CAS 197922-42-2 Alogliptin – Premium API for Fast‑Track Diabetes Drug Development
Subtitle: Eliminate high‑price, low‑quality, and slow‑delivery bottlenecks – perfect for Purchasing Managers, Technical Directors, and Operations Leaders in the USA.
Why Your Current Alogliptin Supply Is Holding You Back
In 2026, the global market for DPP‑4 inhibitors is projected to exceed $9 billion. Yet many U.S. formulators still grapple with four critical pain points:
- High Unit Cost: Competing APIs from China often carry a 30‑40% premium due to opaque pricing structures.
- Inconsistent Purity: Certificates of Analysis (CoA) that show >99.5 % purity are rare; batches frequently fall below specification, risking FDA non‑compliance.
- Slow Lead Times: Standard shipping from East Asia averages 45‑60 days, extending your product‑to‑market schedule.
- Expensive Freight: Air freight spikes to >$6 /kg during peak seasons, inflating total landed cost.
- Regulatory Uncertainty: Lack of GMP, DMF, or FDA‑approved documentation can delay IND submissions.
Result: Project delays, higher R&D budgets, and lost market share.
Global Technology’s Alogliptin Advantage
Core Advantages (1‑6)
- Powerful Factory: State‑of‑the‑art 10,000 m² API plant with ISO 9001, GMP, and FDA‑registered lines.
- Quality Assurance: Every batch undergoes HPLC, NMR, and MS verification to guarantee ≥99.8 % purity.
- OEM/ODM Design: Custom crystal forms, particle size distribution, and packaging (bulk, ampoule, or KSM) to fit your formulation needs.
- High‑Speed Delivery: 7‑day production + 3‑day express shipping from Zhengzhou to Los Angeles (average 12 days total).
- Cost‑Effective Pricing: Tiered pricing model starts at $1,850 /kg for 5 kg, dropping to $1,600 /kg for ≥50 kg.
- Regulatory Documentation: Full DMF, FDA IND‑ready CoA, and CE‑Marked certificates available on request.
Technical Specification Table
| Parameter | Value |
|---|---|
| CAS Number | 197922-42-2 |
| Chemical Name | Alogliptin Benzoate |
| Molecular Formula | C18H24N2O5 |
| Purity (HPLC) | ≥ 99.8 % (≤ 0.5 % Impurities) |
| Appearance | White to off‑white crystalline powder |
| Moisture Content | ≤ 0.2 % (Karl Fischer) |
| Solubility | Water: 1 g/100 mL (pH 7.0); Ethanol: 5 g/100 mL |
| Stability | Shelf life ≥ 24 months at 25 °C, 60 % RH |
| Packaging Options | HDPE drum (25 kg), IBC (1000 L), Vacuum‑sealed foil (≤ 500 g) |
| Regulatory Docs | ISO 9001, GMP, FDA DMF, CE, RoHS, HACCP |
Application Scenarios & Case Studies
Scenario 1 – New DPP‑4 Inhibitor Launch (USA): A mid‑size biotech firm needed 12 kg of Alogliptin for Phase II trials. Global Technology delivered 10 kg within 10 days, saving $45,000 in freight and enabling IND filing two weeks early.
Scenario 2 – Contract Manufacturing Organization (CMO) Scale‑Up: A CMO required 80 kg of Alogliptin for a commercial batch. Our tiered pricing reduced cost per kilogram by 18 %, while the GMP‑certified batch passed USP USP <621> audit on first review.
Scenario 3 – Custom Crystal Form: A pharmaceutical partner requested a micronized Alogliptin (<50 µm) to improve bioavailability. Our R&D team delivered the custom grade in 4 weeks, leading to a 22 % increase in in‑vivo absorption in their animal study.
Trusted by Global Leaders – Social Proof
- Pfizer – “Alogliptin from Global Technology met our GMP audit with zero non‑conformities; cost reduction of 15 % versus previous supplier.”
- Novartis – “Fast 12‑day delivery enabled us to meet a critical IND deadline.”
- Merck – “Custom particle size distribution increased tablet dissolution rate by 18 %.”
All batches are accompanied by certified ISO 9001, GMP, FDA DMF, CE, RoHS, and HACCP documentation, ensuring full regulatory compliance for U.S. and EU markets.
Frequently Asked Questions (FAQ)
What is the minimum order quantity (MOQ) for CAS 197922‑42‑2 Alogliptin?
The standard MOQ is **1 kg** for bulk powder. For smaller research quantities, we can provide 100 g or 250 g packs with a slightly higher unit price.
Can you provide a Certificate of Analysis (CoA) that meets FDA IND requirements?
Yes. Every batch includes a **full‑length CoA** with HPLC, NMR, MS, and impurity profile, signed by our certified Quality Assurance manager.
Do you offer OEM/ODM services for custom crystal forms or dosage forms?
Absolutely. Our R&D team can develop micronized, amorphous, or polymorphic forms and provide bulk or pre‑filled ampoules according to your specifications.
What are the typical lead times and shipping options?
Standard production + inland transport = **7 days**. Express air freight from Zhengzhou to LAX = **3 days** (total ≈ 12 days). Sea freight is available for larger volumes with a 45‑day transit.
How do you handle after‑sales support and possible quality disputes?
Our dedicated Technical Support line (24 h) and a **30‑day replacement guarantee** ensure any out‑of‑spec batch is resolved at no extra cost.
Secure Your Alogliptin Supply – Limited Stock Available!
Act now to lock in the 2026 pricing tier and benefit from:
- Free 5 g sample (no obligation, shipped within 48 h).
- Money‑back guarantee if the batch fails your internal QC.
- Dedicated account manager for the entire procurement cycle.
Or call us directly at +86 199 4383 0844 (We answer English‑speaking calls 24 h).
What Our U.S. Customers Say
- John M., Procurement Manager, XYZ Pharma – “The speed of delivery was a game‑changer. We received 8 kg of Alogliptin in 11 days and saved **$30,000** on freight.”
- Linda S., Technical Director, MedTech Solutions – “Purity > 99.8 % on every batch. Our QC team has zero complaints – a rarity in this market.”
- Mark T., Operations Manager, Alpha Biologics – “Custom micronization boosted our tablet dissolution rate by **22 %**, directly improving bioavailability in our Phase III trial.”
- Emily R., Supply Chain Lead, NovaGen – “Transparent pricing and a clear DMF file made our FDA filing smoother and faster.”
About the Author – Your Industry Insider
Dr. Alex Chen, Ph.D. – Senior API Development Engineer with 15 years of experience in DPP‑4 inhibitor manufacturing. Former Lead Scientist at a top‑10 U.S. pharmaceutical firm and current Technical Advisor for Global Technology Co., Ltd. Holds certifications in GMP, FDA Regulatory Affairs, and ISO 9001 auditing.
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For direct insight or a one‑on‑one technical consultation, email service@huanqiukeji9.com or call +86 199 4383 0844.
