Accelerate your oncology pipeline with a reliable, GMP‑certified Elacestrant intermediate that meets FDA, EMA, and China NMPA standards.
Get Free Quote in 24 h1. Sky‑rocketing Prices – Global demand for selective estrogen receptor degraders (SERDs) has pushed the average cost of Elacestrant intermediate above $1,200 per kilogram, eroding your R&D budget.
2. Inconsistent Purity – Many suppliers provide batches with ≥98% purity only after extensive recrystallization, causing batch‑to‑batch variability and jeopardizing clinical trial timelines.
3. Lengthy Lead Times – Typical delivery windows range from 45 to 90 days, while your product launch roadmap may only allow 30 days for raw‑material procurement.
4. Complex Regulatory Documentation – Missing or outdated certificates (DMF, GMP, ISO 9001) force you to repeat audits, adding weeks of delay and extra legal costs.
5. Shipping Bottlenecks – International freight for hazardous chemicals often incurs $2,500‑$4,000 in surcharges, inflating total landed cost.
Data Point: A 2025 survey of 112 pharmaceutical procurement managers revealed that 68% cited “unreliable intermediate supply” as the top risk to on‑time trial initiation.
Discover how Global Technology Co., Ltd eliminates these barriers →
| Parameter | Specification |
|---|---|
| CAS Number | 1239011‑60‑9 |
| Chemical Name | Elacestrant Intermediate (C26H30N4O5) |
| Purity (HPLC) | ≥99.8% (Assay) |
| Appearance | White to off‑white crystalline powder |
| Moisture Content | ≤0.5% (Karl Fischer) |
| Solubility | DMSO 10 mg/mL; Methanol 5 mg/mL |
| Stability | Stable ≥24 months at 25 °C/60% RH |
| Packaging | 1 kg HDPE drums, 25 kg bulk bags, or custom‑sealed ampoules |
| Regulatory Status | GMP, FDA‑registered, EMA‑compliant, ISO 9001:2015, CE, RoHS |
Scenario 1 – Early‑Phase Oncology Trials
A mid‑size biotech in Boston needed 2 kg of Elacestrant intermediate for a Phase I trial. Using our 2‑week delivery and pre‑qualified GMP documentation, the client launched the trial 12 days ahead of schedule, saving an estimated $85,000 in study‑site fees.
Scenario 2 – Large‑Scale API Manufacturing
A European contract manufacturing organization (CMO) scaled production to 15 tonnes per year. Our continuous‑flow synthesis platform delivered consistent 99.8% purity, reducing downstream chromatography steps by 30% and cutting overall production cost by 37%.
Standard orders (1‑5 kg) are shipped within 10‑14 business days after payment confirmation. Express production (≤2 kg) can be ready in 7 days.
Yes. Our dedicated pilot‑plant can scale up to 20 tonnes per year with identical purity specifications. OEM/ODM contracts include process‑development, technology transfer, and validation support.
Every batch is accompanied by a Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), GMP batch record, and, upon request, a full DMF excerpt. All certificates are available in English and Chinese.
Absolutely. We offer FOB, CIF, and DDP options. DDP to any US port typically lands within 5‑7 business days after dispatch, inclusive of customs clearance and inland freight.

Our technical service team is on‑call 24 h (UTC+8) for troubleshooting, analytical method transfer, and stability‑study guidance. We also offer a 30‑day satisfaction guarantee or a full refund on any non‑conforming batch.
Limited‑time Offer: Place an order before 31 May 2026 and receive free 1 kg sample plus 20% off your first commercial purchase.
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John D., Procurement Manager – BioGenix
“The sample arrived in 48 hours. Purity was exactly as promised, and the CoA saved us two weeks of regulatory paperwork. We’ll be placing a 10‑kg order next month.”
Linda S., Technical Director – NovaThera
“Their OEM support let us develop a custom salt form that improved solubility by 45%. The partnership feels like an extension of our own R&D team.”
Ahmed K., Operations Manager – EuroPharm
“We needed a 3‑ton batch for a Phase II trial. Global Technology delivered on schedule, and the logistics team handled customs flawlessly. Cost per kilogram was 15% lower than our previous supplier.”
Sofia M., C‑Level Executive – MedBridge
“Risk‑free sampling convinced our board. The quality assurance documentation passed our internal audit without a single comment.”
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
All product information complies with local regulations (FDA, EMA, NMPA) and is provided for B2B procurement only. Prices are FOB unless otherwise stated.
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“Switching to Global Technology’s Elacestrant intermediate cut our raw‑material cost by 28% and shortened batch release from 18 days to 9 days.” – Dr. Emily Chen, Head of Process Development, NovaPharm
“Their GMP‑certified documentation passed our FDA audit on the first attempt – a rarity for overseas suppliers.” – Mark Rivera, Procurement Director, Medix Labs
Certificates & Compliance
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