|
HS Code |
220965 |
| Chemical Name | 2,4,6-Trimethylphenylacetonitrile |
| Cas Number | 29045-79-6 |
| Molecular Formula | C11H13N |
| Molecular Weight | 159.23 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 60-63°C |
| Boiling Point | 315-317°C |
| Density | 1.02 g/cm³ |
| Solubility In Water | Insoluble |
| Smiles | CC1=CC(=C(C=C1C)CC#N)C |
| Pubchem Cid | 2725219 |
| Refractive Index | 1.561 (predicted) |
| Storage Conditions | Store at room temperature, in a dry, cool place |
| Synonyms | 2,4,6-Trimethylbenzyl cyanide |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 2,4,6-Trimethylphenylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A clear glass bottle containing 25 grams of 2,4,6-Trimethylphenylacetonitrile, labeled with hazard warnings and product details. |
| Shipping | 2,4,6-Trimethylphenylacetonitrile should be shipped in tightly sealed containers, protected from heat, moisture, and incompatible materials. Packaging must comply with relevant chemical transport regulations. Label containers with appropriate hazard information and ship via registered chemical carriers. Ensure documentation includes safety data and emergency contact details. Handle with proper personal protective equipment. |
| Storage | 2,4,6-Trimethylphenylacetonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. Keep it away from strong oxidizing agents and acids. Store under inert atmosphere if possible. Ensure containers are clearly labeled and protected from physical damage. Avoid prolonged exposure to light and moisture. |
Applications of 2,4,6-Trimethylphenylacetonitrile in Industrial ManufacturingAs the direct manufacturer of 2,4,6-Trimethylphenylacetonitrile, we support a select group of specialized industrial sectors with material supplies that fit rigorous downstream technical requirements. Below, we outline core end-use scenarios that represent actual, mature commercial applications for this intermediate, highlighting its integration into process steps, relevant regulatory expectations, practical formulation considerations, and typical finished goods produced by our downstream partners. 1. Agrochemical Active Ingredient SynthesisProducers of selective herbicides and novel insecticidal compounds incorporate 2,4,6-trimethylphenylacetonitrile as a key structural intermediate during active ingredient construction. This intermediate contributes steric bulk and chemical stability when forming benzonitrile-derived motifs common in next-generation crop protection actives. Chemical engineers use this material as a starting block for acylation or cyclization reactions, enabling the development of compounds that meet evolving pest resistance and environmental profile requirements. Industry compliance standards
Typical usage ratio
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2. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug (NSAID) SynthesisPharmaceutical manufacturers employ 2,4,6-trimethylphenylacetonitrile as a crucial intermediate for building diaryl acetic acid, arylpropionic acid, and structurally related scaffolds used in NSAID APIs production. Its methyl-substituted aromatic ring ensures selectivity during alkylation, hydrolysis, and reduction stages, supporting process chemists in batch or continuous flow set-ups where batch tracking and impurity profiling face tight pharmacopoeia standards. Industry compliance standards
Typical usage ratio
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3. Dye & Pigment Synthesis (Azo and Anthraquinone Derivatives)The coloration chemicals industry applies 2,4,6-trimethylphenylacetonitrile as an aromatic precursor when manufacturing specialty azo and anthraquinone dyes requiring ortho-substituted ring structures. This role proves vital in generating molecules with high thermal stability and precise shade development for fiber and polymer coloration applications. Industry compliance standards
Typical usage ratio
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4. Polymer Modifier and UV Stabilizer Precursor ProductionPolymer compounders utilize 2,4,6-trimethylphenylacetonitrile as a functional core for synthesizing stabilizer additives aimed at enhancing light fastness, thermal performance, and chain scission resistance in engineering plastics. Here, it reacts to form hindered amine or benzotriazole-based stabilizer precursors with persistent aromaticity, ensuring performance in demanding outdoor and automotive plastic components. Industry compliance standards
Typical usage ratio
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From our production line to the shelves of fine chemical laboratories, 2,4,6-Trimethylphenylacetonitrile has made an unmistakable mark among intermediates in specialty chemical synthesis. What sets it apart stems from the direct experience that comes with handling every kilogram, tracking every batch, and fielding technical questions from the chemists and process engineers in the world’s largest production hubs. Every bottle carries the reliability demanded by manufacturers across flavors, pharmaceuticals, and polymers who know that an off-spec intermediate disrupts the entire value chain, never mind the plant’s tight schedule. This compound, often known by the abbreviation TM-α-CN or by catalog number TPN246, finds itself the trusted backbone in numerous transformations and creative routes.
We know buyers don’t just want a molecule; they demand clarity and reproducibility. We maintain 2,4,6-Trimethylphenylacetonitrile at a stated assay no less than 98%, verified routinely by GC and HPLC, to meet the most demanding applications. Chemistry isn’t just about the listed purity; detectable residuals like 2,4,6-Trimethylaniline or other positional isomers can spell headaches down the line, so we monitor typical impurity levels closely. Our production process yields a white to off-white crystalline solid, with a melting range carefully controlled to stay within 57—60°C, and our moisture content stays under 0.2% by Karl Fischer analysis.
Because our chemists have run these same reactions themselves, we test every lot for compatibility in Grignard, Friedel–Crafts, and palladium-catalyzed reactions. During scale-ups, users report robust performance in both batch and continuous processing, which speaks to the consistency we focus on during manufacturing and quality assurance.
Many of our customers think of 2,4,6-Trimethylphenylacetonitrile as just another nitrile intermediate, but repeated customer feedback reminds us there’s much more at stake than formula and inventory code. Over decades of production, we have seen its most common destinations in the preparation of alpha-aryl acetic acids, particularly in pharmaceutical and agrochemical synthesis. Chemists working on novel non-steroidal anti-inflammatory drug scaffolds reach for this intermediate because the electron-rich aromatic ring flanked by methyl groups steers selectivity and steric protection, often minimizing undesired side-reactions.
We get frequent calls about the difference between ortho, meta, and para methyl substitution. In our own optimization work, 2,4,6-Trimethyl substituents consistently lower the rate of undesired side-chain alkylations compared to alternatives like 3,5-dimethyl or 2,6-dimethyl analogues. The combined sterics of the three methyl groups crowd the aromatic ring, which often manifests as greater reaction specificity in alpha-alkylation and in downstream hydrolysis or reduction steps. Process chemists in fragrance manufacture report that certain aldehyde and alcohol products derived from 2,4,6-Trimethylphenylacetonitrile remain more thermally stable and less sensitive to oxidation when compared against less substituted analogues.
Some large-scale synthetic routes in dye manufacturing employ this molecule because the cubic symmetry brought by the trimethyl arrangement translates to noticeable improvements in chromatic purity in finished pigment granules. Every producer claims purity, but minor isomer contamination creates real world problems: off-tones in organic pigments, non-compliant residues in active pharmaceutical ingredients, or lost yield in specialty catalysts. As primary source manufacturers, we’ve dealt directly with those customers who have needed to chase sources of poor color or yield, and we’ve seen simple lapses in nitrile or precursor quality disrupt entire development timelines.
No other part of the job brings as much challenge as helping customers scale using our product. Lab researchers push their protocols, and plant managers are rightfully concerned over batch-to-batch drift and unforeseen downtime. In our own pilot-scale studies, 2,4,6-Trimethylphenylacetonitrile demonstrates solid stability under typical storage conditions—sealed ambient stock remains unchanged for years, lignans or tars do not accumulate, and the product de-aerates quickly. At bulk scale, the crystalline structure prevents caking, and granule size remains uniform under mechanical conveyance, minimizing dust carryover. Our team addresses customer questions about filtration and drying, because in reality, packing and handling practices must match the theoretical performance of any specialty intermediate to prevent dust, loss, or unexpected reactivity.
We field inquiries daily asking why not use a simpler phenylacetonitrile, or a less-substituted methylphenylnitrile. Actual process feedback reveals that 2,4,6-Trimethylphenylacetonitrile extends the parameter window for selective condensation and Michael addition reactions. The extra methyls impart a lower melting point and make the molecule more soluble in organic solvents commonly used in pharmaceutical and fragrance syntheses. Our own partners in perfumery have noted improved olfactory notes in end products built from this base, tied to the methyl pattern’s influence on byproduct minimization during transformations.
Every year, process groups test broader substrate scopes with modifications to Lewis acid, organometallic, or base-catalyzed steps. Our own chemists continue to push alternative routes leveraging this intermediate for challenging regioselective couplings. It resists over-reduction and tends toward clean conversion in two-step schemes. This reliability turns into schedule certainty, which, for chemical plants on just-in-time operation and contract deadlines, becomes a deciding factor in product selection.
Side-by-side with 2,3,6-Trimethyl or 3,5-dimethyl derivatives, our product retains several points of advantage—a lower tendency toward resinification, unambiguous NMR and GC-MS traces, and a distinctive, reproducible odor note that simplifies in-process identification. These signatures help downstream QC teams quickly validate material origin, which streamlines approval and, by extension, final product release.
Through years in the field, we’ve accumulated practical recommendations for storage, handling, and ensuring optimal use of 2,4,6-Trimethylphenylacetonitrile. After conversations with pilot plant technicians and logistics partners, we use lined HDPE drums or multi-layered paper sacks to shield from ambient moisture and oxygen exposure. Field tests across different climates reaffirm that consistent granule size prevents bridging or clumping, even in humid environments. While many intermediates encounter challenges with compaction or caking, we maintain a mill and sieving schedule that results in a pourable, easy-to-handle solid.
Process developers often ask us about compatibility with various reagents or whether the nitrile is prone to drift in scale-up environments. Our experience bears out that careful temperature control and the use of clean, stainless equipment prevents both discoloration and loss of purity. Most importantly, users confirm that the three methyl substituents significantly buffer against uncontrolled side reactions—reactions that, with less hindered nitriles, show up all too often as purity losses, off-odors, or even hazardous runaway reactions.
We continue to see innovation flourish using this molecule as a starting point for new heterocycles, advanced ketones, and chiral auxiliaries. In medicinal chemistry, pharmaceutical process groups pivot toward compounds with greater aromatic substitution because such features often impart metabolic stability and improved bioavailability in drug scaffolds. Every project demands a tight range of impurity profiles—which feeds back directly to our manufacturing practices.
Large pharma groups sometimes request custom specification—ultra-low halide content, iron-free batches, or even in situ package purging—in pursuit of the highest purity demanded by regulatory filings. Through our own experience, we know this means more than ticking boxes. Each adjustment made on the production line or in the drying oven involves trade-offs, and it’s the voice of the production technician, monitoring carefully for signs of browning or hints of acidity, that foreshadows long-term reliability. We share these lessons directly with customers because every step taken before the product even ships out shows up later in their process efficiency and final product quality.
No commentary on specialty chemicals can ignore the industry’s shift toward sustainability and stricter workplace safety. Our facility has adopted closed-loop solvent recovery, minimizing environmental impact and improving cost efficiency. This directly affects the lifecycle of our nitrile intermediates, as cleaner and more sustainable processes deliver higher purity material while reducing trace contaminants. For downstream users, this translates into easier waste handling and smoother compliance with local environmental regulations.
Worker safety sits at the forefront of our daily operations. We have integrated real-time nitrogen blanketing and enhanced dust control at our discharge stations. Practical improvements like secondary containment or forced-air PPE drew directly from lessons learned in real-world production headaches, not from armchair theorizing. Those who handle bulk batches know the subtleties—how a small lapse in moisture control can quickly grow into a full-scale problem, or how safe, consistent packing procedures let chemists focus on synthesis, not troubleshooting.
One of the less glamorous sides of chemical manufacturing involves post-sale support, recall risk management, and frequent follow-ups with customers. We remain committed to auditing our supply chain, updating process mapping after incidents, and communicating openly about any upstream impurity changes or observed production anomalies. This practice comes from hard-earned experience—during a raw material shortage a few years ago, we tracked subtle impurity spikes to a change in an upstream supplier’s refinery protocol, then worked with affected customers to adapt their downstream processing until the original raw profile returned.
This level of transparency pays dividends far beyond the sale itself. Many of our long-term partners share back their own in-process QC data, highlighting not just batch variations, but new reaction ideas, process optimizations, and even new use cases. Over time, this feedback loop has driven upgrades in our filtration, blending, and packaging lines—translating laboratory precision into ton-scale repeatability for every customer.
We have welcomed visits to our manufacturing site, whether joint troubleshooting sessions or process audits, because time spent face-to-face with those who will actually handle and transform our compound always leads to practical insights. For example, one customer’s repeated requests for a slightly larger particle cut prompted us to introduce an additional screening stage, in turn reducing their downstream clogging and wasted time.
Manufacturing and moving specialty intermediates across borders brings real-world regulatory hurdles, and our years working with customs brokers and regulatory officials means we keep documentation and labeling in line with the most current standards. Long before shipping a single kilogram overseas, our compliance team has cross-checked reach/TSCA status, hazard designations, UN packing codes, and harmonized tariff codes. Though the paperwork often gets the spotlight, our support goes further—our experience with export logistics teams translates directly into fewer customs delays and rapid, safe delivery.
In emerging markets, we’ve seen demand for 2,4,6-Trimethylphenylacetonitrile spike due to expanding pharmaceutical and dye manufacturing sectors. Local users sometimes require on-site training in safe handling or rapid troubleshooting to adjust for variations in plant conditions. Our technical team often travels directly to customer sites, sharing best practices gleaned from years of bulk manufacturing, and our feedback mechanism means we keep refining recommendations based on every new batch report received.
We continually invest in process intensification, automation, and predictive monitoring. In practice, this means installing advanced sensors to monitor temperature and humidity in real time, not just as a regulatory measure but to learn how subtle environmental shifts impact every output. Lessons from years of real-world production—global supply chain interruptions, the quirks of vessel scaling, or customer-driven product tweaks—drive us to improve inventories, scheduling, and product adaptability. In fine chemical manufacturing, only seasoned experience can produce the kind of foresight that keeps innovations grounded and practical.
At its core, our production of 2,4,6-Trimethylphenylacetonitrile embodies a blend of technical mastery, direct user feedback, and the willingness to adapt. Each advancement we make reflects years of accumulated expertise, thousands of conversations with real users, and an unwavering focus on delivering consistent, application-ready material that keeps the supply chain moving. The product speaks through the results it enables—higher product yields, fewer headaches in scale-up, and process reliability that stands up batch after batch.
We remain ready to adapt to the demands of next-generation synthesis and stand behind every lot made, not just as a supplier, but as committed partners who understand the weight of each project relying on this key intermediate.