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HS Code |
571200 |
| Chemicalname | 4-Hydroxy-2,6-Dimethylbenzonitrile |
| Molecularformula | C9H9NO |
| Molecularweight | 147.18 g/mol |
| Casnumber | 6248-21-9 |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | 154-158°C |
| Boilingpoint | Unavailable |
| Solubility | Slightly soluble in water |
| Density | 1.18 g/cm³ |
| Purity | Typically ≥98% |
| Smiles | CC1=CC(=CC(=C1N#C)O)C |
| Inchi | InChI=1S/C9H9NO/c1-6-3-8(2)7(5-10)4-9(6)11/h3-4,11H,1-2H3 |
| Synonyms | 4-Cyano-2,6-dimethylphenol |
| Storagetemperature | Store at 2-8°C |
| Refractiveindex | Unavailable |
As an accredited 4-Hydroxy-2,6-Dimethylbenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a tight-sealing cap, labeled "4-Hydroxy-2,6-Dimethylbenzonitrile, CAS: 50615-76-8, 99% purity." |
| Shipping | 4-Hydroxy-2,6-Dimethylbenzonitrile is shipped in tightly sealed containers to prevent contamination and moisture exposure. It should be transported in compliance with applicable local, national, and international chemical transport regulations. Store and ship in a cool, dry place, protected from direct sunlight, and clearly labeled with hazard information. Handle with appropriate safety precautions. |
| Storage | 4-Hydroxy-2,6-Dimethylbenzonitrile should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizers. Keep the container clearly labeled and protected from moisture. Ensure storage is in accordance with chemical safety guidelines and local regulations, and restrict access to trained personnel only. |
Applications of 4-Hydroxy-2,6-Dimethylbenzonitrile in Industrial ManufacturingAs the original manufacturer, we provide 4-Hydroxy-2,6-Dimethylbenzonitrile specifically engineered to match the strictest process and traceability requirements encountered in advanced chemical synthesis sectors. This intermediate forms an essential building block in several established industrial chains, each with particular compliance, formulation, and operational protocols. Below we outline its role across major real-world downstream routes substantiated by industry demand and regulatory context. 1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug Synthesis4-Hydroxy-2,6-Dimethylbenzonitrile serves as a critical heterocyclic precursor in the synthesis of various non-steroidal anti-inflammatory drugs (NSAIDs). It enters advanced multi-step synthesis routes where precise control over purity and reactivity is mandatory. In this segment, pharmaceutical manufacturers depend on its consistent reactivity profile to achieve high-yield transformations, especially in condensation and cyclization stages that lead to the final active pharmaceutical ingredient (API) core structures. Industry compliance standards
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2. Agrochemical Intermediate for Selective Herbicide ProductionDownstream agrochemical manufacturers utilize this compound as a reactive intermediate within synthesis pathways for aryl nitrile–based selective herbicides. Its hydroxy-substituted benzene ring structure offers targeted reactivity ideal for creating pre-emergent and post-emergent herbicidal formulations focused on specific weed resistance mechanisms. Detailed process tuning allows for structural optimization in the final molecule, contributing to improved field performance and regulated safety margins. Industry compliance standards
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3. Electronic Chemicals Precursor for High-Purity Liquid CrystalsIn liquid crystal manufacturing, especially for display and sensor applications, high-purity hydroxy-substituted benzonitriles provide the necessary foundation for assembling mesogenic cores. This compound offers desirable electron-donating and withdrawing group placement, critical for adjusting phase transition temperatures and dielectric properties in specialty liquid crystals. Manufacturers implement rigorous purification steps at this stage to meet stringent downstream electronic material standards. Industry compliance standards
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4. Dye Intermediate for High-Fastness Disperse Dye SynthesisOur customers in the textile and specialty dye sectors rely on this molecule’s ortho-methyl and hydroxy substitution pattern to create high-performance intermediates for disperse dyes. These downstream products feature superior shade strength, wash, and lightfastness properties, crucial for synthetic fiber dyeing. The compound’s reactivity favors controlled coupling sequences essential for consistent coloration in mass fiber processing. Industry compliance standards
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5. Fine Chemicals Intermediate for UV Filter SynthesisIn ultraviolet absorber and sunscreen manufacturing, downstream formulators exploit the aromatic nitrile and hydroxy structure to build UV-stable benzotriazole and related molecular frameworks. Consistent reactivity mitigates side product risk and ensures predictable absorption spectrum placement, a key demand for UV filter compounds used in advanced coatings and personal care. Industry compliance standards
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For many years, our team has put effort into producing specialty chemicals with tight control over structure and traceability from factory floor to shipment. One of the products we focus on, 4-Hydroxy-2,6-Dimethylbenzonitrile, stands out for several reasons. The compound does not see the kind of demand attached to mainstream intermediates, but it has a dedicated following among researchers and manufacturers who require true consistency batch after batch.
We produce 4-Hydroxy-2,6-Dimethylbenzonitrile with meticulous attention to raw material selection. The most critical factor lies in keeping the process free from secondary contamination, especially since the hydroxy and nitrile groups present handling and reactivity challenges. Our synthesis follows a setup tailored to avoid over-oxidation and side-chain reactions. From our experience, even minor contamination with related isomers will affect color and solubility characteristics, making purification more labor-intensive for our customers.
The typical physical appearance shows up as a pale to off-white crystalline solid, though the shade can change slightly with batch scale and time of storage. Specifications that draw repeated attention from buyers include moisture content, melting point, and residual solvents. We target water content comfortably below one percent, measured with Karl Fischer titration for every lot. Melting range provides a rough but instant assessment of purity, and we calibrate our own differential scanning calorimeter several times monthly for accuracy. As for solvents, we carry out routine GC analysis, since traces of alcohols or halogenated reagents tend to compromise stability — and our long-term clients recognize even the smallest drift from previous batches.
Unlike more commonly traded intermediates, 4-Hydroxy-2,6-Dimethylbenzonitrile fills a precise role in very specific manufacturing chains. The hydroxyl group in the 4-position paired with the cyano group opens up further transformations. Laboratories and plants that run aromatic substitution, etherification, or nitrile reduction appreciate a well-defined starting point. In the pharmaceutical sector, the compound allows custom synthesis of intermediates that conventional benzonitriles cannot match. We've witnessed customers in active ingredient research come back repeatedly, knowing they need the unique substitution profile for their synthetic targets.
Production teams have pointed out that this compound, with two methyl groups flanking the hydroxy moiety, resists unwanted oxidation better than unsubstituted analogs. That physical stability translates into cleaner reactions downstream, saving time lost in post-reaction purification. Chemical manufacturers working on dyes and pigments use it as a scaffold to access color shades not feasible from other benzonitrile variants. This ability to serve as a high-value intermediate, rather than just a basic aromatic, sets it apart in the market.
Chemically, 4-Hydroxy-2,6-Dimethylbenzonitrile differs from products that look similar on paper. For example, the popular 4-hydroxybenzonitrile does not possess the methyl substitutions at 2 and 6, which has significant effects in practice. Those methyl groups block certain electrophilic attacks on the ring, preventing the formation of unwanted side products during downstream reactions. Our technical clients confirm that this leads to predictably higher yields and fewer chromatographic steps, a strong argument for sourcing the exact isomer rather than a general benzonitrile.
Even a single change in substitution pattern alters physical properties such as solubility in different solvent classes or the ability to mix with resins and polymers. We documented clear differences in reactivity with dimethylated versus non-methylated benzonitriles, especially during Mannich or acylation reactions. Our analytical work captured these contrasts—NMR and HPLC purity readings do not match across analogs with even slight variations. For process engineers, this means a more straightforward workflow because the exact substitution pattern removes guesswork.
We have tracked use cases ranging from pharmaceutical intermediate development to specialty polymer innovation. Several clients in the European specialty chemicals sector rely on our product as a key precursor for medical imaging agents. In these cases, both purity and structural integrity define end-product reliability. The compound also appears in research on advanced organic conductors, where the hydroxy-nitrile group pairs well with metals and complex ligands, opening pathways for new material families.
Customized surfactant and additive programs utilize the compound’s functional flexibility. Our product repeatedly supports efforts to build blocks for UV-absorbing agents and antioxidant stabilizers for plastics. In direct syntheses, it offers an anchor for ether and ester formation, supporting experiments where typical benzonitriles show poor performance or incompatibility with harsher conditions.
A handful of fragrance and fine chemical innovators tap into 4-Hydroxy-2,6-Dimethylbenzonitrile for its aromatic structure. The combination of methyl and nitrile influences volatility and sensory impact, giving perfumers more room in their palette. Here, too, batch-to-batch consistency stands out — essential when small differences can shift product tone.
Since introduction of this product, the challenges of handling have defined our manufacturing improvements. The nitrile group demands careful ventilation and material transfer because even minute vapor release causes unnecessary occupational exposure. Over time, we reengineered our loading lines and introduced upgraded personal protective equipment protocols. These steps have led to longer shelf-life, stable storage, and greater protection for both our operators and warehousing partners.
End-users also comment on the packaging. We ship in tightly sealed, light-resistant containers, limiting hydrolysis and photooxidation. Shipping and logistical teams at client sites see reduced caking and easier dispensing. Documentation, including full traceability of raw materials and finished goods, accompanies every order. Copies of analytical test results, including HPLC and moisture determination, serve as confirmation for our partners who operate under strict regulatory audits.
Technical support does not end with a sale. When clients report downstream reaction issues, we collaborate to pinpoint root causes, from suspected micro-contaminants down to minor analytical discrepancies. This ongoing exchange builds confidence between chemists on both sides. Our experience bears out the belief that close feedback directly shapes process improvements — such as when customer reports led us to refine our drying and crystallization steps several production cycles ago.
Shifts in environmental and safety regulations ask more of manufacturers year after year. Our compliance officers and chemists stay ahead of new limits on nitriles and related aromatic intermediates across all regions we supply. Each batch crosses thresholds for heavy metal content and residual solvents far below established maximum values. We track evolving requirements from agencies and integrate feedback in real time.
Many customers now expect a full life-cycle assessment. We document sourcing through the supply chain and publish waste minimization progress in our periodic reports. For 4-Hydroxy-2,6-Dimethylbenzonitrile, we invested in updated filtration and liquid phase workup, which limits organic waste and reduces the need for additional chemical quenching. Our implemented closed-loop recycling for process water cuts freshwater needs. That’s supported by direct data on reduced consumption compared with industry averages for similar products.
Global supply chains for specialty intermediates face disruptions, whether from geopolitical events or logistics bottlenecks. While commodity benzonitriles track with the market, niche compounds like ours need relationship building all the way upstream to raw material producers. During the past two years marked by supply interruptions, advance planning and inventory transparency kept production moving for critical customers. We lean into direct negotiation with raw material suppliers and share planning forecasts ahead of time, smoothing resupply. This flexibility allows us to offer realistic lead times even under challenging global conditions.
Some buyers ask why we rarely keep massive inventory of 4-Hydroxy-2,6-Dimethylbenzonitrile. Due to its value and required certification levels, most orders tie directly to customer timelines. Our factory teams run scheduled campaigns, making batch record-keeping and identification easier. This custom-fit approach benefits quality control as each order receives focused attention, minimizing risk of cross-contamination.
Continuous upgrading of both process technology and analytical methodology strengthens our batches every year. About three years ago, feedback from several large clients highlighted inconsistencies in moisture content across lots. Our teams responded by introducing in-line drying monitors and revising container drying protocols. Direct discussion with customers led to collaboration on setting new process hold points, narrowing specification windows, and gaining further insight into user needs.
After implementing these process changes, internal sample batches showed more predictable melting ranges, matching client assessments with less deviation. Engineers adjusted crystallization periods and vessel agitation, yielding tighter particle size control, improving both ease of handling and flow for automated chemical lines at client sites.
Analytical improvements run in parallel. Newer detection techniques, including LC-MS, brought greater certainty to contaminant identification; internal audits now catch minute levels of unwanted side-products. Documentation updates match or exceed local and international expectations — our partners across multiple regions focus on regulatory filings and compliance audits, which these clear records support.
The wider field of aromatic nitriles continues to evolve, but we see growing demand for tailored intermediates with distinctive properties. Areas such as functional dyes, photoactive materials, and custom drug scaffolds require ever-tighter molecular control. Our R&D group works alongside process engineers to anticipate these shifts. Recent projects include exploring greener reaction conditions and seeking ways to phase out problematic solvents without reducing purity or yield.
We also support clients piloting new downstream applications. In-house technical teams provide data on reaction compatibility, highlighting which processes give the cleanest results. Strong relationships with university research labs give us feedback on novel uses, feeding back into how we refine specifications and analytical scope.
Support sometimes extends beyond direct sales. For research groups and production plants new to the compound, we share handling protocols, reaction optimization tips, and troubleshooting ideas based on our own operational experience. Our staff chemists attend client site visits when process upsets occur, offering perspective that comes only from making the compound at scale.
Competing products often take shortcuts that become apparent only after several batches run through a plant. Unwanted isomers cause headaches for downstream synthesis, especially in regulated applications. Low-purity lots may pass basic tests but fail to perform in demanding syntheses. We invest in additional purification even where the base specification seems “good enough,” because these extra steps head off future complaints and rework.
We have observed that traders and third-party packagers sometimes offer cheaper grades sourced from outside the established supply chain. Our relationships with end users reveal the performance differences first-hand. Once a batch fails to deliver—due to slight shifts in melting point, yellowing, or solubility problems—the argument for direct-from-manufacturer supply becomes obvious. Several multinational partners now stipulate direct sourcing for all benzonitrile derivatives after experiencing the long-term cost of off-spec material.
Production of 4-Hydroxy-2,6-Dimethylbenzonitrile brings daily reminders of the hands-on nature of specialty chemical manufacture. Each step, from synthesis to packaging, relies on the skill and attention of our factory team. Our operators, many with a decade or more of experience, regularly troubleshoot routine and unexpected issues: pump leaks, inconsistent crystallization, or subtle color shifts. Their insights—combined with the technical background of R&D staff—feed directly into steady product improvement.
For us, answering customer queries is not an afterthought. It ties together each part of our business with the needs of those using our compound for their own innovations. We view every batch as a test of our own process and a building block toward longer-lasting partnerships. In a marketplace filled with alternatives, we believe the knowledge and experience embedded in our product supports progress across several industries, whether in the lab or on the factory floor.
In a world increasingly shaped by data-driven choice and compliance, consistency and confidence separate true manufacturers from a crowded field. Our experience with 4-Hydroxy-2,6-Dimethylbenzonitrile has shown that there is no substitute for close observation, honest feedback, and the willingness to adjust both process and attitude. As research and production needs grow more demanding, specialty chemicals like ours will only gain in relevance—provided they are delivered with the same care and rigor that brought them to the market in the first place.