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1-Tert-Butyl-4-Chlorobenzene

    • Product Name 1-Tert-Butyl-4-Chlorobenzene
    • Alias 4-Chloro-tert-butylbenzene
    • Einecs 202-331-1
    • 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

    647251

    Chemical Name 1-Tert-Butyl-4-Chlorobenzene
    Molecular Formula C10H13Cl
    Molecular Weight 168.66 g/mol
    Cas Number 140-38-9
    Appearance Colorless liquid
    Boiling Point 210-212 °C
    Melting Point -25 °C
    Density 0.976 g/cm³ at 25 °C
    Refractive Index 1.513 at 20 °C
    Flash Point 81 °C (closed cup)
    Solubility In Water Insoluble
    Synonyms 4-Chloro-tert-butylbenzene
    Smiles CC(C)(C)C1=CC=C(C=C1)Cl
    Pubchem Cid 81427

    As an accredited 1-Tert-Butyl-4-Chlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 250 mL, screw cap with PTFE liner; clear hazard labeling and product identification for 1-Tert-Butyl-4-Chlorobenzene.
    Shipping 1-Tert-Butyl-4-Chlorobenzene should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must comply with relevant chemical transport regulations. Package with proper labeling, including hazard identification, and use secondary containment if needed. Transport at ambient temperature, ensuring limited exposure to extreme heat or open flames.
    Storage Store 1-Tert-Butyl-4-Chlorobenzene in a tightly closed container in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep away from ignition sources. Use appropriate safety storage cabinets for flammable liquids. Handle under a chemical fume hood and avoid prolonged exposure. Clearly label the storage area and ensure spill control materials are available.
    Application of 1-Tert-Butyl-4-Chlorobenzene

    Applications of 1-Tert-Butyl-4-Chlorobenzene in Industrial Manufacturing

    As an established producer of 1-Tert-Butyl-4-Chlorobenzene, we supply this intermediate to multiple chemical sectors requiring precise aromatic compounds for high-value conversions. Below, we outline our experience in major industry use cases supported by regulatory, process, and product-specific information.

    1. Agrochemical Intermediate Synthesis

    Major crop protection manufacturers utilize this compound as a central aromatic building block in multi-step routes for specialty herbicides and fungicides. It offers high para-selectivity and stability during halogenation or alkylation, enabling efficient scale-up in continuous or batch reactors. Adoption into registered plant protection actives requires tight impurity control, validation under recognized agricultural chemical frameworks, and consistent analytical documentation. Production engineers adjust usage ratios based on desired yield and downstream coupling agent excess to optimize purity and reduce waste streams. End formulation teams incorporate it during the early synthesis step to construct advanced intermediates, often as a precursor for further functional group modifications before eco-toxicological evaluation and regulatory submission.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP)
    • ISO 9001:2015 Quality Management
    • EU REACH Substance Registration
    • FAO/WHO Guidelines for Pesticide Preparation

    Typical usage ratio

    • 0.85 to 1.3 molar equivalents, tailored per target molecule, with ratio dependent on side reaction suppression and reagent recovery efficiency

    Downstream process integration

    • Charged in nitration or alkylation reactors as first aromatic block for further chlorination or side-chain functionalization

    Final product types

    • Selective herbicide intermediates
    • Custom fungicide building blocks
    • Pesticide additive blends
    • Registered agrichemical APIs

    2. Pharmaceutical Intermediate Manufacturing

    Innovators and large-scale API facilities source this aromatic compound for multi-step synthesis of non-steroidal anti-inflammatory drugs and central nervous system therapies. The controlled introduction of the tert-butyl and chlorinated para-arene framework increases the synthetic accessibility of complex molecules while meeting stringent ICH Q7 requirements on raw material traceability, metal residues, and identity verification. QC teams depend on robust process analytics and documented change control during scale-up from pilot to commercial batch sizes. Production chemists implement it in acylation or coupling stages, allowing for precise modification prior to pharmacopoeial specification testing. Its compliant synthesis route and minimal side product formation support easier impurity profiling in final APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF and EP Monographs, where applicable
    • FDA DMF (Drug Master File) or CEP (Certificate of Suitability) documentation for upstream intermediates
    • GMP-compliant traceability

    Typical usage ratio

    • 0.95–1.1 equivalents relative to coupling partners, adjusted according to step yield and impurity threshold in route development

    Downstream process integration

    • Introduced in initial aromatic substitution or alkylation stage, followed by functionalization en route to API

    Final product types

    • Intermediate for anti-inflammatory drugs (NSAIDs)
    • Building blocks for CNS active compounds
    • Precursors for analgesic or anti-allergy actives
    • Custom research molecules for pharma innovation

    3. Polymer Additive and Plasticizer Intermediate

    Thermoplastic and specialty polymer manufacturers incorporate this raw material as a source for tailored additives, high-performance rubber modifiers, and next-generation flame retardant intermediates. With its sterically hindered aromatic structure, process engineers employ it in controlled Friedel–Crafts acylation or further halogenation to target durability and thermal stability in end formulations. Regulatory adherence to regional chemical inventory and product stewardship systems is critical for downstream market entry, especially for consumer-facing polymer compounds. Formulators calibrate dosage ratios according to thermal analysis and migration studies across different substrate batches to balance mechanical strength and processability.

    Industry compliance standards

    • EU REACH and CLP regulations
    • TSCA Inventory (US)
    • ISO 14001 Environmental Management
    • Chemical Substance Control Law (Japan)

    Typical usage ratio

    • 2.5–7.0% by weight in additive or masterbatch solutions, adjusted for target flame retardancy and mechanical testing requirements

    Downstream process integration

    • Added at the compounding stage for masterbatch or during suspension polymerization for enhanced performance polymers

    Final product types

    • Flame-retardant plasticizers
    • Technical rubber additives
    • Specialty resin modifiers
    • Polymer masterbatches for extrusion and molding

    4. Specialty Dye & Pigment Manufacturing

    Dye producers and industrial pigment formulators rely on this aromatic for its unique contribution to electrophilic aromatic substitution routes in high-purity organic pigments. The tert-butyl substituent imparts increased resistance to photodegradation, critical in automotive and industrial coating applications. Regulatory and quality teams align incoming raw material control to ISO colorant testing and environmental emission reporting. Chemists set input ratios based on chromophore evolution monitored via spectroscopic analysis, tuning proportions to achieve target shade, dispersibility, and consistency across production campaigns. The integration stage involves diazotization or condensation coupling, producing robust pigment architectures for advanced coatings and inks.

    Industry compliance standards

    • ISO 9001 and ISO 14001 quality and environmental systems
    • EU REACH Applicability in dyes and pigments
    • APEO-free certification where mandated
    • Compliance with EN71-3 (safety of toys, colorants)

    Typical usage ratio

    • 1.0–2.2 molar equivalents per base chromophore; dosage refined during scale-up by color matching to standard references

    Downstream process integration

    • Activated in primary nucleophilic substitution or condensing cycle in pigment/dye synthesis line

    Final product types

    • High-stability organic pigments
    • Automotive and coil coating colorants
    • Industrial ink base colors
    • Special applications textile dyes

    5. Electronic and Fine Chemical Synthesis

    Semiconductor and fine chemical industries apply this compound as a precursor in the development of specialty intermediates required for photoresist materials, OLED display actives, and electronic-grade coatings. R&D and scale-up teams select it for its defined electronic properties, aromatic rigidity, and low trace metal profile, crucial for minimizing background contamination in ultrapure syntheses. Compliance monitoring includes full traceability and analytical batch release per silicon device fabrication standards and chemical management systems. Process scientists optimize loading based on purity specification, impact on chain propagation, and minimization of structural byproducts in high-throughput routes. Integration occurs at the aromatic precursor polymerization or cross-coupling junctions in electronic chemical synthesis chains.

    Industry compliance standards

    • SEMI S2/S8 semiconductor chemical safety standards
    • RoHS Directive (Restriction of Hazardous Substances, EU)
    • ISO 9001 for electronic material production
    • GHS classification for chemical transport and use

    Typical usage ratio

    • Typically 0.7–1.0 moles per functionalized monomer, corrected for batch purity, stoichiometry, and required electronics-grade specifications

    Downstream process integration

    • Charged in polymer backbone synthesis or as photoreactive arene input in advanced lithography material production

    Final product types

    • Photoresist intermediates for semiconductor fabrication
    • OLED layer precursors
    • Specialty coating resins
    • High-purity fine chemical reagents for electronics
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