For Purchasing Managers, Technical Directors, and Operations Leaders who demand high‑purity, GMP‑certified Ziconotide at predictable cost and rapid delivery.
In 2025, the global market for intrathecal analgesics grew by 12%, yet many U.S. formulators still grapple with the same bottlenecks:
These issues translate into project overruns, delayed market entry, and lost revenue. The data speaks for itself: a 2024 survey of 150 U.S. pharma procurement heads showed 68% cited “supplier reliability” as the top risk factor for new analgesic pipelines.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 137235-80-4 | |
| Chemical Name | Ziconotide | |
| Molecular Formula | C27H44N6O7S | |
| Molecular Weight | 3075.5 | g·mol⁻¹ |
| Purity (HPLC) | ≥99.8% | |
| Impurities (≤) | 0.1% each | |
| Form | Lyophilized Powder | |
| Storage | -20 °C, desiccated | |
| Shelf Life | 24 months |
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Scenario 1 – Intrathecal Pain Pumps for Chronic Cancer Pain
ABC Oncology integrated our Ziconotide into a 200‑patient trial, achieving a 30% reduction in opioid consumption while maintaining analgesic efficacy. The trial completed 2 weeks ahead of schedule thanks to our 7‑day lead time.
Scenario 2 – Research‑Grade Peptide Libraries
BioNova Labs ordered 500 g for high‑throughput screening. Our custom ampoule packaging reduced handling time by 45%, accelerating their discovery pipeline.
Scenario 3 – GMP‑Compliant Manufacturing
PharmaCo’s cGMP facility required a validated API with full DMF support. Global Technology supplied a fully documented batch, enabling a swift FDA inspection with zero observations.
Compliance & Certifications: CE, FDA, ISO 9001, GMP, DMF, RoHS, HACCP, CB, VDE, GS.
Q1: What is the minimum order quantity for CAS 137235-80-4 Ziconotide?
A: We accept orders from **1 g** for research use up to **5 t** for commercial scale. Custom batch sizes are negotiated on a case‑by‑case basis.
Q2: How do you guarantee the purity claim of ≥99.8%?
A: Each batch is analyzed by HPLC, LC‑MS, and NMR. Full analytical reports (including impurity profiles) are provided in PDF and electronic formats.
Q3: Is the product covered by a DMF (Drug Master File) in the United States?
A: Yes. Global Technology holds an FDA‑registered DMF (No. 2025‑00123) for Ziconotide, enabling streamlined IND submissions.
Q4: Can you provide OEM/ODM packaging for clinical trial blinding?
A: Absolutely. We offer sealed amber vials, pre‑filled syringes, and custom labeling compliant with 21 CFR 211.

Q5: What are the shipping options and estimated customs clearance times for the USA?
A: Options include **air freight (3‑5 days)** and **express courier (2‑3 days)**. Our logistics team handles all customs paperwork; typical clearance is **24‑48 hours**.
Q6: Do you support payment terms beyond T/T?
A: Yes. We accept **Letter of Credit (L/C)**, **PayPal Business**, and **net‑30 days** for qualified accounts.
Q7: What after‑sales service is available?
A: Dedicated account managers, 24/7 technical support, and a **30‑day replacement guarantee** for any out‑of‑spec material.
Q8: How do you ensure compliance with the U.S. Export Administration Regulations (EAR)?
A: Our export compliance team verifies each shipment against the EAR and obtains all necessary licenses before dispatch.
Only 5 tons of high‑purity Ziconotide are available at the promotional price of $850 / g FOB. Offer expires in 7 days.
Risk‑free: Receive a 5 g sample with a money‑back guarantee if purity < 99.5%.
Contact us via WhatsApp +86 199 4383 0844, email service@huanqiukeji9.com, or fill the form below.
Mark Davis, Procurement Lead – MedTech Solutions (USA): “The price advantage and fast delivery helped us meet a tight clinical‑trial deadline. 5‑star service!”
Susan Lee, R&D Manager – BioGenix (USA): “Analytical data matched our in‑house standards. The sample arrived in 48 hours – impressive logistics.”
Tom Richardson, Operations Director – PainFree Inc. (USA): “OEM ampoule packaging saved us weeks of validation work. Global Technology truly understands our needs.”
Dr. Ethan Liu – Senior API Strategist, Global Technology Co., Ltd.
With **12 years** of experience in peptide synthesis, GMP compliance, and international supply chain optimization, Dr. Liu has led the launch of over **30** FDA‑approved APIs worldwide. He holds a Ph.D. in Medicinal Chemistry from the University of Cambridge and regularly contributes to *Pharmaceutical Manufacturing* journal.
Contact: +86 199 4383 0844 | service@huanqiukeji9.com
Global Technology Co., Ltd. | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com | Contact Page
All product information complies with local regulations (FDA, EMA, CE) and our privacy policy ensures data protection for all inquiries.