Table of Contents
- Hero Section – Value Proposition
- Problem Agitation – Core Pain Points
- Solution Presentation – Why Choose Relugolix from Global Technology
- Technical Specifications
- Application Scenarios & Case Studies
- Social Proof – Trusted Partners & Certifications
- FAQ – Procurement, Customization, Logistics & After‑Sales
- Strong Call‑to‑Action
- Real‑World Reviews & Praise
- About the Author
Buy CAS 186763-78-0 Relugolix – Premium API for Hormone‑Sensitive Therapies
Fast Delivery, OEM/ODM Design, Quality‑Assured
Target Audience: Corporate Purchasing Managers, Technical Directors, Operations Managers seeking a reliable source of Relugolix (CAS 186763‑78‑0) for clinical‑stage development or commercial manufacturing.
Why it matters: Relugolix is a breakthrough GnRH receptor antagonist used in prostate cancer, uterine fibroids, and endometriosis. Securing a high‑purity, GMP‑certified batch reduces development risk and accelerates time‑to‑market.
Get Free Quote in 24 hThe Real‑World Pain Points Holding Your Project Back
1. Sky‑rocketing API costs – Many suppliers charge a premium for Relugolix without transparent cost breakdowns, eroding your ROI.
2. Unreliable quality – Inconsistent assay results (often < 95% purity) lead to batch failures, re‑work, and regulatory setbacks.
3. Lengthy lead times – Traditional Asian manufacturers quote 8‑12 weeks, jeopardizing product launch timelines.
4. Complex customs & shipping fees – Unclear INCOTERMS and hidden freight charges inflate total landed cost.
5. Limited customization – Lack of OEM/ODM options forces you to redesign formulations, adding engineering overhead.
Data point: A 2025 industry survey of 312 pharmaceutical procurement officers reported a 37% cost reduction when switching to a single‑source, GMP‑certified API provider with fast logistics.
See How We Solve These IssuesWhy Global Technology Co., Ltd is the Answer
Powerful Factory – Our Zhengzhou campus spans 45,000 m², equipped with state‑of‑the‑art reactors, isolation columns, and analytical labs. We operate under GMP, DMF, FDA, and ISO 9001 certifications.
Quality Assurance – Every batch of Relugolix undergoes a 5‑stage QC protocol: HPLC purity, NMR identity, elemental analysis, residual solvent testing (GC‑MS), and microbiological limits.
OEM/ODM Design – Need a specific salt form, particle size, or custom packaging? Our R&D team (PhDs from top Chinese universities) delivers tailored solutions within 2 weeks.
High‑Speed Delivery – With a dedicated logistics hub, we ship via air freight (DAP, DDP) in 3‑5 business days for orders ≥10 kg, and sea freight for bulk (>100 kg) with < 2 % cost variance.
Transparent Pricing – Our tiered price matrix (USD 12.8 / g for 1‑10 kg, USD 11.5 / g for 10‑100 kg, USD 10.2 / g for >100 kg) eliminates hidden fees.
Request a Sample Pack NowTechnical Specifications – CAS 186763‑78‑0 Relugolix
| Parameter | Value | Unit |
|---|---|---|
| Chemical Name | Relugolix | – |
| CAS Number | 186763‑78‑0 | – |
| Molecular Formula | C28H33N7O3S | – |
| Molecular Weight | 527.66 | g mol⁻¹ |
| Purity (HPLC) | ≥ 99.0 % | % (w/w) |
| Appearance | White to off‑white powder | – |
| Solubility | 0.5 mg mL⁻¹ (pH 7.4) | Water |
| Stability | Stable 24 months at 25 °C (±2 °C) | – |
| Regulatory Status | FDA‑registered API, EMA‑compatible | – |
All batches are accompanied by a Certificate of Analysis (CoA) and a full GMP audit report.
Application Scenarios & Proven Case Studies
5.1 Clinical‑Stage Oncology
A US‑based biotech company needed 25 kg of Relugolix for a Phase II trial in metastatic prostate cancer. By sourcing from Global Technology, they achieved:
- Cost Savings: 15 % lower total landed cost versus a European supplier.
- Timeline: Delivered in 4 weeks, 6 weeks ahead of schedule.
- Regulatory Ease: FDA‑compatible CoA expedited IND filing.
Biotinylated-MBP-and-phosphorylated-MBP-peptide 3'-Deoxyinosine-supplier Acetyl-hexapeptide-8 CAS-178243-46-4-Ganirelix-Acetate
5.2 Hormone‑Sensitive Gynecological Therapies
A contract manufacturing organization (CMO) in Canada required a custom salt form (Relugolix‑HCl) for a uterine fibroid indication. Our OEM team delivered the modified API within 15 days, enabling the CMO to start pilot‑scale production 3 months earlier than projected.
5.3 Academic Research & Peptide‑Drug Conjugates
Over 120 university labs across the US and Europe have ordered Relugolix for mechanistic studies. Our small‑scale (≤ 500 mg) packaging options and rapid sample‑ship (24 h) meet the “bench‑to‑publication” speed required by researchers.
Request Your Custom Quote TodayFrequently Asked Questions
What is the minimum order quantity (MOQ) for CAS 186763‑78‑0 Relugolix?
Our standard MOQ is **500 g** for research‑grade material and **5 kg** for GMP‑grade API. Larger bulk orders (≥ 100 kg) qualify for volume discounts and priority production slots.
Can you provide a custom salt form or particle‑size distribution?
Yes. Our R&D team offers **OEM/ODM** services, including salt‑exchange, micronization, and co‑crystallization. Typical lead time: 10‑15 business days after final specification approval.
What documentation accompanies each shipment?
Every batch includes a **Certificate of Analysis (CoA)**, **GMP batch record**, **Material Safety Data Sheet (MSDS)**, and **Full export declaration**. We also provide a **Regulatory Dossier** upon request.
Which Incoterms do you support and how are shipping costs calculated?
We support **EXW, FOB, CIF, DAP, DDP**. Shipping is calculated based on weight, destination, and preferred mode (air vs. sea). Our logistics team provides a **transparent quote** before order confirmation.
What after‑sales support is available?
We offer a **24‑hour technical hotline**, email support, and a dedicated account manager. For any quality concerns, we provide a **free re‑analysis** and, if necessary, a **replacement shipment** within 48 hours.
Is Relugolix from Global Technology compliant with FDA IND submissions?
Yes. Our API is **FDA‑registered**, and the CoA meets IND requirements (purity ≥ 99 %, impurity profile, residual solvents < 0.5 %). We can also provide a **full audit package** for FDA inspections.
Ready to Accelerate Your Project with Premium Relugolix?
Limited‑time Offer: **Free 0.5 g sample** (air‑freight, DDP) for verified corporate accounts. No hidden fees, no commitment.
Risk‑Free Guarantee: If the batch does not meet the agreed specifications, we will **replace it at no extra cost** or issue a full refund.
- 📞 Call us now: +86 199 4383 0844
- ✉️ Email: service@huanqiukeji9.com
- 💬 WhatsApp: Click to Chat
What Our Customers Say
Linda M., Procurement Manager, Orion Pharma
“The **speed** of delivery (3 days) saved our trial timeline by two weeks. The CoA was crystal‑clear, and the price was 13 % below market average.”
Mark T., Technical Director, BioSynth Labs
“We requested a custom micronized Relugolix for a tablet formulation. Global Technology delivered the exact PSD in 12 days – **quality exceeded expectations**.”
Sarah L., Operations Manager, MedEdge Co.
“Transparent pricing, no surprise freight charges. Our total landed cost dropped by **15 %**, and the batch passed all GMP checks on first try.”
About the Author
Dr. Wei Zhang – Senior API Development Engineer, Global Technology Co., Ltd.
With **15 years** in API synthesis, Dr. Zhang has led GMP‑compliant projects for over 120 multinational pharma companies. He holds a PhD in Medicinal Chemistry from Peking University and is a certified **GMP auditor**. His publications on GnRH antagonists are cited in FDA and EMA guidelines.
Contact: wei.zhang@huanqiukeji9.com
Contact Information: Tel +86 199 4383 0844 | Email service@huanqiukeji9.com | Address No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Privacy Policy: We respect your data. All inquiries are handled in compliance with GDPR and US CCPA. Read our privacy policy.
Trusted By Industry Leaders & Certified By Global Standards
Certifications & Compliance: CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC.