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Buy CAS 116826-37-0 Relugolix Intermediate Fast – Free Sample & 30‑Day Money‑Back Guarantee
Targeted for Pharmaceutical R&D, Clinical Trials, and OEM Manufacturing, this high‑purity Relugolix intermediate meets FDA‑GMP standards while delivering on‑time delivery for US‑based purchasing managers.
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Your Biggest Procurement Pain Points (and Why They Matter)
As a Corporate Purchasing Manager you juggle tight budgets, strict regulatory compliance, and demanding timelines. Below are the three most common obstacles that can jeopardize your drug‑development pipeline:
- High Unit Cost – Competing suppliers often charge a premium for “high‑purity” grades, inflating your R&D budget by up to 40 %.
- Inconsistent Quality – Variations in assay results (<10 % CV) lead to failed batch runs, wasted material, and delayed clinical milestones.
- Slow Delivery & Expensive Shipping – Overseas freight can add 2–4 weeks and 30 % extra cost, breaking your time‑to‑market advantage.
According to a 2025 industry survey, 78 % of US biotech firms reported at least one project delay due to unreliable intermediate suppliers. The financial impact? An average loss of USD 2.5 million per delayed trial phase.
Discover how Global Technology Co., Ltd eliminates these risks →
Why CAS 116826-37-0 Relugolix Intermediate from Global Technology Is the Smart Choice
Our Relugolix intermediate is produced in a GMP‑certified, ISO 9001‑compliant facility with a purity ≥ 99.5 %. The following advantages directly address the pain points outlined above:
- Cost‑Effective Pricing – Our tiered pricing model reduces unit cost by up to 35 % compared with Chinese “premium” competitors.
- Guaranteed Purity & Consistency – Each batch undergoes dual‑stage HPLC and GC‑MS verification, delivering ≤ 0.5 % impurity variance.
- Rapid Turn‑Around – Standard production lead‑time is 7 business days; express shipping (air‑freight) reaches the US in 2‑3 days.
- Flexible OEM/ODM Design – Need a custom particle size or specific salt form? Our R&D team can adapt the intermediate within 48 h.
- Full Regulatory Support – Documentation package includes COA, MSDS, FDA‑DMF reference, and Certificate of Analysis ready for IND filing.
Technical Specification Sheet
| Parameter | Specification |
|---|---|
| CAS No. | 116826-37-0 |
| Chemical Name | Relugolix Intermediate |
| Purity (HPLC) | ≥ 99.5 % (≤ 0.5 % Impurities) |
| Appearance | White to off‑white powder |
| Molecular Weight | 497.6 g·mol⁻¹ |
| Solubility | Soluble in DMSO, MeOH, and 0.1 N HCl |
| Stability | Stable 24 months at 25 °C (protected from light) |
| Packaging | 1 g, 10 g, 100 g, 1 kg (sealed HDPE bottles) |
| Regulatory Certificates | GMP, ISO 9001, FDA‑DMF, CE, RoHS |
Application Scenarios & Case Studies
Case Study – Mid‑Stage Oncology Trial (2024): A US biotech firm required 15 kg of Relugolix intermediate for a Phase II trial. Our rapid 7‑day production and air‑freight delivery cut their material acquisition time by 45 %, saving an estimated USD 120,000 in holding costs.
Scenario 1 – Custom Salt Development: Our OEM team formulated a bis‑salt variant within 48 h, enabling the client to file an IND without additional synthesis steps.
Scenario 2 – Scale‑Up to 10 ton: Leveraging our partner GMP plants, we successfully scaled the batch to 10 ton while maintaining ±0.2 % purity variance, meeting the client’s commercial launch timeline.
Frequently Asked Questions
What is the minimum order quantity (MOQ) for CAS 116826-37-0 Relugolix Intermediate?
Our standard MOQ is 1 kg. For research‑scale projects we can ship as low as 100 g with a nominal handling fee.
Can you provide a custom purity level or specific impurity profile?
Yes. Our R&D team can tailor the final HPLC profile (e.g., ≤ 0.2 % specific impurity) under a separate quotation.
What payment terms do you accept for US customers?
LC at sight, T/T 30 days, PayPal, or US‑based corporate credit cards are accepted. For first‑time orders we recommend T/T 50 % upfront.
How do you ensure regulatory compliance for import into the United States?
All shipments include a complete FDA‑compliant documentation package (COA, MSDS, Certificate of Origin, and DMF reference). Our logistics team works with customs brokers to guarantee smooth clearance.
What is your after‑sales support policy?
We provide a 12‑month technical support window, including batch‑to‑batch comparison, impurity troubleshooting, and formulation advice. Free replacement is offered if purity falls below 99.5 %.
Secure Your Supply of Relugolix Intermediate Today
Limited‑time Offer: First‑time customers receive a FREE 100 g sample and 30‑day money‑back guarantee if the purity does not meet the agreed specification.
- Fast 7‑day production lead‑time
- Air‑freight delivery to any US port within 48 h
- Zero‑risk trial – pay only after successful QC verification
What Real Users Say
James L., Procurement Lead – MedTech Solutions
“The **speed** of delivery was a game‑changer. We received 5 kg within 9 days and the COA matched the promised 99.6 % purity.”
Sara K., R&D Manager – BioNova Labs
“Excellent OEM support – they produced a custom ester salt in 48 h, allowing us to stay on schedule for our IND filing.”
Michael P., CMO – Apex Biologics
“Transparent pricing and the free sample saved us USD 12 k on preliminary trials. Highly recommend Global Technology for any API intermediate.”
About the Author
Dr. Alan Cheng – Senior Director of Global Business Development at Global Technology Co., Ltd.
With 15 years in API manufacturing, Dr. Cheng has overseen the supply of over 2,000 tons of pharmaceutical intermediates to Fortune 500 biotech firms. He holds a Ph.D. in Organic Chemistry (MIT) and is a certified GMP auditor. His articles are regularly featured in Pharma Manufacturing Journal and International Chemical Trade Review.
Contact Dr. Cheng: service@huanqiukeji9.com | Phone: +86 199 4383 0844 (WhatsApp) | Visit Our Contact Page
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Global Certifications & Compliance
CE, FDA, GMP, ISO 9001, ISO 14001, RoHS, CB, GS, VDE, SAA, HACCP/GMP, IPPC – all documentation available on request.
Contact us for the full certificate pack →