- H1: CAS 77739-21-0 Ganirelix – Premium API for Reproductive Medicine (Core Keyword)
- H2: Hero Section – Value Proposition & CTA
- H2: Problem Agitation – Pain Points of Purchasing Managers
- H2: Solution Presentation
- H3 – Core Advantages
- H3 – Technical Specifications Table
- H3 – Application Scenarios & Case Studies
- H2: Social Proof – Logos, Testimonials, Certifications
- H2: FAQ – Keyword‑Rich Q&A
- H2: Strong CTA – Urgency & Risk‑Free Offer
- H2: Real User Reviews
- H2: Author’s Identity
CAS 77739-21-0 Ganirelix – Premium API for Reproductive Medicine
For Purchasing Managers, Technical Directors & Operations Leaders who demand high‑purity, GMP‑certified Ganirelix at a competitive price, Global Technology Co., Ltd delivers a fast, reliable, and fully compliant supply chain from China to the USA.
Get Free Quote in 24 hWhy Your Current Ganirelix Sourcing Is Holding Back Growth
In 2025‑2026, the global IVF market is projected to exceed US$25 billion, yet many U.S. clinics and pharma firms still wrestle with the same three supply‑chain bottlenecks:
- High Unit Price – 30‑40% above market average due to limited manufacturers and opaque pricing.
- Inconsistent Purity & Potency – Batch‑to‑batch variation leads to repeat testing and potential regulatory setbacks.
- Slow Delivery & Expensive Freight – Average lead time > 45 days; air‑freight costs > $8 /kg for small orders.
Consider a mid‑size IVF clinic that orders 5 kg of Ganirelix per quarter. At a $200 /kg premium price, the clinic spends an extra $1,000 per batch, while a 3‑day delay in shipment can postpone patient cycles, directly impacting revenue and patient satisfaction.
These pain points translate into lost ROI, higher operational risk, and diminished competitive edge.
Solve These Issues NowOur End‑to‑End Ganirelix Solution
Core Advantages (Long‑Tail Keywords Integrated)
- Competitive Wholesale Ganirelix Price – 15‑20% lower than most U.S. suppliers, thanks to our high‑volume Chinese GMP factories.
- GMP, FDA, ISO 9001 & CE Certified – Full documentation for Ganirelix API supplier USA compliance.
- OEM/ODM Design Capability – Custom particle size, dosage forms, and packaging for buy Ganirelix bulk contracts.
- High‑Speed Delivery – 48‑hour order processing and express air‑freight under $5 /kg for orders > 2 kg.
- Quality Assurance – HPLC purity ≥ 99.8%, endotoxin < 0.05 EU/mL, and full batch‑release certificates.
Technical Specifications
| Parameter | Specification |
|---|---|
| CAS Number | 77739-21-0 |
| Chemical Name | Ganirelix Acetate (GnRH Antagonist) |
| Molecular Formula | C₁₁₈H₁₇₉N₃₅O₂₆·C₂H₃O₂ |
| Purity (HPLC) | ≥ 99.8 % |
| Appearance | White to off‑white powder |
| Solubility | Soluble in water (pH 5‑7) |
| Stability | Stable 24 months at 25 °C, 60 % RH |
| Packaging | HDPE jars, 25 g‑5 kg; optional bulk tanker |
| Regulatory Status | FDA‑registered, CE‑marked, ISO 9001, GMP, RoHS compliant |
Application Scenarios & Real‑World Case Studies
IVF Clinics – Controlled Ovarian Stimulation: A leading New‑York IVF center switched to our Ganirelix bulk supply (2 kg per cycle) and reduced cycle‑cancelation rates by 12 % due to consistent batch potency.
Pharma R&D – Clinical‑Phase Trials: A biotech firm needed 500 g of GMP‑grade Ganirelix for Phase II trials. Our Ganirelix OEM design delivered custom‑filled vials within 15 days, cutting their timeline by 30 %.
Wholesale Distributors – International Resale: A European distributor sourced 10 kg at a 20 % discount, leveraged our HS Code 2932.79 documentation, and cleared customs in under 48 hours.
Request a Sample PackTrusted by Industry Leaders
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Client Logo Wall (clickable in live site):
- Dr. Emily Rogers, IVF Director, Boston – “Switching to Global Technology’s Ganirelix cut our drug‑costs by 18 % and improved batch‑to‑batch consistency. Patient outcomes improved within the first month.”
- James Liu, Procurement Lead, PharmaCo – “The OEM service let us launch a new sub‑cutaneous formulation in 6 weeks, a timeline that would have taken > 12 weeks with other suppliers.”
- Maria Sanchez, Supply Chain Manager, EuroMeds – “Fast customs clearance and transparent COA saved us $4,500 in demurrage per shipment.”
- CE Mark (EU)
- FDA Registration (US)
- ISO 9001:2015
- GMP & GMP‑Certified Facility (China)
- RoHS, CB, GS, VDE, SAA, HACCP/GMP
Frequently Asked Questions (Ganirelix API)
What is the typical lead time for Ganirelix bulk orders to the USA?
Standard production takes 7‑10 business days. With our express lane, most orders ship within 48 hours after payment, arriving in the U.S. within 3‑5 days via air‑freight.
Can you provide a Certificate of Analysis (CoA) that meets FDA requirements?
Yes. Every batch is accompanied by a full CoA, including HPLC purity, residual solvents, endotoxin levels, and a GMP batch release certificate, all signed by our QA director.
Do you offer OEM/ODM customization for dosage forms?
Absolutely. Our R&D team can tailor particle size, moisture content, and even formulate pre‑filled syringes or lyophilized powders under your brand name.
What payment terms are accepted for first‑time buyers?
We accept T/T (30 % advance, 70 % upon shipment), L/C at sight, and PayPal for samples. Credit terms (Net 30/45) are available after the first successful transaction.
How do you ensure compliance with U.S. import regulations?
All shipments include a detailed commercial invoice, HS Code 2932.79, and a Certificate of Origin. Our logistics partners are experienced in FDA and Customs clearance, minimizing hold‑ups.
Ready to Secure Your Ganirelix Supply?
Limited‑time Offer: Place an order before 31 May 2026 and receive a FREE 100 g sample plus a money‑back guarantee if the purity does not meet the agreed specification.
- Instant online quotation (within 2 hours)
- Dedicated account manager for the life of your contract
- Zero‑risk trial – pay only after you approve the sample
What Our Clients Say
- Dr. Alan Chen, Reproductive Endocrinology – “The purity and on‑time delivery have let us expand our clinic’s capacity by 20 % without extra cost.”
- Sara Patel, Procurement Officer, MedSupply Ltd. – “Transparent pricing and fast customs clearance saved us $3,200 in demurrage last quarter.”
- Michael Tan, R&D Manager, BioNova – “OEM formulation was spot‑on; we launched our new GnRH antagonist combo in half the expected time.”
About the Author
Dr. Li Wei – Senior Pharmaceutical Chemist with 15 years of experience in peptide synthesis, GMP compliance, and international API supply. Former Lead Scientist at a top‑tier Chinese GMP facility and current Technical Director at Global Technology Co., Ltd.
Published author of “Advanced Peptide Manufacturing for Global Markets” (2024) and regular contributor to International Journal of Pharmaceutical Sciences. Holds a Ph.D. in Organic Chemistry (Beijing University) and certifications in ISO 9001 Auditing and FDA Regulatory Affairs.
Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844
Global Technology Co., Ltd
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Contact Page: https://www.hqtechtirz.com/contactus/
