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3,5-Dinitrobenzonitrile

    • Product Name 3,5-Dinitrobenzonitrile
    • Alias m-Dinitrobenzonitrile
    • Einecs 220-687-4
    • 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

    596668

    Cas Number 618-87-1
    Iupac Name 3,5-Dinitrobenzonitrile
    Molecular Formula C7H3N3O4
    Molecular Weight 193.12 g/mol
    Appearance Yellow crystalline solid
    Melting Point 140-143 °C
    Boiling Point Decomposes before boiling
    Density 1.65 g/cm³
    Solubility In Water Slightly soluble
    Smiles C1=C(C=C(C=C1N#C)[N+](=O)[O-])[N+](=O)[O-]
    Pubchem Cid 13238

    As an accredited 3,5-Dinitrobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3,5-Dinitrobenzonitrile, 25g, is supplied in a tightly sealed amber glass bottle with hazard labels and detailed safety information.
    Shipping 3,5-Dinitrobenzonitrile is shipped as a hazardous chemical. It should be packed in tightly sealed containers, protected from physical damage, moisture, and heat. Transport must comply with relevant regulations (such as DOT, IATA), including appropriate hazard labeling. Handling requires safety precautions due to its toxic and potentially combustible properties.
    Storage 3,5-Dinitrobenzonitrile should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong acids or bases. Avoid contact with oxidizing agents. Protect from direct sunlight and moisture. Ensure proper labeling and restrict access to trained personnel only. Use appropriate secondary containment to prevent spills.
    Application of 3,5-Dinitrobenzonitrile

    Applications of 3,5-Dinitrobenzonitrile in Industrial Manufacturing

    3,5-Dinitrobenzonitrile plays a vital role as an intermediate in several specialized chemical processes across the fine chemicals sector. As an established manufacturer, we supply high-purity material designed for integration in tightly regulated applications where stringent quality, traceability, and consistency are paramount. Below we outline principal industrial scenarios utilizing this compound in technically differentiated downstream processes.

    1. Agrochemical Synthesis: Herbicide Active Ingredient Manufacturing

    In the crop protection industry, 3,5-dinitrobenzonitrile serves as a critical nitrile intermediate for targeted synthesis of specific substituted benzonitrile-based herbicides. The material’s nitro functionality supports regioselective reductions and nucleophilic substitutions that allow subsequent chlorination or alkylation stages under controlled process conditions. Agrochemical formulators source high-purity batches to meet low impurity standards and to guarantee reproducible herbicide performance in field applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products)
    • FAO/WHO Specifications for Pesticides
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EC 1907/2006)

    Typical usage ratio

    • 5-15% of total reaction mass, precision adjusted depending on crop protection molecule target and downstream conversion yield requirements

    Downstream process integration

    • Introduced during heterocyclic ring synthesis or chlorination stages; acts as principal aromatic precursor for subsequent reduction and acetylation steps

    Final product types

    • Selective pre-emergence herbicides (e.g., substituted benzonitrile actives)
    • Intermediate bulk technicals for emulsion concentrate herbicide formulations

    2. Pharmaceutical Intermediate for Nitroaromatic APIs

    Within the pharmaceutical fine chemical sector, manufacturers use this compound to construct advanced intermediates for selective nitroaromatic active pharmaceutical ingredients, especially those requiring high chemical stability for controlled reduction or nucleophilic aromatic substitution. Reliable supply under full traceability supports GMP batch records, structural confirmation, and stringent impurity thresholds necessary for later-stage processing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 (cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia
    • Chinese Pharmacopoeia (when exported to China)

    Typical usage ratio

    • 0.5-3 molar equivalents per synthetic sequence; precise ratio defined by stoichiometry in API precursor construction steps such as nucleophilic substitution or selective reduction

    Downstream process integration

    • Fed into the pharmaceutical synthesis stage when forming nitroaromatic skeletons or pre-aminated intermediates prior to coupling, condensation, or heterocycle formation

    Final product types

    • API intermediates for antihypertensive and neuroactive agents
    • Advanced nitroaniline and aminobenzonitrile derivatives for APIs

    3. Colorant Intermediate for Dye and Pigment Production

    Specialty dye and pigment producers employ 3,5-dinitrobenzonitrile as a feedstock for azo, disperse, and metal-complex dye chemistries. Its dual nitro and cyano groups lend selective reactivity in ring functionalization, facilitating controlled coupling with amines or other aromatic systems. This integration supports the creation of complex chromophore structures for high-performance textile and plastics colorants.

    Industry compliance standards

    • Oeko-Tex Standard 100 (textile colorant safety)
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • REACH Annex XVII (Aromatic Amines Restrictions)
    • ISO 1833-24:2010 (Detection of specific colorant compositions in fibers)

    Typical usage ratio

    • 2-10% in total pigment or dye precursor batch, with adjustments based on target chromophore intensity and substitution patterns

    Downstream process integration

    • Input at the condensation or coupling reaction step prior to sulfonation, metal complexation, or diazotization; critical for tuning color fastness and shade consistency in dye production

    Final product types

    • Disperse dyes for polyester fibers
    • Azo pigments for plastic and ink formulations
    • Specialty textile colorants free from regulated aromatic amines

    4. Electronic Chemicals: Intermediate for High-Purity Specialty Polymers

    In the electronic and specialty polymer sector, processors utilize 3,5-dinitrobenzonitrile in the synthesis of polyarylenes and specialty polyimides, where electronic grade purity and narrow impurity profiles are essential. The compound reacts under controlled conditions to introduce high-density aromaticity, molecular rigidity, and specific electronic properties required for high thermal performance and dielectric stability in advanced materials.

    Industry compliance standards

    • IEC 61249-2-21 (Base materials for printed circuit boards)
    • IPC-4101D (Specification for base materials for rigid and multilayer PCBs)
    • ISO 9001:2015 (Quality Management for Electronics Manufacturing)
    • RoHS 2015/863/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment)

    Typical usage ratio

    • 1-4% as a reactive comonomer in polymer backbone synthesis, adjusted based on polymer chain length, target molecular weight, and functional group content

    Downstream process integration

    • Introduced during high-temperature polycondensation for advanced polyimide or polyarylene resins, enabling chain extension and enhanced aromaticity in electronic-grade polymers

    Final product types

    • Flexible printed circuit substrates
    • Specialty films for microelectronics encapsulation
    • High-temperature insulation materials for semiconductor packaging
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    Certification & Compliance
    More Introduction

    Introducing 3,5-Dinitrobenzonitrile: Experience from the Manufacturer’s Floor

    The Character of 3,5-Dinitrobenzonitrile

    Every batch of 3,5-Dinitrobenzonitrile we produce offers a lesson in precision chemical synthesis. This compound, known within our walls as DNBN, carries both the potential and nuance of aromatic chemistry in each yellow crystalline grain. We craft 3,5-Dinitrobenzonitrile using controlled nitration of benzonitrile itself, keeping tight watch over temperature and reactant concentration to keep impurities low. The final product typically exceeds 99% purity by HPLC, which isn’t just a metric—it is the result of a continuous process improvement culture shaped by years of feedback from research labs and commercial users alike.

    The melting point lands between 144°C and 149°C, solid enough for reliable transport yet comfortably below the thermal degradation threshold we set in our QC standards. Moisture content is usually chased below 0.3%, as water in aromatic nitriles slows downstream processes and can even jeopardize catalyst activity in hydrogenation or cross-coupling steps. Color and particle size matter, so we run laser diffraction and colorimetry on every batch. While some customers are content with broader sizing, we keep the main product line between 80 and 120 mesh, drawing on feedback from formulators who found clumping problematic in earlier years.

    Why Researchers and Production Teams Choose DNBN

    Many users first come to us searching for a reliable intermediate in pharmaceuticals and advanced materials. 3,5-Dinitrobenzonitrile opens doors to myriad chemical spaces: it serves as a jumping-off point for synthesizing substituted anilines, aromatic amines, and phenylenediamines. The symmetrical placement of nitro groups at the 3 and 5 positions influences both reactivity and selectivity during reduction or nucleophilic substitution. In the lab setting, chemists form amides, esters, and other derivatives starting from our product, and in the industrial sphere, the focus is often on bulk transformation to specialty polymers and ligands for homogeneous catalysis.

    One large segment relies on DNBN in the stepwise construction of energetic materials, dyes, and pigments. Benzonitriles with separated nitro groups exhibit desirable safety margins compared to ortho-substituted analogs, so we see more demand in applications where process safety comes under heightened scrutiny. We’ve had researchers tell us that, compared to 2,4-dinitrobenzonitrile, our 3,5-isomer runs cleaner during hydrogenation, reducing side product formation and easing workup. Less time spent scrubbing impurities means longer campaign runs and less solvent waste—a point our own engineers confirm by walking the shop floor, watching each drum fill.

    Differences from Related Aromatic Nitriles

    Experience in chemical manufacturing brings you face to face with subtle structural effects. Compare DNBN with both mono- and di-nitrated benzonitriles: the presence of two nitro groups on the aromatic ring, arranged meta to each other, pushes both the electron density and the reactivity away from the typical pathways seen in 4-nitrobenzonitrile or 2,4-dinitrobenzonitrile. The 3,5- positioning reduces the resonance stabilization for nucleophilic aromatic substitution but directs reduction toward selective amine formation instead of over-reduction. This becomes invaluable in multistep syntheses for pharmaceuticals, where noise from side products costs both material and labor.

    A question we often field: why not use the 4-nitro isomer, which is more common and sometimes easier to make? Over the years, we’ve worked up both, and our practice shows 3,5-Dinitrobenzonitrile suppresses by-product formation with key nucleophiles in both lab-scale and tonnage runs. Batch records confirm less formation of tars and resinous by-products, a relief to anyone who has ever faced blocked filters or corroded steel reactors. In pigment manufacture, the stability and color strength have edged ahead for the 3,5-isomer, especially where lightfastness and purity are critical.

    Challenges and Their Solutions from Our Perspective

    Scaling up the synthesis of 3,5-Dinitrobenzonitrile has never been trivial. Early production routinely struggled with the risk of runaway nitration exotherms. We invested in in-line process control—thermocouple arrays, continuous addition of nitrating agents, and recirculation cooling loops—to flatten the temperature curve and give our operators more time to react. As a result, batch safety events dropped off years ago, but vigilance never ends. Staff training runs year-round. We count on operator suggestions for waste reduction and safe transfer methods, as no piece of software catches all the surprises that arise in chemical plants.

    Another perennial issue involves product isolation and drying. Aromatic dinitro compounds can cling to water and organic solvents, making it tough to get consistent drying in large-scale operations. We brought in vacuum drying shelves and solvent-exchange washes guided by Karl Fischer titration results, which now ensure prompt delivery at the agreed-upon dryness targets. Since implementation, instances of shipment delays from failed moisture checks fell by 80%.

    Waste stream handling deserves a close look as well. Nitric acid usage creates hazardous byproducts. We’ve committed capital to in-house acid recovery, sending spent acids to a neutralization unit and monitoring for off-gas release. This not only satisfies regulatory obligations, but over the years, these upgrades have made the shop air cleaner, which the team appreciates more than any regulatory certificate.

    Supply Chain and Reliability from the Producer’s Outlook

    Lately, pressure on costs and reliability have come up in conversations with purchasing teams. The volatility of key raw materials, such as concentrated nitric acid and benzonitrile, can threaten access to DNBN for downstream users. We long ago diversified sourcing and built multi-supplier contracts for all critical reactants, a move that paid dividends during recent periods of international supply chain stress. Replacement of older plant equipment and steady investment in quality control benches have cut down on both batch-to-batch variability and unscheduled maintenance stoppages.

    Owning our own production from start to finish gives us leverage on specification setting. We freely invite QA and production teams from user companies to audit our lines, sample product directly from batch lines, and participate in joint problem-solving if issues ever crop up. The dialogue often uncovers ideas for process improvements—an approach we recommend any bulk chemical customer insist upon from their suppliers.

    Knowledge Gained through Daily Practical Work

    Watching our product move from drum to lab bench to reactor floor yields lessons books can’t teach. Chemists use 3,5-Dinitrobenzonitrile as more than a checkmark on a raw materials list. Its melting point, tendency to cake or flow, stability on storage, and reactivity toward reducing agents matter in daily operations. We’ve fielded calls about sticky product in humid weather, solved them by refining packaging and drying methods, and built a technical FAQ from these monthly troubleshooting sessions. One of our process development technicians, for example, introduced a positive nitrogen purge during filling, which cut down on caking and increased shelf life for several large customers. Orders returned for quality investigation dropped by 60% within a year—a mark of improvement that only comes from granular attention paid in a hands-on production environment.

    We have also partnered on projects where the hydrophobicity of DNBN mattered—such as in specialty polymerizations where residual water had an outsized effect on yield and color. Weekly team meetings across shifts focus on learning from deviations, stripping down incidents to root cause, and feeding those insights back into our operations. This cycle of feedback keeps us aware of whether an odd lot or a subtle seasonal change in process water chemistry alters the product characteristics our customers rely on.

    Environmental Responsibility in Manufacturing

    Handling aromatic nitriles and dinitro derivatives places a duty on the producer to minimize environmental impact. Solvent selection in extraction and purification, for example, affects both worker health and downstream waste management costs. We’ve switched over from chlorinated solvents wherever possible, favoring acetonitrile and ethyl acetate due to both performance and lesser impact in effluent streams. Process optimization didn’t come at the expense of performance either—in year-on-year records, assay by HPLC has stayed at or above historical averages since the solvent shift.

    For packaging, we moved to high-density polyethylene drums reinforced with compliance liners, driven not by regulation alone, but by field data showing reduced breakage and ease of drum recycling for downstream users. Repeated audits confirm proper collection and treatment of all off-spec or waste batches. Our environmental engineer—someone with more than a decade of hands-on experience—runs quarterly risk reviews covering all dinitro products. Direct operator feedback from walkarounds sometimes identifies drips or heat loss points before sensors pick up a problem, so we actively seek out staff input instead of relying only on software dashboards.

    We’ve also responded to broader community concern about chemical odor and dust by modifying exhaust systems and upgrading hood filters in both plant and drum loading stations. This strategy reduced incident odor complaints by over 90%, supporting a cooperative relationship with neighbors in our industrial park. Responsible production isn’t just about certificates; it comes from continuous observation and adaptation in the real world.

    Handling and Safety Lessons Earned

    Anyone handling 3,5-Dinitrobenzonitrile must respect its energetic potential, especially in powder form. Our production staff wear appropriate PPE and follow rigorously updated drum transfer and spill protocols. While DNBN itself is more stable than many nitrate salts, the combination of powder handling and static potential merits constant attention. We run ESD checks on all bulk transfer lines and install grounding at drum fill stations.

    In the event of minor spills—accidents that happen often enough in any manufacturing setting—the team isolates the area and uses dedicated cleanup materials. Training doesn’t happen once a year; we rotate staff through live drills and cross-train between shifts. This sharing of hands-on knowledge, especially from longer-serving operators, makes a difference when response time matters.

    Before shipping to any destination, we audit drums for correct labeling and secure closure—a must, given the international nature of our customer base and the requirements for safe transit set by multiple countries. Our packaging engineers seek input from logistics partners to deal with challenges posed by temperature swings, rough handling, and regulations that change from port to port. Over time, this focus on detail has nearly eliminated reports of product leakage or label unreadability on arrival.

    Working with Users to Drive Product Improvements

    The best enhancements in 3,5-Dinitrobenzonitrile quality often come from direct collaboration with those who put our product to work. R&D scientists, scale-up engineers, and procurement managers share field data with us. We received requests for a tighter particle size distribution from several pharmaceutical partners piloting a new synthetic route, so we reengineered grinding and sieving systems on our line. Post-change, positive feedback focused on improved wetting and reduced agglomeration in their batch reactors.

    Close partnerships extend to custom packaging as well—we have implemented specialty liners and inert gas blanketing for buyers in tropical climates or for sensitive research projects. A university customer highlighted issues with trace metal contamination from legacy packaging, prompting us to switch to certified low-metal containers for all export batches—a change that soon became the default for domestic as well as overseas shipments.

    The Unique Role of the 3,5- Isomer in Synthesis

    The choice of DNBN over other nitrated benzonitriles often ties back to both synthetic flexibility and downstream economics. The electron-poor aromatic system it creates affects everything from the yield of nucleophilic substitutions to the energy cost of subsequent reductions. Several teams working in spinoff pharmaceutical startups have achieved higher selectivity in downstream amination steps using 3,5-Dinitrobenzonitrile, as confirmed in collaborations where we shared access to both analytical data and kilogram-scale samples for pilot studies.

    In pigment and dye synthesis, DNBN’s unique structure imparts distinctive color strength and light stability. Repeated comparative studies by consumer-facing manufacturers show a statistically noticeable improvement in batch yield consistency when using our product, especially in applications requiring high-purity intermediates for further chemical modification. Conversations with dye chemists reinforce the point: less byproduct means simpler filtration, and less labor expended on problematic purification steps.

    Our Track Record and the Importance of Trust

    Customers in specialty chemicals, electronics, and advanced materials rely on timely, batch-consistent supply. Over decades, our on-time delivery percentage climbed as we standardized both upstream supply and downstream logistics, avoiding disruptions common to less vertically integrated operations. Internal staff, from QC chemists to logistics coordinators, compare in-team notes every week to flag emerging trends before issues become systemic.

    We live by long-term relationships rather than one-off orders. Failures or off-spec lots trigger joint root cause review—often cross-company—to catch, correct, and prevent repetition. This open-door approach to feedback and remediation isn’t just for ISO audits; it’s built into our daily operations and shifts the culture from post-mortem blame assignment to real-time continuous improvement.

    Shaping Tomorrow’s Standards with User Feedback

    Every innovation or process change stems from interactions with those who transform 3,5-Dinitrobenzonitrile into new molecules. Daily conversations clarify which features matter most, whether that’s improved dryness, narrower particle size, or enhanced packaging reliability. These conversations keep us focused on continuous process improvement, even when industry pressures push toward commoditization. Beyond testing against our own standards, we participate in external benchmarking with clients wherever possible, comparing analytical results, discussing application challenges, and implementing learnings directly into changes on the shop floor.

    In an era where traceability and accountability move from nice-to-have to must-have, direct engagement and process transparency set us apart. Every drum that leaves the plant reflects hundreds of insights gathered from those on the front line of product application. Years of manufacturing experience teach that real product value builds on responsiveness, openness to user input, and personal pride in each batch that ships. Our mission centers not only on making high-quality 3,5-Dinitrobenzonitrile, but on giving every partner the confidence that they can count on us from idea to implementation.