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3-Chloro-4-Fluorobenzoyl Chloride

    • Product Name 3-Chloro-4-Fluorobenzoyl Chloride
    • Alias 3-Chloro-4-fluorobenzoyl chloride
    • Einecs 412-110-6
    • 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

    940692

    Product Name 3-Chloro-4-Fluorobenzoyl Chloride
    Cas Number 162012-74-6
    Molecular Formula C7H3Cl2FO
    Molecular Weight 193.01 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 241 °C (estimated)
    Density 1.46 g/cm³ (at 20 °C, estimated)
    Purity Typically ≥98%
    Solubility Reacts with water, soluble in organic solvents
    Chemical Structure ClC6H3(F)COCl
    Synonyms 3-Chloro-4-fluorobenzoic acid chloride
    Storage Conditions Store at 2-8°C, keep container tightly closed

    As an accredited 3-Chloro-4-Fluorobenzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled “3-Chloro-4-Fluorobenzoyl Chloride, 100g.” Bottle features hazard symbols, lot number, and tightly sealed cap.
    Shipping 3-Chloro-4-Fluorobenzoyl Chloride is shipped in tightly sealed, chemical-resistant containers to prevent moisture and air exposure. It is classified as a hazardous material and transported according to international chemical safety regulations, with clear hazard labeling and appropriate documentation. Strict temperature and handling controls are observed to ensure stability and safety during transit.
    Storage **3-Chloro-4-Fluorobenzoyl Chloride** should be stored in a cool, dry, well-ventilated area, away from sources of moisture, heat, and incompatible substances such as bases, oxidizing agents, and water. Keep the container tightly closed and properly labeled. Protect from physical damage and direct sunlight. Handle and store under an inert atmosphere, such as nitrogen, to minimize hydrolysis and degradation.
    Application of 3-Chloro-4-Fluorobenzoyl Chloride

    Applications of 3-Chloro-4-Fluorobenzoyl Chloride in Industrial Manufacturing

    3-Chloro-4-Fluorobenzoyl Chloride stands as a key intermediate in advanced industrial syntheses, supporting specialized processes in the agrochemical, pharmaceutical, pigment, specialty polymer, and fine chemical industries. Below, we outline critical downstream applications where this material fulfills distinct technical and regulatory roles.

    1. Agrochemical Synthesis: Herbicide Intermediate

    Major multinational crop protection companies utilize this compound in the synthesis of novel herbicide active ingredients, particularly amide or triazine derivatives. The intermediate reacts in acylation steps, forming the benzoyl backbone needed for target molecule assembly. Large-scale processes employ closed-system reactors to ensure operator safety and prevent hydrolysis. Process engineering teams must validate residue limits and monitor for byproduct formation through in-process controls, supporting regulatory petitions. Reliability and lot-to-lot reproducibility prove essential, as failure to meet agrochemical compliance leads to batch rejection and significant economic losses.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • EPA 40 CFR Part 167 (Pesticide Production Report)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products Registration)
    • REACH Annex VII–X requirements for intermediates

    Typical usage ratio

    • 10–35% w/w relative to co-reactant in acylation steps; producers adjust for molecular design and process yield optimization

    Downstream process integration

    • Introduced after amine or hydrazine substrate addition; batch or semi-batch reactors under inert gas protection; continuous pH and purity monitoring during reaction

    Final product types

    • Selective post-emergent herbicides
    • Pre-emergent weed control active ingredients
    • Formulated suspension concentrates (SC)
    • Active substance technical concentrates

    2. Pharmaceutical Manufacturing: API Gatekeeper Intermediate

    Pharmaceutical companies incorporate this substance in the synthesis of fluorinated benzamide intermediates used for API development in oncology and CNS therapeutics. Material handling follows GMP protocols, with process chemists specifying acid chloride scale-in based on route scouting and impurity profile assessments. The material's halogenation pattern proves essential for receptor-binding modulation, influencing clinical lead success. Control laboratories track residual acid chlorides, while serialization systems support batch traceability for regulatory submission.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • EDQM CEP standards for starting materials
    • USP <467> Residual Solvents Guidance

    Typical usage ratio

    • 8–22% molar equivalent relative to active-amino precursors; adjusted based on impurity control and yield in multi-step synthesis

    Downstream process integration

    • Fed during early- or mid-stage API building block assembly; isolation under nitrogen atmosphere; followed by immediate downstream coupling or cyclization

    Final product types

    • Clinical trial materials for novel oncologics
    • Pilot-plant batches of CNS-active pharmaceuticals
    • Small-molecule research APIs
    • Reference standards for regulatory dossiers

    3. Colorants & Pigment Industry: Benzoyl Chloride Building Block

    Specialty pigment manufacturers use this ingredient to synthesize halogenated diaryl pigments and high-performance colorants for plastics and inks. Its precise substitution pattern provides thermal and light stability critical for demanding polymer processing conditions. Strict environmental controls govern acid chloride use, with automated fume scrubbing and closed-transfer technology to minimize operator exposure. Final pigment quality depends on feedstock purity and batch consistency, as impurities can cause unwanted color shifts or loss of dispersion efficiency in masterbatch applications.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management System
    • EU Regulation (EC) No 1907/2006 (REACH)
    • EN 71-3 (Toy Safety—Migration of Certain Elements)
    • ASTM D5965 (Colorant Testing Protocol)

    Typical usage ratio

    • 5–18% w/w depending on pigment synthesis step; adjustments made for target chroma and substrate compatibility

    Downstream process integration

    • Blended with specific aromatic amines during condensation or coupling stages; purification steps follow to remove unreacted chlorides

    Final product types

    • High-stability organic pigments for engineering plastics
    • Inks and coatings for packaging applications
    • Dispersed colorant masterbatches
    • Automotive and industrial paints

    4. Advanced Polymers: Specialty Monomer Synthesis

    Producers of advanced fluorinated and halogenated polymers use this product as a functionalized monomer precursor. Reaction schemes incorporate it to achieve precise backbone modification for high-performance polymers demanded in wire & cable, electronics, and filtration membrane markets. Polymerization engineers focus on monomer incorporation ratios and work in controlled environments with strong anhydrous discipline. Strict analytical protocols verify the absence of free acid chloride in the final monomer batch, ensuring safe downstream polymerization and consistent dielectric or chemical resistance properties in finished goods.

    Industry compliance standards

    • ISO 9001:2015 for quality assurance
    • RoHS Directive 2011/65/EU (for E&E uses)
    • UL 94 (Flammability of polymeric materials, as applicable)
    • ASTM E2409 (Standard Performance Specification for Fluoropolymers)

    Typical usage ratio

    • Typically 3–10% w/w of the initial batch depending on polymer backbone requirements; higher ratios for advanced specialty copolymer grades

    Downstream process integration

    • Charged during monomer functionalization under controlled atmosphere; subsequent purification removes hydrolyzable residues; polymerization proceeds after in-process GC/HPLC confirmation

    Final product types

    • Fluorinated specialty copolymers
    • High-performance films for electronics
    • Wire and cable insulations
    • Membranes for chemical-resistant applications

    5. Fine Chemicals: Custom Synthesis Reagent

    Leading fine chemical manufacturers employ this material for custom syntheses involving halogenated aromatic compounds with specific substitution patterns. Reactive stepwise addition allows production of tailored intermediates for fragrance, UV absorber, photoinitiator, or advanced catalyst segments. Experienced process chemists manage all handling in contained vessels with rapid transfer systems, minimizing exposure to moisture and oxygen. Documentation of feedstock traceability and batch-specific impurity profiles remains central for fine chemical clients requiring reproducible custom molecules with stringent QC release testing.

    Industry compliance standards

    • Responsible Care® Management System
    • ISO 9001:2015 and ISO 17025 for laboratory testing
    • REACH and TSCA (when exporting to Europe and US)
    • Japanese Chemical Substances Control Law (Kashinhou)

    Typical usage ratio

    • Variable: typically 6–15% w/w relative to co-reactant in custom syntheses, adjusted by target molecule and scale

    Downstream process integration

    • Added at specific condensation or acylation stages in multi-step fine chemical production; precise dosing via metered addition ensuring control over reaction exotherms and byproduct formation

    Final product types

    • Custom aromatic intermediates for electronics
    • Photoinitiators for UV-curable coatings
    • Fragrance and UV-absorbing molecules
    • Research and development fine chemicals
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