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2-(4-Chlorophenyl)-3-(Trifluoromethyl)Pyrazole-4-Carboxylic Acid

    • Product Name 2-(4-Chlorophenyl)-3-(Trifluoromethyl)Pyrazole-4-Carboxylic Acid
    • Alias Bixafen
    • Einecs 694-179-3
    • 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
    VTB
    Specifications

    HS Code

    860637

    Chemical Name 2-(4-Chlorophenyl)-3-(Trifluoromethyl)Pyrazole-4-Carboxylic Acid
    Molecular Formula C11H6ClF3N2O2
    Molecular Weight 290.63 g/mol
    Cas Number 1042066-98-7
    Appearance White to off-white solid
    Solubility Slightly soluble in organic solvents (e.g., DMSO, methanol)
    Smiles C1=CC(=CC=C1C2=NN=C(C2C(=O)O)C(F)(F)F)Cl
    Inchi InChI=1S/C11H6ClF3N2O2/c12-8-3-1-7(2-4-8)10-16-15-6(11(13,14)15)9(17)5-18/h1-4H,5H2,(H,17,18)
    Purity Typically >98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 4-Carboxy-2-(4-chlorophenyl)-3-(trifluoromethyl)pyrazole

    As an accredited 2-(4-Chlorophenyl)-3-(Trifluoromethyl)Pyrazole-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-(4-Chlorophenyl)-3-(Trifluoromethyl)Pyrazole-4-Carboxylic Acid, sealed with a screw cap.
    Shipping Shipping for 2-(4-Chlorophenyl)-3-(Trifluoromethyl)pyrazole-4-carboxylic acid follows standard procedures for laboratory chemicals. The compound is securely packaged in sealed containers, clearly labeled, and shipped via authorized carriers, complying with all local and international hazardous materials regulations to ensure safe and compliant delivery. Documentation accompanies every shipment.
    Storage Store 2-(4-Chlorophenyl)-3-(Trifluoromethyl)pyrazole-4-carboxylic acid in a cool, dry, and well-ventilated area, tightly sealed in a clearly labeled container. Keep away from incompatible substances such as strong oxidizing agents. Protect from moisture, direct sunlight, and sources of ignition. Always follow all safety guidelines for handling and storage, using appropriate personal protective equipment (PPE).
    Application of 2-(4-Chlorophenyl)-3-(Trifluoromethyl)Pyrazole-4-Carboxylic Acid

    Applications of 2-(4-Chlorophenyl)-3-(Trifluoromethyl)Pyrazole-4-Carboxylic Acid in Industrial Manufacturing

    As a dedicated producer, we support downstream industrial sectors by supplying high-purity 2-(4-Chlorophenyl)-3-(Trifluoromethyl)Pyrazole-4-Carboxylic Acid, a key intermediate in advanced synthesis. Our technical team collaborates with formulation and process specialists to help customers achieve consistent quality, compliance, and performance in each target application. Below are the principal application channels for this compound, reflecting its specialized use in established markets.

    1. Synthesis of Advanced Agrochemical Fungicides

    This compound supports synthesis routes for triazole and pyrazole-based fungicide actives, especially in crop protection formulations designed for resistance management. Formulators incorporate it as a primary building block in the preparation of active ingredients with enhanced efficacy against cereal and vegetable pathogens. Downstream manufacturers use proprietary methods to create new-generation pesticide products while meeting global safety benchmarks.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 on plant protection product authorization
    • China GB/T 1604 Pesticide Standards
    • Good Laboratory Practice (GLP, OECD)

    Typical usage ratio

    • Used at 0.4–0.8 molar equivalents per fungicide synthesis batch, adjusted according to the desired active compound yield and purity targets

    Downstream process integration

    • Introduced during the key cyclization or condensation reaction step to assemble the pharmacophore core of triazole or related fungicides; followed by purification and formulation

    Final product types

    • Technical grade active fungicide ingredients
    • Wettable powders and emulsifiable concentrates
    • Suspension concentrates for broadacre and specialty crop use

    2. Pharmaceutical Intermediate for Novel Antimicrobial Agents

    Our material serves as an essential coupling component for the creation of pyrazole-carboxylic acid derivatives in pharmaceutical research and scale-up. Medicinal chemistry laboratories and API manufacturers introduce this intermediate into multistep syntheses to develop new small-molecule antimicrobial candidates with improved metabolic stability.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP, FDA 21 CFR Part 210/211)
    • ICH Q7 Guidelines for Active Pharmaceutical Ingredients
    • USP General Chapters on process impurities
    • EMEA Guideline on Setting Specifications for New Drug Substances

    Typical usage ratio

    • Applied at 1.1 to 1.3 molar equivalents in heterocyclic coupling steps, with slight excess to compensate for downstream purification yield losses

    Downstream process integration

    • Charged in the amidation or esterification stage following initial scaffold construction, then carried through crystallization and chromatographic refinement

    Final product types

    • Preclinical and clinical-stage active pharmaceutical ingredient intermediates
    • Registered drug substance starting materials
    • Reference standards for antimicrobial API development

    3. Synthesis of Specialty Polymerization Catalysts

    This carboxylic acid derivative functions as a ligand precursor in the manufacture of highly selective, transition-metal-based polymerization catalysts. Downstream catalyst producers rely on its chemical stability to enable efficient formation of complex organometallic structures, streamlining the production of specialty plastics for high-value applications.

    Industry compliance standards

    • ISO 9001 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 for chemical hazard evaluation
    • Environmental, Health, and Safety Management (EHS, ISO 14001)

    Typical usage ratio

    • Employed at 0.2–0.5 parts per part of metal precursor, tailored to catalyst performance requirements in polyethylene and specialty copolymer production

    Downstream process integration

    • Incorporated into the catalyst complexation reaction as a ligand donor, followed by filtration and activation steps before final catalyst formulation

    Final product types

    • Single-site polymerization catalysts
    • Modified Ziegler-Natta catalysts
    • Metallocene and post-metallocene catalyst systems

    4. Building Block for Veterinary API Synthesis

    Veterinary drug chemical suppliers utilize this compound within key synthetic stages when constructing active molecules for animal pharmaceuticals. The stability of both the chlorophenyl and trifluoromethyl functional groups enables reliable scale-up and minimizes byproduct formation during the synthesis of pyrazole-based veterinary agents.

    Industry compliance standards

    • Good Manufacturing Practices for Veterinary Drugs (VICH GL35, GL19)
    • European Pharmacopoeia (Ph. Eur.) Monograph requirements
    • US FDA CVM Guidance on Veterinary APIs
    • Quality assurance documentation (Batch Records, CoA, MSDS)

    Typical usage ratio

    • Used at 0.5–0.7 molar ratios in API backbone assembly steps, adjusted for specific synthesis route and impurity threshold controls

    Downstream process integration

    • Added to coupling or cyclization reactions for pyrazole ring closure, then subjected to downstream isolation, drying, and milling before API finishing

    Final product types

    • Finished veterinary drug substances
    • Premixed formulations for dosage preparation
    • Stabilized bulk powder APIs for animal health manufacturers

    5. Precursor in Crop Growth Regulator Manufacturing

    This pyrazole-carboxylic acid supports synthesis of certain growth regulation agents used for field crops and horticulture. Downstream manufacturers employ it in selective transformation reactions to introduce functional groups that modulate plant metabolism under stress or promote resistance to adverse environments.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • ISO 17025 Laboratory Accreditation for Agrochemical Analysis
    • EPA FIFRA Registration Requirements (for U.S. markets)

    Typical usage ratio

    • Integrated at 0.3–0.6 molar proportion of the total active ingredient mass, with batch-specific tuning based on plant metabolism studies

    Downstream process integration

    • Participates in final side-chain introduction or ester hydrolysis stages, followed by formulation into water-dispersible granules or concentrates

    Final product types

    • Plant growth regulator actives (technical grade)
    • Liquid and solid growth regulator formulations
    • Seed treatment additive products
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