Cas 1239011 60 9 Elacestrant Intermediate

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Cas 1239011 60 9 Elacestrant Intermediate

Accelerate your oncology pipeline with a reliable, GMP‑certified Elacestrant intermediate that meets FDA, EMA, and China NMPA standards. 1. Sky‑rocketing Prices – Global demand for selective estrogen receptor degraders (SERDs) has pushed the average




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CAS 1239011‑60‑9 Elacestrant Intermediate – High‑Purity, Fast‑Track Supply for API Manufacturers

Accelerate your oncology pipeline with a reliable, GMP‑certified Elacestrant intermediate that meets FDA, EMA, and China NMPA standards.

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Why Procurement Teams Keep Stumbling Over Elacestrant Supply

1. 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 Complex Regulatory Documentation – Missing or outdated certificates (DMF, GMP, ISO 9001) force you to repeat audits, adding weeks of delay and extra legal costs.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 →

Our Competitive Edge – The Elacestrant Intermediate You Can Trust

Key Advantages (Long‑Tail Keywords Integrated)

  • Premium Purity – 99.8% (HPLC): Consistent batch quality reduces downstream purification steps.
  • Fast‑Track Production – 2‑Week Turnaround: Our high‑speed reactors and dedicated line cut lead time by 55%.
  • Transparent Pricing – FOB, CIF, DDP Options: Competitive rates with no hidden fees; volume discounts start at 5 kg.
  • Full Regulatory Package: GMP, ISO 9001, DMF, FDA ANDA‑ready certificates, plus CE & RoHS compliance.
  • OEM/ODM Design Support: Tailor‑made salt forms, particle size, and polymorph selection for your formulation needs.

Technical Specifications

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

Application Scenarios & Case Studies

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%.

Start your own cost‑saving project today →

Trusted by Industry Leaders

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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

  • ISO 9001:2015
  • GMP (China, EU, US)
  • FDA DMF (Active Pharmaceutical Ingredient)
  • CE Marking (Medical Device Compatibility)
  • RoHS, REACH, FCC, GS, CB, VDE, SAA

Request a compliance package now →

Frequently Asked Questions

What is the typical lead time for CAS 1239011‑60‑9 Elacestrant Intermediate?

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.

Do you provide custom‑scale synthesis (tonnage level)?

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.

What documentation is included with each shipment?

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.

Can you arrange DDP (Delivered Duty Paid) shipping to the United States?

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.

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What after‑sales support do you provide?

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.

Still have questions? Contact us now →

Ready to Secure Premium Elacestrant Intermediate for Your Next Project?

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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All quotations are confidential. No‑obligation, risk‑free inquiry.

What Our Clients Say

John D.

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.

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.

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.

Sofia M., C‑Level Executive – MedBridge

“Risk‑free sampling convinced our board. The quality assurance documentation passed our internal audit without a single comment.”

About the Author

Author Avatar

Dr. Victor Liang – Senior Process Chemist & Technical Marketing Lead at Global Technology Co., Ltd.

With **12 years** of experience in API development for oncology and endocrine therapies, Victor has authored 35 peer‑reviewed papers and holds a Ph.D. in Medicinal Chemistry (University of Cambridge). He oversees the Elacestrant platform, ensuring GMP compliance, scale‑up feasibility, and cost‑optimization for worldwide clients.

Contact: service@huanqiukeji9.com | Tel: +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 | 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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