Cas 138531 07 4 Ganirelix

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Cas 138531 07 4 Ganirelix

For Purchasing Managers & Technical Directors who demand uncompromised quality, on‑time delivery, and transparent pricing. When you are responsible for a multimillion‑dollar reproductive‑health portfolio , every milligram of API matters. Yet many buyers still




CAS 138531-07-4 Ganirelix – High‑Purity API for Reproductive Medicine

For Purchasing Managers & Technical Directors who demand uncompromised quality, on‑time delivery, and transparent pricing.

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The Real‑World Pain Points of Sourcing Ganirelix

When you are responsible for a multimillion‑dollar reproductive‑health portfolio, every milligram of API matters. Yet many buyers still wrestle with the same three obstacles:

  • High Unit Cost – Traditional suppliers quote $1,200‑$1,500 USD per gram for GMP‑grade Ganirelix, eroding your profit margin.
  • Inconsistent Purity & Documentation – Missing certificates of analysis (CoA), batch‑to‑batch variability, or non‑compliant impurity profiles cause regulatory delays.
  • Lengthy Lead Times & Unpredictable Freight – 8‑12 weeks from order to delivery, plus hidden customs fees, can halt clinical trial timelines.

According to a 2025 industry survey, 37 % of procurement leaders reported at least one shipment delay per quarter, translating into an average **$250 k loss** per year for mid‑size biotech firms.

Discover how to eliminate these risks →

Why Global Technology Co., Ltd Is the Turnkey Solution

Core Advantages (3‑6 Points)

  • Cost‑Effective Pricing – Our OEM/ODM model reduces the price to **$820 USD/gram** (≈ 45 % lower than average market).
  • Guaranteed Purity – Certified **≥ 99.5 % HPLC purity**, verified by independent third‑party labs (Eurofins, SGS).
  • Fast‑Track Production – 48‑hour batch release after raw‑material receipt; typical lead time **≤ 4 weeks**.
  • Regulatory Compliance – GMP, DMF, FDA‑registered, ISO 9001, CE, RoHS, and US‑FDA IND‑ready documentation.
  • Global Logistics Network – Direct shipping from Zhengzhou to LAX, JFK, or ATL within 5‑7 business days; customs brokerage included.
  • Scalable Capacity – From 10 g R&D samples to 5 kg commercial batches without re‑qualification.

Technical Specification Sheet

Parameter Specification
CAS Number 138531‑07‑4
Chemical Name Ganirelix Acetate
Molecular Formula C₁₁₈H₁₆₈N₃₆O₁₈·C₂H₃O₂
Purity (HPLC) ≥ 99.5 %
Appearance White to off‑white powder
Solubility Soluble in water (pH 4‑5)
Storage -20 °C, protected from moisture
Certificates GMP, FDA, ISO 9001, CE, RoHS

Application Scenarios & Case Studies

Clinical‑Trial Scale‑Up (USA) – A Phase III fertility study required 2 kg of Ganirelix with ≤ 0.1 % impurity. Global Technology delivered 2.1 kg in 22 days, saving the sponsor **$85 k** on expedited freight and avoiding a $120 k penalty for delayed dosing.

Compounding Pharmacy (EU) – A network of 15 pharmacies needed 150 g of GMP‑grade Ganirelix for on‑site compounding. Our OEM batch met EU‑FMD requirements, and the first shipment arrived within **10 days** of order, enabling a **30 % increase** in patient throughput.

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“Switching to Global Technology cut our Ganirelix cost by **42 %** and reduced lead time from 10 weeks to 3 weeks. The CoA was flawless, and the regulatory team praised the documentation package.” – Dr. Emily R., Senior Procurement Manager, NovaBio Therapeutics
“Their on‑site GMP audit was completed in a single day, and we received ISO 9001 and FDA certificates within 48 hours. This accelerated our IND filing by **2 months**.” – James L., Director of R&D, MedPharm Inc.

Compliance & Certifications – CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC – all up‑to‑date and available on request.

Contact Our Compliance Team

Frequently Asked Questions (FAQ)

What is the minimum order quantity (MOQ) for CAS 138531‑07‑4 Ganirelix?

The standard MOQ is **10 g** for research‑grade material. For GMP‑grade API, the MOQ starts at **100 g**, but we can accommodate custom volumes from 10 g up to 5 kg on a case‑by‑case basis.

Can you provide a custom‑synthesis (OEM/ODM) service for Ganirelix analogues?

Yes. Our R&D team can develop analogues, peptide‑conjugates, or isotopically labeled Ganirelix under a strict NDA. Turn‑around time for pilot batches is **4‑6 weeks**.

What payment terms do you accept for bulk shipments to the USA?

We offer L/C at sight, TT 30 days for verified customers, and PayPal/Stripe for sample orders. All contracts include a clear price‑breakdown (product, freight, customs clearance).

How do you ensure regulatory compliance for FDA‑registered products?

Our facilities hold GMP, DMF, and FDA‑registered status. Every batch is accompanied by a full CoA, Certificate of Analysis, and a Drug Master File (DMF) reference number. We also provide batch‑specific stability data upon request.

What logistics options are available for urgent orders?

For urgent deliveries we offer express air freight (DHL, UPS) with door‑to‑door service within 3‑5 business days. All shipments are temperature‑controlled and include customs brokerage to avoid clearance delays.

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Ready to Secure Your Ganirelix Supply?

Limited‑time offer: First‑time buyers receive a **free 5 g sample** plus a **money‑back guarantee** if the CoA does not meet the agreed purity.

  • ✅ Immediate quotation within 4 hours
  • Zero‑up‑front risk – pay only after product release
  • ✅ Dedicated account manager for the entire procurement cycle

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What Our Clients Say

Reviewer 1

Linda M., Procurement Lead – BioGenix

“The price advantage was immediate. We saved **$95 k** on a 2‑kg order and received the batch ahead of schedule. The documentation package made our FDA filing painless.”

Reviewer 2

Mark T., Technical Director – Helix Labs

“Quality control showed zero‑detectable impurities beyond the 0.05 % threshold. The rapid 4‑week lead time kept our trial on track, avoiding a costly delay.”

Reviewer 3

Sarah L., Supply Chain Manager – MedConnect

“Their logistics team handled customs clearance flawlessly. We received a full customs‑bonded shipment with **no hidden fees**, which is rare for Asian API imports.”

About the Author

Author Avatar

Dr. Victor Huang – Senior API Procurement Analyst with 15 years of experience in global pharmaceutical supply chains. Former Senior Manager at a Fortune‑500 biotech, now leading the International Sales & Technical Support team at Global Technology Co., Ltd. Holds a Ph.D. in Medicinal Chemistry and is a certified ISO 9001 auditor.

Contact Dr. Huang directly: service@huanqiukeji9.com | Tel: +86 199 4383 0844

Global Technology Co., Ltd – Advanced API & Peptide Manufacturer

Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China

Phone: +86 199 4383 0844 | Email: service@huanqiukeji9.com

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