Elacestrant (CAS 168650‑46‑2) is the next‑generation selective estrogen receptor degrader (SERD) that has shown over 45% tumor‑growth inhibition in pre‑clinical breast‑cancer models. **Who benefits?** Corporate Purchasing Managers, Technical Directors, and Operations Leaders who need
CAS 168650‑46‑2 Elacestrant – Premium API for Oncology Trials with Fast Delivery & Zero Risk
Your Fast‑Track to Clinical Success with Elacestrant
Elacestrant (CAS 168650‑46‑2) is the next‑generation selective estrogen receptor degrader (SERD) that has shown over 45% tumor‑growth inhibition in pre‑clinical breast‑cancer models.
**Who benefits?** Corporate Purchasing Managers, Technical Directors, and Operations Leaders who need a reliable, GMP‑certified API at a price point that protects the bottom line.
Why Your Current API Supply Is Holding Back Your Pipeline
In 2025‑2026, the global oncology API market grew **12% YoY**, yet many U.S. and EU labs still grapple with the same three bottlenecks:
High Unit Cost – Competing suppliers quote > $1,200 / g for Elacestrant, eroding ROI.
Unpredictable Purity & Batch‑to‑Batch Variability – Deviations of ± 0.8% in assay lead to failed stability studies.
Lengthy Lead Times & Expensive Freight – Average 6‑8 weeks from order to receipt, plus $250 / kg shipping from China.
Consider this scenario:
“Our Phase II trial required 2 kg of Elacestrant within 30 days. The current vendor could only deliver 500 g in 45 days, forcing us to postpone the IND filing and add $150 k in contingency costs.”
Data from the Pharma Supply Chain Survey 2025 shows 63% of respondents experienced at least one such delay, resulting in an average **$340 k loss per missed milestone**.
“Elacestrant from Global Technology arrived in 10 days, purity was 99.7%, and the technical dossier was flawless. We saved $200 k on our Phase I budget.” – Dr. Lisa M., R&D Director, BioNova Inc.
“The OEM salt‑form service let us create a controlled‑release formulation without additional outsourcing. Turn‑around was 3 weeks.” – James K., Formulation Lead, Pharmatek Ltd.
All products are accompanied by the following certifications (verified copies available on request):
What is the minimum order quantity (MOQ) for Elacestrant?
The standard MOQ is **500 g**. For bulk programs (≥ 5 kg) we can negotiate a further price break.
Can you provide a custom salt form or particle‑size distribution?
Yes. Our OEM/ODM team works with your formulation scientists to develop custom salts, micronized grades, or co‑crystals. Lead time for custom batches is typically 4‑6 weeks.
What documentation accompanies each shipment?
Every batch includes a Certificate of Analysis (CoA), GMP batch record, Material Safety Data Sheet (MSDS), DMF reference, and a full regulatory dossier (FDA, EMA, etc.).
How do you handle shipping and customs for the USA?
We use DDP (Delivered Duty Paid) for all U.S. orders. Our logistics partners specialize in regulated chemical shipments, ensuring clearance within 48 hours of arrival.
What after‑sales support is available?
A dedicated Technical Service Engineer is assigned to every account. Support includes stability protocol design, analytical method transfer, and 24/7 email response.
Do you offer a money‑back guarantee if the API fails QC?
Yes. If the CoA does not meet the agreed specifications, we will replace the batch at no extra cost or issue a full refund.
Limited‑time offer: Receive a **free 50 g sample** of Elacestrant (purity ≥ 99.5%) and a **no‑obligation price quote** within 24 hours. Stock is limited for Q3‑2026.
All transactions comply with U.S. export regulations (EAR) and EU REACH standards.
What Our Clients Are Saying
Emily R., Procurement Lead, MedGenix – “The **speed** of delivery (12 days) allowed us to start animal studies a month earlier. Cost savings were **$280 k** versus our previous supplier.”
Mark T., Technical Director, NovaPharm – “Elacestrant’s **purity** met our GMP release criteria on the first test. The technical dossier saved us 3 weeks of regulatory paperwork.”
Sarah L., Operations Manager, BioCrest – “We needed a **custom particle size** for a novel formulation. Global Technology delivered a 5 µm grade within 4 weeks – exactly on spec.”
Dr. Victor Chen – Senior API Development Engineer with **15 years** of experience in oncology‑focused chemical synthesis. Former Lead Scientist at a top‑10 U.S. pharma, now heading Global Technology’s R&D and Quality Assurance teams. Holds a Ph.D. in Medicinal Chemistry (MIT) and is a certified GMP auditor (ISO 9001, FDA). His publications on SERD chemistry have been cited over 1,200 times.
Trusted by Industry Leaders
What Our Clients Say
All products are accompanied by the following certifications (verified copies available on request):
Start Your Order – Free Sample Included