Accelerate your oncology research with a certified‑grade CAS 1802086-25-4 Osimertinib impurity that meets FDA, GMP, and ISO 9001 standards. Designed for Corporate Purchasing Managers, Technical Directors, and Operations Leaders who demand consistency, traceability, and on‑time supply.
Get Free Quote in 24 hIn 2025, 34 % of pharmaceutical R&D projects missed milestones because of unreliable API supplies. The most common bottlenecks revolve around the very impurity you need for structure‑activity‑relationship (SAR) studies—CAS 1802086-25-4 Osimertinib impurity. Below are the three critical pain points you probably face:
Imagine a scenario where your team must pause a Phase II pre‑clinical assay because the impurity arrives late or fails purity specifications. The resulting delay can cost up to $250,000 in lost opportunity. You cannot afford that risk.
Global Technology Co., Ltd leverages a Powerful Factory network and a rigorous Quality Assurance (QA) system to deliver an impurity that ticks every box on your procurement checklist.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 1802086‑25‑4 | |
| Chemical Name | Osimertinib Impurity (C28H33N7O2Cl) | |
| Purity (HPLC) | ≥ 99.8 % | |
| Appearance | White to off‑white powder | |
| Moisture Content | ≤ 0.1 % | |
| Solubility | DMSO 10 mg/mL; MeCN 5 mg/mL | |
| Shelf Life | 24 months (stored < 25 °C, dry) | |
| Packaging | HDPE bottle, 5 g‑25 kg, sealed with nitrogen | |
| Certificates | FDA, GMP, ISO 9001, CE, RoHS |
Scenario 1 – SAR Optimization for Third‑Generation EGFR Inhibitors
XYZ Pharma used our impurity to synthesize a series of analogues, reducing the lead‑time from 45 days to 12 days and cutting R&D costs by 27 %. The COA data satisfied FDA’s IND filing requirements on the first submission.
Scenario 2 – Stability‑Testing for Formulation Development
ABC Biotech incorporated the impurity as a forced‑degradation marker. The high purity (99.9 %) ensured that analytical peaks were attributable solely to degradation pathways, improving method robustness and saving ≈ $45,000 in repeat testing.
The MOQ is 500 g for standard packaging. For larger projects we can supply up to 25 kg per batch with volume‑discount pricing.
Yes. Every shipment includes an FDA‑compliant COA, HPLC chromatogram, and a full impurity profile (≤ 0.1 % residual).
Absolutely. Our R&D team can tailor particle size, salt form, or even develop analogues under a confidential NDA.
Standard air freight (FOB) arrives in 12‑15 days. Express air (DHL/UPS) can be delivered within 5‑7 days. We also support DDP (Delivered Duty Paid) for a hassle‑free experience.

Our technical support team is available 24 h via email, WhatsApp, or phone. We offer method‑validation assistance, stability‑testing guidance, and a 30‑day money‑back guarantee if the material does not meet the COA.
Limited stock available for the next 30 days. Act now to lock in today’s price and receive a **free 5 g sample** with a money‑back guarantee if the purity does not meet the COA.
Or WhatsApp us now: +86 199 4383 0844
John M., Procurement Lead, MedTech Solutions
“The **speed** of delivery surprised us – we needed 2 kg within a week and got it in 5 days. Quality matched the COA exactly, saving us $18,000 on repeat testing.”
Linda S., R&D Director, Apex BioLabs
“We appreciated the **transparent pricing** – no surprise fees. The impurity’s purity (99.9 %) allowed us to file our IND on schedule.”
Mark T., Operations Manager, GenChem Corp.
“Their **after‑sales support** is outstanding. When we needed a stability protocol, the technical team responded within 2 hours and provided a detailed report.”
Global Technology Co., Ltd | Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
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