Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2,6-Bis(Trifluoromethyl)Benzonitrile

    • Product Name 2,6-Bis(Trifluoromethyl)Benzonitrile
    • Alias BTBN
    • Einecs 245-139-6
    • 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
    VTB
    Specifications

    HS Code

    447844

    Chemicalname 2,6-Bis(Trifluoromethyl)Benzonitrile
    Casnumber 328-74-5
    Molecularformula C9H3F6N
    Molecularweight 241.12
    Appearance White to off-white solid
    Meltingpoint 60-64°C
    Boilingpoint 224°C at 760 mmHg
    Density 1.54 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CC(=C(C(=C1)C#N)C(F)(F)F)C(F)(F)F
    Inchi InChI=1S/C9H3F6N/c10-8(11,12)6-2-1-5(4-16)7(3-6)9(13,14)15/h1-3H

    As an accredited 2,6-Bis(Trifluoromethyl)Benzonitrile 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 25 grams of 2,6-Bis(Trifluoromethyl)Benzonitrile, tightly sealed, labeled with hazard warnings and product details.
    Shipping 2,6-Bis(Trifluoromethyl)Benzonitrile is shipped in tightly sealed, chemically resistant containers to prevent moisture and environmental exposure. The package is clearly labeled with appropriate hazard warnings. Transport complies with all relevant regulations for organic chemicals, including temperature control and protection from physical damage during transit to ensure safe delivery.
    Storage **2,6-Bis(Trifluoromethyl)Benzonitrile** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, ignition sources, and direct sunlight. Keep it separated from incompatible materials such as strong oxidizers and acids. Use proper chemical storage practices, including secondary containment, and ensure that access is restricted to trained personnel wearing appropriate PPE.
    Application of 2,6-Bis(Trifluoromethyl)Benzonitrile

    Applications of 2,6-Bis(Trifluoromethyl)Benzonitrile in Industrial Manufacturing

    2,6-Bis(Trifluoromethyl)Benzonitrile is an advanced fluorinated aromatic intermediate with widespread adoption in industries demanding high-performance materials. Our experience as a direct manufacturer ensures tight control over purity, particle size distribution, and trace residuals, meeting the precise needs of downstream processors. Below we outline distinct application areas where this raw material demonstrates industrial significance, detailing typical use patterns, compliance demands, and integration into established production chains.

    1. Synthesis of Agrochemical Active Ingredients

    Major multinational crop protection companies utilize this compound as an electron-withdrawing intermediate for constructing selective fungicidal and herbicidal actives. The trifluoromethyl substitution facilitates design of molecules targeting disease resistance, while enabling dense molecular packing for formulation stability. Our supply is consistent in purity specification to maintain batch reproducibility and bioavailability, as required by industry protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients (for dual agro-pharma use)
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • ISO 9001:2015 Quality Management System
    • EPA 40 CFR Part 180—US Tolerances and Exemptions for Pesticide Chemical Residues

    Typical usage ratio

    • 5–15% w/w as an intermediate; actual ratio depends on desired degree of fluorination and crop species target.

    Downstream process integration

    • Condensation or Suzuki coupling in the API synthesis stage
    • Subsequent hydrolysis or halogenation for bioactive formation
    • Final formulation through granulation, microencapsulation, or suspension concentrate blending

    Final product types

    • Systemic fungicidal active ingredients
    • Selective pre-emergence herbicides
    • Seed treatment concentrates
    • Crop-specific blended formulations

    2. Liquid Crystal Display (LCD) Material Intermediates

    Display manufacturers incorporate this compound as a core building block for tailored nematic and smectic liquid crystal monomers. Its strong electron-withdrawing nature enables highly stable mesogenic structures required for sharp switching speeds and extended operating temperature ranges. Our strict particle filtration controls contamination, maintaining uniform alignment throughout LCD production.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for display component safety
    • IEC 62321 for hazardous material testing in electronic materials
    • ISO 14001:2015 Environmental Management System for chemical supply

    Typical usage ratio

    • 2–8% w/w based on molecular weight of the target liquid crystal phase; adjusted according to desired optical birefringence and viscosity profile.

    Downstream process integration

    • Grignard reaction to introduce further aromatic extension
    • Integrated into the core structure via alkylation or cyanation reactions
    • Final purification before polymerization or physical blending into LC mixtures

    Final product types

    • Nematic LC monomers for TFT and IPS screens
    • Advanced dichroic dye additives
    • Specialty LC pre-polymers for hi-res panel substrates

    3. High-Performance Polymer Precursors

    Producers of specialty engineering plastics use this molecule for introducing fluorinated aromatic moieties, which deliver enhanced chemical and thermal resistance in demanding environments. It is frequently integrated into synthesis of polyaryletherketones (PAEKs), polyimides, and fluorinated copolymers, where even low-level incorporation can substantially increase lifespan under aggressive conditions.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for polymer intermediates
    • UL 94 Flammability testing for electrical applications
    • ASTM D5203 for high-temperature polymers
    • ISO 9001:2015 facility quality assurance

    Typical usage ratio

    • 1–7% molar equivalent relative to main monomer; higher loading only in high-fluorine-performance segments as dictated by customer’s final product requirements.

    Downstream process integration

    • Monomer synthesis via nucleophilic aromatic substitution
    • Copolymerization with ether or imide chains through melt or solution polymerization
    • Purification prior to extrusion, molding, or film casting

    Final product types

    • Films and laminates for electronic insulation
    • Extruded rods and profiles for semiconductor manufacturing
    • Composite sheets for aerospace or transportation

    4. Pharmaceutical Intermediate for Anti-Inflammatory Agents

    API manufacturers apply this compound in the multi-step synthesis of specific fluorinated non-steroidal anti-inflammatory drug (NSAID) candidates. Its nitrile group and trifluoromethyl segments facilitate precise molecular tuning for improved metabolic stability and prolonged half-life. We ensure reagent grades appropriate for cGMP and batch traceability required for pharmaceutical use.

    Industry compliance standards

    • ICH Q7 GMP for API Manufacturing
    • USP/NF Monographs for API purity and residual solvents
    • FDA 21 CFR Parts 210/211 for finished pharmaceuticals
    • EDQM CEP (Certificate of Suitability to the monographs of the European Pharmacopoeia), where applicable

    Typical usage ratio

    • 5–10% molar equivalent as a synthesis intermediate; precise percentage controlled by target compound and regulatory filing dossier.

    Downstream process integration

    • Aromatic ring functionalization during core structure assembly
    • Selective reduction or further halogenation for side-chain elaboration
    • Final conversion to carboxylic acid or ester as finishing step before API crystallization

    Final product types

    • Fluorinated NSAID bulk drug substances
    • Registered pharmaceutical intermediates supplied to contract manufacturing organizations
    • Anti-inflammatory API for prescription medications

    5. Synthesis of Specialty Dye Intermediates

    Producers of high-stability dyes for technical textiles and inks rely on this raw material for building highly fluorinated chromophores that provide strong photostability and chemical resistance. These properties allow final dyes to maintain fastness and color intensity in outdoor, automotive, and harsh processing applications, where ordinary aromatic intermediates fail to deliver acceptable durability.

    Industry compliance standards

    • OEKO-TEX Standard 100 for harmful substance exclusion in textile dyes
    • ISO 105-B02 for color fastness to light
    • REACH Annex XVII (Entry 43, azo dyes restriction) for colorant safety
    • ISO 9001:2015 process quality

    Typical usage ratio

    • 2–6% relative to other aromatic units in chromophore design; adjustment based on lightfastness testing and application-specific resistance criteria.

    Downstream process integration

    • Condensation into azo or anthraquinone dye backbones
    • Subsequent sulfonation or halogenation for solubility adjustment
    • Spray drying or granulation for finished dye formulation

    Final product types

    • Sunlight-resistant dyes for automotive textiles
    • High-performance inkjet pigments
    • Outdoor and industrial-grade textile colorants
    Free Quote

    Competitive 2,6-Bis(Trifluoromethyl)Benzonitrile prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Practical Insights Into 2,6-Bis(Trifluoromethyl)Benzonitrile

    Understanding the Material From the Manufacturing Floor

    Real production environments shape how we view and handle chemicals. In the context of fluorinated intermediates, 2,6-Bis(Trifluoromethyl)Benzonitrile holds a place for its particular behavior in tough syntheses. Everyday, our operators and process specialists see how this molecule’s structural quirks influence workflow, yields, and downstream chemistry. Connecting real tasks with the properties of this intermediate offers more value than a textbook definition.

    What Makes 2,6-Bis(Trifluoromethyl)Benzonitrile Stand Out?

    Unique among aromatic nitriles, this compound’s structure — with trifluoromethyl groups firmly anchored on both ortho positions — brings two major changes. First, it dramatically reduces electron density around the benzene ring. In traditional electrophilic aromatic substitution steps, hardly any reactivity remains. Second, its strong electron-withdrawing power not only alters the chemical neighborhood, but also bumps up the resistance of this compound to oxidation and hydrolysis. Our lab techs respect it for being stubbornly stable, even under punishing synthetic conditions.

    Visually, the powder form provides a clue to its nature: a faintly off-white, free-flowing solid at room temperature. Our analytical chemists have demonstrated time and again the importance of keeping batch purity consistent; even a subtle impurity can tangle up later process steps, especially in pharmaceutical or crop-protection routes. Routine GC-MS and NMR confirm this compound’s distinct spectral signature, and our in-house standards eliminate most guesswork in product acceptance.

    Production Realities and Batch Reliability

    Large-scale preparation of this benzonitrile needs precise management of reaction exotherms. The trifluoromethyl groups come from specialized reagents, and any stray moisture or batch-to-batch variability in those intermediates directly impacts the outcome. Our experience with pilot plant campaigns showed stubborn clumping issues if drying is rushed or uneven. Solvent choice and cooling regime matter more than most realize at first glance. Every synthesis has forced our teams to revisit standard procedures, learning by adjusting feed rates and agitation. Neither off-the-shelf nor “cookbook” approaches deliver the narrow purity windows required downstream.

    Shipment and storage get their own attention. This compound, thanks to its low volatility and inertness, stores well in lined drums or HDPE pails. Even so, open-air handling invites cross-contamination — so we stick to sealed bags under nitrogen, straight from finished lot to final loading. These procedures avoid “mystery” deposits or unexplained shifts in downstream product quality. Even one mishandled pail in the chain can mean an entire batch cascades into off-specification territory.

    Where It Enters Key Industrial Pathways

    Synthetic chemists who build complex molecules out of basic blocks reach for 2,6-Bis(Trifluoromethyl)Benzonitrile due to its versatility. The nitrile group works as a springboard: it converts to amides, esters, or carboxylic acids, feeding diverse targets in pharma and agrochemicals. The double trifluoromethyl arrangement isn’t only decorative — it pushes the compound’s boiling point, suppresses unwanted side reactions, and increases overall molecular rigidity.

    Pharmaceutical researchers often report that this building block resists metabolic degradation. That’s no accident — the fluorinated arms shield positions on the ring that would otherwise attract enzymatic attack. Our collaboration with veteran process chemists led to significant breakthroughs in fluorinated fungicides, where routine nitriles failed. This molecule simply delivers a tougher backbone; stability under acidic, basic, and oxidative conditions extends the useful lifetime of derived actives in field use.

    Real Differences From Other Benzonitriles and Analogues

    Plenty of aromatic nitriles are available, but few behave like this one in reaction vessels. The 2,6-bis(trifluoromethyl) motif blocks access to the ortho positions; catalytic hydrogenation likewise demands elevated pressure and selectivity becomes far more predictable. By contrast, mono-substituted or para-substituted trifluoromethyl derivatives exhibit both higher reactivity and a greater tendency toward byproduct formation.

    For instance, 4-trifluoromethylbenzonitrile — which we also manufacture — remains more prone to nucleophilic aromatic substitution, and will react with amines under moderate heat. In our experience, that difference dramatically simplifies purification when dealing with the bis-substituted material. Several customers trying to scale up para-substituted routes have reported intractable gum formation, while those switching to the bis-substituted route noted reduced tars and improved filtration rates. Less time cleaning, more time producing.

    Another real difference involves volatility and odor. Many nitriles emit a sharp almond or industrial aroma that lingers in plant air despite robust scrubbing. With 2,6-Bis(Trifluoromethyl)Benzonitrile, even large weighing jobs stay odor-neutral. Line operators appreciate this, and incident investigations have found far fewer worker complaints, even over multiple batches.

    Specification Benchmarks That Matter

    We trust our own production results more than generic claims. In our workflow, every batch undergoes detailed NMR analysis alongside purity check by GC and HPLC. Experienced staff look for trace fluorinated byproducts, even below 0.1 percent. Particle size affects reaction mixing and charging, so we maintain an average between 100 and 300 microns to suit common reactor types. Moisture remains below 0.2 percent — higher levels proved problematic on scale-up with Grignard or lithium reagents, sometimes causing whole campaigns to stall.

    Residual solvents tell their own story. Some plants struggle with chlorinated leftover compounds, but our process eliminates these with controlled distillation. Each lot arrives free from halogenated solvent background, reducing downstream hazards and extra purification steps. To our customers, these tangible differences translate into fewer filtration hiccups and less rework per shipment.

    Direct Applications We’ve Enabled

    Over the last decade, our chemists have contributed to launches of several fluorinated herbicides and pharmaceutical scaffolds. A common theme: standard nitriles faltered in process or final formulation stability, jeopardizing regulatory approval. The bis(trifluoromethyl) upgrade consistently improved photostability in field formulations and extended shelf life under warehouse storage, especially in hot climates. Local customers in agrochemicals often push for extended field stability, and these batches meet that challenge while remaining cost-competitive.

    In polymer synthesis, specialty fluorinated monomers based on our benzonitrile create higher thermal resistance and lower dielectric constant materials. Compounds based on this structure serve in high-frequency circuit boards and chemical-resistant linings. Technical staff from the electronics field rank the ability to tune dielectric performance as a key edge. The double trifluoromethyl substitution gives greater control over end properties, letting formulators hit demanding targets.

    Medicinal chemistry groups trust our product for preparing kinase inhibitors and central-nervous system candidates. Their feedback highlights that metabolism studies with animal models show slower decomposition, which sheets directly back to the shielding from double CF3 groups. Our direct supply from the reactor floor, rather than through any middlemen, allows rapid problem-solving as their targets evolve.

    Operational Challenges and Lessons Learned

    Handling this compound brings quirks best managed through experience. During packaging, any static buildup turns this powder stubborn, attracting dust and slowing automated dosing. Early attempts at continuous packaging led to jamming, so we integrated anti-static measures in drum loading. On the warehouse floor, temperature swings didn’t cause caking or melting, but operators noticed that poorly sealed bags eventually absorbed plant odors, requiring tighter sealing specs.

    Cleaning reactor lines post-campaign once posed a pain. This powder deposits a fine residue along baffles and transfer pipes, more persistent than simpler benzonitriles. We switched to dedicated cleaning solvents and added compressed air flushes after each sequence, cutting plant downtime in half over several months. The lessons here didn’t come out of books but from hands-on troubleshooting.

    Years in the business taught us that cost isn’t only measured in raw materials, but also in solve-it-on-the-spot plant decisions. A batch might look fine on dry spec sheets but fail to dissolve cleanly in the customer’s reactor. Regular discussions and visits with our users uncovered surfactant compatibility issues in a few field sites; coarser lots proved easier to disperse, especially in automated dosing setups, eliminating bottlenecks on line.

    Safety and Environmental Factors as Seen On Site

    Despite its stability, prudent controls rule our workplace. This compound behaves as a low volatility solid, but the manufacturing process releases acids and perfluorinated byproducts that require robust scrubbing. Training our plant staff to check for odors, visible mists, and pressure swings has paid off: no reportable emissions in three years over dozens of tons shipped. Fire risk sits low due to the high boiling point, yet all waste drums stay double-lined and clearly segregated.

    As public scrutiny on PFAS (per- and polyfluoroalkyl substances) grows, raw materials with heavy fluorine content draw new regulatory interest. Our waste minimization team recycles spent catalysts and captures minor byproduct streams, sending them for off-site destruction — never landfill. Both our site inspectors and external environmental auditors regularly test ground and air for traces, and so far, none have breached detection limits.

    Experience keeps reinforcing that skipping checks even on routine products risks long-term consequences. New staff join every season, so our trainers always stress dust minimization and direct exposure avoidance. Protective gear remains standard inside all loading zones, not because this specific compound poses a high acute hazard, but because safe handling habits cut incident rates across all product lines.

    Continuous Improvement and Insights From End Users

    Regular feedback loops with large customers have helped shape unit operations. Analytical folks in pharma firms demanded tighter limits on trace organic acids, pressing us to upgrade both our in-process controls and purification skid design. Our plant teams responded by extending column flushes, and as a result, our product now meets even the most stringent impurity limits seen in drug master file submissions.

    On the technical side, batch-to-batch repeatability remains a sticking point in more ambitious syntheses. Partnering closely with key customers allowed us to rapidly test alternative reagents and variant routes, identifying the conditions that avoid troublesome oligomeric byproducts common in higher-volume runs. Rather than hiding behind paperwork or generic specs, our operations staff speak directly with the chemists writing the procedures. This sort of chemistry shop-floor relationship delivers better results for everyone involved.

    Market Comparison: Not Just Another Nitrile

    Discussions with purchasing departments sometimes question the premium over more basic nitriles. The explanation comes down to consistency, stability, and fewer surprises in the lab and plant. Downtime from process disruptions or failed regulatory review easily dwarfs any up-front savings. Users focusing on target APIs, advanced agrochemicals, or performance polymers see the real difference at the technical and operational level, not just on price sheets.

    Early development groups value small lots with tight specs, while scale-up teams require large, consistent lots that retain their properties from kilo to ton scale. Both groups agree that saving pennies by accepting lower-purity lots ends up costing hours in cleanup and lost product at the end of the process chain. The voice of experience rings clear through customer audits and repeat orders; the reliability and traceability we offer has become a strong differentiator.

    Bridging R&D Ambitions and Plant-Level Execution

    Research platforms in drug discovery or material science lean toward short cycles, changing preferences on synthetic strategies with each project. While academic groups might tolerate broader speciation in their solvents or intermediates, process researchers in manufacturing FTE programs focus on downstream compatibility and impurity knock-on effects. Our knowledge of how this compound interacts during scale-up — influencing mixing times, filtration rates, and reactor fouling — comes from years on the line rather than theory.

    For R&D users testing new approaches, we frequently pilot custom batch sizes or adjusted particle ranges. Feedback from these small campaigns often uncovers hidden factors: for example, a slight shift in melting range hints at trace inclusion of partially fluorinated byproducts, impacting downstream hydrogenation performance. Working side by side with these teams, we fine-tune conditions, not to chase lab legends, but to enable practical, repeatable results for both small-batch and full-scale production.

    Future Directions and Industry Trends

    Current conversations in specialty chemicals reveal growing demand for performance intermediates with higher durability, enhanced electronic properties, and resistance to UV and chemical attack. Our investments in process automation and inline quality checks position us to deliver on these expectations, expanding both volume and quality consistency at the same time. We observe strong growth in fields like OLED precursors and novel antimicrobial coatings, which value the unique attributes native to this molecule: stability, inertness, and fluorinated protection.

    Regulatory and sustainability topics increasingly shape purchasing decisions. Customers across markets express more concern about eco-toxicity, exposure potential, and waste minimization. We see continued momentum for greener chemistries that avoid problematic solvents or persistent byproducts. Having mapped out supply chain footprints for our main feedstocks, we are investing in greener alternatives and closed-loop solvent recovery systems. While cost pressures will always matter, conversation is shifting to life cycle assessment and regulatory readiness — areas where source-to-dock control and continuous process improvement matter most.

    Closing Reflections From the Production Side

    Insights into 2,6-Bis(Trifluoromethyl)Benzonitrile grow from cumulative real-world work, not claims made in marketing copy. From tank farm to final packout, this compound challenges operators and rewards careful process control. Its unique structure opens doors for tough synthetic challenges that stymie less tailored intermediates. For those seeking technical edge, pursuing tighter specs, higher consistency, or cleaner downstream chemistry, the lessons gleaned from years on the factory floor carry more weight than theory alone. As specialty chemistry evolves, direct and open conversations between maker and user will define which products actually deliver on their promise, shaping how industries address tomorrow’s molecular challenges.