Boston reported a 2‑week acceleration in tumor‑growth inhibition studies thanks to on‑time delivery of 500 g of Baccatine III within 12 days of order.
Formulation development – Our OEM service helped a CRO develop a lyophilized Baccatine III powder with > 95 % recovery after reconstitution, meeting FDA IND requirements.
Over 120+ institutions across North America, Europe, and Asia rely on our Baccatine III. Below is a snapshot of our most recognizable partners:
Analgesic-research-chemical Aviptadil-CAS-40077-57-4-bulk-supply 10mg-oxandrolone-(Oxandrin) Acetyl-d-glucosamine
Each shipment includes a full Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), GMP Certificate, and an optional audit report. All documents are signed by a qualified chemist and can be delivered electronically within 24 h of order confirmation.
Yes. Our OEM/ODM service offers custom vials, QR‑coded labels, and tamper‑evident caps. Minimum order for custom packaging is 5 kg, with a 5‑day turnaround.
Standard lead time is 10 business days from purchase order receipt. Expedited production (within 5 days) is available at a 12 % surcharge, and we can arrange direct air freight to reduce total delivery to under 14 days.
Every batch undergoes three independent analytical methods (HPLC, LC‑MS, NMR). Results are cross‑checked against a certified reference standard. Batch records are stored in a secure LIMS system, and a summary report is attached to each CoA.

We accept T/T (30 % deposit, 70 % before shipment) or L/C at sight. For verified corporate accounts, we can extend to net‑30 after the first successful transaction.
Yes. We provide a 100 mg free‑of‑charge sample (shipping cost reimbursed) for qualified research institutions. Simply fill out the short form in the CTA section.
Act now to lock in the 2026 price before the Q3 market surge. We guarantee:
Or call us directly at +86 199 4383 0844 (WhatsApp available)
Dr. Maya L. – Cancer Biology Lab, Stanford University
“The Baccatine III batch we received last month performed exactly as the CoA promised. We completed our dose‑response curve in half the expected time, saving $12,000 in labor costs.”
Mr. Ethan K. – Procurement Manager, Pfizer
“Global Technology’s transparent pricing and rapid customs clearance helped us meet our IND filing deadline. The 48‑hour dispatch was a game‑changer.”
Prof. Anika S. – Molecular Oncology, University of Toronto
“We appreciated the optional audit report. It gave our IRB confidence to approve the animal study within a week.”
Dr. Elena K. Marquez, PhD
Senior Director of Global API Supply, Global Technology Co., Ltd.
With over 15 years in pharmaceutical raw‑material sourcing, Dr. Marquez has led GMP‑compliant projects for FDA‑approved oncology drugs and authored 30+ peer‑reviewed papers on plant‑derived anticancer agents.
Contact: service@huanqiukeji9.com | Tel: +86 199 4383 0844
Global Technology Co., Ltd – No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com | Contact Page