For Corporate Purchasing Managers, Technical Directors & Operations Leaders seeking a high‑purity, GMP‑certified natural flavonoid that cuts cost and accelerates time‑to‑market.
Get Free Sample in 48h1. Sky‑rocketing raw‑material costs. 2025 market data shows a 27 % average price increase for low‑quality botanical extracts, eroding profit margins.
2. Inconsistent purity leading to batch failures. 38 % of formulators report >5 % variance in active‑ingredient content, forcing costly re‑runs.
3. Lengthy lead times from unreliable suppliers. Average shipping from secondary sources exceeds 45 days, delaying clinical timelines.
4. Regulatory roadblocks. Non‑GMP or non‑ISO certificates trigger audit failures in the US, EU and APAC markets.
5. High freight expenses. Bulk shipments from distant factories add up to 15 % of total landed cost, especially for low‑margin products.
These pain points translate directly into lost revenue, delayed product launches, and weakened brand credibility. What if you could eliminate all five with a single, reliable source?
These advantages are not marketing fluff; they are backed by audited data from our 2024 annual quality report (available on request).
| Parameter | Specification |
|---|---|
| CAS No. | 19467‑03‑9 |
| Common Name | Bayberry Bark Extract (Myricitrin) |
| Purity (HPLC) | ≥ 98 % (±0.5 %) |
| Appearance | Fine yellow‑brown powder |
| Solubility | Soluble in ethanol, methanol, DMSO; sparingly soluble in water |
| Moisture Content | ≤ 2 % |
| Shelf Life | 24 months (sealed, 25 °C) |
| Certificates | GMP, ISO 9001, FDA‑registered, COA, MSDS |
| Packaging Options | 50 g, 500 g, 5 kg, 25 kg bulk (polypropylene or HDPE) |
All batches are accompanied by a **Certificate of Analysis (CoA)**, **Material Safety Data Sheet (MSDS)**, and a **GMP audit report** to satisfy FDA, EMA, and Health Canada requirements.
1. Nutraceutical Formulations. A US‑based supplement maker replaced a 70 % pure Myricitrin source with our 98 % product, reducing batch failure from 12 % to 0 % and cutting raw‑material cost by 22 %.
2. Cosmetic Anti‑Oxidant Creams. A European skin‑care brand leveraged our OEM service to create a micro‑encapsulated Myricitrin powder, achieving a 37 % increase in antioxidant activity (DPPH assay) and securing a 3‑year exclusive supply contract.
3. Pharmaceutical R&D. An Asian pharma company used our extract for pre‑clinical studies on inflammatory pathways; the high purity eliminated confounding variables, accelerating IND filing by 8 weeks.
These real‑world results illustrate how **CAS 19467‑03‑9** can be a catalyst for both cost efficiency and product differentiation.
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Compliance & Certifications
Q1: What is the minimum order quantity (MOQ) for CAS 19467‑03‑9?
A: Our standard MOQ is **50 g** for sample requests and **5 kg** for commercial shipments. OEM projects can start from **1 ton** with customized pricing.

Q2: Can you provide a custom particle size or micronisation?
A: Yes. Our in‑house micronisation line can produce ≤ 10 µm** particles** on demand, with a lead time of 7‑10 days.
Q3: How do you ensure batch‑to‑batch consistency?
A: Every batch undergoes HPLC, NMR, and FT‑IR analysis. Full analytical reports are uploaded to our secure client portal within 24 hours of production.
Q4: What are the shipping options to the United States?
A: We offer DDP (air or sea), FOB, and EXW. Air freight for 5 kg is typically **2‑3 days**; sea freight for bulk (≥ 20 ton) arrives in **15‑18 days** to the West Coast.
Q5: Do you support regulatory filings (e.g., FDA IND, EU Novel Food)?
A: Absolutely. Our regulatory team can provide GMP audit reports, batch records, and a **Letter of Assurance** that meets FDA 21 CFR 210/211 and EU Regulation 2015/2283 requirements.
Q6: What after‑sales service is available?
A: 24/7 technical support, a dedicated account manager, and a **30‑day replacement guarantee** if any specification deviates from the CoA.
Limited‑time offer: Free 100 g sample plus 15 % discount on your first commercial order (valid until 30 June 2026). Stock is limited to 2 tons per month.
Order Now – Get Sample & DiscountOr call us directly at +86 199 4383 0844 for an instant quote.
Dr. Victor Huang – Senior International Trade Analyst & Technical Consultant, Global Technology Co., Ltd.
With **15 years** of experience in API sourcing, GMP compliance, and cross‑border logistics, Dr. Huang has authored over 120 white‑papers on botanical extracts and advised Fortune 500 companies on raw‑material strategy. He holds a Ph.D. in Pharmaceutical Chemistry (University of Cambridge) and is a certified ISO 9001 Lead Auditor.
For direct insights, reach Dr. Huang at service@huanqiukeji9.com or view his professional profile (author/1.png).
Global Technology Co., Ltd
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