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HS Code |
829079 |
| Name | 4-N-Butoxynitrobenzene |
| Cas Number | 104-45-0 |
| Molecular Formula | C10H13NO3 |
| Molecular Weight | 195.22 g/mol |
| Appearance | Yellow crystalline solid |
| Boiling Point | 302 °C |
| Melting Point | 44-46 °C |
| Density | 1.19 g/cm³ |
| Solubility In Water | Insoluble |
| Flash Point | 148.3 °C |
| Smiles | CCCCOc1ccc(cc1)[N+](=O)[O-] |
| Pubchem Cid | 8168 |
As an accredited 4-N-Butoxynitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with screw cap, hazard labels, product name “4-N-Butoxynitrobenzene”, safety instructions, supplier details. |
| Shipping | **Shipping Description for 4-N-Butoxynitrobenzene:** Ship 4-N-Butoxynitrobenzene in tightly sealed containers, protected from light, heat, and moisture. Use approved packaging according to local and international regulations. Label as a hazardous chemical (if applicable), and handle with care to avoid spills or exposure. Transport via ground, air, or sea as per chemical transportation guidelines. |
| Storage | 4-N-Butoxynitrobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Store separately from strong oxidizers, acids, and reducing agents. Ensure appropriate labeling and secondary containment to prevent leaks or spills. Use only in chemical storage areas with access controls and suitable chemical safety protocols. |
Applications of 4-N-Butoxynitrobenzene in Industrial ManufacturingAs the direct producer of 4-N-Butoxynitrobenzene, we supply this specialized intermediate for highly specific segments of the chemical industry. Detailed below are main B2B applications, compliance requirements, formulations, downstream process stages, and resulting end products as verified in real-world practice. 1. Synthesis of Pharmaceutical IntermediatesPharmaceutical manufacturers use 4-N-Butoxynitrobenzene as a key building block for complex heterocyclic intermediates. The process involves catalytic hydrogenation followed by functional group modification to develop advanced substances for Active Pharmaceutical Ingredient (API) synthesis. Downstream partners require traceable sourcing, impurity profile control, and precise handling protocols to achieve regulatory-grade purity, integrating the nitro compound at early synthetic steps for ultimate yield optimization in finished APIs like antibacterial agents and selective CNS drugs. Industry compliance standards
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2. Advanced Agrochemical SynthesisMajor agrochemical producers incorporate this nitroaromatic in the assembly of selective herbicides and fungicides. Through nucleophilic aromatic substitution routes, it participates in the creation of high-value crop protection active components. Industrial processes demand assured batch-to-batch reproducibility and adherence to field residue standards. End-use applications require formulated blends maintaining stable release rates suitable for modern integrated pest management systems. Industry compliance standards
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3. Electrochemical Material ProductionThe electronics and specialty battery sectors employ 4-N-Butoxynitrobenzene for the synthesis of high-purity aromatic intermediates in the fabrication of advanced electroactive materials. Downstream users require controlled particle size, low residual solvent content, and predictable electrochemical behavior. The compound is introduced as a film precursor or a cathodic material base, impacting the capacity and cycle stability in consumer and industrial battery systems. Industry compliance standards
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4. Dyes and Pigments ManufacturingProducers of specialty dyes and pigments rely on 4-N-Butoxynitrobenzene for the synthesis of azo and anthraquinone colorants. The nitroaromatic serves as a stable intermediate enabling clean diazotization and coupling reactions, achieving the depth and lightfastness required in technical textile treatments, plastics coloration, and printing ink applications. Formulators seek batch records ensuring consistent chromophore assembly, especially for applications in regulated commodity chains such as food packaging or medical textiles. Industry compliance standards
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5. Synthesis of Specialty PolymersIn the resin and engineering plastics industry, 4-N-Butoxynitrobenzene functions as a reactive monomer or modifying agent to impart targeted electronic and mechanical properties to polymers. Polymer chemists introduce it during step-growth or free-radical polymerization, facilitating the design of dielectric resins and surface-active copolymers with nitroaromatic segments. Strict process control ensures minimal oligomer residue and meets industry-specific product qualification inspections, particularly in the electronics, composites, and packaging sectors. Industry compliance standards
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For years, we have committed ourselves to producing high-purity 4-N-Butoxynitrobenzene, a nitroaromatic intermediate valued by manufacturers in the fine chemicals sector. This compound, classified as a substituted nitrobenzene, features a butoxy group fixed para to the nitro function. Chemists use it not just for its structure, but for what it brings to the synthesis of dyes, pigments, pharmaceuticals, and even specialty polymer additives.
Each batch of 4-n-butoxynitrobenzene, bearing the CAS number 104-45-0, draws from our refined liquid-phase nitration process. We control reaction parameters at every stage, monitoring color, melting point, and by-product limits. Typical purity measures above 99%, and trace impurities—such as related positional isomers and starting anilines—stay well below detectable thresholds.
Physical inspection shows a pale yellow crystalline appearance, with a melting point between 43℃ and 46℃, aligning with key reference data. Moisture content often determines shelf stability; we maintain water below 0.2%, verified using Karl Fischer titration. Only samples conforming to set melting point, GC purity profiles, and minimal residual solvents go forward for packaging.
Nitrobenzene derivatives present hazards in their manufacture, handling, and use. Over the decades, we have seen process upsets stemming from exothermicity during nitration reactions. Our plant has tackled runaway events and learnt to implement incremental acid dosing, coupled with jacketed reactor monitoring. Waste acid neutralization and scrubbing, both issues with legacy types of production, led us to design more contained operations. Few intermediates respond to process fingerprints as sensitively as 4-n-butoxynitrobenzene—color shifts or subtle odor changes signal in-process deviations. Workers recognize these cues through years spent in the plant, not lab-scale theory.
The value of this compound lies less in its basic chemical properties and more in the transformations it enables. In the dye industry, 4-n-butoxynitrobenzene undergoes reduction and coupling to yield intermediates for azo, anthraquinone, and phthalocyanine dyes. These finished products appear in textiles, printing inks, and even electronic materials.
Our pharmaceutical partners use this molecule as a substrate in multi-step syntheses. The butoxy group selectively participates in nucleophilic substitution and reduction, leading to functionalized amines—or acts as a protected tether for constructing complex heterocyclic scaffolds. Sometimes the nitro group must be transformed under mild hydrogenation; we have worked closely with customers optimizing their reduction protocols, sharing lessons about solvent choice and catalyst passivation seen in plant routines.
Other routes take advantage of the nitro functionality itself, for instance in agrochemical actives. Locally, some partners have converted 4-n-butoxynitrobenzene to its corresponding aniline derivative, further acylated for specialty fungicidal compounds. This highlights the importance of high isomeric purity and free amine absence, both recurring requests we receive from this sector.
The difference may appear minor between 4-n-butoxynitrobenzene and other nitrobenzenes substituted with ethoxy, propoxy, or methoxy groups. From a purely structural viewpoint, n-butoxy substitution increases lipophilicity and changes solubility profiles in common solvents, which matters when fine-tuning dye or drug synthesis processes. For some downstream reactions—where steric factors help control regioselectivity—our product enables cleaner reactions, less by-product formation, and easier separations.
Over the years, we have also processed orders for substituted isomers such as 2-n-butoxynitrobenzene, but almost every synthetic chemist we serve eventually settles on the para compound for the balance of reactivity and handling. The longer side chain offers a lower vapor pressure compared with the ethoxy or methoxy derivatives, contributing to safer handling on the plant floor.
Experience has taught us that subtle production differences impact every downstream process. In one project, a global dye maker struggled with yield loss because of undetectable levels of meta isomer contamination in their intermediate supply. Our team worked directly with their analytical lab, compared spectral fingerprints, and helped identify the root cause: process drift at the nitration stage. Regular dialogue between technical teams, not just product managers or brokers, keeps us trustworthy and our partners competitive.
Maintaining quality requires both modern analytical tools—HPLC, GC-MS, and NMR—and skilled operators who know how to read a process sheet, troubleshoot changes, and document deviations. We run stability trials and stress tests that go beyond basic batch release specifications. Recognizing that supply reliability and impurity fingerprints can influence not just regulatory approvals but patent challenges in the downstream marketplace, we preserve batch records for years and refer back to earlier runs whenever questions arise.
Handling nitrobenzenes involves more than regulatory compliance—these chemicals require cultural discipline at every layer of production. We keep in touch with regulatory updates on handling and environmental controls, working with local and international agencies for safe waste management. We invest in closed-loop processes that reduce fugitive emissions, monitor workplace exposure, and maintain full traceability for each drum leaving our premises. This approach did not appear overnight; only repeated audits, both internal and external, force a manufacturer to refine its routines.
Again and again, we are reminded of the difference between theoretical chemistry and actual factory practice. Many common issues occur only on scale-up: agitation limits, temperature gradients, or even batch inhomogeneity. Powdered samples may cake or absorb moisture if left exposed, so packaging and storage methods receive as much attention as upstream chemistry. Logistics also require forward thinking: export-size drum packaging, temperature-controlled containers in hot climates, and clear material identification labeling to avoid customs holdups.
We have adapted bottle sizes and packaging liners based on direct feedback from our customers. Pharmaceutical plants in humid regions wanted improved tamper-proof seals and double liners, because moisture alters reaction outcomes and blocks approvals in regulated environments. Large dye works requested bigger batches with tighter particle size distributions for faster downstream dissolving. Each of these changes owes more to hands-on collaboration than to one-size-fits-all specifications.
Supply shortages in major aromatic feedstocks—nitrobenzene and n-butanol—influence our lead times and lot sizes. Fluctuating regulatory restrictions on benzene derivatives in various regions push us to diversify sourcing and minimize bottlenecks. Decades of relationships with upstream suppliers, paired with new risk-screening protocols, allow us to flag and mitigate most disruptions before orders get involved. Transparent communication with users about evolving situations has earned us trust, even through raw material shortages or logistics slowdowns.
We often assist our partners in planning inventory safety stocks or adjusting order schedules to match cyclical swings in their own production forecasts. Our technical and commercial teams work side by side, sharing process updates, advising on long-term storage, and warning about minor contaminant risks that only surface in certain reactions. These facts weigh more than distant assurances from faceless middlemen or sites disconnected from the realities of custom synthesis.
We witness ongoing requests from buyers for greener, safer, and more sustainable nitrobenzene derivatives. Our team revises process flows to minimize energy usage, cut down on non-recyclable process aids, and enhance spent acid recovery. With the adoption of closed-filtration and solvent recovery systems, workplace exposure and chemical loss decrease. Overseas, we have helped clients scale pilot runs using our tailored grades of 4-n-butoxynitrobenzene developed by modifying melting range and flow properties.
Some of our competitors attempt short-term cost savings through shortcut process routes or relaxed purification steps, aiming for fast and cheap output. In real-world conditions, this introduces more unanticipated impurities, batch losses, or even safety incidents. Our view remains rooted in robust QC, staged plant upgrades, and robust staff retention. The cost of saving a few minutes on line-cleaning fades compared to the impact of a contamination recall or reputational hit—something every seasoned chemical plant manager learns the hard way.
Some of our loyal customers are specialty chemical research teams that seek small custom lots for exploratory syntheses. We assign technical experts to guide order development. Custom batch production includes thorough impurity analysis, and real-time troubleshooting if downstream reactions behave abnormally. Problems might range from incomplete reduction to unexpected by-product formation—issues best solved through direct technical dialog rather than generic specification exchanges.
Supporting R&D goes both ways. Customers often feed back data to us, especially if they encounter unexpected outcomes with a particular lot. These learning cycles improve our own manufacturing and inspire targeted process tweaks, making for a virtuous feedback loop. The close partnership between plant floor and customer lab yields far greater progress than any rigid spec sheet.
There is growing demand for sustainable approaches to aromatic nitro compounds, both due to market pressures and regulatory scrutiny. We have invested in improved vapor scrubbing, solid waste containment upgrades, and new water treatment systems. Every change follows from recognized issues—fugitive vapor complaints from neighbors, rising effluent monitoring costs, or the simple logic that solvent recovery can fund itself in under a year. Closed-system investments started as a regulatory demand but have paid off by improving both plant safety and product yields.
We are aware that chemical intermediates such as 4-n-butoxynitrobenzene must earn their place in end-use products, which in turn face rising sustainability expectations. In response, we continually audit our own environmental performance, benchmark competitors, and keep dialogue open with user groups—industry, regulators, and the wider community.
Distributors and brokers may focus on competitive pricing or fast turnarounds, yet repeat business in specialty chemicals always circles back to technical knowledge and honest support. Our best supply agreements depend on clear technical exchanges—whether discussing impurity management, specific packaging preferences, or custom lot production.
We welcome customer audits, onsite visits, and full disclosure. This builds mutual confidence and problem-solving ties that let both sides weather tough markets, regulatory shifts, or sudden plant outages. Long-standing customers know the difference between manufacturer-supplied material and third-party goods that lack manufacturing traceability.
The chemical industry faces shifts driven by regulation, supply dynamics, and consumer trends. 4-n-butoxynitrobenzene remains a niche yet essential intermediate for industries pushing toward better, safer, and more sustainable finished products. We are committed to evolving in step with new technical requirements, product safety demands, and environmental responsibilities that shape our sector.
Building on years in the sector, we know that real progress—and business stability—come through close engagement with both production realities and downstream user needs. Reliable supply, deep technical memory, and a commitment to quality matter more to users than a fleeting price advantage. Through active problem-solving and open sharing of plant experience, we continue to improve our process, support our partners, and prepare for a chemical industry that asks more from its intermediates every year.
Some of our most valuable process breakthroughs have come from feedback—sometimes a phone call about a minor color difference, other times a technical report of unexpected reactivity in a new process. We keep these communication lines open and encourage frequent engagement from every customer group. Only by listening closely and adapting can a manufacturer evolve past routine production and play a key role in advancing downstream innovation.
Every successful plant visit or technical call reinforces the value of direct relationships, open technical discussion, and honest reporting. We invite all users, from long-standing partners to newcomers, to see firsthand how our 4-n-butoxynitrobenzene is produced, managed, and released to the market. This approach secures both product quality and customer confidence—two outcomes that no shortcut or templated sales pitch can match.