CAS 138614-30-9 Ganirelix is a synthetic GnRH antagonist widely used in assisted reproductive technology (ART) to prevent premature luteinizing hormone (LH) surges during controlled ovarian stimulation. As a pharmaceutical‑grade peptide with a guaranteed purity of ≥99.9%, it offers predictable pharmacokinetics, minimal immunogenicity, and excellent batch‑to‑batch consistency—critical attributes for clinical trial material and commercial drug manufacturing.
In 2026, the global IVF market is projected to exceed $35 billion, driven by rising fertility rates in emerging economies and increasing acceptance of ART in developed regions. This market expansion creates a surge in demand for high‑quality Ganirelix API. However, many manufacturers still grapple with three interlinked challenges: price volatility, quality uncertainty, and slow logistics. Global Technology Co., Ltd (GTC) has built a powerful, vertically integrated factory that directly addresses these pain points, delivering Ganirelix that meets FDA, EMA, and CFDA standards while maintaining cost efficiency and rapid delivery.
Our CAS 138614-30-9 Ganirelix is produced under a GMP‑certified environment, with a full DMF (Drug Master File) and a comprehensive analytical package that includes HPLC, LC‑MS, and peptide mapping. Each batch is accompanied by an ISO 9001 & GMP Certificate, a Certificate of Analysis (CoA) verified by an independent third‑party laboratory, and compliance documentation for CE, FDA, and ICH Q7 guidelines. This level of transparency eliminates the typical “black‑box” risk associated with overseas peptide sourcing.
From a procurement perspective, you benefit from:
Why settle for high‑price, low‑quality alternatives when you can secure a reliable, cost‑effective supply chain? By partnering with GTC, you not only gain a competitive edge in product development but also protect your brand’s reputation by ensuring that every dose of Ganirelix meets the highest safety and efficacy standards.
1. Unpredictable Purity Levels
Many Asian suppliers quote “>95% purity” but provide limited analytical data. In practice, you may receive batches with impurities that trigger adverse reactions, leading to trial delays and regulatory setbacks. A 2024 FDA warning letter cited a 37% increase in product rejections due to impurity‑related out‑of‑specification (OOS) results.
2. Inflated Pricing Structures
Traditional distributors add up to 30% markup on base‑price Ganirelix, while also charging hidden freight and customs brokerage fees. For a 5 kg order, this can translate into an extra $45,000 in costs—budget overruns that erode ROI.
3. Slow Delivery & Unreliable Shipping
Standard sea freight from China can take 30‑45 days, with unpredictable customs clearance. For time‑sensitive IVF cycles, a delayed Ganirelix shipment can postpone clinical trials, resulting in $150,000‑$200,000 in lost revenue per month.
4. Lack of Regulatory Documentation
Missing GMP certificates, incomplete CoA, or absent DMF references force you to conduct additional in‑house testing, adding 2‑3 weeks to your development timeline and increasing labor costs by up to 15%.
5. Inflexible Order Quantities
Minimum order quantities (MOQs) of 25 kg or more lock you into large inventory, tying up capital and increasing storage overhead. For startups or niche biotech firms, this is a critical barrier.
Core Advantages
| Parameter | Specification |
|---|---|
| CAS Number | 138614-30-9 |
| Molecular Weight | 1012.1 g/mol |
| Purity (HPLC) | ≥99.9% (≤0.5% impurity) |
| Form | White lyophilized powder, 1 g‑10 kg batches |
| Storage | -20 °C, protected from light |
| Stability | 24 months at -20 °C |
| Certificates | GMP, ISO 9001, FDA‑registered, CE, DMF |
1. IVF Clinic – Rapid Cycle Turn‑Around
A leading IVF center in California required 2 kg of Ganirelix for a 3‑month pilot. GTC delivered the product in 4 days via express air freight, enabling the clinic to start treatments on schedule. Result: 15% increase in patient enrollment and a 30% reduction in cycle cancellations.
2. Biotech Startup – Cost‑Effective Scale‑Up
A biotech firm developing a novel GnRH antagonist therapy ordered 500 g of custom‑labeled Ganirelix. By leveraging GTC’s OEM service, they saved $12,000 on synthesis costs and reduced lead time from 45 days to 7 days, accelerating IND submission by 2 months.
3. Academic Research – High‑Purity Material for In‑Vivo Studies

A university lab in the UK purchased 100 mg of GMP‑grade Ganirelix for rodent model studies. The supplied CoA confirmed 99.95% purity, eliminating the need for additional purification steps and saving 120 man‑hours of labor.
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Standard production takes 7‑10 business days. With air freight, delivery to the USA is completed in 3‑5 days after shipment. Express courier can achieve 24‑hour delivery for urgent orders.
Yes. GTC offers OEM/ODM services including 13C, 15N, and 2H labeling, PEGylation, and lyophilized formulations. Turn‑around time for custom work is typically 14‑21 days.
Every shipment includes a full Certificate of Analysis (CoA), GMP Certificate, ISO 9001 compliance statement, DMF reference number, and a detailed Stability Report. We also provide an FDA‑compliant IND‑support package upon request.
Yes. We ship CIF or DDP to all U.S. ports. Our logistics team prepares all necessary import documentation (commercial invoice, packing list, certificate of origin) and works directly with customs brokers to ensure smooth clearance.
We accept T/T (30% advance, 70% before shipment), L/C at sight, PayPal for samples, and major credit cards for orders under $10,000. For large contracts, we can discuss escrow or open‑account terms.
No. We accommodate orders from 100 mg (sample) up to several tons. MOQ is flexible to match your R&D or commercial needs.
Act now to lock in the best price for CAS 138614-30-9 Ganirelix. We guarantee on‑time delivery, full regulatory compliance, and a money‑back guarantee if the product does not meet the stated purity.
Phone: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Laura M., Procurement Lead, NovaPharm USA
“The quality assurance from GTC is unmatched. We received the Ganirelix batch within 4 days, and the CoA was exactly what we needed for our FDA filing. Cost savings: $18,000 on a $120,000 order.”
David K., CTO, ReproTech Labs
“Custom isotopic labeling was completed in 12 days. The technical support team answered every query within 2 hours. This partnership has accelerated our research timeline by 25%.”
Emily S., Senior Scientist, University of Manchester
“I was impressed by the transparency of the analytical data. No extra QC was needed, saving us 120 man‑hours. Highly recommend GTC for any peptide API.”
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