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3,5-Dinitrobenzotrifluoride

    • Product Name 3,5-Dinitrobenzotrifluoride
    • Alias 1,3-Dinitro-5-(trifluoromethyl)benzene
    • Einecs 209-026-6
    • 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
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    Specifications

    HS Code

    915733

    Chemical Name 3,5-Dinitrobenzotrifluoride
    Cas Number 401-99-0
    Molecular Formula C7H3F3N2O4
    Molecular Weight 252.11 g/mol
    Appearance Yellow crystalline solid
    Melting Point 54-57°C
    Density 1.66 g/cm³
    Solubility In Water Poorly soluble
    Flash Point 119°C
    Pubchem Cid 12289

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

    Packing & Storage
    Packing Brown glass bottle, 100 grams, sealed with a plastic screw cap. Features hazard labels, product name, and chemical company branding.
    Shipping 3,5-Dinitrobenzotrifluoride is shipped as a hazardous chemical, typically in sealed, UN-approved containers. It must be labeled as an irritant and handled under dry, cool conditions, away from heat and incompatible substances. Appropriate safety documentation, such as an SDS, must accompany all shipments according to local and international transport regulations.
    Storage 3,5-Dinitrobenzotrifluoride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases and oxidizers. Protect from heat, sunlight, and sources of ignition. Use secondary containment, and label storage clearly. Keep away from food, beverages, and combustible materials to prevent contamination or hazardous reactions.
    Application of 3,5-Dinitrobenzotrifluoride

    Applications of 3,5-Dinitrobenzotrifluoride in Industrial Manufacturing

    3,5-Dinitrobenzotrifluoride serves critical roles in multiple chemical manufacturing sectors due to its reliability as an intermediate. As a direct manufacturer, we supply this material for downstream processes where high-purity input, precise reaction control, and compliance with rigorous industry standards define production success. The following segments highlight proven and regulated applications within the industrial landscape.

    1. Agrochemical Active Ingredient Synthesis

    Many crop protection product manufacturers rely on 3,5-Dinitrobenzotrifluoride as a key aromatic building block for synthesizing herbicide and pesticide actives, particularly those requiring fluorinated nitroaromatic intermediates. The material enters nitration and halogenation sequences, undergoing reactions with phenol, amine, or urea derivatives, leading to core structures found in leading herbicidal products. Only manufacturers with integrated quality systems can guarantee low impurity profiles required for downstream environmental approval. Each batch mandates strict process control to attain expected conversion rates, and downstream yields depend on precise feed ratios matched to catalyst and solvent systems. Crop protection molecules derived from this intermediate must pass global residue limits and stability tests prior to field use.

    Industry compliance standards

    • FAO/WHO specification for pesticide technical materials
    • OECD Good Laboratory Practice (GLP)
    • EU REACH regulations for agricultural chemicals
    • US EPA registration requirements (40 CFR Part 158 Subpart A, F)

    Typical usage ratio

    • Serves as 20–40% by weight of starting material in the active ingredient synthesis stage, adjusted by process scale and targeted product composition.

    Downstream process integration

    • Feeds directly into batch or flow reactors after raw material quality validation; enters as initial substrate in multi-step N-alkylation, nitration, or condensation reactions.

    Final product types

    • Selective pre-emergence herbicides (e.g., fluorinated triazine derivatives)
    • Broad-spectrum insecticides where nitroaromatic scaffolds are required
    • Industrial fungicidal agents
    • Crop-specific pesticide formulations

    2. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    GMP-certified pharmaceutical manufacturers use 3,5-Dinitrobenzotrifluoride to build fluorinated aromatic cores for specific API families, such as certain kinase inhibitors and anti-inflammatory agents. This material acts as a crucial aromatic substitution reagent during early synthetic steps, dictating downstream yield and impurity profile. Process chemists carefully monitor reaction temperatures, solvent ratios, and rigorous in-process checks to conform with pharmacopoeial monograph limits. Batch records and analytical COAs accompany all shipments for regulatory audits. Residual solvents, genotoxins, and elemental impurities directly link to the quality of the raw intermediate, underscoring the necessity for robust supplier QC.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for active pharmaceutical ingredients
    • USP/NF monograph standards for raw pharmaceutical materials
    • European Pharmacopoeia (Ph. Eur.) testing parameters
    • 21 CFR Part 211 cGMP (FDA)

    Typical usage ratio

    • Ranges from 5–30% of the overall input for API intermediate synthesis depending on the molecular weight and stoichiometry of the target drug substance.

    Downstream process integration

    • Introduced after initial condensation reactions; often undergoes reduction, halogenation, or coupling for further transformation into active pharmaceutical intermediate structures.

    Final product types

    • Anti-cancer compounds synthesized from fluoronitroaromatics
    • Anti-inflammatory API drugs
    • Intermediates for CNS (central nervous system) pharmaceuticals
    • Custom medicinal building blocks for clinical R&D batches

    3. Dye and Pigment Synthesis for Specialty Textiles

    Colorant manufacturers employ 3,5-Dinitrobenzotrifluoride in the formulation of specialty dyes and pigments, especially those requiring strong chromophoric groups with enhanced fastness properties. The nitro and trifluoromethyl substituents introduce electron-withdrawing effects, stabilizing pigment molecules and improving color intensity and sunlight resistance. Integration of this raw material takes place during the arylation or azo coupling stage, where specific molar ratios ensure consistent hue and yield. Downstream QA testing assesses hue consistency, lightfastness, and residual solvent content as demanded by fiber industry standards. Finished pigment lots must meet formaldehyde-free and heavy metal exclusion criteria prior to downstream compounding.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile dyes
    • ZDHC MRSL v2.0 (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • REACH Annex XVII restrictions on azo dyes
    • ISO 105-B02 light fastness for colorants

    Typical usage ratio

    • Present at 7–25% in pigment or dye synthesis stages; precise loading determined by desired color strength and downstream compatibility with textile substrates.

    Downstream process integration

    • Added during arylation, azo coupling, or sulfonation stage; carefully metered into acid or alkaline media within closed system reactors to manage fume and dust generation.

    Final product types

    • Disperse dyes for polyester textiles
    • Acid dyes for nylon and wool blending
    • Fluorinated pigments for outdoor fabrics and automotive interiors
    • Inkjet colorants for industrial printing applications

    4. High-Performance Polymer Manufacturing

    Producers of performance polymers and specialty plastics integrate 3,5-Dinitrobenzotrifluoride as a reactive monomer in the synthesis of high-gloss, chemically resistant fluoropolymers. The electron-deficient nitro and trifluoromethyl groups confer improved dielectric properties and oxidative stability, critical for end uses in electronics and aggressive chemical environments. This material feeds into co-polymerization or insertion stages at elevated temperatures under nitrogen shielding. Consistent batch purity assures reliable molecular weight distribution and surface finish in polymerized products. Downstream converters require that precursor residual levels remain within tight technical ranges to ensure final product reliability and regulatory acceptability.

    Industry compliance standards

    • UL 94 and IEC 60695 fire resistance testing
    • RoHS Directive for heavy metal and halogen content
    • ISO 9001:2015 certified production and traceability systems
    • ASTM D3299 for fluoropolymer chemical resistance

    Typical usage ratio

    • Applied at 3–15% as a co-monomer or chain terminator, with dosage adjusted according to film thickness, molecular chain length, and electrical requirements.

    Downstream process integration

    • Charged into pressurized polymerization reactors prior to initiator addition; participates in condensation or free-radical copolymerization steps, forming targeted side-chain or backbone linkages.

    Final product types

    • Fluorinated engineering plastics for electronics enclosures
    • Protective chemical-resistant coatings
    • Membranes for specialty filter media
    • Wire and cable insulation for industrial automation
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    Certification & Compliance
    More Introduction

    3,5-Dinitrobenzotrifluoride: The Value of Precision-Made Intermediates

    Real-World Experience in Making 3,5-Dinitrobenzotrifluoride

    Years behind reactors and in front of market trends have shaped our relationship with 3,5-Dinitrobenzotrifluoride. Each batch that leaves our facility stands as the result of incremental improvements, labor, and lessons learned from the challenges of large-scale nitration and purification. We approach 3,5-Dinitrobenzotrifluoride as more than a commodity. It’s a pivotal aromatic intermediate with a role in a wide range of value-added chemical syntheses.

    Shaping a molecule like 3,5-Dinitrobenzotrifluoride (CAS: 328-75-6) is not a matter of simple mixing. The process starts with carefully selected benzotrifluoride, and precise handling becomes essential as nitration takes place at both the 3- and 5-positions of the aromatic ring. We track the progress with chromatography and in-process analytical control, not simply for compliance, but because our downstream partners expect reproducibility batch after batch. In our facility, staff have become adept at recognizing the subtle cues of a high-purity product well before final analytical sign-off. If our LC-MS flags any significant impurities, we isolate and solve the process root cause so next time the product meets expectations tighter than any stated certificate.

    Purity, Consistency, and Traceability from the Manufacturer

    Customers tend to focus on purity levels and trace impurities, but from the manufacturer's side, attention never drifts from actual molecular consistency. 3,5-Dinitrobenzotrifluoride’s pale-yellow crystalline appearance in the drum speaks both to how we’ve refined our separation process and how we store and package the material. Clean breaks between fractions and proper wash procedures keep colored byproducts out of the final product. Each drum we produce gets a unique batch record, not just for paperwork but so we can instantly review the precise lot, raw materials, and even the hours spent on that specific run.

    Over the years we’ve listened to stories from coating manufacturers, agrochemical formulators, and pharmaceutical innovator teams who experienced trouble with non-uniform intermediates or inconsistent melting points. We take these stories seriously. Our quality control team routinely runs melting point determinations and checks against reference standards. FTIR and HPLC readings get crosschecked, all with the goal that each kilogram matches the last. Problems spotted early, whether an off-spec melting range or even a small trace of a side product, can mean the difference between a multi-ton process moving forward or stalling out.

    Common and Distinctive Uses in Synthesis

    Most inquiries about 3,5-Dinitrobenzotrifluoride come from the need for a solid building block that tolerates aggressive reaction conditions. In our experience, demand follows its specialized use in pharmaceuticals and crop protection actives, where both the electron-withdrawing dinitro groups and the trifluoromethyl moiety deliver unique reactivity. Chemists ask for this compound specifically when designing intermediates that demand strong aromatic stability, halogen compatibility, or improved metabolic resistance in a final molecule.

    We’ve witnessed the molecule’s popularity spike as a precursor for 3-amino-5-nitrobenzotrifluoride and its derivatives. The nucleophilic aromatic substitution on the dinitrobenzotrifluoride core allows amination and reduction routes that favor the trifluoromethyl-substituted ring. Specialty pigments, fine chemical synthesis, and advanced materials development also rely on this exact substitution pattern, where minor shifts in position or isomer count can shut down a synthetic route or trigger costly process modifications.

    Technical Specifications that Matter in the Real World

    There’s no substitute for a full suite of analytical data that demonstrates purity, but some customers, especially formulators and process chemists, dig deeper into melting point, solubility, and stability profiles. Melting points typically come in at 80-83°C, which gives clear guidance for downstream crystallization and handling. Our runs maintain water content at a level where crystallinity is preserved and storage risks are kept minimized.

    The molecular structure, C7H2F3N2O4, brings together a rigid aromatic backbone with strong electron-withdrawing potential, tailored for cross-coupling or nucleophilic aromatic substitution. Our internal team watches especially for chloro-substituted congeners or mono-nitro isomers that may slip through due to small shifts in reaction heat or acid ratios. Removal of these isomers is one of the biggest differentiators in technical grade vs. fine chemical grade 3,5-Dinitrobenzotrifluoride.

    Special attention is given to storage. Moisture might seem like a minor enemy, but years of shipping experience have shown that caked material, if not dried thoroughly or properly sealed, can complicate loading in industrial dissolvers or reactors. That is why we take extra precautions on drying, inert gas packaging, and double-layered LDPE drum liners whenever customers request extended storage or ocean freight handling.

    Why 3,5-Dinitrobenzotrifluoride Stands Apart from Other Aromatic Nitro Compounds

    Comparing 3,5-Dinitrobenzotrifluoride with simpler dinitrobenzenes or with mononitrobenzotrifluorides exposes some important differences. The strong electron-withdrawing effect of the trifluoromethyl group at the para position shifts reactivity, giving more control in multi-step syntheses where selectivity can make or break a campaign. We’ve had customers who switched from standard dinitrobenzenes and saw sharper yields or better process safety after incorporating the trifluoromethylated analog.

    Where other nitrobenzene derivatives might fall short in terms of metabolic stability or environmental robustness, the -CF3 group of 3,5-Dinitrobenzotrifluoride helps deliver important gains. We’ve watched pharmaceutical partners achieve longer half-lives in active molecules through direct transformation of this intermediate. In the pigment sector, the molecule’s brilliant contribution to fastness properties has drawn continued attention. It’s not simply about purity, but about what the specific substitution brings to the end molecule that makes this intermediate more valuable or even indispensable.

    Lessons Learned from Years of Production

    Anyone managing a reactor for the nitration process learns fast that batch control, temperature ramping, and mixing all have to align to avoid undesired byproducts. If caustic neutralization happens too quickly, or if temperatures spike, secondary products like 2,6- or 2,4-dinitro isomers can form. Over time, our technicians have developed a precise sense of the process, balancing oxidizing agent addition with cooling capacity and agitation power.

    We pay attention to not just yields, but to the shifting ratio of desired molecules. Small trials early on taught us that the purification profile for 3,5-Dinitrobenzotrifluoride is much sharper than for related mono-nitro analogs, which drives our decision to invest in better phase separators and serial crystallizers. That investment pays off in lower waste, better sustainability record, and customer confidence in every delivered drum.

    Supporting Responsible Handling and Environmental Best Practices

    The process safety profile and environmental stewardship around nitroaromatic production cannot be neglected. We have seen that consistent staff training, diligent waste management, and responsible emissions control ensure compliance and long-term viability for our whole site. The real story is in our investment in closed-system acid recovery, which captures and recycles excess nitrating acid, and our use of real-time VOC monitors to keep solvent emissions in check.

    Waste treatment matters to us because downstream processors—not only regulatory authorities—ask for proof of best practice. We track each effluent’s organic content before and after in-plant treatment. Sludge containing residual nitroaromatics never leaves our site untreated. We share reports with partners willing to audit, and in some cases, have adjusted our neutralization cycles in collaboration with customers who have stricter internal environmental targets.

    Solving Common Problems in the Field

    We hear from plenty of users who have struggled with material that clogs feed lines or refuses to dissolve properly during scale-up. Our technical support team has stood behind more than one customer as they worked through dissolution profiles or adjusted their solvent composition during formulation. Based on past challenges, we recommend direct-feed approaches and small-scale solubility trials before ramping up to production quantities.

    Downstream issues sometimes arise when trace acidity remains from the final nitration wash. We’ve improved our rinsing and drying steps to reduce acid carryover to well below detection thresholds. Our analytics team remains on call to provide pH measurements for any suspicious batch report.

    Some customers also require reprocessing services, particularly those in pharmaceuticals who must minimize the risk of cross-contamination or side reactions. We run dedicated lines for fluorinated nitroaromatics to protect both the product and customer trust. Labeling every drum with traceability codes makes future investigations swift, and partners have thanked us for the transparency that avoids the finger-pointing seen with less rigorous suppliers.

    Market Trends and Our Response

    The cost pressure on intermediates like 3,5-Dinitrobenzotrifluoride has only grown. Raw material volatility for fluorinated and nitrated aromatics can swing wildly. Instead of passing every cost directly on, we bulk-purchase benzotrifluoride and nitric acids well ahead of known demand cycles. We cross-train production staff so that equipment turnover during maintenance doesn’t slow output. Longstanding relationships with logistics partners ensure we buffer for shipping disruptions, fueling the reliability downstream partners depend on.

    Regulatory trends influence not only safety protocols but how we map future investments. As global hazard awareness for nitroaromatics grows, we have overhauled storage area ventilation, adopted explosion-proof handling systems, and revised product safety messaging to be more transparent and useful. Customers today request not simply a product, but proof of origin, proof of compliance, and proof of repeatability. We have responded by offering full product dossiers—analytical, safety, and compliance summaries—backed by our historical manufacturing data.

    Direct Support from the Plant Floor

    Far from the image of a remote supplier, we operate with an open-door policy for audit teams and technical specialists from our partners. We believe that working hand-in-glove with end-users—including site visits, process demonstrations, and troubleshooting—keeps our learning loop strong and the finished product as close to expectation as possible.

    A few years back, a major coatings customer flagged an unexpected crystallization issue during a seasonal temperature swing. Rather than lean on technical documents, we sent our product manager and plant technician to observe their formula preparation on-site. The root cause traced back to a localized moisture ingress during winter storage, which changed the crystallization dynamics during pre-mix. We’ve since revised our winter packaging protocol and include anti-caking recommendations in customer guides.

    We see this collaboration spirit as core to serving not just direct clients but the entire chemical development ecosystem. The learning from these interactions cycles back to our production planning and product development. Feedback from a pharmaceutical innovator chasing an ultra-filtration process, or from a pigment user who demanded red-shifted spectra from their product, helped us refine not only batch quality but also the specific analytics we make available.

    Building for Tomorrow with Root-Level Manufacturing

    Supply reliability in the intermediate market is all about foundation work at the manufacturing level. Process stability, raw material sourcing, and end-to-end transparency build a reputation far more enduring than any badge or standard. Stepwise optimization, process troubleshooting, and willingness to learn from setbacks define the track record of a manufacturer committed to evolution.

    3,5-Dinitrobenzotrifluoride production has challenged us to perfect not just chemistry, but business resiliency, technical support, and the fine details that bring a specialty intermediate from drawing board to reactor and into final customer projects.

    Our path with 3,5-Dinitrobenzotrifluoride is built on hard-won expertise, direct technical engagement, and a willingness to invest in both process and people. We stand behind every shipment with full traceability, technical documentation, and readiness to collaborate on any challenge thrown our way.