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Postion:Product Catalog >Pharmaceutical intermediates>Heterocyclic compound>5-(2-fluorophenyl)-1H-pyrrole-3-carbonitrile
5-(2-fluorophenyl)-1H-pyrrole-3-carbonitrile
  • 5-(2-fluorophenyl)-1H-pyrrole-3-carbonitrile
  • 5-(2-fluorophenyl)-1H-pyrrole-3-carbonitrile
  • 5-(2-fluorophenyl)-1H-pyrrole-3-carbonitrile

5-(2-fluorophenyl)-1H-pyrrole-3-carbonitrile NEW

Price Get Latest Price
Package 1kg 25kg
Min. Order: 1kg
Supply Ability: 900kg
Update Time: 2025-05-19

Product Details

Product Name: 5-(2-fluorophenyl)-1H-pyrrole-3-carbonitrile CAS No.: 1240948-77-9
Min. Order: 1kg Purity: 0.99
Supply Ability: 900kg Release date: 2025/05/19

?Vonoprazan Fumarate Intermediate (CAS 1240948-77-9)?
Google Keywords: Vonoprazan Intermediate, CAS 1240948-77-9, Gastrointestinal Drug Synthesis, P-CAB API Manufacturing, GMP Pharmaceutical Intermediates


?? ?Product Overview?

?Vonoprazan Fumarate Intermediate? (CAS 1240948-77-9) is a critical high-purity chemical intermediate used in synthesizing ?Vonoprazan Fumarate?, a potassium-competitive acid blocker (P-CAB) approved for treating acid-related gastrointestinal disorders, including gastric ulcers and reflux esophagitis. This intermediate ensures precise and scalable production of the API, aligning with global pharmaceutical quality standards.

  • ?Primary Function?: Key building block for Vonoprazan Fumarate API synthesis, enabling robust and selective chemical transformations.

  • ?Applications?: Gastrointestinal drug development, acid suppression therapies, and large-scale API manufacturing.


? ?Key Advantages?

?? ?Ultra-High Purity? | ≥99.5% (HPLC/GC verified) | Complies with ICH Q11 guidelines for pharmaceutical intermediates.
?? ?Scalable Process? | Optimized for high-yield synthesis (>85% efficiency) with minimal byproducts, reducing production costs.
?? ?Regulatory Ready? | Fully characterized (NMR, HRMS, FTIR) to support FDA/EMA filings and GMP compliance.


?? ?Applications?

  1. ?API Manufacturing?: Enables efficient synthesis of Vonoprazan Fumarate with consistent batch-to-batch quality.

  2. ?Process Development?: Accelerates R&D for optimizing synthetic routes and enhancing production sustainability.

  3. ?Quality Assurance?: Used in analytical method validation and stability testing during API release.


?? ?Quality Assurance?

  • ?Testing Methods?: HPLC, GC, NMR, HRMS, and FTIR for structural verification and impurity profiling.

  • ?Standards?: Meets USP <1086>, EP 10.0, and ISO 9001:2015 certified production protocols.


?? ?Market Trends?

The ?global acid-related disorder treatment market? is projected to reach ?$6.8 billion by 2030? (CAGR 4.9%), driven by rising prevalence of GERD and demand for fast-acting therapies like Vonoprazan. This intermediate supports rapid scaling of P-CAB drug production to meet global healthcare needs.


Power your gastrointestinal drug pipeline with Vonoprazan Fumarate Intermediate – precision-engineered for purity, scalability, and compliance.


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Company Profile Introduction

Wuhan Biocar Pharmaceutical Co., Ltd. is a high-tech and innovative enterprise specializing in the research, development, production, and sales of APIs and pharmaceutical intermediates (excluding finished drugs). Located in the heart of Optics Valley Biological City, our company leverages the cutting-edge facilities of the Wuhan University Scientific Research Laboratory and benefits from the region's favorable policies to advance the field of biomedicine. Guided by our business philosophy—"Driven by market demand, powered by technological innovation, and enabled by e-commerce"—we are committed to delivering biomedical products that are precise, high-quality, fast, and reliable. Our offerings serve pharmaceutical companies, university research institutions, hospital outpatient services, reagent providers, and distributors worldwide.

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