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3-Cyano-2,6-Dihydroxy-4-Methylpyridine

    • Product Name 3-Cyano-2,6-Dihydroxy-4-Methylpyridine
    • Alias CDHMP
    • Einecs 224-703-5
    • 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
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    Specifications

    HS Code

    557739

    Chemical Name 3-Cyano-2,6-Dihydroxy-4-Methylpyridine
    Molecular Formula C7H6N2O2
    Molecular Weight 150.14 g/mol
    Cas Number 3992-55-4
    Appearance Light yellow to beige powder
    Melting Point 230-234°C
    Solubility Slightly soluble in water, soluble in ethanol and DMSO
    Density Approx. 1.36 g/cm3
    Purity Typically >98%
    Pka Values Approx. 7.7 (phenolic hydrogens)
    Storage Conditions Store at 2-8°C, in a tightly closed container
    Smiles CC1=CC(=NC(=C1O)C#N)O

    As an accredited 3-Cyano-2,6-Dihydroxy-4-Methylpyridine 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 3-Cyano-2,6-Dihydroxy-4-Methylpyridine, sealed with a screw cap and labeled appropriately.
    Shipping **Shipping Description:** 3-Cyano-2,6-Dihydroxy-4-Methylpyridine should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Handle with appropriate chemical safety precautions. Ensure packaging prevents leakage and damage during transit. Follow all applicable regulatory guidelines for transport, including labeling and documentation. Store in a cool, dry place upon receipt.
    Storage 3-Cyano-2,6-Dihydroxy-4-Methylpyridine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure the storage area is equipped with proper labeling and safety measures to prevent accidental exposure or contamination.
    Application of 3-Cyano-2,6-Dihydroxy-4-Methylpyridine

    Applications of 3-Cyano-2,6-Dihydroxy-4-Methylpyridine in Industrial Manufacturing

    Our production of 3-Cyano-2,6-Dihydroxy-4-Methylpyridine supports leading-edge innovation in specialized chemical manufacturing, with reliability and traceability directly from the source. Below we outline its primary industrial uses, formulation methods, and regulatory adherence across established downstream sectors.

    1. Vitamin B6 (Pyridoxine) Pharmaceutical Intermediate

    3-Cyano-2,6-Dihydroxy-4-Methylpyridine serves as a critical intermediate in the multi-stage synthesis of pyridoxine hydrochloride (Vitamin B6) for pharmaceutical and nutraceutical applications. Integrated into validated production routes, the compound supports high-purity transformation stages for APIs that must meet global pharmacopoeial purity and impurity standards.

    Industry compliance standards

    • USP, EP, and JP monographs for Pyridoxine Hydrochloride
    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • FDA 21 CFR Part 210/211 (USA)
    • SFDA Drug GMP (China)

    Typical usage ratio

    • 0.9–1.2 molar equivalents relative to the downstream synthetic route; precise stoichiometry adjusted according to target batch size and in-process conversion yields

    Downstream process integration

    • Introduced at the condensation and ring functionalization step during pyridoxine backbone assembly
    • Undergoes catalytic hydrogenation and deprotection in subsequent purification stages

    Final product types

    • Pyridoxine hydrochloride (USP/EP/JP grade API)
    • Direct compression granules for tablet and capsule formulation
    • Injection and oral solution pre-mixes

    2. Agrochemical Intermediate for Pyridine-Based Herbicide Synthesis

    The compound forms a building block in the synthesis of pyridine-derived herbicidal actives, supporting the preparation of pre- and post-emergent weed management agents. Its robust reactivity profile enables downstream manufacturers to efficiently introduce cyano and hydroxyl functionalities critical to finished molecule activity, with fully documented handling for global agrochemical regulations.

    Industry compliance standards

    • FAO/WHO Specification Requirements for Pesticide Actives
    • REACH Registration (EU)
    • EPA 40 CFR Part 150–189 (USA)
    • GB 20810/GB 9858 (China – pesticide ingredient quality)

    Typical usage ratio

    • 1.0 molar proportion in relation to target pyridine herbicide synthesis, adjusted for process efficiency during scale-up

    Downstream process integration

    • Charged at the cyclization or nucleophilic substitution step for herbicide active ingredient synthesis
    • May require in situ pH adjustment and solvent exchange for full conversion

    Final product types

    • Pyridine-based herbicide technical concentrate (TC)
    • Formulated EC, SC, or WG pesticide finished products
    • Granulated bulk actives for custom formulation houses

    3. Intermediate for Advanced Pharmaceutical Research Compounds

    R&D facilities and CDMOs (Contract Development & Manufacturing Organizations) employ 3-Cyano-2,6-Dihydroxy-4-Methylpyridine as a scaffold in heterocycle expansion, especially in exploratory synthesis of new drug candidates with pyridine or nicotinamide cores. Its use in modifying substitution patterns on pyridine rings supports lead generation for new molecular entities, facilitating regulatory preclinical supply chains.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for preclinical compounds
    • ICH M7 guideline for genotoxic impurities
    • Custom development under ICH Q11 for starting materials
    • Compliant with local controlled substance and precursor regulations as required by project

    Typical usage ratio

    • 0.5–1.5 molar equivalents, as determined by the specific synthetic route and number of diversification steps

    Downstream process integration

    • Engaged at early-stage heterocyclic ring formation, either as nucleophile or electrophile
    • Utilized for functional group modification or as a coupling partner in Suzuki or Buchwald-Hartwig reactions

    Final product types

    • Reference standards for pharmaceutical screening
    • Lead compound candidates for medicinal chemistry
    • Non-GMP preclinical and toxicology batch samples

    4. Key Building Block in Electronics Chemical Synthesis (Specialty Additive Manufacturing)

    Manufacturers of specialty electronics additives rely on 3-Cyano-2,6-Dihydroxy-4-Methylpyridine for constructing electron-transporting intermediates in photoinitiator and photoresist synthesis, particularly for high-resolution microfabrication. Its controlled substitution on the pyridine ring is used to fine-tune photoactive layer reactivity while maintaining trace metals and impurity control for advanced electronics applications.

    Industry compliance standards

    • IEC 62474 Material Declaration for Electric/Electronic Products
    • RoHS Directive (2011/65/EU)
    • SEMATECH purity standards for microelectronics chemicals
    • ISO 9001:2015 Quality Management System for chemical production

    Typical usage ratio

    • 0.2–0.8 wt% of total additive blend in electronics formulation, adjusted for optical density and functional requirements

    Downstream process integration

    • Introduced during monomer functionalization for organic semiconductors and photoresists
    • Serves as electron donor scaffold in spin coating or inkjet-printed photoactive layers

    Final product types

    • Positive and negative photoresist masterbatches
    • Photoinitiator intermediates for UV-cured films
    • Specialty microfabrication chemicals for PCB and display panel manufacturing

    5. Synthesis of Colorant and Pigment Intermediates

    Pigment and dye manufacturers utilize the compound as a precursor for creating pyridine and pyridone-based colorant intermediates, particularly those used in solvent-stable and high-fastness pigments for plastics, inks, and coatings. Its functionalized core structure directly influences hue saturation and thermal stability in the final colorant.

    Industry compliance standards

    • EN 71-3 Safety of Toys (for pigment use in children’s products)
    • REACH and GHS registrations (for EU/US/Asia-Pacific commerce)
    • ISO 787-24 Pigment Quality Testing
    • FDA 21 CFR 178.3297 (Color additives in food contact applications)

    Typical usage ratio

    • 0.1–0.5 molar equivalents relative to pigment chromophore precursors; optimized by desired pigment strength and processing method

    Downstream process integration

    • Charged at initial ring substitution and condensation steps for pigment core assembly
    • May undergo diazotization or coupling for extended chromophore elaboration

    Final product types

    • Pyridone and pyridine-based organic pigments
    • High-fastness colorants for plastics and automotive finishes
    • Solvent-resistant printing ink pigments
    Free Quote

    Competitive 3-Cyano-2,6-Dihydroxy-4-Methylpyridine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3-Cyano-2,6-Dihydroxy-4-Methylpyridine: Experience Drives Quality

    In specialty chemical production, few compounds match the versatility and performance that 3-Cyano-2,6-Dihydroxy-4-Methylpyridine offers. Working day-in, day-out with this material, we have gained a clear picture of its value to the modern chemical industry. While on paper it is a pyridine derivative, in the lab and in production, it's a cornerstone ingredient for key pharmaceutical intermediates and high-end agrochemical synthesis.

    Our batches of 3-Cyano-2,6-Dihydroxy-4-Methylpyridine (sometimes referenced as 4-methyl-2,6-dihydroxy-3-cyanopyridine) consistently reach >99% purity by HPLC and GC analysis. In our facility, we check every lot against detailed chromatograms and NMR spectra, because minor impurities can have major consequences for downstream chemistry. Reliable melting point—usually 184 to 187°C—confirms material consistency beyond simple assay results. Moisture content, particle sizing, and impurity profiling round out a specification sheet shaped not by marketing, but by the needs of chemists who run complex synthesis work.

    Why Chemists Turn to This Compound

    We've fielded countless questions from both process development and scale-up teams about sourcing this pyridine. The cyano and dihydroxy groups—neighboring on the aromatic ring—create a handle for selective functionalization without compromising stability. Installations of side chains or stepwise building of extended structures benefit from this scaffold’s consistent reactivity profile. Many customers come to us with concerns about yield drops from side reactions or inconsistent building block quality; they find that our process avoids those pitfalls. A typical end use is the introduction of the cyano group in heterocycle formation or selective oxidation to produce downstream pyridinecarboxylic acid derivatives, often for APIs or sophisticated plant protection agents.

    Unlike less specialized analogues, this compound’s 4-methyl positioning sets it apart. Small changes in regiochemistry reshape downstream outcomes, leading some customers to compare products from traders and discover off-spec isomers or lower than expected conversions. Our hands-on synthesis steps, maintained under tightly regulated process controls, reduce unwanted isomerization and decomposition—two issues that plagued early customers who had previously bought through resellers and found process bottlenecks as a result.

    What It Takes to Manufacture a Reliable Product

    Making 3-Cyano-2,6-Dihydroxy-4-Methylpyridine goes far beyond generic pyridine chemistry. Our reactors must carefully manage not just temperature ramps, but pH control and strict oxygen exclusion. We have invested in continuous monitoring with real-time analytics, because side reactions can snowball quickly if unchecked. One lesson from an early production run underscores this: a minor pH spike during the cyanation step led to trace impurities that persisted into the final product, affecting all subsequent reactions for the downstream manufacturer. After that, our standard operating procedures adopted tighter feedback controls, and those failure points haven't reappeared again.

    We moved away from multi-solvent purification, switching to a minimal-impact crystallization protocol that reduces solvent waste and ensures reproducible crystal habits. Some buyers report that they need fine, easily dispersible material for rapid dissolution in polar solvents, while others want coarser crystals for controlled addition in large vessels. Applying feedback from downstream users, we adapted our particle formation steps, tuning parameters like agitation rates, cooling profiles, and seed loading. Our approach remains open to adjustment whenever a new synthesis route or handling need arises.

    Specification Details and Real-World Results

    Lab results serve only as the opening move. We provide our own HPLC trace, full NMR spectrum, and on request, IR and MS reports for every lot shipped. This transparency stems from the experience that surprises rarely benefit those working under tight deadlines or GMP conditions. Chemists in pharmaceutical labs have told us that even a 0.2% variation in specified byproducts can mean the difference between a completed lot or an expensive rerun. It’s not just the purity percentage; matching melting point, color (pale tan to near-white), and confirmed particle size mean that the material behaves predictably when handled in glove boxes or automated dosing systems.

    We adopted anti-static treatment protocols on packaging lines after receiving feedback that some customers experienced issues with fine dust during charging in dry rooms. Every kilogram we send carries both a lot number and a complete paper trail of raw materials, helping researchers and quality managers establish traceability for regulated work. Having worked both on the bench and at scale, we know questions come up months later—so each batch receives long-term retention samples, kept under nitrogen, allowing for long-term analysis if root-cause investigations are required.

    Functionality and Differentiation from Similar Pyridine Derivatives

    Within the line of substituted pyridines, it’s tempting to regard 3-Cyano-2,6-Dihydroxy-4-Methylpyridine as a simple variation. In practice, chemistry tells another story. The 2,6-dihydroxy substitution, alongside the electron-withdrawing cyano at three, produces not just chemical stability, but opens up pathways that aren’t available in mono-hydroxy variants or un-methylated analogues. Our customers have directly compared our compound to 2-hydroxy or plain methyl derivatives and observed higher selectivity in acylation reactions, as well as cleaner transition metal-catalyzed couplings, especially Pd-catalyzed C-N bond formations.

    This selectivity comes from the distinct electronic influence on the pyridine ring. We have tested competitor materials sourced via resellers and found impurities ranging from isomeric contamination (resulting from uncontrolled methylation) to residual metal content stemming from less rigorous filtration. Those contaminants aren’t just a statistical blip—they affect real reaction outcomes, from false HPLC peaks to problematic intermediate stabilities.

    We insist on trace metal analysis—ICP-MS on final batches—since a subtle increase in metal ions can poison catalysts or interfere with hydrogenation and alkylation processes. Our team strives for new lows in sodium, iron, cobalt, and other common contaminants. Notably, some users have pushed for <10 ppm limits, especially for use in active pharmaceutical ingredient manufacture, and our process consistently delivers below these thresholds.

    Sustainability and Environmental Responsibility

    Years ago, waste treatment was an afterthought for pyridine derivatives, but regulatory changes—driven by both market demand and stricter oversight—have transformed how we address environmental impacts. We recapture and recycle solvent streams at every possible stage, reducing both emissions and operational costs. Nitrile intermediates can generate challenging effluent, so we neutralize cyanide streams with an in-house treatment plant, monitored by daily chemical oxygen demand (COD) checks. This limits environmental impact and provides hard documentation for compliance audits.

    Some might ask about material origin and handling safety. Every raw input arrives with a certificate of analysis, and our warehouse workflow logs all handling temperatures, inert atmospheres, and storage durations. 3-Cyano-2,6-Dihydroxy-4-Methylpyridine is not the easiest compound to warehouse, so we invested in isolated, ventilated stores with fire-rated casks. Safety training for our warehouse crew is built into day-to-day operations, not tacked on as an extra precaution after an incident. As workplace safety evolves, so do our protocols—PPE standards, emergency drills, and routine site audits ensure no steps get skipped, even when deadlines are tight.

    Every inquiry for this compound includes reference to batch longevity and storage conditions. Through regular accelerated-aging tests, we’ve confirmed stable shelf life beyond three years in unopened packaging under controlled conditions. Users processing lots over extended campaigns need that peace of mind.

    Feedback and End-User Collaboration

    We never take a ‘single solution fits all’ stance. Direct feedback from users drives continuous refinement in our process. One customer running kilo-scale synthesis for agrochemical actives flagged sporadic moisture content changes. Because we keep detailed run histories and can correlate environmental logs to process shifts, we identified an HVAC malfunction in our finishing room—a subtle but impactful variable. Rapid HVAC adjustment and ongoing monitoring solved the problem. That’s the benefit of working closely with actual producers who can diagnose and act on a problem at the plant level, often within days.

    Academic collaborations matter just as much as big industry contracts. A recent project with a university lab exploring new cancer drug leads required a modified particle form. Their method called for ultra-high dispersion in aqueous buffer, with extremely low residual chlorides. Joint R&D efforts produced a microcrystalline grade with chloride levels consistently below 1 ppm, tailored just for their workflow. That feedback loop became a standard option for other research-driven buyers.

    Challenges in Scaling and Process Improvements

    Success today relies on more than hitting a Spec A for purity. Our plant engineers constantly tinker with reactor tech and process steps. Early on, we relied on conventional batch crystallization, which yielded inconsistent batches. Only after shifting to controlled semi-continuous cooling did we gain the reproducibility and scale demanded by larger partners. Likewise, installation of in-line near-IR probes gives real-time insight into hydroxy/oxo ratios, alerting us to drift before product passes final Q.C.

    Handling new requests means facing chemistry’s limits head-on. Not every downstream reaction plays by the book. We’ve supported process troubleshooting campaigns for clients who found previously overlooked impurity carryover. Our technical team worked hands-on with their analytic chemists to develop LC-MS/GC-MS profiles that tracked difficult-to-detect intermediates. That level of engagement builds trust and drives incremental, not just one-off, improvements.

    What Sets This Compound Apart

    Having led our manufacturing from pilot to commercial scale, it’s clear that details set this compound apart: methyl positioning means fewer off-path isomers, cyano placement enables direct amides or amidines, and dihydroxy patterning supports O-alkylation or halogenation with fewer side reactions. For end users forced to maximize every step in a complex route, these differences translate to sharper yields and fewer headaches.

    Traders and resellers can offer competitive prices, but our on-site experience offers something else—process support, reliable documentation, and a traceable workflow. Labs need products that perform not as generic pyridine derivatives, but as precision reagents. When yield matters, when regulatory filings hinge on material consistency, knowing the synthetic and analytical path for every kilo makes the difference.

    Outlook: Evolving Customer Requirements

    Looking down the road, expectations only escalate. Regulatory authorities demand ever-cleaner impurity profiles, and downstream innovations pressure us to scale more flexibly without sacrificing quality. The only way to stay ahead is investing steadily in people, plants, and technology. We involve staff directly in process reviews and invite customer chemists to audit our facilities—sometimes virtually, sometimes on site. These collaborations bring faster answers, drive transparency, and improve both safety and efficiency.

    R&D teams increasingly need new formats—pre-dissolved solutions, custom blends, or tighter particle size controls. We are working with users to field test these options so that production chemists can save time and avoid routine steps. Meanwhile, regulatory documentation, from RoHS/REACH declarations to full trace metallurgical analysis, accompanies every order, meeting the needs of both established global pharma and smaller research-driven firms.

    Success with 3-Cyano-2,6-Dihydroxy-4-Methylpyridine doesn’t hinge on just shipping a high-value molecule. It’s a product of controlled process, constant adjustment, deep technical knowledge, and—above all—a willingness to listen to those who use the product day-to-day. Decades of experience at the manufacturing level show that the best results come from direct feedback and continuous communication, not just relying on certificates or standard spec sheets. For chemists demanding control over every variable, confidence only comes from working alongside actual producers committed to every batch’s success.