CAS 551‑15‑5 Oridonin – High‑Purity API for Fast‑Track R&D & Commercial Production
Accelerate drug discovery, lower total cost of ownership, and guarantee regulatory compliance – **the solution every pharmaceutical R&D manager, technical director, and operations leader needs**.
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- The Critical Challenges Facing Your Oridonin Procurement
- Why Global Technology’s Oridonin Is the Definitive Solution
- Technical Specification Sheet
- Real‑World Applications & Success Stories
- Trusted By Industry Leaders
- Frequently Asked Questions (FAQ)
- Take Action Now – Secure Your Supply
- Customer Reviews & Praise
- About the Author
The Critical Challenges Facing Your Oridonin Procurement
When you are sourcing CAS 551‑15‑5 Oridonin for pre‑clinical studies or large‑scale manufacturing, three pain points dominate the decision‑making process:
- Price volatility – Traditional Asian suppliers quote high unit prices for small batches, eroding your R&D budget.
- Inconsistent purity & batch‑to‑batch reproducibility – A 2‑3 % impurity swing can invalidate toxicology data and trigger regulatory delays.
- Lengthy lead times & unpredictable shipping – 6‑8 weeks from order to delivery is common, jeopardizing trial timelines and causing costly stock‑outs.
According to a 2025 industry survey, **37 % of pharmaceutical R&D managers** reported that supply‑chain instability increased project timelines by more than 30 days. Moreover, the same study highlighted that **over 42 % of procurement teams** switched suppliers after experiencing a single batch that failed USP USP 1 specifications.
These data points illustrate why a reliable, cost‑effective, and fast‑delivering Oridonin source is not a luxury—it is a competitive necessity.
Why Global Technology’s Oridonin Is the Definitive Solution
Global Technology Co., Ltd. combines a **state‑of‑the‑art production line** with a **GMP‑certified, FDA‑registered supply chain** to deliver Oridonin that meets the most stringent pharmaceutical standards.
- Unmatched Purity – Certified ≥ 99.5 % (HPLC) with ≤ 0.1 % heavy metals (ICP‑MS) and full‑traceability batch records.
- Cost Leadership – Our vertical integration reduces raw‑material markup, delivering a **15 % lower unit price** versus average market rates.
- Rapid Turn‑Around – Standard 3‑week production + 2‑day air freight; express 48‑hour delivery** available for urgent trials.
- Custom OEM/ODM Design – From gram‑scale research lots to tonnage‑scale commercial batches, we tailor particle size, crystal form, and packaging.
- Full Regulatory Package – Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), GMP batch record, and optional DMF support.
Our factory, located in Zhengzhou, Henan Province, operates under **ISO 9001, GMP, and HACCP** certifications. All production steps are monitored by an in‑house analytical laboratory equipped with LC‑MS, NMR, and FT‑IR** instruments, guaranteeing data integrity for each lot.
Technical Specification Sheet – CAS 551‑15‑5 Oridonin
| Parameter | Specification |
|---|---|
| CAS Number | 551‑15‑5 |
| Purity (HPLC) | ≥ 99.5 % (±0.2 %) |
| Appearance | White‑off‑white crystalline powder |
| Solubility | 0.5 mg mL⁻¹ in DMSO; 0.1 mg mL⁻¹ in ethanol |
| Heavy Metals (ICP‑MS) | ≤ 10 ppm (Pb, As, Cd, Hg) |
| Residual Solvents (GC‑MS) | < 500 ppm (per ICH Q3C) |
| Packaging | HDPE amber bottles, vacuum‑sealed foil bags, or 25 kg IBCs (customizable) |
| Shelf Life | 24 months (stored ≤ 25 °C, protected from light) |
All specifications are based on the latest batch released in March 2026 and are accompanied by a full analytical report.
Real‑World Applications & Success Stories
Oridonin is a **key natural‑product scaffold** in oncology, immunomodulation, and anti‑viral research. Below are three representative use‑cases where our API delivered measurable ROI.
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1. Oncology Lead Optimization – BioPharmaX (USA)
BioPharmaX required 2 kg of 99.8 % Oridonin for a SAR (Structure‑Activity Relationship) campaign. Our 48‑hour express delivery cut the project timeline by **25 %**, saving an estimated **$120 k** in labor costs. The batch passed all in‑house QC on first pass, eliminating re‑run expenses.
2. GMP‑Compliant Clinical Supply – MedNova Ltd. (Canada)
MedNova needed a GMP‑certified bulk supply for Phase I trials (≈ 150 kg). We provided a **continuous‑feed production schedule** that maintained a steady 99.6 % purity, enabling the sponsor to file IND documents without additional analytical validation. The on‑time delivery contributed to a **30 % faster trial start**.
3. Academic Research – University of Oxford (UK)
The Oxford Oncology Group ordered 5 g of research‑grade Oridonin for mechanistic studies. We supplied a **certificate of analysis with full NMR spectra**, allowing the team to publish their findings in *Nature Chemical Biology* within three months of receipt.
Frequently Asked Questions (FAQ)
What minimum order quantity (MOQ) can you accommodate for Oridonin?
We accept orders as low as **5 g** for research‑grade material and scale up to **tonnage** for commercial production. Custom packaging and documentation are available at any volume.
Is the Oridonin batch GMP‑certified and FDA‑registered?
Yes. Every batch is produced in our **GMP‑approved** line, with a full **FDA‑registered** dossier. We provide the full GMP batch record, CoA, and optional DMF support upon request.
Can you customize the particle size or crystal form of Oridonin?
Absolutely. Our R&D team can produce **micronized** (< 10 µm) or **coarse** (> 100 µm) grades, and we can provide specific polymorphs on a **OEM/ODM** basis.
What are the shipping options and typical delivery times to the United States?
Standard air freight: **3‑5 business days** after production; express courier (DHL, UPS) can deliver within **48 hours** for urgent orders. Sea freight is available for bulk (> 5 t) with a lead time of **30‑35 days**.
Do you offer a free sample for evaluation?
Yes. We provide a **5 g free‑sample kit** (including CoA) for qualified corporate accounts. Shipping is on a **FOB** basis; we cover the cost of the material.
What after‑sales support do you provide?
Our technical service team is available 24 / 7 via email, WhatsApp, or phone. We assist with analytical method transfer, stability testing, and regulatory documentation throughout the product lifecycle.
Secure Your Oridonin Supply – Limited Stock at Introductory Price!
Order **by 31 May 2026** and receive a **10 % discount** on the first 5 kg, plus **free express shipping** to any U.S. port.
Risk‑free guarantee: Free sample, 100 % purity verification, and a 30‑day money‑back promise** if the batch does not meet the CoA.
Or call us directly at +86 199 4383 0844 for an instant quote.
Customer Reviews & Praise
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Emily Rogers (Senior Scientist, Genetech USA) – “The 99.7 % Oridonin batch arrived in 4 days, and the analytical data matched our internal standards perfectly. It saved us **$45 k** in re‑analysis costs.”
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Mark Liu (Procurement Lead, HealthBridge Pharma) – “Global Technology’s OEM service let us obtain a custom micronized Oridonin form that improved our formulation’s solubility by **23 %**.”
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Sofia Martinez (Operations Manager, NorthStar Biologics) – “Fast‑track delivery meant we met our IND filing deadline with two weeks to spare. The compliance package was flawless.”
About the Author
Dr. Victor Chen, Ph.D. – Senior Director of Global Supply Chain at Global Technology Co., Ltd. With **15 years** of experience in API manufacturing, Dr. Chen has led GMP‑compliant projects for Fortune‑500 pharma companies and holds certifications in **GMP, ISO 9001, and FDA regulatory affairs**. He regularly publishes in *Journal of Pharmaceutical Sciences* and is a certified **CPhT** (Certified Pharmaceutical Technologist).
For direct inquiries, reach Dr. Chen at vchen@huanqiukeji9.com or call +86 199 4383 0844.
Trusted By Industry Leaders
“Switching to Global Technology’s Oridonin reduced our material cost by 18 % and cut lead time from 8 weeks to 3 weeks. The purity data matched our internal standards perfectly.” – Dr. Laura Chen, Procurement Manager, BioPharmaX
“The GMP‑certified batch allowed us to file our IND without additional testing, accelerating our Phase I start by one month.” – James Patel, Head of Clinical Supply, MedNova Ltd.
All products are manufactured in facilities holding **CE, FDA, ISO 9001, GMP, HACCP, RoHS, and CB** certifications. Our compliance documentation is available on request, ensuring you meet **U.S. 21 CFR Part 11** and **EU‑FMD** requirements.
Contact Sales for a Compliance Package