1-Cyclopropyl-6-Fluoro-1,4-Dihydro-4-Oxo-7-(1-Piperazinyl)- Quinoline Intermediate

Fluoro

Product Overview

    • 1-Cyclopropyl-6-Fluoro-1,4-Dihydro-4-Oxo-7-(1-Piperazinyl)- Quinoline Intermediate, widely identified across international active drug compounding systems as Ciprofloxacin Acid or Cipro Core Intermediate, is a premier synthetic fluoroquinolone organofluorine active compound matrix. Structurally, it fuses a highly functionalized 4-oxoquinoline core ring system substituted with a cyclopropyl ring at position-1, a fluorine atom at position-6, a piperazinyl block at position-7, and a terminal carboxylic acid group at position-3. ProCorBay International directs massive industrial bulk logistics lines of premium, pharmacopoeial-grade and technical-grade Ciprofloxacin intermediates to generic medicine factories, contract blending lines, and anti-infective dosage plants globally.
    • This advanced intermediate compound is typically manufactured through the complex multi-step organic synthesis assembly linking fluorinated nitrobenzoic acids with cyclopropylamine, followed by internal cyclic condensation to build the quinoline nucleus, selective nucleophilic substitution at position-7 using anhydrous piperazine complexes, and high-precision acid precipitation. ProCorBay coordinates strategic supply tracks exclusively with world-class, GMP-aligned chemical refineries to deliver material featuring ultra-low decarboxylated byproduct traces, zero heavy metal profiles, and exceptional particle distribution parameters.
    • Within the global anti-infective healthcare framework, this bicyclic fluoroquinolone core represents an indispensable regulatory milestone. It acts as the direct regulatory structural predecessor and certified analytical reference standard for manufacturing the blockbuster broad-spectrum antibiotic Ciprofloxacin Hydrochloride. The localized fluorine and piperazine configurations deliver highly targeted bacterial DNA gyrase and topoisomerase IV enzyme inhibition pathways when converted into the finalized dosage salt form. ProCorBay handles deep, multi-ton inventory lines to guarantee commercial pricing safety and reliable supply continuity for leading generic medicine brands.

Applications

    • API Finished Synthesis: Core active raw input and advanced regulatory intermediate utilized to manufacture generic Ciprofloxacin Hydrochloride tablets, eye drops, and intravenous liquid infusions.
    • Analytical Reference Standards: Key tracking compound used for high-performance liquid chromatography (HPLC) validation methods and systematic impurity profiling.

Benefits

    • Targeted Fluoroquinolone Core: Provides the exact chemical heterocyclic framework required for step-efficient broad-spectrum antibiotic compounding.
    • High Chemical Assay: ≥ 99.0% high active purity minimizes processing catalyst residues, streamlining lab validations.
    • Low Volatile Residues: Advanced vacuum drying loops eliminate unreacted piperazine traces and volatile reaction artifacts completely.
    • Optimized Granulometry: Regular granular properties ensure uniform blending traits inside automated factory direct-compression and wet-granulation setups.
    • Comprehensive Regulatory Files: Backed by deep technical validation records, including verified NMR mappings, to ease registration pathways.

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Frequently Asked Questions

No. This is the pure free acid core matrix (Ciprofloxacin Base); it requires downstream salt formation using hydrochloric acid solutions to match finalized dosage monograph lines.

Fluoroquinolone ring architectures naturally exhibit subtle, light-yellow color shades due to their dense conjugated electron system. This is fully within normal specification baselines.