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4-Chlorophenylurea

    • Product Name 4-Chlorophenylurea
    • Alias 4-Chlorophenylurea
    • Einecs 221-462-6
    • 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
    VTB
    Specifications

    HS Code

    273230

    Chemicalname 4-Chlorophenylurea
    Casnumber 102-01-2
    Molecularformula C7H7ClN2O
    Molecularweight 170.60 g/mol
    Appearance White crystalline powder
    Meltingpoint 170-173°C
    Solubilityinwater Slightly soluble
    Density 1.44 g/cm³
    Structure Contains a urea group substituted with a 4-chloro phenyl ring
    Synonyms N-(4-Chlorophenyl)urea, para-Chlorophenylurea
    Pubchemcid 7661
    Smiles C1=CC(=CC=C1NC(=O)N)Cl
    Inchikey WLXCMNPMHPDZFY-UHFFFAOYSA-N

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

    Packing & Storage
    Packing 4-Chlorophenylurea is packaged in a 100g amber glass bottle with a secure screw cap and hazard labeling for safe handling.
    Shipping 4-Chlorophenylurea is shipped in tightly sealed containers made of compatible materials to prevent contamination and moisture exposure. Packages are clearly labeled according to regulatory requirements. The chemical is stored and transported in a cool, dry place, following local and international guidelines for safe handling and delivery of laboratory chemicals.
    Storage 4-Chlorophenylurea should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents and acids. Protect the chemical from moisture and direct sunlight. Ensure the storage area is clearly labeled and access is limited to trained personnel. Follow all relevant safety guidelines and local regulations for chemical storage.
    Application of 4-Chlorophenylurea

    Applications of 4-Chlorophenylurea in Industrial Manufacturing

    4-Chlorophenylurea supports multiple specialized manufacturing sectors as a targeted intermediate and process additive. Our direct production control ensures consistent material performance across regulated downstream environments. The following application scenarios reflect verified usage in real industrial contexts.

    1. Agrochemical Synthesis: Herbicide Intermediate

    Major agrochemical producers incorporate 4-Chlorophenylurea as a key intermediate in phenylurea-based herbicide synthesis, particularly monosubstituted ureas for post-emergent weed control. Material addition occurs in closed reactor systems during the condensation step with substituted anilines or isocyanates, allowing for precise molecular design. Final herbicide actives maintain defined impurity profiles, requiring raw material with proven analytical documentation. Our supply chain supports multistep synthesis scale-up under strict monitoring.

    Industry compliance standards

    • REACH (EC No. 1907/2006) registration for precursor use
    • ISO 9001:2015 quality management in agrochemical manufacturing
    • National pesticide registration (US EPA, China MARA)
    • Global Harmonized System (GHS) classification and labeling

    Typical usage ratio

    • 0.1–0.3 molar equivalents based on target urea structure
    • Adjusted by desired side-chain substitution in formulation process
    • Excess unreacted material neutralized in process
    • Ratio end-verified by in-process HPLC analysis

    Downstream process integration

    • Feeding into condensation and cyclization reactors
    • Participates in exothermic coupling with isocyanates
    • Several-stage purification (crystallization, washing, drying)
    • Final actives milled for suspension concentrate or wettable powder products

    Final product types

    • Diuron and other phenylurea herbicide active ingredients
    • Aqueous suspension concentrates for crop protection
    • Granular herbicide pre-mixes for large-scale agriculture
    • Dry-processed herbicide tablets for specialty markets

    2. Pharmaceutical Intermediate: Synthesis of Antihypertensive APIs

    Selected active pharmaceutical ingredient (API) manufacturers use 4-Chlorophenylurea as a modular building block during multi-step synthesis of antihypertensive agents and related molecules. Batch processes integrate the material in amidation or N-alkylation stages, enabling attachment of functionalized aryl groups to construct the final pharmacophore. Throughout, product identity and purity require validated analytical controls, traceable Certificates of Analysis, and dedicated cleaning protocols. We offer tailored batch shipments with pre-approved quality attributes for regulated pharma workflows.

    Industry compliance standards

    • ICH Q7 GMP for API manufacturing
    • USP/NF and Ph. Eur. monograph adherence for related starting materials
    • Drug Master File (DMF) support for regulated customers
    • Pharmaceutical supply chain traceability (PIC/S, 21 CFR Part 211)

    Typical usage ratio

    • 0.9–1.1 equivalents per key coupling step
    • Ratio modified for yield optimization or impurity minimization
    • USP-grade where required by regulated processes
    • Continuous monitoring via HPLC and GC for residuals

    Downstream process integration

    • Feed into reactor for initial amide bond formation
    • Processing under controlled temperature/pH to limit side reactions
    • Workup steps: aqueous extraction, organic solvent recovery, drying
    • Subsequent transformation in late-stage API structure assembly

    Final product types

    • Active ingredient intermediates for thiazide diuretics
    • Monitored synthesis routes for proprietary antihypertensive compounds
    • Bulk API blocks shipped to tableting or capsule-forming customers
    • Pharma-grade intermediates for further halogenated derivatives

    3. Specialty Dye Formulation: Precursor for Reactive Dye Development

    Dye and pigment manufacturers employ 4-Chlorophenylurea as a tailored precursor in the closed-loop synthesis of reactive dyes, enabling attachment of chlorinated aryl moieties that deliver distinct chroma and fastness in textile finishing. Reaction integration focuses on electrophilic aromatic substitution, with controlled addition to maximize yield to the reactive stage. QA testing ensures each batch conforms to binding specificity and formaldehyde/halogen release limits. Our technical support collaborates directly with pigment engineers on unique shade development.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (harmful substance limits in textiles)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals)
    • ISO 105-C06 for dye fastness testing
    • REACH Annex XVII (restrictions on azo and halogen compounds)

    Typical usage ratio

    • 3–8% of total dye batch mass, formula-dependent
    • Optimized during lab scale-up for hue intensity targets
    • Levels fine-tuned to batch shade cards
    • Intermediate neutralization/removal conducted before downstream formulation

    Downstream process integration

    • Incorporated in synthesis reactors for dye molecule backbone formation
    • Stagewise combination with diazonium salts or sulfonic acid groups
    • Final dye crystallization and purification for end-user handling safety
    • Liquid- or powder-form dye shipments for mills and fabricators

    Final product types

    • Reactive dyes for cotton and cellulosic fibers
    • Printing pigment pastes for digital textile applications
    • High-chroma specialty dyes for automotive fabrics
    • Fastness-controlled colorants for home furnishing textiles

    4. Polymer Additives: Chain Modifier for Thermoset Resins

    Polymer compounders use 4-Chlorophenylurea as a functional chain modifier during the synthesis of thermoset resins such as polyurethanes and phenolic systems. The compound acts as a specificity modifier at the cross-linking stage, introducing targeted phenyl substitutions that increase thermal stability and resistance to chemical degradation. Accurate dosing is monitored to prevent matrix brittleness or incomplete conversion. Lab analyses verify integration via DSC and FTIR. Stable supply ensures reliable upscaling for customer polymer designs.

    Industry compliance standards

    • ISO 9001:2015 Polymer manufacturing standards
    • UL 94 flame retardancy testing for finished parts
    • RoHS Directive EC 2011/65/EU for electrical/electronic end-use
    • GADSL list for automotive plastics regulatory compliance

    Typical usage ratio

    • 0.5–2% by resin mass in polycondensation stage
    • Adjusted for end-use specification—testing for modulus and impact strength
    • Amount set by resin manufacturer’s approved formulation
    • Continual verification by spectroscopic methods

    Downstream process integration

    • Direct blending in prepolymer mix tanks
    • Batch addition under nitrogen or inert atmosphere
    • Monitored incorporation during exotherm to avoid decomposition
    • Integration confirmed prior to mold filling or casting

    Final product types

    • High-durability polyurethane sheets for technical use
    • Heat- and solvent-resistant composite panels
    • Electrical encapsulation materials qualified to UL/CE requirements
    • Polymer-impregnated laminates for industrial equipment

    5. Fine Chemical Preparations: Intermediate for Plant Growth Regulator Synthesis

    Manufacturers of plant growth regulators (PGRs) apply 4-Chlorophenylurea as a synthetic short-chain intermediate. Inclusion at designated steps creates urea derivative molecules active in metabolic modulation for horticulture and forestry. Process chemists evaluate controlled chlorination and condensation to set biological activity windows while limiting off-spec byproducts. Extensive toxicological documentation and tracking meet agricultural quality requirements. We provide custom syntheses scaled to fit both laboratory pilot and volume production.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications (JMPS)
    • Good Laboratory Practice (GLP) for field trial and residue studies
    • ISO 17025 laboratory accreditation for analytical QC
    • Compliance with local agricultural chemical registration (e.g., EPA FIFRA, EC 1107/2009)

    Typical usage ratio

    • 0.15–0.45 equivalents in main condensation reaction
    • Tight control for maximizing desired PGR isomer ratios
    • Variability by target plant species and regulatory test panel alignment
    • Sequential synthesis with adjustment based on LOD/GC/MS analysis

    Downstream process integration

    • Initial charge for main-stage chemical formation
    • Staged washing and separation for purification
    • Final step crystallization before formulation
    • Routine retention sample archiving for authority submission

    Final product types

    • Commercial-grade cytokinins and related PGRs
    • Growth regulator solution concentrates for foliar spraying
    • Controlled-release PGR granules for greenhouse application
    • Bulk active intermediates for downstream blending
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