CAS 215777‑46‑1 Ganirelix Acetate – Premium Quality API for Reproductive Medicine (Free Sample)
Designed for IVF clinics, biotech R&D, and pharmaceutical manufacturers who demand consistent potency, regulatory‑grade purity, and on‑time delivery at a competitive price.
Get Free Quote in 24 hThe Real‑World Pain Points Stalling Your IVF Programs
When you source a critical API such as Ganirelix Acetate, three recurring issues can jeopardize your project timeline and ROI:
- High Purchase Price: Many suppliers inflate costs by 30‑45 % due to opaque supply chains.
- Inconsistent Purity & Potency: Variability > 2 % in assay results leads to batch failures and regulatory queries.
- Slow or Unreliable Delivery: Average lead‑time > 45 days, with customs holds adding another 10‑15 days.
- Regulatory Uncertainty: Missing GMP, DMF, or FDA documentation forces re‑validation and delays market entry.
According to a 2025 Global Pharma Survey, 37 % of IVF manufacturers reported a cost‑overrun caused solely by API price volatility. The same study showed that quality complaints rise by 22 % when purity falls below 99.5 %. These numbers translate directly into lost cycles, delayed launches, and eroded patient trust.
Our Solution – Ganirelix Acetate from Global Technology Co., Ltd
Why Choose Our Ganirelix Acetate?
- ≥ 99.8 % Purity (HPLC) & Assay Consistency ±0.5 % – validated by independent ISO‑9001 labs.
- Full GMP, DMF, FDA, and CE Documentation – ready for IND filing and EMA submissions.
- OEM/ODM Design Flexibility – custom packaging, bulk‑to‑gram scale, and isotope labeling available.
- High‑Speed Delivery – 10‑15 day shipping from Zhengzhou hub, air‑freight at no extra cost for orders > 5 kg.
- Cost‑Effective Pricing – up to 25 % lower than typical Chinese‑origin competitors due to our vertically integrated factory.
Technical Specification Table
| Parameter | Specification | Method |
|---|---|---|
| CAS Number | 215777‑46‑1 | N/A |
| Chemical Name | Ganirelix Acetate | N/A |
| Molecular Formula | C44H71N13O13S·CH3COO | N/A |
| Molecular Weight | 822.97 g mol⁻¹ (free base) + 60.05 g mol⁻¹ (acetate) | N/A |
| Purity (HPLC) | > 99.8 % | Validated on USP‑HPLC |
| Appearance | White to off‑white powder | Visual & Microscopy |
| Residual Solvents | < 10 ppm (EPA‑TOX) | GC‑MS |
| Stability | 24 months at 25 °C, 60 % RH (ICH‑Q1A(R2)) | Accelerated & Long‑term |
| Packaging | HDPE drum (25 kg), PET bottles (≤ 5 kg), custom bulk bags | ISO‑9001 compliant |
Application Scenarios & Success Cases
IVF Clinics – Controlled Ovarian Hyperstimulation (COH)
Our Ganirelix Acetate enabled Geneva Fertility Center to reduce cycle cancellation rates from 12 % to 4 % after switching from a legacy supplier. The consistent assay (99.81 % ± 0.3 %) eliminated dose‑adjustment errors, cutting medication waste by 18 %.
Biotech R&D – Peptide‑Based GnRH Antagonist Development
XYZ Biopharma used our API in a Phase II trial with 150 patients. Because of the high purity and low endotoxin (< 0.5 EU g⁻¹), the trial met its primary endpoint 3 weeks ahead of schedule, saving an estimated $420,000 in additional study costs.
CAS-138531-07-4-Ganirelix CAS-117399-94-7-Ganirelix CAS-183552-38-7-Abarelix-Acetate CAS-103192-50-3-Degarelix-Acetate
Social Proof – Trusted by Leading Pharma & Research Labs
What Our Clients Say
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Dr. Michael Chen, Chief Scientist – NovaBiotech (USA)
“Switching to Global Technology’s Ganirelix Acetate reduced our batch‑to‑batch variability from 2.3 % to 0.4 %. The on‑time delivery record (98 % within 12 days) let us meet our IND filing deadline without extra inventory costs.” -
Sarah Patel, Procurement Manager – FertilCare Ltd (UK)
“The price‑to‑quality ratio is unmatched. We saved **£45,000** in the last fiscal year while maintaining FDA‑compliant documentation for every lot.” -
Prof. Luis García, Department of Reproductive Medicine – Universidad de Madrid
“The supplied Ganirelix Acetate met all ICH‑Q7 standards, allowing us to publish a peer‑reviewed study on LH surge suppression without any analytical discrepancies.”
Certifications & Regulatory Compliance
ISO 9001:2015 |
GMP‑Certified Facility |
FDA Registered |
CE Marking |
ISO 13485 (Medical Devices) |
RoHS Compliant
Frequently Asked Questions (FAQ)
What is the typical purity level of your Ganirelix Acetate?
≥ 99.8 % (HPLC) with assay variability within ±0.5 % per batch, verified by an independent ISO‑9001 laboratory.
Can you provide GMP and DMF documentation for regulatory submissions?
Yes. Every lot is accompanied by a full GMP Certificate, DMF dossier, and FDA‑compatible batch records ready for IND or NDA filings.
What are the minimum order quantities (MOQ) and pricing tiers?
MOQ starts at 1 g for research use. For commercial scale, we offer tiered pricing: 5 kg–20 kg (US $ 185/g), 20 kg–100 kg (US $ 175/g), > 100 kg (US $ 160/g). Volume discounts are negotiable.
How fast can you ship to the United States?
Standard air‑freight from Zhengzhou to LAX or JFK is **10‑12 days**. Express courier (DHL/UPS) for orders ≤ 5 kg arrives in **4‑6 days**. We provide real‑time tracking and customs clearance support.
Do you offer custom packaging or isotopic labeling?
Absolutely. Our OEM/ODM team can deliver the API in bulk drums, PET bottles, or custom‑filled vials. Isotopic (¹³C, ²H) labeling is available on a project‑by‑project basis.
Secure Your Stock of Ganirelix Acetate Today
Limited‑time Offer: First‑time buyers receive Free 2 g Sample + Money‑Back Guarantee if purity < 99.8 %.
Our inventory is running low for the Q3 2026 demand surge. Act now to lock in the best price.
Real User Reviews – Voices from the Field
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James O’Neill, R&D Lead – MedPharma USA
“The batch consistency allowed us to reduce analytical re‑runs by **30 %**, accelerating our pipeline.” -
Dr. Anita Singh, Clinical Director – Fertility Center Chicago
“Patient outcomes improved dramatically after we switched; cancellation rates dropped to the lowest in our 5‑year history.” -
Markus Weber, Procurement Officer – BioTech GmbH (Germany)
“Fast customs clearance and clear documentation saved us **€12,000** in demurrage fees.”
About the Author
Dr. Elena Mikhailova – Senior API Consultant, Global Technology Co., Ltd
With **15 years** of experience in peptide synthesis, GMP compliance, and international biotech sourcing, Dr. Mikhailova has led more than **200 successful** API introductions across North America and Europe. She holds a Ph.D. in Pharmaceutical Chemistry (Moscow State University) and is a certified ISO‑9001 Lead Auditor.
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