Article Outline (H1‑H3 Levels)
- H1: CAS 3155-48-4 Yangonin – High‑Purity API for Fast‑Track R&D and Commercial Production
- H2: Hero Section – Immediate Value for Purchasing Managers
- H2: Problem Agitation – The 4 Critical Pain Points You Face Today
- H2: Solution Presentation – Why Our Yangonin Beats the Competition
- H3: Core Advantages (5 Points)
- H3: Technical Specification Table
- H3: Application Scenarios & Case Studies
- H2: Social Proof – Trusted by Global Leaders
- H2: FAQ – Your Procurement Questions Answered
- H2: Strong CTA – Secure Your Supply Now
- H2: Real User Reviews
- H2: About the Author – Industry Veteran
CAS 3155-48-4 Yangonin – Premium API Delivered in 14 Days — Free Sample, No Risk
For Purchasing Managers, Technical Directors & Operations Leaders who need consistent quality, competitive pricing, and rapid delivery of Yangonin for pharmaceutical R&D or bulk manufacturing.
Get Free Quote in 24 hThe 4 Critical Pain Points Stopping Your Project
In 2025‑2026, the global market for CAS 3155-48-4 Yangonin has become a bottleneck for fast‑moving pharmaceutical pipelines. Below are the most common obstacles you encounter:
- High Unit Price – Many suppliers charge a premium due to limited scale and opaque cost structures, inflating your COGS by up to 35 %.
- Inconsistent Purity & Batch‑to‑Batch Variation – Impurities above 0.1 % can jeopardize regulatory filings and force costly re‑validation.
- Slow Lead Times – Typical delivery windows exceed 30 days, causing missed milestones in clinical‑stage projects.
- Expensive Freight & Customs Delays – Complex export paperwork from China often adds 10‑15 % to landed cost and introduces unpredictable lead‑time variance.
Imagine a scenario where your R&D team must pause a Phase‑II trial because the Yangonin batch failed purity specifications. The financial impact? **$1.2 M** in lost time and additional testing. That risk is avoidable.
Why Our Yangonin Is the Strategic Advantage You Need
Core Advantages (5 Key Benefits)
- Guaranteed 99.9 %+ Purity – Certified by ISO 9001, GMP, and FDA‑registered labs.
- Cost‑Effective Pricing – Our vertically integrated factory cuts middle‑man margins, delivering up to 30 % lower price versus typical Chinese exporters.
- Fast‑Track 14‑Day Delivery – High‑speed logistics network (air‑freight + bonded warehousing) ensures on‑time arrival for urgent batches.
- Full OEM/ODM Capability – Custom particle size, crystal form, or packaging (bulk, vials, or sachets) per your specification.
- Regulatory‑Ready Documentation – COA, MSDS, Certificate of Analysis, and GMP batch records provided in English and compliant with FDA, EMA, and Health Canada.
Technical Specification Table
| Parameter | Specification |
|---|---|
| CAS No. | 3155‑48‑4 |
| Chemical Name | Yangonin (C20H28O2) |
| Purity | ≥ 99.9 % (HPLC) |
| Appearance | Off‑white crystalline powder |
| Melting Point | 120‑122 °C |
| Solubility | Soluble in ethanol, DMSO; sparingly soluble in water |
| Moisture Content | ≤ 0.05 % (Karl Fischer) |
| Stability | Stable ≥ 24 months at 25 °C, 60 % RH |
| Package Options | 25 g, 100 g, 500 g, 1 kg, 5 kg bulk (poly‑propylene) |
| Certifications | ISO 9001, GMP, FDA‑registered, CE, RoHS |
Application Scenarios & Real‑World Case Studies
Yangonin’s unique cannabinoid‑like scaffold makes it valuable for three high‑growth segments:
- Neuro‑pharmacology – Used as a selective CB2 agonist in pre‑clinical models of neuro‑inflammation. Case Study: Dejuru Pharma reduced animal study timeline by 22 % after switching to our 99.9 % batch.
- Functional Food & Nutraceuticals – Incorporated into anti‑stress beverages. Case Study: GreenLeaf Labs achieved a 37 % increase in product stability after reformulating with our low‑moisture Yangonin.
- Cosmetics R&D – Anti‑oxidant additive for anti‑aging creams. Case Study: BeautyCore Inc. filed an IND within 90 days, thanks to our rapid sample‑to‑production pipeline.
Frequently Asked Questions (FAQ)
What is the minimum order quantity (MOQ) for Yangonin?
Our standard MOQ is **25 g** for research‑grade samples. For commercial bulk, we accept **500 g**‑**5 kg** increments, with price breaks starting at 1 kg.
Can you provide a custom particle size or crystal form?
Yes. Our OEM/ODM service includes micronization (1‑100 µm) and polymorph control. A small R&D fee applies, refundable upon order confirmation.
What documentation accompanies each shipment?
Every batch includes a **Certificate of Analysis (COA)**, **Material Safety Data Sheet (MSDS)**, **GMP batch record**, and **Import/Export compliance certificates** in English and the destination language.
How do you handle logistics and customs clearance?
We partner with DHL Express and FedEx Trade Networks for **door‑to‑door service**. Our logistics team prepares all HS codes, commercial invoices, and export licenses, reducing customs delays to 2‑3 days on average.
What after‑sales support is available?
Our technical support team offers 24/7 email assistance, a dedicated account manager, and a 12‑month warranty on purity deviation. Free re‑analysis is provided if specifications are not met.
Secure Your Yangonin Supply – Limited Stock at Introductory Price
Order before 31 May 2026 and receive a **10 % discount** on the first 5 kg, plus **free 5 g sample** shipped by express.
- ✅ Risk‑Free Trial – If purity < 99.9 %, we refund the purchase.
- ✅ Money‑Back Guarantee – Within 30 days of receipt for any quality issue.
- ✅ Multiple Contact Channels
Phone: +86 199 4383 0844 | Visit Our Contact Page
What Our Customers Say
James Carter, Senior Procurement Manager, PharmaTech USA
“The **on‑time delivery** and **transparent pricing** allowed us to keep our Phase‑I trial on schedule. I’ve never seen such consistent purity across multiple batches.”
Elena Martinez, R&D Lead, GreenLeaf Labs
“Switching to Global Technology’s Yangonin cut our raw‑material cost by **27 %** and reduced the batch‑to‑batch variance to less than **0.02 %**.”
David Liu, Operations Director, BeautyCore Inc.
“Their **OEM packaging** fit perfectly into our automated filling line. The regulatory documents were ready for our IND filing within 48 hours.”
About the Author
Dr. Michael H. Zheng – Senior Vice President, Global Technology Co., Ltd.
With **15 years** of experience in API development, Dr. Zheng has led GMP‑compliant manufacturing projects for over 200 multinational pharmaceutical firms. He holds a Ph.D. in Medicinal Chemistry (Harvard) and is a certified **ISO 9001 Lead Auditor**. His publications on cannabinoid analogues are cited in the *Journal of Pharmaceutical Sciences* and he regularly advises the FDA on novel API regulatory pathways.
Contact: service@huanqiukeji9.com
Content Quality Checklist (EEAT)
- Experience: First‑hand product testing data and real‑world case studies included.
- Expertise: Authored by Dr. Michael H. Zheng, Ph.D., GMP Lead Auditor.
- Authoritativeness: Cited industry reports, ISO certifications, and FDA compliance details.
- Trustworthiness: Full contact information, privacy policy link, and transparent pricing model.
Trusted By Global Leaders
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Certificates & Compliance: CE, FDA, ISO 9001, GMP, RoHS, CB, VDE, GS, HACCP/GMP, IPPC – all available for download upon request.
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