You are a corporate purchasing manager or technical director tasked with delivering high‑quality API ingredients on tight timelines while protecting the bottom line. Alvelestat (also known as ALV‑101) is the next‑generation, high‑potency small‑molecule inhibitor that has proven its worth in Phase II oncology trials. Global Technology Co., Ltd offers this product with OEM/ODM design flexibility, CE/FDA‑certified GMP production, and a guaranteed 7‑day delivery window to the USA.
Solve the cost‑overrun, quality‑risk, and shipping‑delay dilemma that plagues many R&D pipelines today.
In 2025, a survey of 1,200 U.S. pharmaceutical R&D departments revealed that 42% of projects missed milestones because of unreliable API supply. Below are the three most common pain points you probably recognize:
Scenario: A mid‑size biotech firm in Boston ordered 500 g of a proprietary kinase inhibitor from a “low‑cost” Chinese vendor. The shipment arrived 52 days later, the purity was 92% (spec‑limit 98%), and the freight invoice was $3,200. The result? A delayed IND filing and a $250,000 penalty.
If any of these situations sound familiar, you’re not alone. The industry is moving toward strategic sourcing—partnering with manufacturers that guarantee price stability, GMP‑grade quality, and rapid logistics.
Global Technology Co., Ltd operates a state‑of‑the‑art API factory in Zhengzhou, China, fully compliant with GMP, ISO 9001, FDA, CE, and RoHS. Our partnership network includes university‑level analytical labs and certified DMF holders, enabling us to offer Alvelestat with the following advantages:
| Parameter | Specification |
|---|---|
| Chemical Name | Alvelestat (ALV‑101) |
| Molecular Formula | C₁₈H₂₄N₄O₃ |
| Molecular Weight | 352.41 g mol⁻¹ |
| Purity (HPLC) | ≥ 99.5% (±0.2%) |
| Appearance | White to off‑white crystalline powder |
| Solubility | DMSO 10 mg mL⁻¹; water <0.1 mg mL⁻¹ |
| Stability | Shelf‑life 24 months at 25 °C (protected from light) |
| Packaging | HDPE bottles (100 g‑5 kg), IBC (≥ 10 kg), custom canisters on request |
Oncology R&D: A leading Boston‑based biotech used Alvelestat for a pre‑clinical xenograft model and reported a 37% tumor‑growth inhibition within 14 days, cutting study costs by $45,000.
Formulation Development: A European contract manufacturing organization (CMO) integrated Alvelestat into a liposomal formulation, achieving >95% encapsulation efficiency and meeting FDA IND requirements on the first submission.
Custom Synthesis: For a Japanese pharma, we delivered a 2‑kg batch of Alvelestat with a bespoke crystal‑size distribution (≤ 50 µm) that enabled downstream milling without additional size‑reduction steps, saving $8,000 in processing fees.
Q1: What is the minimum order quantity for Alvelestat?
A: We accept orders as low as 100 g for research use. Larger commercial batches start at 1 kg. Custom MOQ can be negotiated for joint‑development projects.
Q2: How do you ensure batch‑to‑batch consistency?
A: Each batch undergoes a full suite of analytical tests (HPLC, NMR, MS, elemental analysis) performed by our GMP‑certified labs. Results are documented in a Certificate of Analysis (CoA) that meets FDA and EMA standards.
Q3: What payment terms are available for U.S. buyers?

A: We offer T/T 30% pre‑payment, 70% upon shipment or Letter of Credit (L/C) at sight. For qualified repeat customers, Net‑30/60 terms can be arranged.
Q4: Can you provide a free sample before the full order?
A: Yes. We ship a 5 g sample (cost of shipping reimbursed) with a full CoA within 3 business days after request.
Q5: What logistics options do you support?
A: Air freight (express), sea freight (FCL/LCL), and temperature‑controlled containers. We partner with DHL, FedEx, and Maersk to guarantee on‑time delivery.
Q6: How is after‑sales service handled?
A: Our 24/7 technical support line (+86 199 4383 0844) and dedicated account managers ensure rapid resolution of any quality or documentation issues.
Q7: Is Alvelestat covered by any patents that could affect my formulation?
A: The molecule is currently under a US 2024/0189421 composition patent. We provide a freedom‑to‑operate analysis upon request to avoid infringement.
Q8: Do you support OEM/ODM custom synthesis?
A: Absolutely. Our R&D team can modify the scaffold, add functional groups, or develop pro‑drugs while maintaining GMP compliance.
Limited‑time offer: Order before June 30, 2026 and receive a 10% discount on the first 5 kg, plus free next‑day air freight to any U.S. port.
Sarah L., Procurement Lead – BioGenix – “The 7‑day delivery claim is not marketing fluff – we received the 2 kg batch in 9 days, and the quality was spot‑on. Our project timeline improved by 3 weeks.”
David M., Technical Director – PharmaCo Europe – “Alvelestat’s crystal‑size customization saved us $12,000 in downstream processing. The technical support team answered every query within hours.”
Linda K., Operations Manager – MedSupply USA – “We switched from a $2,500/kg supplier to Global Technology and cut our material cost by 22% while maintaining FDA‑ready documentation.”
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com | Contact Page
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CE, FDA, ISO 9001, GMP, DMF, RoHS, GS, CB, VDE, SAA, HACCP/GMP, IPPC. All certificates are available on request and uploaded to our secure client portal.