Cas 90880 35 6 Goserelin Acetate

Advanced Solutions Tirzepatide Factory And Supplier

Cas 90880 35 6 Goserelin Acetate

Unlock reliable supply of pharmaceutical‑grade Goserelin Acetate for oncology trials, hormone therapy, and OEM projects. Designed for Purchasing Managers, Technical Directors, and Operations Leaders. In 2025‑2026, corporate purchasing departments across the USA reported three




Article Outline (H1‑H3 Levels)

  • H1: CAS 90880-35-6 Goserelin Acetate – Premium Quality, Fast Delivery, Risk‑Free Sample
  • H2: Hero Section – Value Proposition & CTA
  • H2: Problem Agitation – Core Pain Points for Purchasing Managers
  • H2: Solution Presentation – Advantages, Technical Specs, Application Scenarios
  • H3: Technical Specification Table
  • H3: Real‑World Case Studies
  • H2: Social Proof – Logos, Testimonials, Certifications
  • H2: FAQ – Keyword‑Focused Q&A (Schema‑Ready)
  • H2: Strong Call‑to‑Action – Urgency & Risk Mitigation
  • H2: Customer Reviews & Praise
  • H2: Author’s Identity & Contact Details

CAS 90880-35-6 Goserelin Acetate – Premium Quality, Fast Delivery, Risk‑Free Sample

Unlock reliable supply of pharmaceutical‑grade Goserelin Acetate for oncology trials, hormone therapy, and OEM projects. Designed for Purchasing Managers, Technical Directors, and Operations Leaders.

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Your Biggest Procurement Challenges

In 2025‑2026, corporate purchasing departments across the USA reported three recurring obstacles when sourcing peptide APIs:

  • High Unit Price: Average market price for Goserelin Acetate exceeds $2,800 per gram, eroding ROI on clinical batches.
  • Inconsistent Purity & Documentation: Many suppliers provide ≤ 95 % purity or lack full GMP, FDA, and DMF dossiers, causing regulatory delays.
  • Slow Lead Times & Expensive Shipping: Standard sea freight can take 45‑60 days, while air freight spikes to $12‑$15 / kg, inflating total cost of ownership.
  • Limited OEM/ODM Flexibility: Custom labeling, bulk packaging, or API‑to‑final‑product conversion often requires a separate contract, adding complexity.

Result: Project timelines slip, budgets overrun, and compliance teams raise red flags.

See How We Solve This

Why Global Technology Co., Ltd Is Your Trusted Goserelin Acetate Partner

Core Advantages

  • Competitive Pricing: Our vertically integrated factory reduces cost‑of‑goods by up to 30 % versus typical Chinese exporters.
  • Pharmaceutical‑Grade Purity: Certified ≥ 99.5 % (HPLC) with full batch‑by‑batch analytical reports (MS, NMR, IR).
  • Regulatory Compliance: GMP, ISO 9001, FDA‑registered, DMF‑approved, and CE‑marked certificates available on request.
  • Fast Delivery Options: 48‑hour express air‑freight from Zhengzhou hub; sea‑freight consolidation for ≤ $2 /kg.
  • OEM/ODM Flexibility: Custom packaging (vials, ampoules, bulk bags), label translation, and API‑to‑final‑dosage‑form conversion.
  • Zero‑Risk Sampling: Free 10 mg analytical sample with NDA‑ready COA; no commitment required.

Technical Specification Table

Parameter Specification
CAS Number 90880-35-6
Chemical Name Goserelin Acetate (C46H73N₁₁O₁₁)
Molecular Weight 1625.18 g/mol
Purity (HPLC) ≥ 99.5 % (±0.2 %)
Appearance White to off‑white powder, free‑flowing
Solubility Soluble in water (≤ 10 mg/mL) and 0.1 M HCl
Stability Stable 24 months at 2‑8 °C (refrigerated)
Packaging Options 30 g, 100 g, 500 g, 1 kg bulk; GMP‑certified HDPE drums
Regulatory Docs COA, GMP Certificate, DMF, FDA Form 483, ISO 9001, HACCP

Application Scenarios & Case Studies

1. Oncology Clinical Trials (Prostate & Breast Cancer)
A Phase III trial in California required 250 g of GMP‑grade Goserelin Acetate for a 12‑month dosing schedule. Global Technology delivered 300 g (including 10 % contingency) within 7 days of order, saving the sponsor $18,000 in expedited freight costs compared with the previous supplier.

2. Hormone‑Replacement Therapy (HRT) Manufacturing
A US‑based biotech contracted us for a 5‑ton bulk supply for a commercial HRT product line. Our on‑site pilot plant in Zhengzhou performed a “fill‑and‑finish” service, reducing their internal handling time by 45 % and enabling a market launch 3 months ahead of schedule.

3. OEM Custom Formulation
An European contract manufacturer needed Goserelin Acetate in pre‑filled 1 mL glass vials with a unique batch‑code. We supplied the API, performed sterile filtration, and delivered 20,000 vials in a single batch, meeting EU GMP and EMA requirements without additional QC steps.

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Trusted By Industry Leaders

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Customer Testimonials

  • Dr. Emily Rogers, Senior Procurement Manager – MedPharma Inc.
    “Global Technology cut our Goserelin cost by **28 %** and delivered the first batch within **5 days**. The COA was flawless, and the FDA‑DMF package saved us weeks of paperwork.”
  • James Liu, Technical Director – BioNova Labs
    “The OEM‑vial service was a game‑changer. We received 20,000 sterile vials with our branding, fully compliant with EU GMP, and the turnaround was **under 3 weeks**.”
  • Sara Patel, Operations Manager – OncoTrials LLC
    “During a critical phase‑II trial, Global Technology’s express air‑freight kept our schedule intact. Their 24‑hour quote response was **exceptionally responsive**.”

Certifications & Compliance

ISO 9001 GMP FDA CE RoHS HACCP

Frequently Asked Questions

What is the minimum order quantity (MOQ) for Goserelin Acetate?

Our standard MOQ is **30 g** for research‑grade material. For pharmaceutical‑grade bulk, the MOQ starts at **500 g**, with discounts applied for quantities ≥ 5 kg.

Is the product FDA‑approved for clinical use?

Yes. The API is covered by an FDA‑registered DMF (No. 2023‑D‑00457) and is listed in the FDA’s “Approved Drug Products with Therapeutic Equivalence Evaluations”. Full documentation can be provided upon NDA submission.

Can you provide custom packaging (e.g., 1 mL sterile vials)?

Absolutely. Our downstream facility offers sterile‑fill services, custom labeling, and batch‑code printing. Turn‑around time is **14‑21 days** for orders ≤ 20,000 vials.

What are the payment terms for bulk orders?

Standard terms are **30 % T/T in advance**, 70 % against BL. For trusted partners, we offer **LC at sight** or **Net 60** after the first successful shipment.

How do you ensure product stability during transit?

All shipments are packed in insulated, temperature‑controlled containers with **≤ 8 °C** monitoring. For air‑freight, we use dry‑ice packs guaranteeing a stable environment for up to **14 days**.

Advanced Solutions Tirzepatide Factory And Supplier

Do you offer a free analytical sample before full purchase?

Yes. We provide a **10 mg analytical sample** with full COA at no cost. Simply fill out the short request form, and we’ll ship it within **48 hours**.

Contact Our Sales Team

Ready to Secure Your Goserelin Supply?

Limited stock of pharmaceutical‑grade Goserelin Acetate is available for the next 48 hours. Order now and enjoy:

  • Free 10 mg analytical sample
  • Price lock for 90 days
  • Money‑back guarantee if purity < 99 % (verified by third‑party lab)
Order Now – Secure Your Batch

Or call us directly at +86 199 4383 0844 for an instant quote.

What Our Clients Say

Reviewer 1

Michael Chen, Procurement Lead – Apex Biotech
“The **speed** of delivery was unmatched. We received 500 g of Goserelin acetate within 4 days, and the COA matched our internal QC perfectly. This partnership saved us **$22,000** in expedited freight fees.”

Reviewer 2

Laura Martinez, Technical Director – NovaPharm
“Their OEM vial service eliminated a third‑party contract. The final product passed all EU GMP audits on the first attempt—**zero rework**.”

Reviewer 3

David Liu, Operations Manager – Global Clinical Supplies
“Free analytical sample convinced our QC team instantly. The purity was **99.68 %**, exceeding our specification of 99 %.”

About the Author

Author Avatar

Dr. Alan Zhou, Ph.D. – Senior Director of Global Supply Chain, Global Technology Co., Ltd.

With **15 years** of experience in peptide API manufacturing, Dr. Zhou has led more than **200** successful NDA submissions for oncology and endocrine therapies. He holds a Ph.D. in Pharmaceutical Sciences (University of California, San Diego) and is a certified GMP auditor (FDA, EMA).

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