Targeted for: Corporate Purchasing Managers, Technical Directors, Operations Managers in the United States who demand consistent quality, fast delivery, and regulatory compliance for peptide‑based therapeutics.
Get Your Free Quote in 24 HoursWhen you source Goserelin (CAS 91485‑02‑8) from low‑cost vendors, three recurring issues often surface:
According to a 2025 industry survey, 68 % of pharma procurement teams reported at least one delayed trial due to peptide supply issues. Your competitive edge depends on eliminating these bottlenecks.
Discover how Global Technology Co., Ltd can turn these pain points into advantages →
We combine a powerful Chinese manufacturing base with Western‑grade quality systems to deliver a peptide that meets both regulatory rigor and cost‑effectiveness.
| Parameter | Value | Unit | Compliance |
|---|---|---|---|
| CAS Number | 91485‑02‑8 | ‑ | EPA |
| Chemical Name | Goserelin Acetate | ‑ | IUPAC |
| Purity (HPLC) | ≥ 99.5 | % | GMP, FDA |
| Molecular Weight | 1558.75 | g·mol⁻¹ | ‑ |
| Form | Lyophilized powder / Aqueous solution (5 mg mL⁻¹) | ‑ | ISO 13485 |
| Stability | ≥ 24 months at 2‑8 °C (dry) | ‑ | ICH Q1A(R2) |
| Packaging | Amber glass vials, HDPE bottles, or bulk drums | ‑ | FDA, CE |
| Regulatory Documents | CoA, DMF, GMP Certificate, ISO 9001 | ‑ | FDA, EMA, TGA |
Goserelin is a synthetic analogue of the natural luteinizing hormone‑releasing hormone (LHRH). Its primary commercial uses include:
Client: Midwest Oncology Research (USA)
Biotinylated-MBP-and-phosphorylated-MBP-peptide 3'-Deoxyinosine-supplier CAS-178243-46-4-Ganirelix-Acetate CAS-255710-51-1-Degarelix-Acetate
Challenge: The sponsor required 5 kg of GMP‑grade Goserelin within 30 days to meet FDA IND timelines.
Solution: Global Technology allocated dedicated production lines, performed in‑process HPLC monitoring, and shipped the bulk in two air‑freight consignments.
Result: The trial started on schedule, and the client reported a 22 % reduction in overall study cost due to lower peptide price and avoided re‑purification steps.
Answer: All batches are tested by HPLC and meet **≥ 99.5 % purity**. A full CoA is provided with each shipment.
Yes. We offer OEM/ODM services for lyophilized powders, aqueous solutions (5 mg mL⁻¹), and pre‑filled syringes. Minimum order for custom packaging is 500 g.
Standard terms are 30 % T/T in advance, 70 % against copy of B/L. For trusted partners we can arrange L/C, open account, or PayPal for smaller quantities.
With air freight, typical transit is **7‑10 days** from our Zhengzhou hub to Los Angeles, plus 1‑2 days customs clearance.
Our regulatory team can supply GMP certificates, batch records, stability data, and even draft the Chemistry, Manufacturing & Controls (CMC) section for your IND.
Zero‑risk guarantee: If the CoA shows purity < 99.5 %, we will replace the batch at no extra cost or issue a full refund.
Why wait? Secure your high‑purity Goserelin today, reduce your R&D cost by up to 37 %, and keep your clinical timelines on track.
Email Us Now WhatsApp ChatOffer valid until 30 days from your first contact. Stock is limited – act fast!
Emily R. – Senior Procurement Manager, NovaPharm USA
“The consistency of Goserelin purity saved us 2 weeks of re‑testing. The free sample let us validate before committing a $80k purchase.”
James L. – Technical Director, MedCore Labs
“Fast air‑freight and detailed CoA meant we could start our animal study on day 1. No delays, no surprises.”
Sara K. – Operations Manager, TheraGen
“OEM packaging in pre‑filled vials cut our downstream processing cost by 18 %. Global Technology truly understands our needs.”
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