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4-Chlorobenzenamine Hydrochloride

    • Product Name 4-Chlorobenzenamine Hydrochloride
    • Alias 4-Chloroaniline hydrochloride
    • Einecs 219-406-4
    • 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

    168047

    Product Name 4-Chlorobenzenamine Hydrochloride
    Cas Number 20265-97-8
    Molecular Formula C6H7Cl2N
    Molecular Weight 164.04 g/mol
    Appearance White to off-white powder
    Melting Point 236-240°C
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 4-Chloroaniline hydrochloride, p-Chloroaniline hydrochloride
    Ec Number 243-640-0

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

    Packing & Storage
    Packing White, tightly sealed, HDPE bottle labeled "4-Chlorobenzenamine Hydrochloride, 100g," with hazard symbols and batch/expiry details, tamper-evident seal.
    Shipping 4-Chlorobenzenamine Hydrochloride is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with regulatory standards for hazardous chemicals. During transit, temperature and handling guidelines are followed to ensure safety and preserve product integrity. Shipping documentation includes safety data and labeling in accordance with international transport regulations.
    Storage Store 4-Chlorobenzenamine Hydrochloride in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture. Use corrosion-resistant shelves or cabinets. Label the storage area clearly, and ensure access is restricted to trained personnel equipped with proper protective equipment.
    Application of 4-Chlorobenzenamine Hydrochloride

    Applications of 4-Chlorobenzenamine Hydrochloride in Industrial Manufacturing

    As the direct manufacturer of 4-Chlorobenzenamine Hydrochloride, we supply this intermediate exclusively for downstream chemical sectors with established markets and compliant production requirements. Below are verified application scenarios with dedicated process integration, regulatory standards, and manufacturing usage details, referencing both current export client feedback and core industry documentation as of 2026.

    1. Production of Pharmaceutical Intermediates for Active Pharmaceutical Ingredients (APIs)

    Major pharmaceutical synthesis facilities use 4-Chlorobenzenamine Hydrochloride as a key intermediate in the multi-step synthesis pathways for several regulated APIs, especially in the manufacture of certain antihypertensive and anti-inflammatory drug classes. Here, process engineers introduce it as a nucleophilic building block in early or mid-stage reactions, often controlling purity and reactivity for subsequent purification stages under strict compliance. Downstream production batches adjust the addition rate depending on targeted output and reaction kinetics, as validated in scale-up manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP (United States Pharmacopeia) and Ph. Eur. (European Pharmacopoeia) for relevant APIs
    • CFDA (NMPA) GMP guidelines for China-based API production
    • FDA 21 CFR Part 211 for Finished Pharmaceuticals

    Typical usage ratio

    • 0.15–0.35 molar equivalents relative to core substrate in multi-step batches, adjusted based on stoichiometry and desired output yield.

    Downstream process integration

    • Combined directly in aromatic substitution and amidation steps, typically dissolved in controlled solvent systems prior to addition to reactor vessels at 70–120°C.

    Final product types

    • Antihypertensive bulk APIs (e.g., chlorobenzamide derivatives)
    • Anti-inflammatory pharmaceutical intermediates
    • Related fine chemicals for advanced intermediate synthesis

    2. Dyes and Pigments Manufacturing

    Leading colorant manufacturers employ this compound in the synthesis of azo and other chlorinated aromatic dyes. Here, it acts as a primary aryl amine precursor in diazotization reactions to create stable colorant frameworks. Industrial formulations calibrate the input ratio based on the specific pigment shade and batch size, as well as dye compatibility with regulatory requirements for textile and printing inks. The chemical enters early in the process to ensure homogenous diazonium salt formation and is crucial for consistent color fastness.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006
    • OEKO-TEX® Standard 100 for certified textiles
    • China's GB 18401 National General Safety Technical Code for Textile Products
    • ISO 9001:2015 (Quality Management Systems for colorant production)

    Typical usage ratio

    • Ranging from 2% to 8% by weight in the primary dye batch; ratios adjusted for molecular weight and dye intensity standards.

    Downstream process integration

    • Introduced as the amine source in in situ diazotization under acidic aqueous media, before coupling with phenols or naphthols to yield azo dye molecules.

    Final product types

    • Azo textile dyes for cotton and polyester
    • Chlorinated colorants for solvent-based inks
    • Industrial grade pigments for plastics coloration

    3. Agrochemical Synthesis (Pesticide Intermediates)

    Controlled-use agrochemical plants utilize 4-Chlorobenzenamine Hydrochloride for synthesizing selective pesticide active ingredients where chlorinated aromatic amines are vital structural elements. The raw material integrates into coupling reactions for the manufacture of herbicides and insecticide precursors. Formulators account for yield optimization and environmental safety when calculating addition dosages, using validated batch processes with mandatory traceability.

    Industry compliance standards

    • ISO 9001:2015 (process quality for agrochemicals)
    • FAO/WHO Guidelines on Pesticide Specifications
    • EPA 40 CFR Part 158 (U.S. Pesticide Registration Process)
    • China GB/T 1604-2016 for pesticide intermediates

    Typical usage ratio

    • 0.08–0.22 molar equivalents relative to the halogenated substrate; optimized for complete reaction progression while minimizing residual precursor.

    Downstream process integration

    • Fed into condensation and cyclization steps when constructing heterocyclic moieties in pesticide precursor synthesis, predominantly under basic or neutral aqueous conditions.

    Final product types

    • Herbicide intermediates (e.g., chlorobenzamide-based compounds)
    • Insecticide precursors for further functionalization
    • Fungicide building blocks

    4. Specialty Polymers and Monomer Preparation

    Polymer manufacturers integrate this compound in the synthesis of high-value specialty monomers where the presence of a chlorinated aromatic amine influences polymer backbone properties. It is often present as a functional comonomer, especially in copolymer and resin manufacture for electrical and coating applications. Production managers fine-tune input levels based on molecular weight targets and cross-linking efficiency, with the material typically introduced at the monomerization stage and closely monitored by in-process control labs.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for restricted substances in electrical/electronic polymers
    • ISO 14001 for Environmental Management in synthetic resin production
    • REACH Annex XVII for polymer chemical management
    • UL 94 standards for flame retardant plastics, where applicable

    Typical usage ratio

    • 0.5–2.0% by weight in monomer blends, dependent on desired polymer characteristics and downstream fabrication process.

    Downstream process integration

    • Employed in the initial stage as a reactive monomer component during free-radical or condensation polymerization, influencing final resin morphology and performance.

    Final product types

    • Electrically insulating coatings
    • High-resistance plastics for automotive connectors
    • Specialty copolymers for wire and cable sheathing

    5. Chemical Synthesis of Fine Organic Compounds

    Chemical and contract synthesis companies employ 4-Chlorobenzenamine Hydrochloride to prepare fine organic intermediates used in laboratory, R&D, and select industrial manufacturing contexts. Its reactivity supports the introduction of the para-chloroamino motif in complex aromatic scaffolds. Technicians adjust the addition based on job order scale and synthesis requirements, with the process frequently relying on high-purity raw material lots for low-impurity final outputs.

    Industry compliance standards

    • ISO 9001:2015 for custom synthesis
    • Responsible Care® principles as outlined by the ICCA
    • Applicable local customs and environmental safety regulations

    Typical usage ratio

    • Typically 0.1–1.0 molar equivalents, depending on target compound and reaction stoichiometry, with exact quantities mandated by the synthetic route.

    Downstream process integration

    • Introduced during nucleophilic aromatic substitution, reductive amination, or oxidative coupling steps in specialty organic synthesis reactors.

    Final product types

    • Reference standards and fine chemicals for analytical use
    • Research compounds for pharmaceutical development
    • Intermediates for performance materials synthesis
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