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1-Tert-Butyl-3-Nitro-4-Chlorobenzene

    • Product Name 1-Tert-Butyl-3-Nitro-4-Chlorobenzene
    • Alias 1-tert-Butyl-3-nitro-4-chlorobenzene
    • Einecs 619-527-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    440203

    Productname 1-Tert-Butyl-3-Nitro-4-Chlorobenzene
    Casnumber 75137-99-0
    Molecularformula C10H12ClNO2
    Molecularweight 213.66
    Appearance Yellow solid
    Meltingpoint 52-56°C
    Density 1.21 g/cm3
    Solubility Insoluble in water
    Purity Typically ≥98%
    Smiles CC(C)(C)c1cc(ccc1Cl)[N+](=O)[O-]
    Synonyms 3-Nitro-4-chloro-tert-butylbenzene
    Storagetemperature Store at room temperature
    Hazardclass Irritant

    As an accredited 1-Tert-Butyl-3-Nitro-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, tightly sealed, labeled with hazard symbols, containing 25 grams of 1-Tert-Butyl-3-Nitro-4-Chlorobenzene, for laboratory use.
    Shipping 1-Tert-Butyl-3-Nitro-4-Chlorobenzene should be shipped in secure, sealed containers, clearly labeled according to hazardous materials regulations. Protect from heat, moisture, and physical damage. Use appropriate cushioning and secondary containment. Accompany with safety data sheets (SDS). Transportation must comply with local, national, and international chemical safety and shipping guidelines.
    Storage 1-Tert-Butyl-3-Nitro-4-Chlorobenzene should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and reducing agents. Keep the container tightly closed, protected from direct sunlight and sources of ignition. Store in a chemical-resistant, labeled container, and avoid exposure to heat, moisture, and open flames. Use secondary containment for added safety.
    Application of 1-Tert-Butyl-3-Nitro-4-Chlorobenzene

    Applications of 1-Tert-Butyl-3-Nitro-4-Chlorobenzene in Industrial Manufacturing

    As a direct manufacturer of 1-Tert-Butyl-3-Nitro-4-Chlorobenzene, we supply this advanced aromatic intermediate to specialized downstream sectors. The following application scenarios reflect real industrial uses that demand stringent quality control, precise formulation, and compliance with sector-specific regulations. Each application harnesses the unique electron-withdrawing and steric characteristics of this compound, supporting specialty chemical synthesis with high purity requirements. Explore dedicated use cases below.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)

    API producers integrate 1-Tert-Butyl-3-Nitro-4-Chlorobenzene as a key substrate in the custom synthesis of molecular scaffolds for drug discovery and scale-up. It finds particular adoption in the production of heterocyclic building blocks through aromatic substitution and condensation reactions, serving as a precursor for compounds targeting CNS and anti-inflammatory indications. Stringent raw material controls apply throughout the route from intermediate production to final API batch release.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) General Chapters – Impurities testing
    • European Pharmacopeia monographs (as referenced in end-use API dossiers)
    • 21 CFR Part 211 – US FDA cGMP for finished pharmaceuticals

    Typical usage ratio

    • 0.9–1.2 molar equivalents, precisely adjusted based on the stoichiometric requirements of the target intermediate; final subsample purity determined per production batch by HPLC/GC-MS.

    Downstream process integration

    • Integrated during the primary aromatic nucleophilic substitution or as a nitration substrate in multi-step synthesis, typically during early-stage intermediate construction or core scaffold assembly, prior to final deprotection and coupling.

    Final product types

    • Custom-developed pharmaceutical active ingredients for CNS, anti-inflammatory, or oncology APIs
    • Protected heterocyclic intermediates for medicinal research applications

    2. Agrochemical Active Ingredient and Intermediate Manufacturing

    Leading crop protection manufacturers employ this compound as a specialized aromatic core in the synthesis of selective herbicide and insecticide intermediates. The tert-butyl group increases steric bulk, influencing the final molecule’s metabolic stability and target selectivity. The raw material enters amidation or reduction sequences pivotal in the design of new agrochemical actives.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products (JMPR)
    • ISO 9001:2015 Quality Management Systems for agrochemical technical production
    • REACH Registration (Europe): Full chemical safety assessment
    • China GB/T 16631 Pesticide Production Hygiene Standards

    Typical usage ratio

    • 5–15% by weight in the technical-grade intermediate batch; often adjusted between pilot and full-scale based on yield optimization and process selectivity tests.

    Downstream process integration

    • Charged during aromatic substitution or reduction stages, preceding final purification of agrochemical technical concentrate; further formulated with co-actives or inert carriers post-purification.

    Final product types

    • Technical-grade herbicide intermediates for acetolactate synthase inhibitors
    • Precursor molecules for selective insecticide formulations
    • Base structures for fungicide actives with chlorinated aromatic motifs

    3. Specialty Dye and Pigment Intermediate Formulation

    Specialty pigment manufacturers source this material as an advanced aromatic structure in the production of high-performance organic dyestuff precursors. The nitro and halogen functionalization facilitate downstream coupling with amines or phenols, leading to pigments with tailored chromatic and fastness profiles for technical textiles and industrial coatings. Usage depends on both color target and solvent compatibility requirements.

    Industry compliance standards

    • Oeko-Tex® Standard 100 for harmful substances (relevant for textile dyes)
    • ISO 9001:2015 for pigment technical quality assurance
    • EU REACH restricted substance lists (pigment sector)
    • ASTM D4236 labeling for artists’ materials

    Typical usage ratio

    • 2–10% by weight based on total dye/pigment mass, depending on coupling reaction yield and target pigment strength; modified for solvent-based vs. water-based systems.

    Downstream process integration

    • Used as an aromatic precursor during diazotization or nucleophilic aromatic substitution, followed by coupling and oxidation to form final dye structure, then purified, milled, and standardized for textile or coating application.

    Final product types

    • Monoazo textile dyestuffs with enhanced lightfastness
    • Chlorinated organo-pigment intermediates for high-durability coatings
    • Precursors for printing ink colorant manufacture

    4. Electronic and Liquid Crystal Material Precursor Synthesis

    Producers of performance materials for the display and electronics industry exploit the halogenated nitrobenzene structure to synthesize photoresponsive or liquid crystalline intermediates. The tert-butyl group provides increased bulk, impacting phase transition temperatures and solubility profiles, with the nitro function available for further reduction or substitution in display-grade materials design.

    Industry compliance standards

    • IEC 61249-2-21: Halogen-free materials assessment (where applicable)
    • GB/T 19001—ISO 9001 certification for functional material production
    • RoHS Directive 2011/65/EU for restricted substance content
    • Sony SS-00259 Standard for electronic component supply chains

    Typical usage ratio

    • 0.5–2.5 molar equivalents, formulated based on downstream compatibility with mesogen or aryl substituent targets, with process adaptation for low-ion, high-purity requirements.

    Downstream process integration

    • Introduced in early coupling or reduction reactions for design of liquid crystal base structures, integrated under controlled reaction atmospheres, followed by extensive purification for optoelectronic-grade purity assurance.

    Final product types

    • Intermediate structures for thermotropic liquid crystals in advanced display manufacturing
    • Monomeric precursors for electronic photoresist material synthesis
    • Specialty aromatic cores for organic semiconductor material development

    5. Fine Chemical Synthesis for Advanced Material Additives

    R&D-scale and commercial fine chemical producers use this material as a building block in the design of specialty additives for lubricants, adhesives, and advanced polymers. Its dual functionality supports targeted modification of bulk and specialty polymers, incorporating thermal resistance and chemical stability attributes. Integration often requires custom development and validation of downstream performance.

    Industry compliance standards

    • ISO 9001:2015 for specialty additive manufacturing
    • REACH Annex XVII: Registration and restriction of chemical use
    • ASTM D4761 for polymer additive testing
    • Customer-applied proprietary QC specifications

    Typical usage ratio

    • 1–7% by weight in additive masterbatches or polymer blends; optimized in pilot formulations according to required performance characteristics and compatibility studies.

    Downstream process integration

    • Blended post-polymerization or co-extruded with resin matrix; in lubricant chemicals, introduced during additive synthesis just before final blending and filtering for product clarity and purity control.

    Final product types

    • Polymer impact modifiers for engineering plastics
    • High-temperature lubricant additive packages
    • Specialty adhesive resins for industrial assembly lines
    Free Quote

    Competitive 1-Tert-Butyl-3-Nitro-4-Chlorobenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Tel: +8615371019725

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    Certification & Compliance
    More Introduction

    Introducing Our 1-Tert-Butyl-3-Nitro-4-Chlorobenzene

    Quality Rooted in Experience

    In the specialty chemicals field, quality isn’t a buzzword—it forms from years of lab trials, discussions with clients, and seeing molecules perform in places from research benches to industrial reactors. As a chemical manufacturer producing 1-tert-butyl-3-nitro-4-chlorobenzene, every process point, from raw material assessment to finished crystallization, has been hammered out through stubborn troubleshooting and listening to customers who build things that matter. We began producing this compound not as an arm’s-length supplier but out of demand from syntheses where reliability counts, especially at scale. Seeing a nitroaromatic like this one make downstream steps easier for a mid-sized agrochemical company or shelf-life longer for an ambitious pharmaceutical startup always adds purpose to what we do.

    Why 1-Tert-Butyl-3-Nitro-4-Chlorobenzene Stands Out

    This molecule comes up again and again for a reason—its tert-butyl group, nitro functionalization, and chloro position set it apart chemically and in the way it sits in a formulated product. Compared with other nitrochlorobenzenes or tert-butylated ring systems, it resists degradation in harsher synthetic routes. There’s more to it than a fleeting yield improvement. Researchers tell us that downstream steps, like nucleophilic substitutions and coupling reactions, run cleaner when they switch to our material. That’s not luck. Part of it is purity, owing to purification steps developed right here. Each time we receive feedback—maybe an impurity profile appearing by high-resolution chromatography—we dig through root causes, tweak solvent choices, or refine distillation points.

    The difference becomes clear during workup in a typical organic synthesis. Substitute in a similar compound lacking the tert-butyl group, and undesired side reactions turn into a headache, particularly in the presence of strong bases or acids. Similar issues arise if the nitro and chloro groups shift locations—reactivity jumps, and control drops. Over time, chemists notice which building blocks feel forgiving in unpredictable day-to-day runs. This specific substitution pattern performs as designed, not just under textbook conditions but in the hands of graduate students and plant engineers alike. That reliability comes from more than a clean COA—it’s an echo of all the times we’ve worked through issues alongside end-users who need consistent outcomes, not surprises.

    Applications Shaped by Real-World Performance

    Let’s get concrete about what sets 1-tert-butyl-3-nitro-4-chlorobenzene apart in use. Our customers include small molecule drug developers, contract research organizations, and specialty chemical firms. For those pursuing complex aromatic intermediates, the chlorine atom opens doors for site-selective transformations. The nitro group, with its electron-withdrawing power, tunes the aromatic ring for later chemistry. Playing off the bulky tert-butyl at the para position, you get steric protection, reducing overreaction in catalytic cross-couplings or directed ortho metalation.

    Compare this to using meta- or para-chloro-nitrobenzenes without added tert-butyl—side products pop up, yields need reworking, and purification gets expensive. One long-standing pharmaceutical partner reported cleaner final API crystallizations after swapping to our compound from a less hindered analog. They no longer saw trace over-nitration that once required repetitive column runs. This isn’t by accident. The dense, nonpolar tert-butyl group acts like a physical shield in synthesis, funneling selectivity into the hands of a patient chemist.

    Some agrochemical developers use this arene as a scaffold for new herbicide candidates. Their synthetic routes put stress on starting materials throughout halogenations, nucleophilic substitutions, and coupling steps. Each functional group on this molecule serves a purpose: the chloro for leaving-group chemistry, the nitro for reactivity balance, and the tert-butyl to stop unwanted para-attack. By fine-tuning these positions, the compound can lead to new structures impossible or costly with less hindered building blocks. Even outside of pharma or agchem, specialty polymer and specialty dye manufacturers draw on the same reactivity suite. Their process chemists want intermediates that withstand scale-up, tolerate variable moisture, and blend without unpredictable exotherms. In each of these uses, having a high-purity, predictable material saves days of troubleshooting and cuts down on waste.

    From Manufacturing Floor to Finished Product

    Our plant staff engage in regular training to meet the detailed requirements of products like 1-tert-butyl-3-nitro-4-chlorobenzene. Small batch sample runs let us screen each reaction step under the same temperature, agitation, and pressure conditions every production lot will face. If byproducts appear, we run root-cause analysis rather than shortcutting to the next lot. Over time, that discipline means less batch-to-batch variance—not just a tight loss on drying or melting range, but side impurities out of the quantifiable range by NMR or GC-MS.

    Water content, residual solvents, and trace metals drop because of investments in fractional distillation, activated carbon steps, and cleanroom packing on the tail end. Our technical team fields questions directly from buyers and formulators, not through intermediaries. Direct dialogue convinced us to adopt tighter particle control during milling, which meant smoother dissolutions in the field and cleaner reactor charges for clients who scale products to kilos or tonnes.

    We select packaging based on how this nitroaromatic travels. For some customers, material heads to humid, hot climates, and double-sealed drums block moisture ingress. For others running small syntheses, kilogram containers with advanced cap liners reduce exposure to air during sample removal. This feedback loop—hearing not just which specs work on paper, but what fails during actual use—drives design on packaging as much as it does on the product itself.

    Product Integrity: Not Just a Claim, but a Practice

    Building trust with chemists doesn’t happen through glossy brochures or brochure-ware claims. It happens when someone calls about an off-smell or a small color shift and our team owns the investigation. Chemists care about trace differences, and even micro-amounts of oxidation or byproduct shift how reliably a reaction proceeds. Our team re-tests retain samples from every order, drawing on libraries of spectra and process logs. If a deviation appears, solutions come in the form of updated cleaning cycles, tweaked crystallization, or sometimes raw material source changes. Every improvement goes straight into the next batch.

    Regulatory bodies focus on trace contaminants, particularly whenever aromatic nitro compounds move into food-contact or pharmaceutical applications. In response, we track every intermediate and handle transportation with compliance from package integrity to certification paperwork. Each regulatory year brings new expectations—trace solvents, lower detection limits, or emerging impurity classes. Our lab pivots to meet these with the same energy as any R&D group facing a new synthesis challenge.

    What Sets Our Product Apart

    In markets where lowest price sometimes drives choices, we stuck to a different path. Our product never leaves the plant without lot-specific analytics and a level of documentation drawn from regular dialogue with actual users. If a new spectral impurity appears, especially during scale-up, formulas and procedures adapt—sometimes overnight. Statistical process control flagging means a batch trending outside historical specs doesn’t go to customers. While some see this as cost, decades of client retention show that customers stick with predictable suppliers after a few missteps with unvetted ones. Other suppliers outsource pieces of the process or blend intermediates on the fly, but our lines run full circle from raw input to finished drum under one roof, with complete in-house traceability and staff who see feedback as fuel for the next improvement.

    Years ago, we found a minor stream generated an off-spec impurity. Rather than masking it or blending away the problem, our engineers rebuilt part of the reactor setup, installing additional cooling controls and inline monitoring. That new step caught the issue before it could enter finished goods, and clients who once experienced irregular color changes shared their appreciation for frankness and commitment to traceability. Not many trace where each lot originated, but our QC and QA labs can match any complaint to actual people, lots, and steps within hours, not weeks.

    Reliability in Diverse Synthetic Protocols

    Laboratories and commercial plants handle 1-tert-butyl-3-nitro-4-chlorobenzene differently. Scale brings new challenges—reactions that work perfectly in 5 mL may gum up at 50 L. Shelf-life, storage, and container compatibility each get real testing. We’ve supported clients as they move from bench synthesis to full-scale preparation, troubleshooting what happens as mixers get larger, temperature gradients sharpen, and unexpected solvent/water contacts arise. Our technical team shares not just data but process walk-throughs and start-up guidance. That transparency with partners brings a sense of shared investment—if a batch doesn’t meet performance targets during a pilot trial, we want to know before it lands in a final product.

    At the heart of commercial chemistry sits a triangle of reactivity, work-up, and purification. The configuration of our benzene ring—tert-butyl, nitro, and chloro at distinct positions—affects each layer. A nitro group boosts electrophilicity and slows unwanted side processes, while the chloro stands ready for SNAr or Pd-catalyzed transformations. By comparison, analogs with differently placed substituents swing too far toward instability or excessive inertness. The tert-butyl cap shields the aromatic core through harsher synthetic steps, so users get to the next intermediate with less cleanup.

    Consistent Innovation Based on Customer Feedback

    Process not only involves adhering to written procedures but also adapting based on user feedback. Several years back we noticed recurring requests for different particle sizes from research clients scaling up chromatographic separations. Our production chemists collaborated with end-users, ran application tests, and found that gently modified crystallization temperatures could tighten particle distribution while preserving overall purity. Those improvements allowed for smoother integration into next-step chemistry and saved users time post-delivery.

    Another sector, dye developers, struggled with lingering color tint in their downstream purification. Instead of brushing off complaints, our product team traced the tint back to an upstream minor contaminant liberated during extended storage. Rather than treating it as a logistics issue, adjustments in drying time and post-packing inert gas flushes nearly eliminated the problem. This dialogue, troubleshooting, and adaptation mindset underpins our strategy—treating each delivery as a partnership, not just a transaction.

    Safety and Compliance

    Working with nitroaromatics brings unique handling and safety requirements. Our production floors implement layered containment, regular sensor calibration, and employee PPE training that matches responsible care protocols. We keep real-time logs on solvent emissions and contain dust at multiple points, knowing that trace exposure matters. Each team member participates in regular refresher courses, because sustainability and worker safety come from daily choices, not slogans.

    We follow strict waste tracking guidelines; disposal routes use licensed handlers, and every outgoing batch matches regional regulatory requirements for hazardous goods. This isn’t an afterthought—for companies seeking ISO or equivalent certification, transparent records and rigorous environmental controls support global shipment and reduce customer risk. Our approach—monitoring air, water, and solid discharge—has survived third-party audits and always aims higher with each review cycle.

    Our Commitment to Supporting Science and Industry

    Every time we ship a lot of 1-tert-butyl-3-nitro-4-chlorobenzene, we recognize the project behind the order. Sometimes it’s pushing a novel drug candidate to its next step. Other times, it’s about enabling a greener synthesis or building safer crop protection solutions. By responding with agility to both problems and suggestions, we maintain technical leadership in the face of shifting market and regulatory pressures.

    Our technical and production teams stay up to date on developments in synthetic methodology. We tap into preprints, attend technical workshops, and invite feedback from industrial partners who challenge us with new process conditions. Informed by this ongoing learning loop, refinements enter production, eliminating manual bottlenecks, preventing cross-lot contamination, and boosting purity beyond minimum specs.

    Choosing Experience and Accountability in a Competitive World

    Decades of building and refining production lines for nitroaromatics led us to one conclusion: consistency earns trust. Each incoming order for 1-tert-butyl-3-nitro-4-chlorobenzene activates the same rigorous screening, QC testing, and order tracking as every high-profile client. Companies seeking to eliminate downtime, cut purification headaches, or accelerate route optimization benefit from a partner who sweats the details—from starting material to sealed drum.

    If unexpected issues do occur, we answer with full transparency, bringing in plant managers, technical staff, and decision-makers to own both cause and solution. That accountability defines our family-owned culture and shapes the trust we enjoy with repeat partners. For those who want more than a commodity product, our track record shows why direct-from-manufacturer support impacts not only production schedules, but also bottom line and innovation.

    The Path Forward

    Markets continue to evolve. Synthesis protocols grow more complex, safety and sustainability challenges evolve, and regulatory scrutiny intensifies. Our role as a dedicated manufacturer of 1-tert-butyl-3-nitro-4-chlorobenzene is to anticipate these shifts and adapt in step with our customers’ goals. We invest in process improvement, transparent data, and open dialogue. That approach moves the molecule from a line item on a PO to a dependable enabler in innovation.

    Whether supporting cornerstone pharmaceutical syntheses, shaping agrochemical pipelines, or fueling exploratory research in high-value specialties, our 1-tert-butyl-3-nitro-4-chlorobenzene stands ready for the next chemical challenge—backed by years of know-how, openness to improvement, and the drive to keep chemistry working smarter every day.