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2,4,6-Trimethylbenzonitrile

    • Product Name 2,4,6-Trimethylbenzonitrile
    • Alias 2,4,6-TriMethylBenzeneCarbonitrile
    • Einecs 242-799-0
    • 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

    589054

    Cas Number 13654-82-5
    Molecular Formula C10H11N
    Molecular Weight 145.20 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 75-77 °C
    Boiling Point 274-276 °C
    Density 1.031 g/cm3
    Solubility In Water Insoluble
    Refractive Index 1.544
    Purity Typically ≥98%
    Flash Point 124 °C
    Synonyms 2,4,6-Trimethylbenzenecarbonitrile
    Smiles CC1=CC(=C(C=C1C)C#N)C
    Iupac Name 2,4,6-trimethylbenzonitrile
    Storage Temperature Store at room temperature

    As an accredited 2,4,6-Trimethylbenzonitrile 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 2,4,6-Trimethylbenzonitrile; features a secure, chemical-resistant cap and hazard labeling.
    Shipping 2,4,6-Trimethylbenzonitrile should be shipped in tightly sealed containers, protected from moisture, heat, and incompatible substances. It is classified as a hazardous chemical, so compliant packaging, labeling, and documentation according to relevant transport regulations (such as DOT, IATA, or IMDG) are mandatory. Handle with appropriate personal protective equipment (PPE).
    Storage 2,4,6-Trimethylbenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. It should be kept away from ignition sources as it is combustible. Proper labeling and secondary containment are recommended to prevent accidental spills or exposure.
    Application of 2,4,6-Trimethylbenzonitrile

    Applications of 2,4,6-Trimethylbenzonitrile in Industrial Manufacturing

    As an established producer of 2,4,6-Trimethylbenzonitrile, we support global industries with direct supply for high-value chemical synthesis, fine chemical intermediates, and specialty compound production. Below, we outline differentiated, real-world applications where our material achieves both high selectivity and processing reliability in downstream manufacturing environments.

    1. Pharmaceutical Intermediate Synthesis

    Process chemists incorporate 2,4,6-Trimethylbenzonitrile as a key intermediate during multi-step synthesis of APIs, particularly for selective aromatic amide and substituted benzonitrile frameworks in antihypertensive and central nervous system drug classes. The compound enters acylation, reduction, or cross-coupling steps, where its substitution pattern supports specific steric and electronic profiles required by patented actives. Batch-to-batch traceability and impurity control meet stringent regulatory scrutiny, ensuring reliable supply for GMP production scale.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monograph specifications for process intermediates
    • FDA 21 CFR Part 211 for API manufacture
    • EU GMP Directive 2003/94/EC applicable to medicinal chemistry reactors

    Typical usage ratio

    • Employed at 1.1–1.5 molar equivalents versus main substrate per synthesis step; process chemist determines precise stoichiometry based on route efficiency and byproduct minimization.

    Downstream process integration

    • Added at post-activation or nucleophilic substitution stages under inert atmosphere; inclusion in reflux, pressure vessel, or catalytic hydrogenation setups depending on step requirements.

    Final product types

    • Active pharmaceutical ingredients for antihypertensive, CNS, and anti-inflammatory medications
    • Protected intermediates for subsequent coupling or reduction
    • Regulatory-submitted process intermediates with validated impurity profiles

    2. Agrochemical Active Ingredient Building Blocks

    Major crop protection manufacturers use 2,4,6-Trimethylbenzonitrile as a nitrile-based scaffold in the synthesis of pyrazole-, pyridine-, and triazine-type active substances. Its methyl-substitution pattern confers desired hydrophobicity and metabolic resistance, aligning with EPA and EU-restricted compound development. Material enters as a core skeleton modifier during early process stages, impacting synthesis efficiency and patent-compliant molecular designs.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Regulation (EC) No 1907/2006 for chemical intermediates
    • EPA 40 CFR Part 174 Pesticide Registration

    Typical usage ratio

    • Utilized at 0.8–1.2 molar equivalents relative to reactive partner, with adjustments made according to target molecule substitution patterns and yield optimization studies.

    Downstream process integration

    • Fed directly in cyclization, condensation, or substitution stages preceding heterocycle ring closure, performed in closed-system reactors equipped for effluent control.

    Final product types

    • Herbicide actives for cereal and broadleaf crops
    • Fungicide intermediates for proprietary blends
    • Insecticide subcomponents with high selectivity for regulatory submissions

    3. Liquid Crystal Material Synthesis

    Manufacturers in the advanced display sector rely on 2,4,6-Trimethylbenzonitrile to construct mesogenic molecules for nematic and smectic liquid crystal blends. The raw material’s steric bulk and electron-withdrawing cyano group contribute directly to the phase transition temperatures and birefringence parameters of finished LC mixtures, which are critical for TFT-LCD and OLED panel performance. Laboratory-scale optimization transitions to bulk chemical integration as part of scalable, QC-driven production lines.

    Industry compliance standards

    • RoHS Directive (EU) 2015/863 compliance for electronic materials
    • IEC 61249-2-21 for liquid crystal device components
    • ISO 9001:2015 quality management for fine chemical production

    Typical usage ratio

    • Engineers introduce at 2–7% by weight in custom mesogen core ingredient formulations; ratio varies to tailor viscosity and dielectric constants according to display application.

    Downstream process integration

    • Reacted in controlled synthesis steps forming biaryl or biphenyl-cyano core units; transferred to subsequent blending and alignment agent addition under nitrogen atmosphere before cell encapsulation.

    Final product types

    • Nematic and smectic liquid crystal compounds
    • TFT-LCD and OLED display material blends
    • Specialty LC mixtures for scientific instrumentation and medical imaging

    4. Advanced Polymer Additive and Monomer Precursor

    Specialty polymer manufacturers adopt 2,4,6-Trimethylbenzonitrile in the synthesis of polymers requiring rigid, hydrophobic aromatic units for engineered property control such as thermal stability and solvent resistance. It functions as a controlled-chain end group or co-monomer precursor before polymerization, affecting polymer architecture and end-use characteristics in technical films, high-performance coatings, and specialty fibers. Quality parameters such as residual nitrile content and byproduct removal are tightly monitored to adhere to downstream industry requirements.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for substances in polymers
    • ISO 14001:2015 Environmental Management relevant to polymer plant operation
    • ASTM D6287 for polymer additive evaluation

    Typical usage ratio

    • Used as 0.5–3% by mol in co-monomer feedstock, or as the sole aromatic nitrile source up to 12% in specialty polymer syntheses; process adjusted to target molecular weight and desired end-group composition.

    Downstream process integration

    • Dosed during pre-polymerization or melt phase as a chain terminator, or in initial monomer-charging sequence; integrated with in-line monitoring of residuals for continuous quality improvement.

    Final product types

    • High-performance polyamides and polyesters
    • Technical films for electrical and chemical resistance
    • Engineered fibers and coatings for automotive and aerospace sectors

    5. Fine Chemical Synthesis for Dye and Pigment Manufacture

    Dye and pigment producers employ 2,4,6-Trimethylbenzonitrile as a synthon for designing aromatic cores with specific chromophoric properties. The molecule enables synthesis of specialty azo and anthraquinone dyes, impacting hue sharpness, fastness, and solvent compatibility. It serves as a substitution and chain extension precursor prior to final dye coupling, where its methyl substitution pattern dictates lightfastness and application-specific performance in high-end plastics and textile coloration.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Guidelines
    • REACH Registration for colorant intermediates
    • ISO 9001:2015 for pigment manufacturing systems

    Typical usage ratio

    • Applied at 1.0–2.5 molar equivalents relative to dye core; margin for adjustment exists depending on target color strength and chromophore substitution density.

    Downstream process integration

    • Enters as an aryl nitrile in nucleophilic aromatic substitution or coupling reactions; processed in jacketed reactors with temperature and pH control ahead of pigment precipitation or dye salt formation.

    Final product types

    • High-strength organic pigments for plastics, inks, and coatings
    • Specialty dyes for fibers, films, and technical textiles
    • Intermediates for high-stability colorant systems in automotive and electronics paints
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    Certification & Compliance
    More Introduction

    2,4,6-Trimethylbenzonitrile: A Look Behind the Label

    Those of us who work hands-on with aromatic nitriles know the subtleties of each compound’s role in downstream chemistry. 2,4,6-Trimethylbenzonitrile isn’t a backyard name, but to the folks shaping specialty chemicals, it’s clear how much difference a single molecular tweak makes. Over the past decade, we’ve seen demand shift; where once the plain benzonitrile sufficed, customers now request the trimethyl variant for its reliable stability and compatibility with tight reaction conditions.

    Understanding the Product

    The molecule itself rewards close inspection. Sporting three methyl groups at the 2, 4, and 6 positions of the benzene ring, this compound resists unwanted side reactions better than its mono- or di-methyl cousins. Seasoned process chemists appreciate its improved steric protection around the cyano group, compared with unsubstituted benzonitrile or o- and p-tolunitriles. In practice, every added methyl introduces incremental hydrophobicity, leading to lower water solubility but enhancing its performance in reactions where trace moisture disrupts yield.

    From our own batches, the product crystals appear as faintly off-white solids, consistent and free from persistent trace color. Our most demanded material ranges in purity above 99%. Sometimes a customer pushes for a particularly low metal content if their synthesis can’t tolerate transition metal traces; we handle that through targeted scrubbing and filtration steps, verified along the way using ICP-MS. Each ton we prepare faces repeat GC and NMR before it moves to labeling, because only by double-checking both volatile and non-volatile impurities do we guarantee confidence at scale. Local teams follow a tight housekeeping protocol to avoid cross-contamination, especially for pharma-grade shipments.

    What Sets 2,4,6-Trimethylbenzonitrile Apart

    Having spent years refining our workflows, the value of this compound stands out most during downstream transformations. Where ortho- or para-tolunitrile might serve as a starting point for specialty dyes, cosmetics, or certain antioxidants, our trimethylbenzonitrile shines where higher selectivity or resistance to oxidation matters. Many academic labs first explored its capacity for withstanding oxidative functionalization. Now, manufacturers in agrochemical and advanced material sectors routinely specify this exact structure to dial in targeted properties.

    Every methyl group on the ring makes direct aromatic substitution slower. In our own benchtop trials, the rate difference compared to benzonitrile becomes obvious with even basic nucleophilic or electrophilic attack conditions. That slight reactivity drop protects downstream intermediates from early decomposition in large or complex multi-step syntheses. In practical terms, using the trimethyl variant gives you a more predictable, robust substrate, especially valuable in process workflows where reliability trumps cost for critical runs.

    Applications in Our Customers’ Workflows

    Our regular client base spans electronics, pigments, fragrance intermediates, and—more recently—pharmaceutical intermediates. Multiple producers count on trimethylbenzonitrile as a protected building block in difficult carbon-carbon and carbon-nitrogen coupling reactions. For example, Suzuki couplings benefit from a stable aromatic core that avoids side precipitation, which significantly improves batch yield.

    Certain colorant brands have championed this compound for the tight hue and purity control it brings to blue and violet pigments. The methyl group placement leads to final product shades less sensitive to trace impurities or variable solvent qualities. We’ve even received feedback from resin manufacturers that small changes in methylation pattern impact polymer backbone rigidity—subtle advantages until you’re shooting for materials exposure-tested through years of sunlight or solvent splash.

    Process Details and Practical Insights

    We’ve improved each lot by years of tightening our nitrile formation conditions. Most commercial runs begin with mesitylene, which already places methyl groups at 2, 4, and 6. Careful ammoxidation introduces the cyano group directly, but copper-catalyst traces can ruin purity. Our continuous-flow platform enables quicker heat-up and cool-down, minimizing byproduct formation that complicates downstream QC. This kind of batch discipline only develops through live-day repetition.

    In our experience, the switch from classic batch to flow nitrilation halved our average impurity burden and eliminated frequent batch-to-batch color drift. Customers working in high-throughput screening have reported that lots from the older process left micro-precipitates or slight yellowing when solubilized; this virtually disappears with the new routine, so long as solvent drying stands up to spec.

    Temperature and oxygen control matter just as much as starter material quality. Sloppy process controls let in isomeric side products or oxidized fragments, shifting both melting point and spectral fingerprint. We test every batch under dry nitrogen to monitor for off-target formation, especially near the end of each run. Only after spectral checks meet both our internal thresholds and the specific requirements from customers’ MSDS filings will we label a batch ready for dispatch.

    How Quality Delivers Reliable Downstream Performance

    Compared to benzonitrile or o-tolunitrile, our trimethylbenzonitrile brings improved shelf life and higher thermal resilience. Customers often store their stocks under ambient or mild sub-zero conditions; over multiple years, the trimethyl groups reduce both hydrolytic and oxidative degradation. For pilot plant operators juggling inventory cycles and unpredictable demand swings, this can sidestep waste penalties and delayed project starts. More than one partner has mentioned their switch to this grade made their storage planning easier, trimming re-analysis runs and saving up-front lab hours.

    Cross-checking analytical records tells a similar story. NMR and GC consistently show cleaner signatures over time for aged trimethylbenzonitrile samples, compared to plain benzonitrile or less substituted analogs. Even after exposure to routine temperature fluctuations—transit, cross dock, warehouse load-in—our product retains its initial profile with minimal increase in baseline contaminants.

    Handling safety features also come into play. The higher methylation drops the compound’s volatility, so vapors during sampling or transfer are notably less pungent than plain benzonitrile. We’ve connected with process technicians who value this small but meaningful difference, especially over dozens of repeated transfer cycles per quarter.

    Environment and Regulatory Footprint

    Many buyers want assurances that specialty chemicals arrive and leave the supply chain capped, logged, and waste-tracked to code. The synthesis of 2,4,6-trimethylbenzonitrile, like all nitriles, generates some ammonium salts and requires careful control of effluent. Our wastewater is treated on-site, split for salt removal, and monitored for aromatic signature before release to external treaters; local permits require us to log every kilogram passing the plant’s drains.

    Use patterns in the European Union and Japan reflect rising expectations on both product purity and process emissions. Our best practice uses a combination of in-line monitoring for any off-gassing and real-time catalysis adjustment, helping catch any spikes before they impact finished product or local compliance limits. Based on collected results, no persistent residues from copper or vanadium catalysts remain above required ppm thresholds; this directly benefits customers producing food-contact materials or high-purity colorants bound for regulated markets.

    Comparisons With Other Benzonitrile Products

    In our shop, quality inspectors regularly compare incoming and outgoing samples of benzonitrile variants. While the base benzonitrile excels at general solvent or intermediate roles, the trimethyl derivative delivers extra robustness and batch-to-batch reproducibility under challenging synthesis. Ortho- and para-methyl derivatives have their own fans in dyes or flavor chemistry but fall short of the trimethyl standard once oxidation risk or reaction temperature climbs. Every turn of the distillation column highlights differences: less substituted nitriles break down faster or discolor in multi-week storage.

    Industrial scale-up further accentuates the differences. Customers relying on older, less tamed grades often report variable endpoint conversion rates, where either underreacted starting material or gradual product darkening logs hours of rework. Switching to our refined 2,4,6-trimethylbenzonitrile addresses these headaches directly by ensuring tighter process windows and by reducing volatility loss through vapor lines and exhaust.

    Why Manufacturers Value Traceability and Batch Consistency

    Down the line, traceability proves its worth every time. Oversight bodies and large end-users expect far more than a certificate of analysis stapled to a drum. Our plant’s batch records trace sources back to starter chemicals and even environmental control records, so all relevant data—temperature, humidity, equipment cleaning logs—move with every lot number. Process teams notice the difference when investigations into a rogue impurity become necessary. By tracing a blip to a specific catalyst batch or an errant piece of plant equipment, downtime drops and corrective action stays straightforward.

    Longer-term customers have remarked on the subtle savings that come from this level of rigor. Instead of scrambling for answers to missing paperwork or out-of-range test results, they receive clear digital audit trails supporting every year’s record. Supply auditors appreciate having supplier records that stand up to close inspection, and end-users rest easier with every bottle in their supply room knowing exactly where, how, and under what conditions it was made.

    Real Challenges in Making and Supplying This Grade

    No chemical is truly plug-and-play. Through years of experience, we’ve learned where hiccups turn into headaches. Raw materials must pass continuous screening, as seasonal and vendor shifts in mesitylene purity alter outcomes even before the first reaction. Cross-shipment of solvents and shared storage tanks can introduce hard-to-catch impurities, so we built up staged storage and dedicated lines for key materials. Our technical team meets weekly to review batch deviations, focusing on trace impurity signatures and rejects. These checks spot bottlenecks or supplier trends early, saving headaches for everyone downstream.

    Keeping the cold chain unbroken makes a big difference. Our logistics crews use insulated containers if ambient temperatures threaten to swing outside the compound’s stability window during long-haul transit. We track each shipment until customer sign-off, logging time, temp, and handling all the way. For high-purity grades, any breach in the cold chain prompts a hold for incoming inspection. If a drum’s history doesn’t match the required spec, it’s flagged and returned for reprocessing—even if it’s just one out of an entire shipping lot.

    Future Developments and On-the-Ground Solutions

    In upstream chemistry, efficiency and safety will keep guiding the direction. Interest in greener synthesis pushes us to trim back catalyst loadings and recover more input materials for reuse. We’re piloting a catalyst recycling loop that drops fresh metal ion use and tightens our control of final product residuals, a win for both economics and compliance. Field trials with alternate oxides continue as environmental standards nudge the bar higher. All major changes roll out only after we compile a year of batch results showing tighter purity, cleaner waste, and better recovery rates.

    Customers now ask about energy usage per ton produced, so our operations group tracks every reactor’s demand across shifts and seasons. Smart-metering and heat integration projects lower our natural gas and steam bills, which passes through to more favorable pricing and a smaller carbon footprint. A handful of process tweaks in recent years—early solvent recovery, better scrubber tuning—have pushed waste reductions beyond initial targets. On the packaging side, our team sources returnable drums for frequent buyers, cutting both landfill and emissions from single-use plastics.

    Education plays its part. We invest hours in open conversations with formulators, helping teams troubleshoot with real material data or adapt new process techniques. These exchanges have exposed hidden bottlenecks in some buyers’ setups—clogged transfer lines, miscalibrated drying ovens, or weak points in air control. Our tech support group partners with customers’ chemists for deeper dive calls or even on-site troubleshooting for high-value projects. Each honest conversation shortens the learning curve and often lifts performance for both sides.

    Reflections From the Factory Floor

    Every pallet of 2,4,6-trimethylbenzonitrile leaving our plant carries layers of hands-on know-how: how to coax a clean product from raw materials, how to keep it tight from lab to logistics, and how to help end-users reap the full benefits of this molecular fine-tuning. Over time, we’ve grown as much from customer feedback as from internal process tweaks. Where chemists care about clean spectra and repeatable performance, we answer with disciplined planning and live tracking. Where product stewards need waste logs and residual records, we meet that with transparent batch and waste data to back the paperwork. This compound shows, better than most, how tailored manufacturing couples daily vigilance with a wider push for smarter, safer, and more responsive chemical supply chains.

    The journey hasn’t been linear. Each production run brings fresh details: the grain of a crystal, the drift of a spectral line, a raw material shipment needing extra scrutiny. By keeping boots on the ground and eyes on the samples, we deliver more than a drum of nitrile—the result is a ledger of experience, owned and shared through every lot that moves from our plant to the world’s R&D labs and pilot reactors. The devil lives in the details, and we spend our working lives learning, adjusting, and improving—all on behalf of customers who trust us not just for a name on a label, but for results in every box and bottle shipped.