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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 | 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. |
Applications of 1-Tert-Butyl-4-Chlorobenzene in Industrial ManufacturingAs 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 SynthesisMajor 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
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2. Pharmaceutical Intermediate ManufacturingInnovators 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
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3. Polymer Additive and Plasticizer IntermediateThermoplastic 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
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4. Specialty Dye & Pigment ManufacturingDye 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
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5. Electronic and Fine Chemical SynthesisSemiconductor 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
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