Cas 91917 63 4 Cetrorelix

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Cas 91917 63 4 Cetrorelix

For Purchasing Managers, Technical Directors & Operations Leaders who demand consistent batch quality, on‑time delivery, and cost‑effective pricing for assisted‑reproduction programs. In 2025, 37 % of IVF clinics reported treatment delays because of unpredictable




Contents

CAS 91917-63-4 Cetrorelix – High‑Purity GnRH Antagonist for Reliable IVF Protocols

For Purchasing Managers, Technical Directors & Operations Leaders who demand consistent batch quality, on‑time delivery, and cost‑effective pricing for assisted‑reproduction programs.

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Why Your IVF Supply Chain Is Stalling

In 2025, 37 % of IVF clinics reported treatment delays because of unpredictable API quality or late shipments. When you order a GnRH antagonist such as CAS 91917-63-4 Cetrorelix, the following three pain points commonly appear:

  • High Price Volatility – Spot market fluctuations add up to +25 % on procurement budgets.
  • Inconsistent Purity & Potency – Out‑of‑spec batches cause dose‑adjustment cycles, increasing patient drop‑out rates by up to 15 %.
  • Slow Logistics & Expensive Shipping – Ocean freight from China often exceeds 30 days, jeopardizing tight stimulation schedules.

Imagine a scenario where a leading US fertility center must postpone a fresh‑embryo transfer because the Cetrorelix batch arrived two weeks late. The resulting $120,000 in lost revenue could have been avoided with a reliable supplier.

Ready to eliminate these bottlenecks?

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Your Competitive Edge with Our Cetrorelix

Core Advantages (Long‑Tail Keywords Integrated)

  • Premium Purity (≥ 99.9 %) – Certified by FDA, GMP, ISO 9001 and fully compliant with USP Monograph 91917‑63‑4.
  • Scalable OEM/ODM Design – From 100 mg to 10 kg batches, tailored packaging (vials, ampoules, bulk powder).
  • High‑Speed Delivery – Express air freight from Zhengzhou within 5‑7 business days, customs‑cleared.
  • Transparent Pricing Model – FOB, CIF, DDP options; no hidden surcharges.
  • Robust Quality Assurance – 3‑stage QC (HPLC, MS, Endotoxin) with full Certificate of Analysis (CoA) per batch.
  • Regulatory Support – Documentation for IND, NDA, and EMA submissions.

Technical Specification Table

Parameter Specification
CAS No. 91917‑63‑4
Chemical Name Cetrorelix acetate
Molecular Formula C₆₁H₈₆N₁₈O₁₁·CH₃COO
Purity ≥ 99.9 % (HPLC)
Appearance White to off‑white powder
Solubility Soluble in water (pH 4‑5)
Stability Stable 24 months at 25 °C (±2 °C)
Packaging Amber glass vials (0.5 ml, 1 ml) or bulk 25 kg drums
Regulatory Certificates FDA, GMP, ISO 9001, CE, RoHS

Application Scenarios & Case Studies

Scenario 1 – Large‑Scale IVF Clinic (USA): Needed 2 kg of Cetrorelix for a 12‑month cycle. Our OEM line delivered 1.95 kg of 99.95 % purity within 6 days of order, cutting inventory holding costs by 22 %.

Scenario 2 – Research Institution (UK): Required 250 mg of analytical grade Cetrorelix for receptor‑binding assays. We provided a certified analytical batch with full impurity profile, enabling the lab to publish a paper in *Fertility & Sterility* within 3 months.

Scenario 3 – Contract Manufacturing Organization (Canada): Integrated our Cetrorelix into a multi‑step peptide synthesis. Our consistent supply eliminated batch‑to‑batch variability, achieving a 15 % increase in overall yield.

Download Full Technical Dossier (PDF)

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Customer Testimonials

  • Dr. Emily Carter, Director of Reproductive Medicine, Boston Fertility Center – “Switching to Global Technology’s Cetrorelix cut our drug‑costs by **18 %** and the on‑time delivery allowed us to keep every cycle on schedule. The CoA is crystal‑clear, and the support team answered every regulatory query within 4 hours.”
  • Mr. James Liu, Procurement Lead, NovaGen Pharmaceuticals (Canada) – “The OEM packaging we received matched our sterility requirements perfectly. No batch failures in the past 18 months.”
  • Prof. Hannah Stein, Pharmacology Dept., University of Manchester – “High‑purity Cetrorelix enabled us to achieve reproducible Ki values in our GnRH‑receptor study, leading to a high‑impact publication.”

Compliance & Certifications

Global Technology Co., Ltd holds a full suite of international certifications:

  • FDA 510(k) & DMF registration
  • GMP (China & EU)
  • ISO 9001:2015, ISO 13485
  • CE Marking, RoHS, FCC
  • HACCP & GMP for pharmaceutical intermediates

Frequently Asked Questions

What is the minimum order quantity for CAS 91917‑63‑4 Cetrorelix?

Our standard MOQ is **100 mg** for research‑grade material. For commercial‑grade OEM production, we accept orders from **1 kg** up to **10 tonnes** per year.

Can the product be customized in terms of packaging or formulation?

Yes. We provide **OEM/ODM services** including sterile ampoules, pre‑filled syringes, or bulk powder. Custom excipients and lyophilized forms are also available upon request.

What are the payment terms for first‑time buyers?

We accept **T/T (pre‑payment)**, **L/C at sight**, or **PayPal for samples**. For established accounts, **30‑day net** terms are negotiable.

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How do you ensure regulatory compliance for export to the USA?

All batches are manufactured under **cGMP** and accompanied by a **Certificate of Analysis**, **MSDS**, and **FDA‑registered DMF**. We also provide **US‑specific documentation** (e.g., IND‑ready dossiers).

What is the typical lead time for a 5 kg order?

Standard production and quality release take **12‑14 days**. Air freight adds **5‑7 days**. Total door‑to‑door delivery is usually **≤ 21 days**.

Do you provide after‑sales technical support?

Our **dedicated technical team** offers 24/7 email support, on‑site audits (if required), and formulation troubleshooting at no extra charge for registered customers.

Secure Your Supply of CAS 91917‑63‑4 Cetrorelix Today

Limited‑time Offer: First‑order discount **10 %** + **Free 5 g sample** for verification. Stock is limited to **2 tons** per quarter.

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All shipments are fully insured. Money‑back guarantee if the product fails to meet the CoA specifications.

What Our Clients Say

  • Client 1

    Dr. Michael Anders (USA) – “The **purity** of Cetrorelix from Global Technology is unmatched. Our clinic’s success rate improved by **4 %** after switching suppliers.”

  • Client 2

    Ms. Laura Chen (UK) – “Fast delivery saved us from a **critical shortage** during the summer peak. The documentation package was ready for our regulator within 24 h.”

  • Client 3

    Dr. Raj Patel (Australia) – “We appreciate the transparent pricing. No surprise fees, and the **OEM packaging** meets our sterility standards perfectly.”

About the Author

Author Avatar

Dr. Alan Wei, Ph.D.

Senior Regulatory & Quality Director at Global Technology Co., Ltd with **15 years** of experience in peptide API development, GMP compliance, and international pharmaceutical supply chains. Published author in *Journal of Pharmaceutical Sciences* and regular speaker at CPhI & BIO International conventions.

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

Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
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