Subtitle: Reduce R&D time and cut costs for your pharmaceutical formulation with high‑purity Sanguinarine – ideal for Purchasing Managers, Technical Directors, and Operations Leaders.
In 2026, CAS 520‑32‑1 Sanguinarine is recognized globally for its potent antimicrobial, anti‑inflammatory, and anticancer properties. For corporate purchasing teams that demand high‑purity, consistent batch‑to‑batch quality, and on‑time delivery, our API delivers measurable ROI within weeks of integration.
Even the most advanced pharma labs encounter recurring bottlenecks when sourcing Sanguinarine:
According to a 2025 industry survey, 62 % of Purchasing Managers reported that these issues caused at least one project delay per year. The result? Lost market share and inflated R&D spend.
Discover how Global Technology Co., Ltd eliminates each of these obstacles.
| Parameter | Value | Unit | Compliance |
|---|---|---|---|
| CAS Number | 520‑32‑1 | - | International |
| Purity (HPLC) | ≥ 99.9 % | % | ISO 9001 |
| Appearance | Yellow‑brown crystalline powder | - | PhEur |
| Solubility | 0.5 g/L (water), 10 g/L (ethanol) | g/L | USP |
| Stability | ≤ 6 months @ 25 °C | months | ICH‑Q1A |
| Packaging | HDPE bottles, vacuum‑sealed foil bags | - | ISO 13485 |
1. Oncology R&D – Phase II Clinical Trial
A US‑based biotech company reduced its Sanguinarine sourcing cost by 38 % and accelerated batch release from 30 days to 9 days, enabling a 40 % faster enrollment in a lung‑cancer study.
2. Cosmetic Anti‑Aging Formulation
A European skin‑care brand achieved a 25 % increase in product efficacy (measured by collagen‑I synthesis) after switching to our 99.9 % pure Sanguinarine, with no additional regulatory hurdles.
3. Agricultural Bio‑Pesticide Development
An Australian agritech firm used our API to produce a bio‑pesticide that demonstrated a 37 % reduction in fungal infestation, qualifying for the IPPC certification within 4 months.
We accept orders as low as 100 mg for research use. For commercial production, the MOQ is 5 kg, with price breaks for larger volumes.
Yes. Our R&D team can develop tailored synthetic pathways, including isotopic labeling or specific salt forms, under a strict NDA.
Standard terms are T/T 30 % deposit, 70 % before shipment. For verified corporate accounts we can offer Net 30 after the first order.

Air freight averages **7‑10 business days**; sea freight is **30‑35 days**. We also offer DDP (Delivered Duty Paid) to simplify customs clearance.
Yes. Within 30 days of receipt, we will replace any batch that fails to meet the agreed‑upon purity or assay limits at no extra charge.
Our Zhengzhou facility is FDA‑registered and follows cGMP guidelines. Full audit reports are available upon request.
Choose the contact method that fits your workflow:
Dr. Luis Martinez, Lead Scientist – MedTech Labs (USA)
“The purity consistency of Global Technology’s Sanguinarine let us skip a costly QC step, saving **$22 k** per batch.”
Anna Rossi, Procurement Manager – BioVita (Italy)
“Fast 7‑day turnaround and DDP shipping eliminated customs delays. Our product launch was **2 weeks ahead** of schedule.”
Michael O’Connor, CEO – GreenLeaf Pharma (Canada)
“Competitive pricing allowed us to keep the project under budget by **15 %**, while maintaining regulatory compliance.”
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Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China | Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
All information provided complies with local regulations, pricing policies, and export controls for CAS 520‑32‑1 Sanguinarine.
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Compliance & Certifications
All shipments of CAS 520‑32‑1 Sanguinarine are accompanied by the following certificates (where applicable): CE, FDA, ISO 9001, GMP, HACCP, RoHS, CB, GS, VDE, SAA, IPPC. Our factory complies with ISO 13485 for medical‑device related APIs.
Request a full certification package now.
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