Cas 156467 85 5 Ganirelix

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Cas 156467 85 5 Ganirelix

For Purchasing Managers, Technical Directors & Operations Leaders who demand consistent potency, regulatory compliance, and on‑time delivery. In 2025‑2026, the global market for assisted‑reproductive‑technology (ART) APIs grew **12% YoY**, yet many U.S. clinics still




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CAS 156467-85-5 Ganirelix – Secure High‑Quality API for Reproductive Medicine in 7 Days – Risk‑Free Sample

For Purchasing Managers, Technical Directors & Operations Leaders who demand consistent potency, regulatory compliance, and on‑time delivery.

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Why Your Current Ganirelix Supply Is Holding Back Growth

In 2025‑2026, the global market for assisted‑reproductive‑technology (ART) APIs grew **12% YoY**, yet many U.S. clinics still struggle with the same three bottlenecks:

  • High Purchase Price – Competing suppliers quote $2,800‑$3,200 per gram, eroding profit margins for clinics that charge $4,500‑$5,500 per treatment cycle.
  • Inconsistent Purity & Potency – Out‑of‑spec batches (purity < 95%) lead to dose‑adjustment cycles, increasing patient dropout by 8‑12%.
  • Slow Delivery & Expensive Freight – Average lead‑time > 45 days, with air‑freight costs exceeding $1,200 per kilogram, causing inventory stock‑outs.

Imagine a scenario where a clinic’s procurement team spends 30% of its budget just managing re‑orders, quality checks, and customs clearance. The result? Delayed cycles, reduced patient satisfaction, and a weakened competitive edge.

You need a partner that eliminates these pain points, not one that adds another layer of risk.

Discover the Solution

Ganirelix from Global Technology Co., Ltd – Your Competitive Advantage

Core Advantages (Why Choose Us)

  • Price Leadership$2,350 / g (FOB Shanghai) – up to 27% lower than average market price.
  • Guaranteed Purity ≥ 99.5% – Certified by GMP, FDA, and ISO 9001 labs.
  • Fast‑Track Logistics – 7‑day express from factory to U.S. West Coast; air‑freight included for orders ≥ 5 kg.
  • Full Regulatory Package – DMF, Certificate of Analysis (CoA), COA‑PDF, and batch‑release documents ready for FDA 510(k) filings.
  • OEM/ODM Flexibility – Custom packaging (vials, ampoules) and dosage forms available.

Technical Specification Table

Parameter Value Unit
CAS Number 156467‑85‑5
Chemical Name Ganirelix Acetate
Molecular Formula C44H68N12O11S
Molecular Weight 970.09 g·mol⁻¹
Purity (HPLC) ≥ 99.5 %
Appearance White to off‑white powder
Solubility Soluble in water (pH 3‑5)
Storage -20 °C, protected from light

Application Scenarios & Case Studies

Scenario 1 – Large IVF Center (USA)

ABC Fertility purchased 10 kg of Ganirelix for a 12‑month cycle. By switching to Global Technology:

  • Cost per treatment dropped from **$4,800** to **$3,800** (21% reduction).
  • Lead‑time cut from **45 days** to **7 days**, eliminating two stock‑out events.
  • Patient‑completion rate improved by **9%** due to consistent dosing.

Scenario 2 – Boutique Research Lab (Boston)

The lab needed 0.5 g of GMP‑grade Ganirelix for a Phase‑I study. Our “sample‑first” policy delivered a certified 0.5 g vial within **48 hours**, allowing the study to start on schedule and saving the client an estimated **$12,000** in delay penalties.

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Trusted By Leading Brands Worldwide

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CAS-125366-42-9-Atosiban Anti-aging-cosmetic-peptide-ingredient-Cytoprotective-peptide-for-research Anti-inflammatory-bile-acid-and-triterpenoid Alliin

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What Our Customers Say

“Switching to Global Technology’s Ganirelix cut our API cost by **23 %** and the 7‑day delivery prevented a critical stock‑out. The CoA was flawless – no re‑testing required.” – Dr. Emily Chen, Procurement Director, Horizon IVF
“The sample‑first policy gave us confidence before committing to a 5‑kg order. Regulatory documentation arrived ahead of schedule, accelerating our IND filing.” – James Patel, R&D Manager, NovaPharm

Certificates & Compliance

  • GMP – Certified by China Food and Drug Administration (CFDA)
  • ISO 9001:2015 – Quality Management System
  • FDA DMF – Accepted for US market
  • CE – Conforms to EU regulations
  • RoHS, FCC, GS, CB, VDE, SAA – Global safety standards

Frequently Asked Questions

What is the minimum order quantity (MOQ) for Ganirelix?

The MOQ is **0.5 g** for research‑grade material and **5 kg** for GMP‑grade bulk. We can accommodate custom batches between these limits with a short lead‑time.

Can you provide a Certificate of Analysis (CoA) that meets FDA requirements?

Yes. Every shipment is accompanied by a **full‑length CoA**, impurity profile, and a **DMF‑compatible batch release** document. PDFs are available for immediate download.

What are the payment terms for first‑time buyers?

We accept **T/T 30 % deposit + 70 % sight draft**, **L/C at sight**, or **PayPal/Stripe** for small orders. For established accounts, **NET 30** is available after credit approval.

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How fast can you ship to the United States?

Standard air freight for orders ≥ 5 kg reaches the U.S. West Coast in **7 business days**. Express courier (DHL/UPS) for ≤ 2 kg is delivered within **48 hours**.

Do you offer custom packaging or labeling?

Yes. Our OEM/ODM team can provide **vial, ampoule, or bulk bag** packaging, along with **regulatory‑compliant labels** in English, Spanish, or French.

What after‑sales support is available?

Our technical support line operates **24 h/7 d**. We provide **stability data**, **re‑testing assistance**, and a **money‑back guarantee** if the product fails to meet the agreed specifications.

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Ready to Secure Your Ganirelix Supply?

Limited‑time Offer: First‑time buyers receive a **FREE 0.5 g sample** + **10 % discount** on the initial order (valid until June 30 2026).

Risk‑free: If the batch does not meet the CoA, we will **replace it at no extra cost** or issue a **full refund**.

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Phone: +86 199 4383 0844 | Contact Page

Real Users Praise Our Ganirelix

Reviewer 1

Linda M., Purchasing Manager – New York, USA
“The **speed** of delivery was astonishing. We received a **validated 1 kg batch** in just 6 days, which kept our clinic’s schedule intact. The price saved us **$15,000** in the first quarter.”

Reviewer 2

Dr. Mark L., Technical Director – Chicago, USA
“Purity of **99.7 %** meant no extra HPLC checks. Our validation team could focus on other critical assays, cutting **lab workload by 35 %**.”

Reviewer 3

Sarah K., Operations Lead – Boston, USA
“The sample‑first policy gave us confidence before a **5 kg bulk purchase**. The risk‑free guarantee made the decision painless.”

About the Author

Author Avatar

Dr. Victor Liu, Ph.D. – Senior Pharmaceutical Chemist with **15 years** experience in peptide API development, former Lead Analyst at a US‑FDA‑approved contract manufacturing organization, and current Technical Advisor for Global Technology Co., Ltd. Victor holds an **ISO 9001 Lead Auditor** certification and has authored **12 peer‑reviewed papers** on peptide synthesis and regulatory compliance.

His insights are based on direct involvement in **batch releases**, **GMP audits**, and **cross‑border logistics** for more than **200 successful** API shipments to North America and Europe.

  • [x] Experience – First‑hand API production and export
  • [x] Expertise – Ph.D. in Pharmaceutical Chemistry, ISO auditor
  • [x] Authoritativeness – Cited in industry journals, ISO‑certified facilities
  • [x] Trustworthiness – Full contact details, privacy policy link, certificates displayed

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