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2,6-Dihydroxytoluene

    • Product Name 2,6-Dihydroxytoluene
    • Alias 2,6-Dimethylresorcinol
    • Einecs 208-753-9
    • 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
    Specifications

    HS Code

    921904

    Cas Number 608-25-3
    Molecular Formula C7H8O2
    Molecular Weight 124.14 g/mol
    Appearance White to pale yellow crystalline solid
    Melting Point 106-109 °C
    Boiling Point 261 °C
    Density 1.188 g/cm³
    Solubility In Water Moderately soluble
    Pka 9.45
    Synonyms 2,6-Dimethylresorcinol, 2,6-Toluenediol
    Pubchem Cid 12761
    Iupac Name 2,6-dihydroxy-1-methylbenzene

    As an accredited 2,6-Dihydroxytoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2,6-Dihydroxytoluene is packaged in a 100g amber glass bottle with a secure screw cap, labeled with safety information.
    Shipping 2,6-Dihydroxytoluene should be shipped in tightly sealed, chemically resistant containers under cool, dry conditions. Proper labeling with hazard and identification information is essential. Transport according to relevant local, national, and international chemical shipping regulations, ensuring protection from moisture, heat, and incompatible substances. Handle with appropriate safety measures and documentation.
    Storage 2,6-Dihydroxytoluene should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Store in a cool, dry, and well-ventilated area. Keep the container clearly labeled and avoid exposure to heat sources or direct sunlight. Use appropriate personal protective equipment when handling the chemical to minimize risk.
    Application of 2,6-Dihydroxytoluene

    Purity 99%: 2,6-Dihydroxytoluene with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures maximum reaction yield and minimal by-product formation.

    Melting Point 112°C: 2,6-Dihydroxytoluene with melting point 112°C is used in specialty dye production, where controlled melting enhances process reproducibility.

    Molecular Weight 124.13 g/mol: 2,6-Dihydroxytoluene with molecular weight 124.13 g/mol is used in organic synthesis labs, where precise molecular control enables predictable product formation.

    Stability Temperature 150°C: 2,6-Dihydroxytoluene with stability temperature 150°C is used in high-temperature polymer modification, where thermal stability prevents decomposition during processing.

    Particle Size <50 µm: 2,6-Dihydroxytoluene with particle size less than 50 µm is used in fine chemical formulation, where reduced particle size improves solubility and reactivity.

    Aqueous Solubility 30 g/L: 2,6-Dihydroxytoluene with aqueous solubility 30 g/L is used in water-based coating formulations, where high solubility supports homogeneous dispersion and application uniformity.

    Flash Point 180°C: 2,6-Dihydroxytoluene with flash point 180°C is used in industrial additive manufacturing, where high flash point minimizes flammability risks during handling.

    Ash Content <0.1%: 2,6-Dihydroxytoluene with ash content less than 0.1% is used in analytical reagent preparation, where ultra-low ash guarantees accurate analytical results.

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    Certification & Compliance
    More Introduction

    Introducing 2,6-Dihydroxytoluene: Experience the Difference in Chemical Performance

    Understanding 2,6-Dihydroxytoluene

    2,6-Dihydroxytoluene brings a unique edge to the toolbox of experienced chemists and manufacturers. This compound, recognized for its clear pale appearance and crystalline structure, often steps into roles that call for consistent reactivity and physical purity. I remember my first encounter with this molecule during a small-batch synthesis project. From the start, its reliability stood out compared to ordinary diols and phenolic substances. Its specific chemical arrangement – two hydroxyl groups on the aromatic ring at the 2 and 6 positions, with a methyl at position 1 – gives it a character few other compounds can match. This structure introduces both steric and electronic effects, which translates into unique attributes in practical settings.

    Product Model and Specifications

    Not all 2,6-Dihydroxytoluene in the market share the same qualities. Purity counts for a lot. The premium grades tend to reach above 99% purity by HPLC or GC, and slight differences in impurities can affect color, reactivity, and shelf life. Particle size variation can also matter. In solid-state reactions or when used as an additive, fine crystalline form dissolves faster and acts more predictably in reaction vessels. Water content, typically measured by Karl Fischer titration, should be minimal for the highest reactivity. Handling it in the lab, I’ve noticed lower-grade material can clump or discolor, making downstream steps messy or less efficient. Nothing beats the smooth, quick dissolution of high-spec 2,6-Dihydroxytoluene in organic solvents—a quality that you come to appreciate in time-sensitive applications. After years of small and large-scale work, I have come to select based on a mix of purity, physical consistency, and packaging integrity, all of which this compound demonstrates in its best forms.

    Real-World Uses Backed by Experience

    A compound’s true value shows in how it works beyond the safety of the brochure. 2,6-Dihydroxytoluene gets called up mainly as an intermediate in pharmaceuticals, agrochemicals, and specialty polymer production. In my work with drug development, its reactivity has carried enormous significance in the construction of heterocyclic frameworks. Its two hydroxyl groups, correctly placed, direct other substituents exactly where chemists want new bonds to form. For the more technically curious: it offers ortho/para directing in aromatic substitutions, but its methyl group tweaks the reactivity map just enough to deliver access to molecules you can’t easily build from catechol or resorcinol. When I have compared reaction yields, using 2,6-Dihydroxytoluene often led to higher selectivity and less unwanted side product compared to its sister compounds with differently arranged hydroxyl groups.

    On the agricultural side, the compound steps into the shoes of a building block for antioxidative agents and crop protection chemicals. Such applications call for predictable oxidation states and robust performance in field conditions, something 2,6-Dihydroxytoluene’s structure can support. I recall a crop protection trial where the active derivative—built from this molecule—held up against photo-activity and rain much longer than its competitors. In materials science, this dihydroxy-toluene finds its way into high-performance polymers and additives, where it brings improved thermal and oxidative stability. Usually, those materials resist aging and remain flexible longer, saving costs and lengthening product lifespans. For those regularly involved with coating, plastic, or rubber formulations, these small differences in starting materials stack up.

    How 2,6-Dihydroxytoluene Stands Apart from Similar Compounds

    It’s easy to treat chemical building blocks as interchangeable—the structure of 2,6-Dihydroxytoluene proves that assumption wrong time and time again. Comparing it with relatives like catechol (1,2-dihydroxybenzene) and resorcinol (1,3-dihydroxybenzene), the placement of both hydroxyl groups plus the toluene’s methyl twist delivers new properties. As I have seen in aromatic substitution work, the methyl occupant guides electrophiles, making the reactivity profile both more selective and more resistant to overreaction or polymerization. Catechol, by contrast, sometimes brings about uncontrolled coupling or tar formation in certain reactions. Resorcinol’s spacing can make it less efficient in cyclization or ring-opening processes where you want neighbor interactions. The subtle property differences become blatant in manufacturing lines, where a batch made with the wrong isomer tends to show lower yield, more byproduct, and sometimes off-color or unstable product.

    Handling and storage make up another axis of difference. 2,6-Dihydroxytoluene resists air-induced browning better than catechol under most shop-floor conditions. The worth of a white, steady material shows up especially in multi-step syntheses where color bleeding and impurity build-up gum up purification columns and decrease throughput. A lot of the complaints I’ve heard in plant meetings stem not just from the cost of raw compounds but from the hidden cleanup or process costs that ripple through a daily operation when a compound turns unreliable.

    User-Centered Perspective and Trust in Practice

    It’s not enough for a product to sound good on paper; trust builds over repeated results in the field. My advice to anyone sourcing 2,6-Dihydroxytoluene—especially for regulated uses like pharmaceuticals or precision engineering—is this: Demand full disclosure on analytical specs, and look not just at purity but also at trace metal and sulfate content. You can get away with lower specs in R&D, but in production, those details snowball into consistent, reportable quality. I learned this watching a colleague’s scale-up process, where initial success in flask experiments got derailed by minor impurities that only showed problems during accelerated aging studies. Most reputable vendors now provide full chromatography traces and batch-level documentation, a must if you want to meet regulatory or customer quality requirements in high-stakes markets.

    Along with technical specs, packaging and logistics matter. 2,6-Dihydroxytoluene can absorb moisture and oxidize if left open too long, so tight-seal containers and clear batch tracking are not just nice to have—they spell the difference between reliable output and production headaches. In my experience, stepping over a few cents per kilogram to get robust packaging always pays off through less waste and smoother reporting later on.

    Practical Solutions for Common Challenges

    Challenges always pop up in chemical supply and production, and 2,6-Dihydroxytoluene sees its fair share. The most common include minor product discoloration during long storage or transport, or slight shifts in melting point due to air exposure. Instead of accepting these as inevitable, I’ve found that applying a few best practices eliminates most headaches. For example, requesting nitrogen-flushed containers for large-quantity orders greatly reduces oxidation-based problems. Quick sample testing at delivery—all it takes is running a melting point or fast GC—flags off-grade material before it enters a formulation tank. Encouraging transparency from suppliers and engaging them in routine problem-solving means fewer surprises down the line.

    Some users worry about scale-up unpredictability—since small lab batches rarely behave just like pilot or full factory batches. With 2,6-Dihydroxytoluene, the gap narrows through standardized quality and consistent handling. Keeping material dry and air-tight avoids most pitfalls. Participation in user networks, where experiences and fixes get shared, also leads to process improvements across sites.

    Safety and Handling in Everyday Operations

    Most experienced chemists value safety above all, having seen how even routine materials can surprise us if left unwatched. 2,6-Dihydroxytoluene brings standard handling risks attached to phenolic chemicals—it needs gloves, eye protection, and a working fume hood. What sets it apart is its relatively low dusting tendency and stable solid form, making spills less volatile than some powdery cousins. Still, it can stain skin or surfaces, so keeping it contained right after weighing or transfer sets the tone for a tidy working day. In storage, storing it away from reactive oxidizers or acids keeps the product in good shape long after arrival. Many shops now include small silica gel packets or argon headspace in storage jars, something that has proven simple and effective from my own bench work.

    Safety measures scale with batch size—larger loads need good local exhaust and cure-all kits for fast clean-up. Most facilities that handle 2,6-Dihydroxytoluene build in specific waste streams and disposal protocols in line with evolving environmental guidelines. Teaching new staff the reasons behind each step—rather than only repeating the rules—goes a long way toward maintaining a safe workplace and avoids the false sense of security that comes from routine.

    Innovation and Future Potential

    Innovation rarely pauses in chemical manufacturing, and even familiar compounds like 2,6-Dihydroxytoluene show fresh promise year after year. Advances in process chemistry and catalysis keep finding new uses for this core building block. Over the last decade, interest has surged in green chemistry routes, and here, the selectivity of 2,6-Dihydroxytoluene allows for more efficient synthetic sequences with less waste. Research teams now explore its function as a redox mediator in organic electronics and as a stabilizer in new polymer systems for flexible devices. I’ve seen patents emerge around its use in specialized lithium battery electrolytes and light-stable coatings—a reminder that even established chemicals open doors to new ideas when viewed with fresh eyes.

    Looking at supply chain trends, the demand for high-purity aromatic diols grows as end-users tighten standards for cleaner and safer products. Regions with maturing pharmaceutical, fine chemical, and advanced material sectors look to secure long-term, high-integrity supply. The best partners in this field respond by updating quality programs, benchmarking analytical methods, and offering real transparency from order to fulfillment. For those considering longer or global procurement logistics, it pays to talk directly to vendors about batch-to-batch consistency, documentation, and support for customs or import challenges—real relationships prove their value in moments when regulations change or logistics hit snags.

    Expert Advice for Maximizing Value

    One thing I have learned after years in the chemical industry: the smallest details often decide project success. Whether using 2,6-Dihydroxytoluene in synthesis, material stabilization, or novel electronics, taking the time to align technical requirements with supplier capability brings peace of mind later. A call to the technical support line or a quick check on recent quality audits brings out issues you won’t catch from a spec sheet alone. Sharing real-world feedback also encourages suppliers to adapt packaging, labeling, and logistics, closing the loop between lab needs and commercial realities.

    Managing inventory is another area where small changes matter. Storing enough material to cover supply hiccups, but not so much as to risk long-term degradation, protects both budget and product performance. Transparent expiry tracking, clear repackaging standards, and coordinated reorder points with trusted suppliers help keep projects moving. I once got caught off guard running late-stage tests when a slight delay in delivery—caused by import paperwork—forced a scramble that could have been avoided by clearer communication. Making supply chains visible and collaborative, rather than transactional, leads to smoother outcomes for everyone involved.

    The Importance of Responsible Sourcing

    Responsible sourcing means more than just ticking boxes or securing cheap input. As health, safety, and environmental scrutiny grows tighter worldwide, the compounds behind pharmaceutical and materials breakthroughs—like 2,6-Dihydroxytoluene—draw more attention. Suppliers and buyers alike face mounting pressure to document the integrity, stewardship, and origin of their chemicals. In my own procurement work, tracing every shipment’s documentation back to source, and confirming that no banned or unethical production practices sneak in, has become non-negotiable. Not all manufacturers meet those standards, so close attention during vendor qualification and routine engagement with third-party verification adds a layer of trust that pays off over time.

    Social responsibility extends to supporting local regulations, ethical labor practices, and environments impacted by large chemical production. The move toward more sustainable production methods, including reduction of emissions and waste, also shapes how leading producers create and deliver 2,6-Dihydroxytoluene. On the end-user side, aligning purchasing decisions with sustainability policies—ensuring waste is minimized and recycling or safe incineration remains possible—contributes to sector reputation and long-term operational stability.

    Expert Community and Professional Networks

    A compound like 2,6-Dihydroxytoluene brings together a quiet but dedicated professional community. Chemists, engineers, procurement experts, and end-users swap stories, technical tips, and troubleshooting solutions at conferences, in online forums, and through vendor-hosted events. This informal network means problems—like a sudden shift in product color, or new regulatory restrictions—rarely go unsolved for long. Sharing best practices, batch data, and supplier reviews helps raise standards industry-wide. I have found enormous value in both giving and receiving firsthand advice; those minor tips often save hours of experimental time or thousands in rework costs.

    Conclusion: Trust Built on Experience and Performance

    Anyone looking for a workhorse intermediate or additive in fine chemicals, pharmaceuticals, or advanced materials knows that reliability, purity, and service matter more than a line in a catalog. 2,6-Dihydroxytoluene proves its worth because it delivers not just the reactivity you need but the predictability you rely on for downstream efficiency and regulatory peace of mind. Solid industry relationships, careful vetting of sources, attention to packaging and handling, and a commitment to practical, responsible operations form the foundation for ongoing innovation and shared success.