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HS Code |
625739 |
| Chemical Name | 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile |
| Molecular Formula | C9H9NO |
| Molecular Weight | 147.18 g/mol |
| Cas Number | 637-15-8 |
| Appearance | Off-white to light beige solid |
| Melting Point | 114-118 °C |
| Solubility In Water | Slightly soluble |
| Synonyms | 3,5-Dimethyl-4-hydroxybenzonitrile |
| Structure Smiles | CC1=CC(=C(C=C1O)C#N)C |
As an accredited 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in a 25g amber glass bottle with a secure screw cap, labeled with product name, purity, hazard symbols, and supplier details. |
| Shipping | 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with chemical transport regulations to prevent leaks or contamination. Appropriate hazard labeling is used if necessary. Shipping is generally conducted via ground or air under controlled temperature conditions, according to the compound’s safety and regulatory requirements. |
| Storage | Store **4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile** in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizers and acids. Protect from moisture, direct sunlight, and sources of ignition. Ensure that storage areas are equipped with proper spill containment and that only trained personnel have access to the chemical. Label containers clearly to avoid confusion. |
Applications of 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile in Industrial Manufacturing4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile serves as a specialized intermediate in several chemical sectors where stringent quality and process control standards are essential. Below, we detail key downstream industrial applications based on direct manufacturing practices and supply chain integration. 1. Pharmaceutical Intermediate for Antihypertensive SynthesisThis compound plays an integral role in synthesizing certain 1,4-dihydropyridine-class antihypertensive agents. Its reactive hydroxy and nitrile groups undergo condensation during heterocyclic ring formation. Manufacturers operate in strict compliance with global pharmacopeial protocols and quality management systems, ensuring each batch meets the trace impurity limits demanded by the finished API sector. Industry compliance standards
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2. Intermediate for Agrochemical SynthesisManufacturers in the agrochemical sector use this molecule for constructing selective herbicide and fungicide structures. The dimethyl and hydroxy functionalities contribute to increased activity and stability of specific pyridine-based and benzene-derived agrochemicals. Production batches require tight control of residual solvents and trace by-products in compliance with international agrochemical registration standards. Industry compliance standards
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3. Dye and Pigment Intermediate ProductionProducers of high-performance dyes and pigments utilize this raw material to introduce electron-donating groups into aromatic systems, enhancing chromophore stability and process compatibility. The compound supports color-fast and temperature-stable dye production required for specialty textile and polymer applications. Precise batch documentation and hazardous substances control remain critical, reflecting downstream user and regulatory requirements. Industry compliance standards
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4. Photoinitiator Precursor for UV-Curing SystemsProducers of UV-curable coatings, inks, and adhesives incorporate this chemical as an aromatic building block during photoinitiator synthesis. Its substitution pattern stabilizes the radical generation needed for consistent polymerization under UV exposure. The resulting photoinitiators must meet strict migration and extraction tests for compliance, especially where food or medical packaging is involved. Industry compliance standards
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5. Advanced Polymer Stabilizer SynthesisThis chemical provides essential building blocks for hindered phenolic antioxidants used as stabilizers in engineering plastics and elastomers. The specific positioning of hydroxy and methyl groups improves compatibility and efficiency in oxidative degradation inhibition during polymer processing. Producers must monitor process contaminants and certificate of analysis (COA) to comply with global material standards. Industry compliance standards
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At the plant, 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile always stands out in our line of aromatic nitriles. Years of handling specialty chemicals have given us a close perspective on the qualities that matter most to customers who expect no-nonsense performance. We offer this compound with a purity that helps chemists avoid headaches when targeting high yields in their custom syntheses, and we understand the tricks of the trade—how batch consistency shapes results, how minor impurities foul up all kinds of downstream reactions, and what it takes for a material to prove itself on the bench.
We manufacture 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile under a controlled synthesis route, making use of high-specification raw materials. Our typical lot purity registers at over 99%, verified through both HPLC and NMR analysis, ensuring minimal levels of byproducts such as methylated phenols or cyano isomers. We pack it in industry-standard containers, sealed against moisture and light to protect shelf life. Granule size follows a consistent distribution to help with weighing and transfer – clients tell us this reduces static clumping on their balances, which comes as a relief when handling large orders in automated lines.
The melting point holds steady within a narrow band, a sign that micro-impurities are kept at bay. We document every kilogram, tracking batch identity, rechecking with QC before shipment. This kind of vigilance helps prevent surprises for formulation chemists, particularly those scaling up from pilot to commercial runs. We know that timelines depend on reliability, and startup delays ripple unhelpfully through the project calendar.
Our colleagues on the application support team keep their ears to the ground, learning from formulators and process chemists how 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile fits into their day-to-day workflows. Most customers buy it as a building block for advanced aromatic chemistry. The hydroxy group, paired with the electron-withdrawing nitrile, makes the ring an attractive scaffold for further functionalization. Medicinal chemistry teams, in particular, lean on its clean profile to help assemble pharmacophores: When they’re screening analogs, they need less noise in their assay plates and fewer surprises during purification. Those who push into agrochemical discovery rely on the same molecular traits—having both methyl and nitrile groups on the ring brings flexibility when designing new bioactive structures.
Material science labs also appreciate this compound. Its stability under common conditions means it serves as a predictable component in specialty polymers or resins, and its structure contributes to color-fastness or resistance to photodegradation in coatings work. Years ago, we saw a spike in interest from companies exploring advanced liquid crystal formulations, drawn by the hydrophobicity and substitution pattern of our product. We observed that some polymer chemists prefer it over less stable or more volatile ring systems for similar reasons: predictable incorporation and clean thermal behavior.
We field frequent questions: “Why not just use regular 4-Hydroxybenzonitrile or another dimethyl phenol?” Our chemists have run those head-to-head tests. The presence of both methyl substituents at the 3 and 5 positions modulates electron density around the ring, tuning reactivity in a way that pure 4-hydroxybenzonitrile does not accomplish. Substitution like this can suppress unwanted side reactions, particularly in metal-catalyzed couplings or directed ortho-lithiation steps, a detail that practitioners notice once their project passes the gram scale. To those who operate kilo plants or multipurpose synthesis modules, less byproduct translates directly to easier clean-up—fewer hours spent on silica columns, less spent solvent, less risk of contaminating downstream intermediates.
Comparing it to similar molecules such as 3,5-dimethylphenol or 4-cyanophenol, we find our product handles moisture and storage stress better over months. The nitrile group stabilizes the structure against oxidative degradation. End-users targeting SAR (structure-activity relationship) explorations for medicinal lead finding value in that blend of aromatic stability and tailored electron density it brings. In the plant, we avoid the excessive odor and volatility associated with lower molecular weight aromatics, resulting in a more pleasant—and safer—work environment for handling.
Scaling up 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile presented its own set of challenges. Early on, we ran into purity issues as small as one-tenth of a percent affecting downstream product color and crystallinity. Our team responded by instituting in-line monitoring steps at multiple points throughout the batch process: infrared spectroscopy after nitrile introduction, GC analysis of distillate, and a final solid-state NMR check. Some industry partners might skip those steps to save on turnaround, but we measure every stage, since one off-batch reverberates through customer production lines and costs everyone more time in the end. As a manufacturer, every day spent on quality assurance saves us from late-night troubleshooting calls and longer-term reputational risk.
Waste minimization always concerns us. Over the years, we’ve tightened process integration – recovering methylated byproducts, capturing excess solvents for reprocessing, and switching to greener oxidants. In conversations with environmental auditors, we share what we've learned about optimizing reaction yields: greater conversion rates mean less off-spec waste to treat, translating to lower disposal fees and safer work routines for our staff. We keep detailed logs and have responded to client requests for more transparency on process improvements, because large downstream buyers increasingly factor source sustainability into their procurement strategies.
One thing about being a manufacturer: you learn a lot by listening. Our sales and technical teams share real feedback from the field. For example, a leading agrochemical company mentioned caking issues during long storage in humid climates. That observation led us to revisit our drying protocols and double-check the desiccant loads in shipment. We found that batch-to-batch consistency on particle size was more important than we realized for customers employing automated pre-weighing systems. Acting on their reports, we fine-tuned both our sieving process and our packaging specification, helping reduce downtime and waste for those end-users. We document all such changes to help purchasers meet audit or regulatory review without friction.
In the specialty chemical world, customer requirements shift faster than most people expect. Global regulations evolve, market needs adapt. For our part, we keep a close watch on industry changes—whether it’s a new REACH restriction or a different purity threshold demanded by pharma clients. We have made it a habit to test every lot against both the strictest specification presently in force and any foreseeable new standards, even if only a minority of our buyers require it. By adopting higher standards before they are mandatory, we’ve avoided emergency retrofitting and last-minute rush jobs, which upset both production lines and working hours.
Quality management shapes every phase of our process. Certifying to ISO 9001 quality standards was not merely a paperwork exercise for us but a matter of day-to-day discipline on the production floor. Our internal guidelines match, and often exceed, what’s required under prevailing international regulations. Regular audits and self-inspections, including random sampling from finished lots, keep us alert to minor fluctuations before they turn into problems. The batch traceability we enforce gives our buyers reassurance—if any anomaly arises, we track its source backwards within hours, not days. This level of discipline ensures that industry clients, from pharma to advanced materials developers, can trust our product in their most sensitive applications.
We also respond to more specific customer needs, such as requests for documentation supporting compliance with restricted substance lists or detailed lab reports for patent filings. We keep ready records on solvent use, batch dates, and measured impurity levels, tailoring delivery of that information according to the unique requirements of each buyer. Our in-house regulatory experts track and interpret new rules in North America, Europe, and Asia, coordinating with production to adapt ahead of time and minimize disruptions.
There’s ongoing discussion these days about green chemistry and its role in specialty chemicals. We take the practical route—minimizing hazardous reagents, recycling where practical, and engaging third-party auditors for periodic environmental checks. Our process generates lower-organic solvent waste than most conventional routes, and our wastewater streams are treated and neutralized onsite before disposal. Occasionally, this means a slightly higher raw material cost or longer synthesis route, but industry clients who have faced permits and audits understand the peace of mind such investments bring.
Efforts to cut our energy use have included engineering upgrades to reduce heating and cooling cycles in product purification. We’ve swapped out aging filtering equipment in favor of faster, more energy-efficient designs; choices like these make a difference when you look at total energy use across batches year after year. We discuss our sustainability practices with buyers who now include environmental metrics in their own supply chain reviews. In the spirit of honest manufacturing, we share shortcomings as well as successes. For example, we still wrestle with minimizing certain waste streams, but steady improvements in reactor yield, coupled with careful process optimization, reduce those challenges over time.
Buyers ask about our supply position all the time, especially in uncertain times. We’re a direct manufacturer, so we control all the core links in the value chain—from sourcing key aromatic feedstocks, right through synthesis and purification to final packing. This translates into real benefits for buyers facing unpredictable shipping lanes, tariff shifts, or last-minute project demands. Thanks to our vertical integration, we offer more accurate lead times, shorter production windows, and the flexibility to tackle custom purity or alternate pack sizes without third-party delays. We keep a buffer stock at our site for urgent orders and offer staggered shipments where long-term contracts require it.
Many of our long-term users point out that our factory-direct model saves them procurement headaches: no unknown intermediaries, no third-party relabeling, direct traceability from our reactor to their warehouse loading dock. If a client calls with a specification shift, we can rapidly adjust at the source, not via a patchwork of subcontractors. This level of flexibility has smoothed over supply interruptions that would otherwise trigger costly production stops for end-users.
We keep close tabs on research trends and commercial shifts. The demand for precision building blocks like 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile only intensifies as custom synthesis work gets more exacting, whether for pharmaceuticals, challenging materials projects, or flavor and fragrance applications. Gradually, we’ve expanded our analytical toolkit to meet new requirements—chiral purity checks, detailed mass spec reports, and certificate formats tailored for regulatory filings. Increasingly, customers look for more than just purity: trace metals, residual solvents, and specific isomer ratios often make or break a project timeline. We’ve updated and upgraded our in-house labs accordingly, always seeking feedback from leading industry users on emerging standards and gaps they’ve encountered with other sources.
A glance across the market landscape suggests a continuing shift toward stricter transparency and tighter quality demands. We see procurement teams increasingly requesting supply chain audits, renewable sourcing information, and deep-dive traceability. These demands fit our company culture well. By sticking to strict internal controls and documenting every step, we anticipate these shifts, rather than being forced to play catch-up.
Years in the industry have taught us that in chemical manufacturing, there’s no substitute for accumulated know-how. The small details—batch records, analytical documentation, regular calibration of every scale, careful planning of every order—deliver real-world value for customers. Feedback from practical users keeps us honest and drives continuing improvement, not wishful marketing claims. Our approach with 4-Hydroxy-3,5-Dimethyl-Benzenecarbonitrile reflects these lessons. Every batch represents our commitment to reliable production, mindful handling, and direct manufacturing expertise that helps research and production teams reach their goals, project after project.
As chemistry continues to evolve and industries press for ever-closer control over their building blocks, we stand ready to help solve new problems and meet higher standards. The trust built over years comes not from advertising, but from delivering on promises, listening to those who work with our product every day, and staying open about both challenges and progress. For us, that’s the only way to build a truly enduring relationship—with every buyer, every batch, and every order we ship.