
5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbonitrile
Price | Get Latest Price | |
Package | 1kg | 25kg |
Min. Order: | 1kg |
Supply Ability: | 800kg |
Update Time: | 2025-05-19 |
Product Details
Product Name: 5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbonitrile | CAS No.: 881677-11-8 |
Min. Order: 1kg | Purity: 0.99 |
Supply Ability: 800kg | Release date: 2025/05/19 |
?Vonoprazan Fumarate Intermediate 2 (CAS 881677-11-8) | High-Purity Building Block for Gastric Drug API Synthesis?
?Google Search Keywords?: Vonoprazan Fumarate Intermediate 2, CAS 881677-11-8, Vonoprazan Synthesis Material, P-CAB Intermediate, Gastric Drug API Precursor
?? ?Product Overview?
Vonoprazan Fumarate Intermediate 2 (CAS 881677-11-8) is a critical chemical component in the synthesis of ?Vonoprazan Fumarate?, a next-generation potassium-competitive acid blocker (P-CAB) used to treat gastric acid-related disorders like gastroesophageal reflux disease (GERD) and peptic ulcers. This intermediate ensures efficient and high-yield production of Vonoprazan Fumarate API, meeting stringent pharmaceutical quality requirements.
?Primary Function?: Enables scalable and impurity-controlled synthesis of Vonoprazan Fumarate API.
?Applications?: Gastrointestinal drug manufacturing, generic P-CAB development, clinical research.
? ?Key Advantages?
? ?Ultra-High Purity?
Purity ≥99% (HPLC/LC-MS validated), minimizing unwanted byproducts and ensuring API quality.
?? ?Optimized Process Efficiency?
Reduces synthesis time by 15-25% through streamlined reaction pathways, enhancing cost-effectiveness.
??? ?Enhanced Stability?
Stable at controlled room temperature (15-25°C), suitable for global logistics and extended storage.
?? ?Regulatory Readiness?
Manufactured under ?ICH Q7? and ?GMP? guidelines, compliant with USP/EP standards for intermediates.
?? ?Applications?
?API Production?: Key precursor in Vonoprazan Fumarate API synthesis for acid suppression therapies.
?Generic Drug Formulations?: Supports cost-effective alternatives to branded P-CAB medications.
?Digestive Health R&D?: Used to study novel P-CAB derivatives with improved pharmacokinetics.
?Clinical Trial Materials?: Critical for scaling up batches during pre-clinical and Phase I-III trials.
?? ?Quality Certifications?
Rigorously tested via ?HPLC, GC, NMR, and Mass Spectrometry? (USP/EP/ICH compliant).
Comprehensive Certificate of Analysis (CoA) with impurity profiles, spectral data, and chromatograms.
?? ?Market Trends?
The global gastric acid-related drug market is projected to grow at ?6.8% CAGR (2024-2030)?, driven by rising GERD prevalence and demand for potent P-CABs like Vonoprazan. Intermediate suppliers are crucial to meeting production needs, especially in Asia-Pacific markets where generic approvals are accelerating.
?? ?Why Choose Us??
?Custom Synthesis?: Tailored purity grades (98%-99.9%) and batch sizes (mg to kg scale).
?Fast Delivery?: Temperature-controlled shipping with real-time tracking and regulatory documentation.
?Technical Expertise?: End-to-end support for API synthesis, impurity control, and regulatory filings.
Company Profile Introduction
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