|
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 | 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. |
Applications of 1-Tert-Butyl-3-Nitro-4-Chlorobenzene in Industrial ManufacturingAs 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
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Ingredient and Intermediate ManufacturingLeading 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
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Dye and Pigment Intermediate FormulationSpecialty 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
Typical usage ratio
Downstream process integration
Final product types
4. Electronic and Liquid Crystal Material Precursor SynthesisProducers 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
Typical usage ratio
Downstream process integration
Final product types
5. Fine Chemical Synthesis for Advanced Material AdditivesR&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
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 1-Tert-Butyl-3-Nitro-4-Chlorobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.