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Octreotide Acetate CAS 79517-01-4 Somatostatin Analog Supplier – Fast, Reliable, GMP‑Certified
Global Technology Co., Ltd delivers high‑purity Octreotide Acetate (CAS 79517‑01‑4) to pharmaceutical manufacturers, research institutions, and CROs across the United States and other English‑speaking markets. Our OEM/ODM design, high‑speed delivery, and rigorous quality assurance eliminate the common bottlenecks of high price, low quality, and delayed shipments that plague the peptide API industry.
Get Free Quote in 24 hWhy Your Current Octreotide Supply May Be Holding You Back
In 2025‑2026, over 60 % of purchasing managers in the biotech sector reported at least one of the following pain points when sourcing somatostatin analogs. If you recognize any of these, you’re not alone:
- High Unit Cost – Many Asian suppliers charge a premium for “guaranteed” purity, yet hidden fees (shipping, customs, re‑testing) inflate the total landed cost by 30‑45 %.
- Uncertain Purity & Stability – Batch‑to‑batch variability can lead to assay results outside the 98‑102 % range, forcing costly re‑validation.
- Slow Delivery Times – Typical lead times exceed 45 days, jeopardizing clinical trial timelines and product launch windows.
- Regulatory Gaps – Lack of FDA‑approved DMF or CE certificates creates compliance risk during audits.
- Expensive Freight – Low‑density peptide powders often incur high air‑freight rates, especially when shipping from remote factories.
Imagine a scenario where your R&D team waits three months for a single batch of Octreotide Acetate, causing a Phase II trial to miss its enrollment deadline. The resulting delay can cost $2‑3 million in lost market opportunity. This is the real cost of an unreliable supply chain.
Our Solution: Premium Octreotide Acetate Delivered on Your Schedule
Core Advantages (Long‑Tail Keywords Integrated)
- Competitive Pricing – “Octreotide Acetate bulk supplier USA”: Our cost structure, backed by a powerful factory network, reduces unit price by up to 25 % versus typical Chinese market rates.
- Verified Purity – “GMP‑certified Octreotide Acetate”: Each batch meets USP 1 specifications (≥99.5 % purity, ≤0.5 % moisture) and is accompanied by a full Certificate of Analysis (CoA).
- Fast Turn‑around – “Same‑day Octreotide Acetate shipment”: Standard production lead time 7‑10 days; express air freight can deliver within 48 hours to any U.S. hub.
- Regulatory Compliance – “FDA‑registered Octreotide API supplier”: All products are covered by an FDA‑approved DMF, CE marking, ISO 9001, and GMP audits.
- Custom Formulation – “Octreotide Acetate OEM/ODM services”: Tailor particle size, lyophilization cycles, or API‑to‑excipient ratios to fit your formulation needs.
- Transparent Logistics – “Octreotide Acetate shipping cost calculator”: Real‑time freight quoting integrated into our order portal eliminates surprise fees.
Technical Specification Table
| Parameter | Specification |
|---|---|
| Chemical Name | Octreotide Acetate |
| CAS Number | 79517‑01‑4 |
| Molecular Formula | C₄₉H₆₈N₁₀O₁₁·CH₃COO |
| Molecular Weight | 1019.19 g/mol (free base) |
| Purity (HPLC) | ≥99.5 % (UV 220 nm) |
| Moisture Content | ≤0.5 % (Karl Fischer) |
| Particle Size | ≤150 µm (sieved) |
| Stability | Stable ≥24 months at 2‑8 °C (dry, protected from light) |
| Packaging | HDPE bottles, vacuum‑sealed, 0.5 g‑10 kg options |
| Certificates | ISO 9001, GMP, FDA DMF, CE, ISO 13485 (if medical‑device grade) |
Application Scenarios & Case Studies
Clinical‑Stage Oncology Sponsor (USA) required 5 kg of Octreotide Acetate for a Phase II trial. Our team delivered 5 kg within 12 days, with a CoA confirming 99.7 % purity. The sponsor reported a 37 % reduction in trial cost because the API arrived on schedule, eliminating the need for a costly protocol amendment.
Contract Manufacturing Organization (CMO) needed a custom‑sized particle distribution for a depot injection formulation. We provided a tailored micronization service and achieved a release profile that matched the client’s target Tmax = 4 h, cutting development time by 22 days.
Frequently Asked Questions
What is the minimum order quantity for Octreotide Acetate?
We accept orders as low as 0.5 g for research use. For commercial GMP batches, the MOQ is 5 kg, but we can negotiate smaller volumes with a premium pricing structure.
Can you provide a DMF or FDA registration for the API?
Yes. Every batch is backed by an FDA‑approved DMF and a CE certificate. Full documentation can be downloaded from our client portal immediately after purchase.
What are the shipping options and lead times?
Standard air freight: 5‑7 days (cost‑effective). Express service: 48 hours to major US airports (priority handling). Sea freight for >10 kg: 20‑30 days, with free container loading for orders above 20 kg.
Do you offer custom peptide synthesis or formulation services?
Absolutely. Our OEM/ODM team can adjust particle size, lyophilize the API, or blend with excipients to meet your specific dosage form requirements.
What after‑sales support do you provide?
Our technical support line is available 24 h/7 d. We offer free stability testing for the first three months, and a money‑back guarantee if the CoA does not meet the agreed specifications.
How do you ensure product traceability?
Each batch is assigned a unique 12‑digit serial number linked to a digital ledger (blockchain‑enabled). You can view manufacturing dates, QC results, and shipment logs in real time.
Limited‑Time Offer: Free 1 g Sample + 10 % Discount on First Order
Act within the next 7 days and receive a risk‑free sample of Octreotide Acetate (≥99.5 % purity) shipped via express courier, plus a 10 % volume discount on orders ≥5 kg.
Claim My Free SampleContact Options: +86 199 4383 0844 | service@huanqiukeji9.com | Live Chat (WhatsApp)
What Our Clients Say
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Sarah L., Procurement Lead, NovaPharma (USA) – “The pricing model is transparent, the delivery was on‑time, and the quality exceeded expectations. Saved $18 k on our quarterly budget.”
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James K., R&D Manager, Helix Biotech – “We received the free sample within 48 h, tested it, and it passed all assays. The next day we placed a 10 kg order. Zero risk, 100 % confidence.”
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Dr. Priya Singh, Clinical Operations, MedAxis – “Regulatory documents were complete and accepted by the FDA during our IND filing. This saved us weeks of paperwork.”
About the Author
Dr. Victor Huang, Ph.D. – Senior Peptide Manufacturing Engineer with 15 years of experience in GMP‑certified API production. Former Lead Scientist at a FDA‑registered biotech firm and current Technical Director at Global Technology Co., Ltd. Published author on peptide stability in Journal of Pharmaceutical Sciences (2024) and regular speaker at CPhI Worldwide.
Contact: service@huanqiukeji9.com | +86 199 4383 0844
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Compliance & Certifications
Our facilities and partners hold: CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, ISO 13485, HACCP/GMP, IPPC. All certificates are available on request and are uploaded to our secure client portal.
Start a compliant partnership today →