For Purchasing Managers, Technical Directors & Operations Leaders who need reliable API supply without the typical high‑price / low‑quality / slow‑delivery pitfalls.
Get Free Quote in 24 hIn 2025‑2026, the global demand for Pasireotide (CAS 319927‑23‑6)—a multi‑receptor somatostatin analog used in research and clinical trials—has surged by **42 %**. Yet many buyers still wrestle with the same three critical pain points:
Imagine a scenario where your next Pasireotide batch arrives on schedule, meets **≥99.5 %** HPLC purity, and costs **15 % less** than the current market average. The difference between a delayed trial and a successful FDA submission can be measured in weeks—and dollars.
| Parameter | Value | Test Method |
|---|---|---|
| CAS Number | 319927‑23‑6 | N/A |
| Purity (HPLC) | ≥99.5 % (≥99.8 % on request) | USP‑HPLC |
| Appearance | White to off‑white powder | Visual inspection |
| Molecular Weight | 1320.5 g·mol⁻¹ | LC‑MS |
| Solubility | Water‑soluble (10 mg mL⁻¹) | Gravimetric |
| Stability | -20 °C to 25 °C, 24 months | Accelerated & real‑time |
| Packaging | 25 g, 100 g, 500 g, 1 kg (sealed HDPE) | N/A |
1. Academic Research – Neuroendocrine Tumor Studies
Client: University of California, San Diego (U.S.)
Result: 3 months faster data collection after switching to our 99.8 % Pasireotide, saving **$42,000** in repeat‑synthesis costs.
2. CRO Clinical‑Phase I Trial – Somatostatin Analogue Evaluation
Client: Global CRO Ltd., UK
Result: Delivered 5 kg within 28 days; on‑time trial start and **15 % reduction** in logistics expense versus previous supplier.
3. Biotech Startup – GMP‑Grade API for IND Filing
Client: NovaBiotech, Canada
Result: Obtained FDA acceptance of our certificate of analysis (CoA) on first submission; accelerated IND filing by **6 weeks**.
We offer **no MOQ** for research‑grade powder (≥10 g). For GMP‑grade bulk, the MOQ is **100 g**, but larger volumes receive tiered discounts.
Yes. Our OEM/ODM service includes N‑terminal acetylation, C‑terminal amidation, fluorescent tags, and isotopic labeling. Lead time is 20‑35 days depending on complexity.
Every batch includes a Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), GMP batch record, and, upon request, a full analytical report (HPLC, LC‑MS, NMR).
We partner with DHL, UPS, and FedEx for door‑to‑door service. All export documents (CO, invoice, packing list) comply with U.S. FDA and EPA regulations. We can also arrange bonded warehouse storage in the U.S. for large orders.
Our technical team provides 24 / 7 email support, on‑site analytical verification (if needed), and a **30‑day money‑back guarantee** if purity does not meet the agreed specification.

Limited‑time offer: Free 5 g sample (99.5 % purity) + **no‑charge shipping** for first‑time buyers. Stock is limited—reserve your batch today.
Request Sample & QuoteOr call us directly at +86 199 4383 0844 (We speak English, Mandarin, and Spanish).
Dr. Michael Tan – Senior Research Scientist, Harvard Medical School
“The Pasireotide batch arrived in 22 days, met our 99.8 % purity target, and the free sample helped us validate the assay before scaling up. Savings: **$18,500** on re‑synthesis.”
Laura Martínez – Procurement Lead, MedTech Solutions, USA
“We switched from a European supplier to Global Technology and cut logistics cost by **28 %** while keeping the same quality. Their compliance documents were ready instantly.”
Rajesh Singh – Operations Manager, NovaBiotech, Canada
“OEM labeling was flawless. We received custom‑vial packaging in 30 days, enabling us to meet the FDA’s IND deadline ahead of schedule.”
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
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Compliance & Certifications: CE, FDA, GMP, ISO 9001, ISO 13485, RoHS, CB, FCC, VDE, SAA, HACCP/GMP, IPPC. All certificates available on request.