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5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine

    • Product Name 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine
    • Alias KNX-002
    • Einecs 629-949-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    273211

    Iupac Name 5-(4-Fluorophenyl)-1H-pyrazol-3-amine
    Molecular Formula C9H8FN3
    Molecular Weight 177.18 g/mol
    Cas Number 864025-11-2
    Appearance Solid (typically off-white to pale yellow powder)
    Melting Point 140-144 °C
    Solubility Soluble in DMSO, slightly soluble in methanol, ethanol
    Smiles C1=CC(=CC=C1C2=CC(=NN2)N)F
    Inchi InChI=1S/C9H8FN3/c10-7-3-1-6(2-4-7)8-5-9(11)13-12-8/h1-5H,11H2,(H,12,13)
    Storage Conditions Store at 2-8 °C, keep container tightly closed
    Purity Typically ≥98%
    Synonyms 4-Fluoro-5-(phenyl)-1H-pyrazol-3-amine

    As an accredited 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Opaque amber glass bottle containing 25 grams of 5-(4-Fluorophenyl)-2H-pyrazol-3-ylamine, labeled with hazard warnings and product details.
    Shipping 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine is shipped in tightly sealed containers, protected from moisture and light, and labeled according to chemical safety regulations. It is transported in compliance with local and international hazardous materials guidelines to ensure safe delivery, with all necessary documentation and safety data sheets included in the shipment.
    Storage Store **5-(4-Fluorophenyl)-2H-pyrazol-3-ylamine** in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and restrict access to authorized personnel. Use personal protective equipment (PPE) when handling to avoid inhalation, ingestion, or direct skin contact.
    Application of 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine

    Applications of 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine in Industrial Manufacturing

    As an established manufacturer of advanced pyrazole derivatives, we supply 5-(4-Fluorophenyl)-2H-Pyrazol-3-Ylamine for specialized applications across the agrochemical, pharmaceutical, dyes, and specialty chemical industries. Each segment below details exact usage contexts, covering regulatory standards, formulation requirements, process integration steps, and the definitive end-uses where this intermediate plays a critical role.

    1. Agrochemical Active Ingredient Synthesis (Herbicides & Fungicides)

    Our material is a key intermediate in the synthesis of certain next-generation crop protection actives. Downstream producers use its pyrazole core to introduce selective weed and fungal resistance properties, especially relevant in high-value fruit and grain production. Its structure allows for targeted functionalization, compatibly integrating with other moieties to build novel agrochemical scaffolds where controlled bioactivity and low mammalian toxicity are essential.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidance for active substance quality and impurities
    • REACH Regulation (EC) No 1907/2006, Annex XVII for restricted substances
    • US EPA OPPTS Harmonized Test Guidelines for pesticide registration intermediates
    • ISO 9001:2015 quality management systems for documented traceability

    Typical usage ratio

    • 15–30% of total agrochemical precursor batch (ratio depends on downstream coupling and derivatization reactions with heterocyclic partners)

    Downstream process integration

    • The intermediate enters as the pyrazole amine core during the second step of multi-stage synthesis—commonly via nucleophilic substitution, then carried into cyclization or acylation sequences under controlled temperature/reaction time conditions

    Final product types

    • Aromatic pyrazole-based herbicides (including selective post-emergent formulas)
    • Systemic fungicide actives targeting triazole resistance strains
    • Customized crop protection agents for cereal and horticultural applications

    2. Pharmaceutical API Intermediate (Antiinflammatory & CNS Compounds)

    This compound serves as an advanced building block in the pharmaceutical sector, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and emerging central nervous system (CNS) therapeutics that target pyrazole receptors. Its fluorinated aromatic ring supports molecular stability and bioavailability profiles needed for regulatory approval in regulated drug synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for active pharmaceutical ingredient intermediates
    • Ph. Eur. (European Pharmacopoeia) 10.0, general monographs for process chemicals
    • US FDA 21 CFR Part 211 for process controls and trace residue limits
    • Japanese Pharmacopeia (JP) for import/export and purity documentation

    Typical usage ratio

    • 20–35% of API precursor batch size (dosage is adjusted based on coupling partner reactivity, especially for pyrazole-ring closure stages)

    Downstream process integration

    • Introduced as an amine nucleophile during protected coupling or direct condensation, preceding final API crystallization and purification steps under GMP-compliant conditions; handled in contained reactors to avoid cross-contamination

    Final product types

    • Active pharmaceutical ingredients in advanced anti-inflammatory drug synthesis
    • Pyrazolyl-aryl CNS actives (anticonvulsant, anxiolytic, and neuroprotective agents)
    • Clinical trial intermediates for oncology pipeline molecules

    3. High-Performance Dye Intermediate (Organic Pigments)

    Major pigment and dye manufacturers use this compound to achieve highly stable color tones and resistance to photobleaching in specialty textile and plastic masterbatches. The fluorinated pyrazole scaffold supports the synthesis of advanced diazo and azo dyes used in the demanding automotive, fashion, and packaging sectors, where colorfastness is non-negotiable.

    Industry compliance standards

    • OEKO-TEX Standard 100 annex chemical restrictions
    • EN 71-3 (European Toy Safety Directive) for dye migration in finished plastics
    • ISO 2846-1 for pigment performance in ink and print systems
    • Global Organic Textile Standard (GOTS) for textile applications

    Typical usage ratio

    • 10–20% of pigment precursor formulation (subject to chromophore optimization, batch-scale validation)

    Downstream process integration

    • Used in the diazotization step to modify colorant scaffolds; enters during intermediary coupling before subsequent sulfonation or halogenation stages in strict batch reactor environments

    Final product types

    • High-stability organic pigments for plastics compounding
    • Direct and reactive textile dyes (high-washfastness grades)
    • Solvent dyes for automotive and industrial coatings

    4. Specialty Chemical Building Block (Heterocycle Synthesis & Electronic Materials)

    Our pyrazole compound is also deployed in specialty chemical operations, particularly in the construction of advanced heterocyclic scaffolds for electronic materials, sensors, or performance coatings. The fluorine substituent confers unique electron-withdrawing properties, valuable in tuning charge transport and thermal stability for downstream polymer or liquid crystal applications.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in specialty chemical manufacturing
    • RoHS Directive 2011/65/EU for use in electrical and electronic components
    • ASTM D543 for chemical resistance of finished plastics
    • Company-specific functional testing protocols for optical/electronic performance

    Typical usage ratio

    • 5–15% of the specialty chemical precursor blend (adjusted in the lab for required electronic/optical properties)

    Downstream process integration

    • Charged as a monomer or functional group donor during heterocycle condensation; enters continuous or batch-mode reactors, followed by solvent removal and purification tailored to low metal and ionic impurity specifications

    Final product types

    • Polymerizable heterocycles for advanced functional coatings
    • Luminescent dyes and charge-transport materials
    • Sensor and electronic substrate formulations (including OLEDs, photoresistors)
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