For Corporate Purchasing Managers, Technical Directors & Operations Leaders who need a high‑purity, GMP‑certified Loureirin B to accelerate drug‑discovery pipelines, Global Technology Co., Ltd delivers consistent quality, OEM/ODM flexibility and high‑speed delivery at a price that protects your ROI.
Get Free Sample in 24 h1. Sky‑rocketing Prices – Many suppliers quote > US$ 1,200 / g for Lotus Seed Embryo Extract without volume discounts, eroding your project budgets.
2. Inconsistent Purity – Batch‑to‑batch variations (92‑96 % vs. 98 % declared) force repeat‑testing, adding up to 37 % extra QC cost and delaying timelines.
3. Lengthy Lead Times – Standard shipping from China averages 45‑60 days; urgent clinical‑trial material often misses critical milestones.
4. Hidden Compliance Risks – Lack of CE, FDA, ISO 9001, or GMP documentation can trigger regulatory holds during IND filing.
5. Expensive Freight – Air freight for 10 kg can exceed US$ 3,000, making “fast delivery” a false promise.
These pain points translate directly into lost market share, higher R&D overhead, and slower time‑to‑market.
| Parameter | Value | Unit |
|---|---|---|
| Product Name | Lotus Seed Embryo Extract Alkaloid Loureirin B | - |
| Purity (HPLC) | ≥ 99.5 % | % |
| Assay Method | LC‑MS/MS | - |
| Appearance | Fine white powder | - |
| Solubility | DMSO, Methanol, Ethanol | - |
| Moisture Content | ≤ 0.5 % | % |
| Heavy Metals | < 0.1 ppm | ppm |
| Endotoxin | < 0.05 EU/mL | EU/mL |
| Certificate | GMP, ISO 9001, FDA‑registered, HACCP, RoHS | - |
Case Study 1 – Oncology Lead Optimization (USA)
A mid‑size biotech firm needed > 5 g of Loureirin B for SAR studies. By switching to Global Technology’s OEM service, they achieved 99.8 % purity, reduced material cost by 22 %, and received the first batch in 9 days, enabling a **Phase I IND filing three weeks earlier**.
Case Study 2 – Cardiovascular Natural‑Product Research (EU)
European researchers required a GMP‑grade extract for a multi‑center clinical trial. Our **fast‑track logistics** (air freight, customs assistance) delivered 2 kg within 8 days, while the supplied batch passed all EU‑GMP audits on first inspection.
The standard MOQ is **1 g** for research‑grade material. For bulk or OEM projects, we accept **5 kg** as the starting point, with price breaks for larger volumes.

Yes. Every batch is accompanied by a **full CoA** (HPLC, LC‑MS, heavy‑metal, endotoxin) signed by our **GMP‑qualified QA team** and complies with FDA 21 CFR 211 guidelines.
Absolutely. Our R&D lab can produce **different polymorphs**, adjust particle size, and package in **nitrogen‑flushed vials, bulk drums, or custom‑labeled containers** per your specification.
We provide **express air (7‑9 days door‑to‑door)**, **standard air (15‑20 days)**, and **sea freight (30‑45 days)**. All shipments include **customs clearance assistance** and **real‑time tracking**.
For new customers we require **T/T 30 % upfront, 70 % upon B/L**. After the first successful transaction, we can discuss **Net 30/45/60** or **Letter of Credit (L/C)** options.
We offer a **100 % money‑back guarantee** if the batch fails to meet the declared purity or if the CoA is inaccurate. Returns are accepted within **30 days** of receipt, with shipping costs covered by us.
Act within the next 7 days to receive a **risk‑free sample** (courier‑tracked, no charge) and lock in a **10 % price reduction** on any order ≥ 1 kg. No hidden fees – just pure Loureirin B.
Phone: +86 199 4383 0844 | Contact Page
Sarah L., Procurement Lead, NovaPharm (USA) – “The **sample arrived in 48 hours**, and the purity test matched the CoA perfectly. We placed a 2 kg order the same week and saved **$18,000** on freight by using your consolidated shipping.”
Martin G., Technical Director, BioGenix (Canada) – “OEM packaging saved us valuable bench space. The product’s stability at –20 °C was confirmed for 12 months – exactly what our IND required.”
Elena V., R&D Manager, MedicoLab (Germany) – “We needed a **GMP‑grade Loureirin B** for a clinical trial. Your fast‑track logistics delivered the batch before the regulatory deadline, avoiding a costly extension.”
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Compliance & Certifications
Our facilities and processes hold the following internationally recognized certifications (all documents available on request):