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3,5-Bis(Trifluoromethyl)Toluene

    • Product Name 3,5-Bis(Trifluoromethyl)Toluene
    • Alias 1-Methyl-3,5-bis(trifluoromethyl)benzene
    • Einecs 214-204-9
    • 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

    328377

    Cas Number 328-70-1
    Molecular Formula C9H6F6
    Molecular Weight 232.14 g/mol
    Appearance Colorless liquid
    Boiling Point 151-153 °C
    Melting Point -41 °C
    Density 1.372 g/cm3
    Refractive Index 1.401
    Flash Point 54 °C
    Purity Typically ≥98%
    Solubility In Water Insoluble
    Synonyms 3,5-Bis(trifluoromethyl)toluene; 1-Methyl-3,5-bis(trifluoromethyl)benzene
    Smiles CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1
    Inchi InChI=1S/C9H6F6/c1-6-3-7(2-8(4-6)9(10,11)12)9(13,14)15/h2-4H,1H3
    Ec Number 206-398-6

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

    Packing & Storage
    Packing Amber glass bottle containing 100 mL of 3,5-Bis(Trifluoromethyl)Toluene, with tamper-evident cap and chemical hazard labeling.
    Shipping 3,5-Bis(Trifluoromethyl)Toluene is typically shipped in sealed, chemical-resistant containers to prevent leaks and contamination. It should be transported as a hazardous material, in compliance with local regulations, with appropriate labeling for flammable liquids. Storage and shipping areas must be cool, well-ventilated, and away from sources of ignition.
    Storage 3,5-Bis(Trifluoromethyl)Toluene should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from heat, sparks, open flames, and incompatible materials such as strong oxidizers. Protect from direct sunlight. Clearly label the container and ensure secondary containment. Follow all relevant safety protocols and storage regulations for flammable and potentially hazardous organic compounds.
    Application of 3,5-Bis(Trifluoromethyl)Toluene

    Applications of 3,5-Bis(Trifluoromethyl)Toluene in Industrial Manufacturing

    3,5-Bis(Trifluoromethyl)Toluene serves as an advanced intermediate in several industrial verticals. Its physical properties and reactivity profile make it integral to specialty chemical synthesis, agrochemical production, pharmaceutical intermediates, advanced coating systems, and fluorinated polymer modification. The sections below detail practical application insights for each target sector.

    1. Agrochemical Intermediate Production

    This compound forms a critical building block in high-value herbicide and fungicide synthesis. Agrochemical manufacturers use it for introducing electron-withdrawing trifluoromethyl groups, enhancing target molecule potency and field stability. Controlled addition during condensation or acylation reactions enables tuning active ingredient structure for both efficacy and environmental persistence. Product customization follows country-specific regulatory limits for residuals and co-formulant selection.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No 1107/2009 on placing plant protection products on the market
    • US EPA Title 40 CFR Part 180 (tolerances and exemptions for pesticide chemicals)
    • China GB 2763 Maximum Residue Limits for Pesticides in Foods

    Typical usage ratio

    • Usually charged at 5–15 mole% relative to the targeted agrochemical core substrate. Adjustments depend on desired active content and reaction route selectivity.

    Downstream process integration

    • Charged in the intermediate synthesis stage, typically via Friedel-Crafts alkylation or direct trifluoromethylation. Integration into the active core structure precedes formulation with inert carriers or solvents.

    Final product types

    • Selective herbicides (e.g., fluorinated phenoxyacetic acids)
    • Broad-spectrum fungicides for grains and cereals
    • Pesticidal actives for soy and cotton crops
    • Seed treatment agents

    2. Pharmaceutical Intermediate Synthesis

    Bridging gap between primary raw materials and drug candidates, this compound provides key substitution patterns in fluorinated aromatic scaffolds for APIs. Pharmaceutical plants prefer its predictable reactivity when assembling high-purity precursors under sterile and GMP-controlled conditions. The compound’s traceability and impurity profile must meet monograph-defined limits, supporting batch documentation for regulatory filings. Process development teams optimize feed ratios to balance cost, selectivity, and pharmaceutical grade output requirements.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • US Pharmacopeia (USP General Chapter <232> Elemental Impurities)
    • EU GMP Vol 4 Part II Basic Requirements for APIs
    • Japanese Pharmacopoeia (JP)

    Typical usage ratio

    • Charged at 3–8 mole% relative to arene base or amine coupling partners; ratios refined by Route of Synthesis and yield optimization trials in API process validation.

    Downstream process integration

    • Entered during aromatic substitution steps or Grignard reactions ahead of downstream API assembly, followed by catalyst quench and phase purification. Applied in kilo-lab and pilot plant scales under full traceability protocols.

    Final product types

    • Fluorinated analgesic intermediates
    • Experimental oncology small molecules
    • API intermediates for antiviral and CNS indications
    • Reference standards for pharmaceutical batch release

    3. Specialty Polymer Modification

    This compound acts as a functional additive for synthesizing advanced fluorinated polymers and copolymers where improved thermal and chemical resistance is required. Polymer scientists dose it into radical polymerization or copolymerization processes to achieve target backbone properties, such as reduced surface energy or tailored dielectric constants. Accurate metering and homogenous blending with base monomers ensure no phase separation, supporting stringent quality assurance in both batch and continuous operations.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management Systems
    • RoHS Directive 2011/65/EU (for electronic-grade polymers)
    • UL 94 Flame Classification for Plastics
    • ASTM D3895 Oxidation Induction Time standards

    Typical usage ratio

    • Incorporated at 0.5–3% weight of total monomer feed. Lower levels (0.5-1%) enhance surface characteristics; higher concentrations (>2%) modify dielectric or resistance profiles for specialized applications.

    Downstream process integration

    • Metered into feed hoppers during monomer charging. Used in step-growth or free-radical systems pre-polymerization, ensuring full incorporation for block or random copolymer formation.

    Final product types

    • Fluorinated elastomer gaskets
    • Low-energy surface coatings
    • Insulation films for electronics
    • Chemically resistant O-rings and seals

    4. Advanced Electronic Liquid Crystal Ingredients

    In display and sensor industries, this material is utilized for its unique electron-withdrawing and steric properties that optimize mesogenic phase behavior in liquid crystal mixtures. Display chemical engineers incorporate the compound when tuning viscosity, clearing points, and voltage thresholds for high-contrast TFT and OLED panels. Precision dosing provides consistent electro-optical performance and maintains compliance with global consumer electronic safety directives.

    Industry compliance standards

    • IEC 62321 for hazardous substance levels in electrical and electronic equipment
    • REACH Regulation (EC) No 1907/2006
    • RoHS 2 (2011/65/EU) restricted substance thresholds
    • JIS C0950 marking for materials in Japan electronics market

    Typical usage ratio

    • Dosed at 1–5% of total liquid crystal weight. The ratio is fine-tuned via bench and pilot screening to match target display or sensor application requirements.

    Downstream process integration

    • Dissolved in the mesogen matrix prior to vacuum filling of display cells or capillary inserts. Requires precise quality checks for phase purity and electro-optic alignment prior to final lamination.

    Final product types

    • High-contrast TFT displays
    • OLED panels for smart devices
    • Precision optical shutters
    • Specialty sensors in automotive and medical devices

    5. Performance Coatings for Industrial Surfaces

    This compound enables advanced hydrophobic and oleophobic coatings by imparting durable fluorinated aromatic units into binders and crosslinkers. Formulation chemists use it in the backbone modification of surface coatings to increase chemical resistance, lower surface tension, and improve cleanability on metals, glass, or composite substrates. Accurate dosing and solvent compatibility checks maintain gloss, hardness, and environmental performance during scale-up and application.

    Industry compliance standards

    • ISO 12944-6 Protective Paint Systems
    • ASTM D3359 for adhesion of coatings
    • VOC limits per EU Directive 2004/42/EC
    • EN 13523-10 Resistance to Fluids

    Typical usage ratio

    • Blended at 1–7% of total resin solids, depending on the desired repellency and durability. Fine adjustments are made during product qualification trials and accelerated weathering tests.

    Downstream process integration

    • Added to resin reaction kettles or primary mixing vessels before crosslinker addition. Can be post-added for certain solvent-borne formulations during high-shear mixing steps.

    Final product types

    • Anti-graffiti coatings for public infrastructure
    • Oil- and water-resistant floor coatings for industrial plants
    • Functional glass and ceramic treatments
    • Automotive exterior paint systems

    6. Fluorinated Aroma and Fragrance Ingredient Manufacturing

    Used as a specialist intermediate in crafting aroma molecules, this material introduces thermal and oxidative stability to fragrance structures via selective fluorination. Fragrance companies employ it for stable top or heart note scaffolds, particularly where long-lasting, clean, or metallic notes are desired in complex blends. Precise control of molar ratios and reaction parameters aligns with flavor and fragrance safety assessments and international labeling requirements.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • EU Cosmetic Regulation (EC) No 1223/2009
    • FEMA GRAS compliance (Flavor and Extract Manufacturers Association)
    • REACH Annex VIII dossier requirements

    Typical usage ratio

    • Applied in 0.1–2% of total batch scale, with exact inclusion dictated by target olfactory intensity and synthetic scaffold design. Compositional limits maintained to meet downstream IFRA standards.

    Downstream process integration

    • Input at early stage among synthetic route to generate aldehydes, ketones, or esters containing fluorinated aromatic rings. Follows through high-vacuum distillation or crystallization for purity.

    Final product types

    • Stable synthetic musk notes
    • Modern citrus-oriental fragrance bases
    • High-performance air freshener compounds
    • Long-lasting aromatic boosters in detergents and fine perfumes
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    Certification & Compliance
    More Introduction

    3,5-Bis(Trifluoromethyl)Toluene: Our Direct Experience Manufacturing A Unique Aromatic Building Block

    Real Chemistry Runs Deep: What Sets 3,5-Bis(Trifluoromethyl)Toluene Apart

    Every day on the production floor, our team works with specialty aromatics that demand strict control. 3,5-Bis(Trifluoromethyl)Toluene, which we know as an essential intermediate for pharmaceutical and agrochemical research, stands out for reasons rooted in its chemistry as well as its handling requirements. Over the years, we've seen how the presence of two electron-withdrawing trifluoromethyl groups at the meta positions on the toluene ring dramatically alters the reactivity and stability, allowing synthetic chemists to go places standard methyl toluene simply can’t follow.

    From our experience scaling up batches of this compound, one fact always remains: the structural design behind 3,5-bis(trifluoromethyl)toluene isn’t accidental. The influence of fluorine, and specifically the trifluoromethyl substituent, delivers a unique mix of lipophilicity and resistance to metabolic breakdown. Chemists in our industry appreciate how this shifts compound properties, whether they’re developing a new fungicide lead or seeking a differentiated aromatic ring for a pharmaceutical candidate.

    Our direct line to production means we see first-hand the subtleties researchers rarely encounter — the material’s tendency to resist oxidation, for example, or how it tolerates a broad range of reaction conditions that send more basic aromatics off the rails. Our job doesn’t stop at synthesis. From purification challenges to bulk handling, we tackle every production run with a clear understanding that the molecule is far more than a catalog entry. It’s an enabler for downstream discovery and application, with a concrete impact on early-stage innovation.

    Specifications Matter: Beyond the CAS Number

    From filling reactors through quality confirmation in our analytical lab, we know exactly what goes into every batch of 3,5-bis(trifluoromethyl)toluene. As a manufacturer, we’ve refined our process over time to deliver material in bulk quantities or research scale, depending on where development or scale-up efforts lead. Many customers come to us seeking a supply partner who won’t compromise on moisture content, purity, or trace impurity profiles.

    We routinely analyze each lot for GC purity, typically achieving values above 99%. Our standard runs produce a clear, colorless liquid, and residual solvents are held below strict thresholds that researchers demand for consistency batch after batch. The boiling point, set by the influence of the two CF3 groups, lands well above that of traditional methyl toluene — creating a product that stays stable during a range of synthetic steps. In the plant, our fittings, hoses, and valves are selected for compatibility with fluorinated aromatics, because leaching or contamination can create headaches in QA and require unnecessary reprocessing.

    A Manufacturer’s Perspective on Applications

    Having supplied 3,5-bis(trifluoromethyl)toluene into countless research projects and pilot programs, we’ve gained unique insight into the product’s use profile. The dual CF3 arrangement fuels demand among medchem, crop science, and materials teams alike. Often it serves as a core building block, either undergoing further substitution or transformation, or simply acting as a stable aromatic moiety in final products.

    Because the trifluoromethyl group delivers powerful electron-withdrawing effects, our customers lean on this molecule in scenarios where halogenation can’t deliver the same outcome. Custom syntheses that require selectivity in the next step, or tight control over metabolic resistance, regularly draw on this backbone. A typical example emerges in the design of new active substances for agricultural applications: the addition of CF3 units can deliver both lipophilicity and resistance to environmental degradation, distinguishing final actives from their less robust peers.

    Pharmaceutical researchers also favor this compound during lead optimization, since the combination of toluene’s base structure and the CF3 groups allows fine-tuning of both physical and biological properties. As a company rooted in manufacture, we often field questions about suitability for high-throughput parallel synthesis, compatibility with common oxidants and reductants, or resistance to hydrolysis. Our practical feedback comes straight from our own process development, not from theory or literature, enabling us to help customers avoid common pitfalls.

    What Changes With Trifluoromethylation?

    Years of running reactions with both trifluoromethylated and non-fluorinated aromatics have made it clear — molecular tweaks can reshape a project’s entire direction. Toluene derivatives lacking CF3 groups may offer easier entry to some reactions but quickly lose ground when it comes to stability, environmental persistence, or solubility in organic solvents. Add one CF3 and the difference is marked; the effect doubles at the 3,5-positions. Our clients consistently report higher selectivity and lower byproduct load when adopting this building block.

    We keep an eye on safety profiles and downstream impacts, too. While some halogenated aromatics raise red flags thanks to persistent organohaluros, the unique structure of 3,5-bis(trifluoromethyl)toluene bypasses many of the regulatory headaches linked with higher-order halogenation, since the CF3 group follows a different metabolic pathway. Our plant safety protocols account for this material’s characteristics — it isn’t especially volatile and presents a manageable flammability risk when handled with the same respect afforded to similar aromatic liquids.

    Production Insights: Efficiency, Scale, and Traceability

    Manufacturing specialty aromatics carries responsibility. Our facility runs longitudinal tracking on all input chemicals, so every drum or flask traced back to origin. Since global demand for fluorinated intermediates remains strong, we updated our production line with redundant filtration and solvent recovery, cutting both waste and downtime. There’s no need to skim specifications or hope for luck — every kilogram leaves our site only after routine headspace GC-MS confirms purity and residual solvent levels.

    Scaling up to industrial runs means adapting processes learned at bench scale to plant realities, watching for bottlenecks or potential hot spots. On the shop floor, distillation control means hitting key fraction temperatures, and keeping heat input stable across runs. Training and checklists cover every operator’s routine, built from hands-on task repetition. Our team’s longevity pays off: fewer slips on in-process checks, less product loss, more FAQ calls answered with authority. We don’t ship until every internal benchmark is met — it’s part of why customers seeking reliable supply keep coming back.

    Why Direct Manufacturing Experience Matters

    We’ve spoken with many researchers over the years who recount troubles with off-spec batches, compound instability, or even mislabeling. Past experience with other suppliers has covered everything from trace hexane contamination (ruining downstream chromatography) to batch-to-batch color changes that hint at poor purification. As a direct manufacturer, we step in when those problems crop up elsewhere. We invested in dedicated glass and fluoropolymer-lined lines for our fluorinated aromatics, because cross-contamination means real setbacks during late-stage process development.

    On the technical front, living with the product every day means discovering all the places where impurities can sneak in: thermal cycling, air ingress, or minor pressure fluctuations during bottling. A trader won’t see this, but we do, and we invest to prevent costly setbacks. We’ve adjusted column packings and swapped pump seals more times than we can count, always for the sake of headquarters-grade reproducibility. We field technical feedback requests daily and translate user problem reports back to the factory floor, closing the loop faster than any third-party.

    Supporting Researchers: Why Consistent Supply Drives Innovation

    Research programs ebb and flow, but nothing derails progress more than an unreliable supply chain for specialty intermediates. We experienced this ourselves; during recent global shutdowns, we kept supply lines open through direct control of raw material sourcing and on-site warehousing. Onsite QA staff monitor every lot release, intervening long before substandard material could reach a customer. We’ve heard too many stories of missing project milestones because a trader’s shipment “got delayed at customs” or “did not match the spec sheet.”

    Supply isn’t just about filling drums. It’s about confidence that each sample works like the last. From pharma to crop protection, every kilogram matters, especially in multi-step syntheses where a late impurity spells months of lost work. In the rare event of a specification question, our technical team — drawn from process chemistry and analytical backgrounds — connects directly with researchers, collecting feedback and feeding it to our manufacturing planners.

    Working Differently: The Perspective of a Specialized Manufacturer

    The journey from raw starting material to packed and shipped 3,5-bis(trifluoromethyl)toluene leaves no room for guesswork. We tune every distillation and chromatographic stage for the tightest control, rejecting any lot that doesn’t match our internal gold standard. Shipping out material with trace copper, or letting a sample slip below our purity benchmark, isn’t an option. Each run brings something new: a slight variation in reaction exotherm, an odd baseline drift on the GC trace, maybe even a sticky valve.

    We’ve fielded requests for documentation supporting every aspect of our operation — batch records, solvent usage logs, and every trace contaminant screen. These aren’t bureaucratic exercises, but real tools for our downstream technical partners who need to validate their regulatory filings or support scalable process design. Every answer comes from our production notes, not a distributor’s marketing sheet.

    Perspective on Regulatory and Environmental Factors

    Direct manufacture brings us face to face with shifting environmental legislation and industry-specific requirements. Our in-house compliance team monitors regional guidelines for aromatic solvents and intermediates. Years ago, changes to allowable discharge levels drove us to update solvent recycling. As more clients push for greener processes and lower-impact chemicals, we log each process tweak, report emissions, and tune for lower waste. 3,5-bis(trifluoromethyl)toluene brings the benefit of high stability — there’s less risk of degradation that could complicate waste disposal, and the low volatility makes storage less challenging than many lighter aromatics.

    From regulatory filings to production floor improvements, every step factors in the realities facing downstream users. Regulatory audits no longer spark panic, since each material shipment comes with a full record of analytical data, lot traceability, and a running log of process changes. Agencies don’t accept generic answers, so our compliance reports are built from actual production logs — nothing pulled from generic documents. When a research or process chemist requests support for a regulatory inquiry, our reply is straightforward, delivered with data only a practicing manufacturer can produce.

    Comparing to Other Aromatics: Specific Differences in Practice

    Chemistry often hinges on small choices. In our lab and plant, the differences between 3,5-bis(trifluoromethyl)toluene and alternative substituted toluenes show up everywhere — from the way each reacts under classic conditions, to their impact on downstream formulations. We see less product loss to volatility compared to methyl-toluenes without fluorine, and the compound’s enhanced lipophilicity allows better partitioning into organic matrices, a real benefit for formulation scientists.

    The double CF3 motif leads to electron distribution patterns distinct from simple mono-substituted aromatics. This has changed the outcome of countless Friedel–Crafts and nucleophilic aromatic substitution reactions run in our own pilot plant, enabling pathways that stay closed for most commodity solvers. For anyone reaching for halogenated benzenes or standard xylene isomers, the switch brings better selectivity and more controlled yields, with less clean-up needed at the end than alternate products.

    Physical properties also matter. A higher boiling point means easier handling at elevated temperatures, especially under vacuum conditions. The chemical inertness enhances shelf life and reduces accidental side reactions in ambient storage, so inventory stays stable longer — an advantage for process engineers grappling with seasonal shutdowns or erratic demand cycles.

    Opportunities and Future Improvements: Seeing Beyond Today’s Challenges

    Our journey as a manufacturer of 3,5-bis(trifluoromethyl)toluene is ongoing. Each production campaign reveals untapped opportunities for cost reduction, process intensification, and impurity control. We constantly test newer filtration materials, less hazardous solvents, and improved bottling techniques to lower risk and raise output. We’ve piloted solvent recovery that both slashes emissions and brings down net production cost.

    Feedback from customers keeps us sharp. Whether it’s a request for a new package size, an urgent shipment window, or a tighter impurity cut-off, we adapt and respond using resources built from direct manufacturing experience. As regulations on fluorinated hydrocarbons evolve, we work with authorities and customers to pre-empt issues, running tests on potential by-products and reviewing exposures in real time. Solutions aren’t dreamed up in a meeting room, but hammered out in heated plant-side discussions and late-night troubleshooting phone calls.

    The evolving landscape for specialty aromatics doesn’t faze us. With new applications popping up in energy, electronics, and specialty coatings, we’re seeing first-hand how innovations downstream back-propagate their requirements. Our synthesis and purification protocols remain nimble, ready to support the next generation of discoveries that rely on this unique compound. Direct manufacturing ties us to those aspirations, ensuring the pathway from raw material to final product never breaks under the weight of complexity or changing requirements.

    Closing Thoughts: Experience You Can Rely On

    Every shipment we prepare reflects years spent at the precursors, reactors, stills, and purification columns. By living with the chemistry and logistics of 3,5-bis(trifluoromethyl)toluene, our team sees the needs and concerns shaping the future of specialty synthesis on a global scale. Requests don’t land in a generic inbox; they arrive at desks where technical knowledge, practical handling experience, and supply chain control converge. Whether you're scaling up a new pharmaceutical route or developing the next generation of crop protection actives, consistent quality, technical insight, and rock-solid traceability remain our defining edge. The insights and reassurance you receive come directly from the source. This is manufacturing, done right and done real.