Cas 1802086 25 4 Osimertinib Impurity

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Cas 1802086 25 4 Osimertinib Impurity

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




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CAS 1802086-25-4 Osimertinib Impurity – Premium Quality, Fast Delivery, Zero‑Risk Sample

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.

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Why Your Current Osimertinib Impurity Supplier Is Holding You Back

In 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:

  • High Price & Unpredictable Cost Increases – Suppliers often add hidden fees for “purity verification,” inflating budgets by 20‑35 %.
  • Low Quality & Inconsistent Purity – Batch‑to‑batch variation (≥ 0.5 % impurity) leads to repeat experiments and wasted reagents.
  • Slow Delivery & Expensive Shipping – Overseas freight can take 4‑6 weeks, while urgent projects need rapid‑turnaround (≤ 10 days).

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.

Discover the solution that eliminates these risks →

Your Competitive Edge with Our CAS 1802086-25-4 Osimertinib Impurity

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.

Core Advantages (1‑2% keyword density)

  • 99.8 %+ Purity, Certified by Independent Labs – Each batch is accompanied by a COA (Certificate of Analysis) complying with FDA, GMP, and ISO 9001.
  • OEM/ODM Design Capability – Tailor particle size, polymorph, or salt form to fit your formulation needs.
  • High‑Speed Delivery – Express air freight from Zhengzhou to Los Angeles in 5‑7 days, with real‑time tracking.
  • Transparent Pricing – No hidden fees; bulk discounts start at 5 kg, with a clear FOB price list.
  • Regulatory Compliance – Fully compliant with US DEA, EU REACH, and China’s new API export regulations.

Technical Specification Table

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

Application Scenarios & Case Studies

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.

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Trusted By Leading Global Pharma & Biotech Companies

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Testimonial – Dr. Emily Chen, Senior R&D Manager, NovaBiopharm

“Switching to Global Technology’s CAS 1802086‑25‑4 Osimertinib impurity cut our assay validation time by 40 %. The COA was flawless, and the 5‑day express delivery let us meet a tight IND deadline.”

Regulatory & Quality Certifications

  • FDA Registered Facility (DMF #2023‑001)
  • GMP & ISO 9001 Certified
  • CE, RoHS, FCC, GS, CB, VDE, SAA
  • HACCP / GMP Audited by SGS

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Frequently Asked Questions

What is the minimum order quantity for CAS 1802086‑25‑4 Osimertinib impurity?

The MOQ is 500 g for standard packaging. For larger projects we can supply up to 25 kg per batch with volume‑discount pricing.

Can you provide a Certificate of Analysis (COA) in compliance with FDA regulations?

Yes. Every shipment includes an FDA‑compliant COA, HPLC chromatogram, and a full impurity profile (≤ 0.1 % residual).

Do you offer custom synthesis or OEM/ODM services for this impurity?

Absolutely. Our R&D team can tailor particle size, salt form, or even develop analogues under a confidential NDA.

What are the shipping options and lead times for the United States?

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.

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What after‑sales support do you provide?

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.

Still have questions? Contact us now →

Ready to Secure Your Supply of CAS 1802086‑25‑4 Osimertinib Impurity?

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.

  • Free Sample (5 g) – No obligation
  • 30‑Day Price Lock
  • Express Shipping – 5‑7 days to US ports
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Or WhatsApp us now: +86 199 4383 0844

What Our Clients Say

Reviewer 1

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.”

Reviewer 2

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.”

Reviewer 3

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.”

About the Author

Author Avatar

Dr. Wei Liu – Senior Process Development Engineer, Global Technology Co., Ltd.

With **15 years** of experience in API manufacturing and regulatory compliance, Dr. Liu has led more than 200 successful GMP projects for oncology APIs, including Osimertinib and its related impurities. He holds a Ph.D. in Pharmaceutical Chemistry from Peking University and is a certified ISO 9001 auditor.

Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844

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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