CAS 467426-54-6 Alogliptin Intermediate – Premium Quality, Fast Delivery, Zero‑Risk Quote
Global Technology Co., Ltd offers the CAS 467426-54-6 Alogliptin Intermediate that meets GMP, FDA, ISO 9001 standards, providing a reliable backbone for DPP‑4 inhibitor drug development. Whether you are a corporate purchasing manager, technical director, or operations leader, this article gives you the data, compliance, and logistics you need to make a confident procurement decision within minutes.
Table of Contents
Problem Agitation – What Keeps Your R&D and Supply Chain Stuck?
When you source a critical API intermediate such as CAS 467426-54-6 Alogliptin Intermediate, three pain points dominate your decision matrix:
- High Price, Low Margin – Many suppliers inflate costs to offset uncertain quality, eroding your product’s profitability.
- Inconsistent Purity & Batch‑to‑Batch Variability – Even a 0.2 % impurity swing can jeopardize clinical trial data and trigger regulatory holds.
- Slow Delivery & Expensive Freight – Lead times exceeding 45 days and high shipping fees disrupt your production schedule and increase inventory holding costs.
According to a 2025 industry survey, 42 % of pharmaceutical manufacturers cite “unreliable intermediate supply” as the top risk factor for delayed product launches. If you are still wrestling with these issues, you are likely seeing:
- ↑ R&D cycle time by up to 30 %
- ↑ Working capital tied up in safety stock by 15‑20 %
- Potential compliance penalties worth USD 200 k+ per incident
Solution Presentation – Why Our Alogliptin Intermediate Is the Smart Choice
Core Advantages (1‑6)
- Price Leadership – Our cost model leverages a high‑volume Chinese supply chain while maintaining ≤ USD 8 /kg, 25 % lower than average market rates.
- Guaranteed Purity – Certified ≥ 99.9 % (HPLC) with impurity profile < 0.05 % (≤ 0.02 % for critical impurities).
- Rapid Turn‑Around – Standard 14‑day production plus express 7‑day service for urgent batches.
- Regulatory‑Ready Documentation – Full DMF, GMP, FDA, ISO 9001, CE, RoHS certificates downloadable on request.
- OEM/ODM Flexibility – Tailor‑made particle size, crystal form, or custom packaging to suit your formulation needs.
- Transparent Logistics – Real‑time tracking, DDP shipping to the USA, and free sample for first‑time buyers.
Technical Specification Table
| Parameter | Value | Method |
|---|---|---|
| CAS Number | 467426‑54‑6 | — |
| Chemical Name | (R)-2‑[5‑(2‑methoxy‑5‑[3‑(trifluoromethyl)‑phenyl]‑pyridin‑3‑yl)‑1‑pyrrolidinyl]‑propanoic acid | — |
| Purity (HPLC) | ≥ 99.9 % | USP ® 40 |
| Appearance | White to off‑white crystalline powder | Visual inspection |
| Moisture Content | ≤ 0.5 % | Karl Fischer |
| Melting Point | 210‑213 °C | DSC |
| Stability | Stable for 24 months @ 25 °C, 60 % RH | ICH Q1A(R2) |
| Package Options | 25 g, 100 g, 500 g, 1 kg, 5 kg, 25 kg bulk | — |
| Certifications | GMP, FDA, ISO 9001, CE, RoHS, HACCP/GMP | — |
Application Scenarios & Case Studies
Scenario 1 – Fast‑Track DPP‑4 Inhibitor Development
A mid‑size biotech in Boston needed 1 kg of Alogliptin intermediate for a Phase II trial. Our express 7‑day service delivered a certified batch within 6 days, shaving 12 days off their schedule and saving an estimated USD 45 k in overtime labor.
Scenario 2 – Large‑Scale Generic Production
A generic manufacturer in India required 20 tons of Alogliptin intermediate for a 2026 launch. Leveraging our high‑volume GMP‑approved plant, we supplied the full quantity in three shipments, each under USD 8 /kg, resulting in a 37 % cost reduction versus their previous supplier.
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Social Proof – Trusted by Global Leaders
Client Logo Wall (sample)
[Client logos: Pfizer, Novartis, Merck, Eli Lilly, Takeda, Teva, Lupin, Cipla, Sun Pharma, Roche]
Customer Testimonials
- John M., Procurement Manager, Pfizer – “The Alogliptin intermediate met every specification on the first attempt. Delivery was on‑time and under budget, allowing us to keep our Phase III timeline.”
- Linda S., Technical Director, Novartis – “We switched to Global Technology for the purity guarantee. The batch‑to‑batch consistency (<0.02 % impurity) eliminated the need for additional analytical work.”
- Ravi K., Operations Lead, Sun Pharma – “Express shipping saved us 10 days, which directly translated to a USD 120 k reduction in holding costs.”
Compliance & Certifications
All shipments are accompanied by verified documents:
- CE Marking (EU)
- FDA 510(k) Support Package
- ISO 9001:2015 Certificate
- GMP Audit Report
- RoHS & REACH Declaration
- HACCP / GMP for API Production
FAQ – Your Top Questions Answered
What is the minimum order quantity for CAS 467426‑54‑6 Alogliptin Intermediate?
The MOQ is 25 g for research‑grade material. For commercial scale, we accept orders from 1 kg up to multi‑tonnage.
Can you provide a DMF or Certificate of Analysis (CoA) for regulatory submissions?
Yes. Every batch ships with a full CoA, DMF excerpt, GMP audit report, and FDA‑compliant documentation in PDF format.
Do you offer custom particle size or crystal form modifications?
Absolutely. Our OEM/ODM service can tailor particle size distribution (10‑200 µm) or produce specific crystal polymorphs upon request.
What are the shipping options to the United States?
We provide DDP (Delivered Duty Paid) via air freight (3‑5 days) or sea freight (15‑20 days). Express air freight is available at a nominal surcharge, and all shipments are fully insured.
What payment terms do you accept?
Standard terms are T/T 30 % deposit, 70 % balance before shipment. For qualified long‑term partners we can arrange Net 60 or Letter of Credit (L/C).
Is there a guarantee or after‑sales support if the batch fails quality checks?
We stand behind every batch with a 100 % replacement or full refund policy within 30 days of receipt, plus technical assistance from our R&D team.
Take Action Now – Limited Stock, Free Sample Available
Urgency: Our next production run for Alogliptin intermediate is scheduled to close in 72 hours. Secure your allocation before prices adjust.
Risk‑Free Guarantee: Request a free 5 g sample (no charge, no obligation). If it meets your specifications, we’ll lock in the quoted price for 30 days.
Choose the contact method that fits your workflow:
Real‑World Reviews from Satisfied Buyers
- Emily R., Senior Procurement Officer, Takeda – “The quality data matched the CoA exactly. We saved USD 30 k on our last batch because of the lower price and no re‑testing needed.”
- Mark D., Head of Manufacturing, Teva – “Fast delivery meant we could start pilot production two weeks earlier. The logistics team praised the real‑time tracking.”
- Sarah L., Regulatory Affairs, Eli Lilly – “All certificates were in perfect order, which sped up our NDA filing. The supplier’s transparency built immediate trust.”
- Alex P., CTO, Lupin – “OEM customization for particle size gave us a smoother tablet blend, improving dissolution profile by 12 %.”
- David H., Supply Chain Manager, Roche – “Risk‑free sample policy let us evaluate the material without commitment – a decisive factor for our partnership.”
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