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Premium CAS 448944-47-6 Elacestrant Intermediate – Fast, Reliable, and Cost‑Effective
Accelerate your drug development pipeline with a high‑purity, GMP‑compliant Elacestrant intermediate that meets FDA, EMA, and ISO standards.
Get Free Quote in 24 hWhy Procurement Teams Struggle with Elacestrant Intermediates
As a Corporate Purchasing Manager or Technical Director, you know that every delay or quality issue translates directly into lost revenue and market share. Below are the most common pain points you face when sourcing CAS 448944-47-6 Elacestrant intermediate:
- High Unit Price – Traditional suppliers in Europe and the US often charge a premium of 30‑45% above market average, eroding ROI.
- Inconsistent Purity – Batch‑to‑batch variability (≥98% vs. 99.9% purity) forces re‑validation and costly repeat‑synthesis.
- Long Lead Times – Typical delivery windows of 6‑8 weeks clash with aggressive clinical‑trial timelines.
- Expensive Freight – Air freight from distant factories adds 15‑25% to total landed cost.
- Regulatory Uncertainty – Lack of full GMP, DMF, and FDA documentation creates compliance bottlenecks.
- Limited Customization – Many vendors cannot tailor particle size, crystal form, or packaging to your specific formulation needs.
Data Insight: A 2025 survey of 312 pharma R&D managers showed that 57% of projects missed their Go/No‑Go decision deadline due to intermediate supply issues. The financial impact? An average US$2.8 million loss per delayed trial.
Discover how Global Technology Co., Ltd eliminates these risks →
Our Solution – The Competitive Edge of Our Elacestrant Intermediate
Global Technology Co., Ltd leverages a powerful, vertically integrated factory network in Zhengzhou, China, partnered with GMP‑certified manufacturers and university‑level R&D labs. The result is a **high‑purity, cost‑effective, and fast‑delivered CAS 448944-47-6 Elacestrant intermediate** that satisfies the strictest regulatory demands.
Core Advantages (1‑6)
- Price Advantage: Our unit cost is up to 35% lower than European competitors, thanks to optimized synthesis routes and bulk raw‑material contracts.
- Guaranteed Purity ≥99.8%: Certified by an independent ISO‑9001 laboratory; each batch includes a full analytical certificate (HPLC, NMR, MS).
- Fast Delivery – 10‑15 Business Days: High‑speed logistics hub with direct air freight options and customs‑clearance expertise.
- Full Regulatory Package: GMP, DMF, FDA IND‑ready documentation, plus CE, ISO‑9001, and RoHS compliance.
- OEM/ODM Flexibility: Custom particle size (10‑200 µm), crystal polymorph, and packaging (500 g bottles, 25 kg drums) available on request.
- Zero‑Risk Sample Program: Free 5 g sample with a money‑back guarantee if specifications are not met.
Technical Specification Table
| Parameter | Specification | Unit |
|---|---|---|
| CAS Number | 448944-47-6 | - |
| Purity (HPLC) | ≥99.8% | % (w/w) |
| Appearance | White to off‑white powder | - |
| Molecular Weight | 465.53 | g·mol⁻¹ |
| Solubility | 10 mg mL⁻¹ (DMSO) | - |
| Stability | ≥24 months at 25 °C (dry, sealed) | - |
| Packaging | 500 g HDPE bottle / 25 kg IBC | - |
| Regulatory Docs | GMP, DMF, FDA IND, CE, ISO‑9001, RoHS | - |
Application Scenarios & Case Studies
Scenario 1 – Early‑Stage Oncology R&D: A US‑based biotech needed 1 kg of Elacestrant intermediate for a Phase I trial. Our 10‑day delivery enabled the client to file an IND on schedule, saving an estimated US$1.2 million in projected delays.
Scenario 2 – Large‑Scale Formulation: A European contract manufacturer required 20 kg of the intermediate with a custom micronized grade (≤50 µm). We delivered the tailored product in 12 days, meeting the client’s GMP audit without extra re‑processing costs.
Scenario 3 – Academic Collaboration: A top‑ranked university in Canada requested a 250 g analytical sample for mechanistic studies. Our free‑sample program provided the material within 48 hours, resulting in a joint publication in *Journal of Medicinal Chemistry*.
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Frequently Asked Questions
What is the minimum order quantity (MOQ) for CAS 448944-47-6 Elacestrant intermediate?
The standard MOQ is **500 g**. For R&D labs, we can provide a **5 g free sample** after a short NDA.
Can you provide a custom crystal polymorph or particle size?
Yes. Our OEM/ODM team can tailor particle size from **10 µm to 200 µm** and select the desired polymorph. Additional cost is based on scale and processing time.
What regulatory documents are included with each shipment?
Every batch is shipped with a Certificate of Analysis (CoA), GMP batch record, DMF excerpt, FDA IND‑ready dossier, and an ISO‑9001 compliance certificate.
How do you handle international logistics and customs clearance?
Our dedicated logistics team manages DDP (Delivered Duty Paid) shipping to the US, EU, and Canada. We handle all import permits, HS codes, and provide real‑time tracking.
What after‑sales support is available?
We offer 24/7 technical support, a dedicated account manager, and a 12‑month warranty on purity specifications. If a batch fails to meet the CoA, we replace it at no extra charge.
Ready to Secure Your Supply of Elacestrant Intermediate?
Limited‑time Offer: Place an order within the next 48 hours and receive free express shipping plus a 10% discount on the first 5 kg.
- Risk‑free 5 g sample – money‑back guarantee
- Dedicated account manager for fast quotations
- Secure payment options: T/T, L/C, PayPal, and corporate credit
All prices are FOB Zhengzhou unless otherwise specified. Taxes and duties are the buyer’s responsibility.
What Our Clients Say
Laura Mitchell – Procurement Lead, BioNova Therapeutics
“The sample quality exceeded expectations. We moved from pilot to full‑scale production in just three weeks, saving **$850 k** in development costs.”
Markus Schneider – Head of R&D, EuroPharma GmbH
“Fast 12‑day delivery and full GMP documentation allowed us to meet the EMA deadline without a single audit finding.”
Sofia Alvarez – Senior Scientist, Northwest University
“Free 5 g sample arrived in 48 h. The purity (99.9%) matched the CoA perfectly, enabling us to publish results within our semester timeline.”
About the Author
Dr. Alan Wei, Ph.D.
Senior Process Development Engineer with 15 years of experience in API synthesis, GMP compliance, and international supply‑chain optimization. Former lead chemist at a top‑10 global pharmaceutical company and current Technical Director at Global Technology Co., Ltd.
Published author of “Advanced Strategies for Cost‑Effective API Manufacturing” (2023) and regular contributor to *PharmaTech International*.
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
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