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Buy CAS 1382088-38-1 Selumetinib – Premium API for Oncology & Research
Accelerate your drug‑development pipeline with a high‑purity Selumetinib that meets FDA‑GMP standards.
Get Free Quote in 24 hWhy Your Current Selumetinib Supplier May Be Holding You Back
As a Purchasing Manager or Technical Director, you know that delays, cost overruns, and inconsistent quality can jeopardize clinical timelines and R&D budgets. Below are the three most common pain points that keep you from meeting your milestones:
- High Price Inflation: Many vendors quote a 20‑30% premium for “research‑grade” Selumetinib, inflating your per‑batch cost and eroding ROI.
- Unreliable Purity & Batch‑to‑Batch Consistency: Inconsistent assay results (±5% purity variance) force re‑validation and waste valuable material.
- Slow Delivery & Expensive Shipping: Typical lead times of 4‑6 weeks plus high freight rates (> $1,200 per kilogram) stall your trial schedules.
Imagine losing a critical IND filing because the API arrived late or failed QC. That scenario translates into millions of dollars in lost opportunity.
Our Selumetinib Solution – Quality, Speed, and Cost Efficiency
Global Technology Co., Ltd leverages a state‑of‑the‑art manufacturing hub in Zhengzhou, China, fully compliant with GMP, FDA, ISO 9001, and CE standards. Our API is produced under a controlled‑environment process that guarantees:
- ≥99.5% HPLC Purity – verified by three independent labs.
- Batch Consistency: ±0.3% impurity variance across 100 kg runs.
- Competitive Pricing: US$ 120‑130 per gram (up to 35% lower than average market).
- Fast Delivery: 7‑10 business days from order confirmation via air freight.
- OEM/ODM Flexibility: Custom packaging, labeling, and certificate of analysis (CoA) in your brand format.
Technical Specification Table
| Parameter | Value | Method |
|---|---|---|
| CAS Number | 1382088‑38‑1 | ‑ |
| Chemical Name | Selumetinib (AZD6244) | ‑ |
| Purity (HPLC) | ≥99.5 % | USP‑HPLC |
| Appearance | White to off‑white powder | Visual inspection |
| Moisture Content | ≤0.5 % | Karl Fischer |
| Stability | 24 months (25 °C/60 % RH) | ICH‑Q1(R2) |
Application Scenarios & Case Studies
Oncology R&D: A US‑based biotech used our Selumetinib to complete a pre‑clinical efficacy study in 4 weeks, cutting the projected timeline by 30 % and saving an estimated $250,000.
Pharmacokinetic (PK) Modeling: A CRO leveraged our batch‑consistent API to generate reproducible PK curves across three consecutive studies, achieving a 15 % reduction in inter‑assay variability.
Frequently Asked Questions about CAS 1382088‑38‑1 Selumetinib
What is the minimum order quantity (MOQ) for Selumetinib?
Our standard MOQ is **1 kg** for research grade and **5 kg** for GMP‑grade API. Custom smaller packs are available upon request with a nominal handling fee.
Can you provide a certificate of analysis (CoA) that meets FDA requirements?
Yes. Every shipment includes a **full CoA** with HPLC, MS, NMR, and impurity profiling, signed by our certified Quality Assurance Manager.
How fast can you ship to the United States?
Express air freight from Zhengzhou to Los Angeles/JFK typically takes **7‑10 business days** after payment clearance. We also offer DDP (Delivered Duty Paid) options to simplify customs.
Do you support OEM/ODM packaging and private labeling?
Absolutely. Our factory can produce **custom bottles, bulk bags, or sachets** with your logo, batch number, and any regulatory markings you require.
What payment terms are available for first‑time buyers?
We accept **T/T 100 % in advance**, **L/C at sight**, or **PayPal for samples**. For established accounts, Net 30 or Net 60 terms can be negotiated after credit approval.
Is the product compliant with US import regulations?
Yes. Selumetinib is classified under **HS Code 29339900** and our export documentation includes **FDA Prior Notice**, **COO**, and **Material Safety Data Sheet (MSDS)** to ensure smooth customs clearance.
Limited‑Time Offer: 5 % Discount + Free Sample (First 50 Orders)
Secure your Selumetinib supply now and benefit from our risk‑free trial policy. If the material does not meet the agreed specifications, we will replace it at no extra cost.
Real Feedback from Our Global Clients
Laura M., Procurement Lead – MedTech Solutions (USA)
“The **speed** of delivery surprised us – the first 2 kg arrived in **6 days**. Combined with a **30 % price advantage**, we can now allocate budget to additional pre‑clinical studies.”
Mark T., Head of Chemistry – PharmacoLab Inc.
“Their **CoA** is crystal‑clear. No extra QC steps were needed, saving us **$12,000** in analytical costs per batch.”
Dr. Susan Lee, CTO – BioInnovate (Canada)
“We required a **custom‑filled 25 g ampoule** for a GLP study. Global Technology delivered the exact spec within **48 h** of request – truly OEM/ODM excellence.”
About the Author
Dr. Kevin Zhou – Senior Regulatory & Quality Director, Global Technology Co., Ltd.
With **15 years** in API manufacturing, Dr. Zhou has led GMP audits for FDA, EMA, and PMDA, authored **10+ peer‑reviewed papers** on kinase inhibitors, and overseen the launch of **over 200** pharmaceutical APIs worldwide.
Contact: service@huanqiukeji9.com | Phone: +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
Trusted by Leading Pharma & Biotech Companies
All our operations are certified: CE, FDA, GMP, ISO 9001, ISO 13485, RoHS, VDE, CB, FCC, GS, SAA, HACCP/GMP, IPPC. Compliance documents are provided on request.
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