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3-Cyano-4,6-Dimethyl-2-Hydroxypyridine

    • Product Name 3-Cyano-4,6-Dimethyl-2-Hydroxypyridine
    • Alias 3-cyano-4,6-dimethyl-2-pyridinol
    • Einecs 622-408-5
    • 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
    VTB
    Specifications

    HS Code

    239629

    Chemical Name 3-Cyano-4,6-Dimethyl-2-Hydroxypyridine
    Molecular Formula C8H8N2O
    Molecular Weight 148.16 g/mol
    Cas Number 110619-22-2
    Appearance Off-white to yellow solid
    Melting Point 174-177°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC1=CC(=NC(=C1O)C#N)C
    Inchi InChI=1S/C8H8N2O/c1-5-3-7(2)10-8(11)6(5)4-9/h3,11H,1-2H3
    Storage Conditions Store at room temperature, tightly closed container, avoid moisture
    Purity Typically ≥98% (may vary by supplier)

    As an accredited 3-Cyano-4,6-Dimethyl-2-Hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled "3-Cyano-4,6-Dimethyl-2-Hydroxypyridine, 25 grams," includes hazard and storage instructions.
    Shipping This chemical, 3-Cyano-4,6-Dimethyl-2-Hydroxypyridine, is shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. Transportation follows applicable regulations for handling organic compounds. Appropriate hazard labeling and documentation are included to ensure safe shipment. Store in a cool, dry location upon arrival to maintain product integrity and safety.
    Storage Store 3-Cyano-4,6-Dimethyl-2-Hydroxypyridine in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep the chemical in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Avoid storing near incompatible substances such as strong oxidizers and acids. Ensure proper labeling and access limited to trained personnel only.
    Application of 3-Cyano-4,6-Dimethyl-2-Hydroxypyridine

    Applications of 3-Cyano-4,6-Dimethyl-2-Hydroxypyridine in Industrial Manufacturing

    3-Cyano-4,6-Dimethyl-2-Hydroxypyridine, as manufactured by our facility, serves as a strategic intermediate for several specialized chemical sectors. Our production controls optimize purity and batch consistency, which enables integration into advanced synthesis and formulation lines. Below we outline verified high-value application scenarios and relevant technical details for downstream users.

    1. Pharmaceutical Intermediate: Antiviral Agents Synthesis

    This compound is widely incorporated into the synthesis route for key antiviral pharmaceutical actives, particularly those containing pyridine-based scaffolds. Production lines employ nucleophilic substitution and cyclization steps, making use of its hydroxypyridine structure to introduce functional groups central to drug efficacy and stability. Integrated batch QC and solvent recovery protocols preserve product integrity throughout processing.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • Ph. Eur., USP, and JP standards for process intermediates
    • European Chemicals Agency (ECHA) REACH compliance
    • FDA 21 CFR Part 211 for process controls

    Typical usage ratio

    • 10–25% w/w relative to total reaction mass, adjusted per target API yield

    Downstream process integration

    • Added as a core reactant in early-stage condensation or substitution steps during pilot and commercial batch synthesis
    • Followed by product isolation and purification via crystallization or solvent extraction

    Final product types

    • Antiviral active pharmaceutical ingredients
    • Precursors for respiratory and influenza therapeutics
    • Patented drug candidates in the pre-clinical stage
    • Custom API derivatives for contract manufacturing

    2. Agrochemical Intermediate: Pyridine-Based Herbicide Production

    Leading agrochemical producers leverage this compound for the manufacture of selective herbicides. Reaction steps typically utilize chlorination or amination, where the cyano and methyl groups play a crucial role in bioactivity modulation. Processing controls align with effluent treatment and hazardous management requirements, with downstream blending frequently tailored for granule or wettable powder formation.

    Industry compliance standards

    • FAO/WHO Specifications and evaluations for pesticide substances
    • ISO 9001-certified manufacturing management
    • EPA (40 CFR Part 152) pesticide registration requirements
    • Globally Harmonized System (GHS) for labeling and transport

    Typical usage ratio

    • 5–15% w/w within herbicidal synthesis batches, subject to end molecule structure and efficacy targets

    Downstream process integration

    • Feeds into initial reaction vessels for heterocyclic building block formation
    • Subjected to chlorination, followed by formulation blending for bulk product prep

    Final product types

    • Pyridine-based herbicidal actives
    • Formulated dry or liquid agrochemical concentrates
    • Bulk granule and suspension concentrates
    • Pre-mix formulations for contract field application

    3. Colorant and Pigment Synthesis: Specialty Dye Manufacturing

    Specialty dye producers employ this compound as a precursor for developing vivid metallic or organo-functional pigments utilized in industrial coatings. Its pyridine base enables coupling with diazonium salts, supporting high-shade and UV-stable pigment attributes. Processing accounts for stringent solvent registration and finished batch heavy metal analysis to meet safety and export requirements.

    Industry compliance standards

    • REACH Annex XVII for colorants and pigments
    • DIN EN ISO 12301 pigment quality testing
    • OEKO-TEX Standard 100 (for applicable textile pigments)
    • US TSCA (Toxic Substances Control Act) registration

    Typical usage ratio

    • 2–8% w/w in pigment precursor formulations; adjusted based on required color depth and application medium

    Downstream process integration

    • Introduced during the diazotization or coupling stage for pigment base formation
    • Undergoes subsequent oxidation, purification, and drying before blending into end-use colorant systems

    Final product types

    • Metal-complex and organic pigments for coatings
    • Textile dyestuffs for high-performance fabrics
    • Plastic coloration masterbatches
    • Industrial ink pigments

    4. Electronic Chemical Synthesis: Liquid Crystal Material Engineering

    Producers of display technology components integrate this compound into the synthesis of key intermediates for liquid crystal material production. Its molecular structure assists in tunable dielectric and viscosity parameters when forming the mesogen core, ensuring stability in panel fabrication. Reaction controls necessitate ultrapure reagents, and integration occurs within closed-loop inert systems to comply with moisture and contamination controls critical to electronic grade standards.

    Industry compliance standards

    • IEC 61249-2 specification for PCB materials
    • ISO 9001:2015 certified production systems
    • RoHS (Restriction of Hazardous Substances) Directive
    • JIS C 6120 for display-grade chemicals

    Typical usage ratio

    • 0.5–3% w/w in liquid crystal core synthesis; tuned according to specific dielectric and optical profile requirements

    Downstream process integration

    • Dosed into intermediate synthesis stages for hybrid mesogen core production
    • Purified through vacuum distillation and filtered to sub-micron specification before incorporation into final liquid mix

    Final product types

    • Nematic, smectic, and cholesteric liquid crystal mixtures
    • Flat panel display liquid crystal modules
    • Organic light-emitting diode (OLED) functional layers
    • Photoalignment materials for LCD production

    5. Fine Chemical Catalysts: Ligand Preparation for Metal Catalysis

    Catalyst manufacturers utilize this compound for constructing pyridine-based ligands, which coordinate selectively in homogeneous catalysis systems. The cyano group serves as a point for further functionalization, influencing electronic properties and catalytic selectivity. Synthesis requires strict process water control and advanced chromatographic purification to ensure ligand purity before metal complexation, supporting consistent performance in pharmaceutical and polymer catalysis processes.

    Industry compliance standards

    • ISO 17025-certified testing laboratories
    • GMP guidelines for catalysts used in fine chemical manufacturing
    • Responsible Care and Process Safety Management (PSM) programs
    • REACH substance registration (where applicable)

    Typical usage ratio

    • 1–5% w/w relative to total ligand batch size, increased or reduced based on desired chelating strength and reaction kinetics

    Downstream process integration

    • Introduced during initial ligand pre-cursor buildup and subjected to purification before metal incorporation
    • Employed in catalyst libraries evaluated for specific process reactions—especially in asymmetric or cross-coupling catalysis

    Final product types

    • Pyridine ligands for transition metal catalysis
    • Fine chemical homogeneous catalyst systems
    • Metal-organic framework (MOF) precursors
    • Polymer synthesis catalyst additives
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    Certification & Compliance
    More Introduction

    Introducing 3-Cyano-4,6-Dimethyl-2-Hydroxypyridine: Proven Value from a Manufacturer’s View

    From the heart of the lab floor to global research benches, the chemistry behind specialty intermediates drives every breakthrough in our industry. Among the roster of complex building blocks, 3-cyano-4,6-dimethyl-2-hydroxypyridine remains a standout. Its structure and value didn’t just pop up one day; years of formulation, repeated small-batch pilots, monitoring chromatograms, checking spectral data in real time, brought meaning to the numeric digits attached to its model and specifications. Not every intermediate meets both the purity requirements and reactivity profile that advanced researchers expect these days. We watch big ideas hinge on the consistency of such a compound, and we know the stakes. There’s no out-of-the-box shortcut when the baseline standard for chemical manufacturing shifts year after year—experience and quality control methods bridge that gap.

    Product Profile and Production: A Manufacturer’s Perspective

    3-cyano-4,6-dimethyl-2-hydroxypyridine takes shape in our reactors as a crisp off-white solid, consistently meeting a purity of no less than 99%. The CAS number alone doesn’t guarantee its traceability, but every lot travels with a full set of COA batch results and our own retention samples. Year-on-year customer audits have shaped our floor practices, so we don’t just talk about process control—we’ve baked traceability and documentation into our operating rhythm. Every charge goes through triple-point moisture analysis and residual solvent checks by headspace GC before shipping. Analytical needs from end-users dictate more than simple specifications; we run custom HPLC methods and support bespoke impurity profiles based on client feedback.

    We see usage patterns evolve in both pharmaceutical and agricultural research, especially where heterocyclic intermediates determine the difference between a successful reaction series or weeks lost to side products. From the earliest scale-up, process chemists want predictable reaction profiles and reliable downstream purification. This molecule’s pyridine nucleus—flanked with cyano, methyl, and hydroxy substitutions—lets chemists perform nucleophilic substitutions, palladium-catalyzed cross-coupling, or condensation reactions without excessive by-product headaches. Clean isolation isn’t just about the structure; it’s about how the compound holds up under various pH loads and solvent exchanges. Researchers care about that, so we invest time validating each change in raw material source or plant process step, logging outcomes batch by batch for client review.

    Why Structure Matters: Practical Roots in Application Chemistry

    A structure like 3-cyano-4,6-dimethyl-2-hydroxypyridine isn't just chemistry on paper. The electron-withdrawing nature of the cyano group, balanced against the activating methyl substitutions and the potential of the ortho-hydroxy group, creates a platform for tailored reactivity. We’ve observed pharmaceutical teams pursue this intermediate to reach new kinase inhibitor scaffolds. Agrochemical researchers pull for it in certain fungicidal lead discoveries. The reality is, only a narrow set of intermediates let medicinal chemists keep side reactions minimal while inserting their creative analogs down the chain. On our production floor, staff see how minor changes to a single parameter—a fraction more water in a wash, a step’s temperature a bit off—affects batch quality. That’s why we don’t work from recipes. Instead, we optimize each input based on tight feedback with partner labs. Each kilo processed represents another micro-adjustment, grounded in lessons drawn from years in the lab and plant.

    Differences that Count: Our Approach Versus Off-the-shelf Sources

    Plenty of catalogs list 3-cyano-4,6-dimethyl-2-hydroxypyridine, but getting a reagent-grade sample doesn’t equal fit for advanced synthesis. Traders and distributers typically grab inventory based on larger suppliers or auction surplus. We oversee the compound’s whole journey—from the first methylpyridine feedstock load to the last bulk pack-off. That means tight control over trace components, such as low-level pyridine impurities, water, or sulfated ash. Our syntheses focus on minimizing potential isomer formation, especially unwanted dihydroxy or polymethyl species that can derail specific transformations. The result is reproducibility: returning customers reference prior batch analytical data, count on repeatability from gram lab batches up to larger multi-kilo runs. For clients running scale-dependent processes, a stable impurity card avoids the dreaded need for scrapped glassware or rushed chromatographic clean-ups at the research bench. We craft our production around user context; internal standards and detailed retained samples back every release for future archiving and repeat testing.

    Supporting Custom Chemistry: More Than a Commodity

    The difference between commodity feedstock and a properly engineered intermediate comes down to experience and the drive for traceability. Supply chain issues throw up more challenges every year—changes to precursor availability, new regulatory expectations, requests for more granular impurity disclosure. In our team’s experience, only a handful of chemical manufacturers keep both small-footprint batch control and full transparency with clients. Shipping out a product doesn’t finish the relationship. We often field technical consultation calls after delivery, where medicinal and process chemists face unique reactivity or solubility scenarios not described in literature. Sharing such troubleshooting bonds our team directly with the innovation lifecycle of our partners.

    Every structure carries a history and a reason for its resurgence in pharma and agro R&D. Back when the demand profile remained steady, researchers expected fewer surprises from their suppliers. Now, with each custom route, each regulatory hurdle, they want deeper disclosure: from possible trace side-products to long-term lot stability. We’ve tracked how sub-ppm levels of certain aromatic impurities can affect high-throughput screens, leading to wasted weeks and budget. Inside each production cycle, our QA signs off only when the compound proves itself both in classic purity tests and modern analytical platforms—plate readers, LC-MS, and NMR sequence matching. We log not just the positive outcomes but near-misses, using this running log to support next-gen problem solving for novel syntheses.

    Meeting Modern Standards: Reliability Built on Past Lessons

    Quality and consistency didn’t show up overnight—plant operators and analytical chemists here voice the setbacks that shaped today’s process parameters. For example, failing to maintain a strict temperature ramp and hold time in the final condensation step once led to measurable by-product drift. That incident prompted a process overhaul, with added in-line sensors and batch-by-batch trend reviews—waste went down, yield climbed, and repeat complaints dropped. We record any detected change in crystalline form or solubility, informing customers in advance if a batch presents a polymorph or habit shift that might alter their downstream processing. Pharma partners highlight just how much uninterrupted production matters: every delayed delivery can mean idle reactors, missed project milestones, and sunk costs in labor and solvent expenditure. We carry those customer concerns into our workflow, settling for nothing less than on-spec, tightly verifiable shipments.

    Shipping sensitive intermediates also invites regulatory scrutiny for every region. Our documentation doesn’t end with standard material safety; stability data, shipping condition assessments, and compliance with evolving transport rules shape how and when we release lots. Early in the supply game, we learned hard lessons from batches failing to meet new REACH or TSCA disclosure needs. Gaps in chain-of-custody proved disruptive for us and end-users alike, so our training for technical staff stays current. That includes refresher sessions for evolving global documentation and in-plant safety practices. Knowing that a new audit or regulatory review may arrive at any time keeps us sharp and detail-oriented at every gate.

    Walking the Fine Line: Beyond Price and Availability

    Pricing wars come and go on chemical markets, but the repeat users of 3-cyano-4,6-dimethyl-2-hydroxypyridine look for more than bottom-dollar numbers. Too often, we hear stories of clients forced to rerun entire syntheses because purity drifted batch-to-batch, or process residues carried through unexpectedly. Those scenarios often arise from excess reliance on generic manufacturing and insufficient analytical follow-up. By retaining production data for years and regularly confirming archived samples, we help project teams troubleshoot unusual TLC spots or aberrant HPLC traces long after delivery. Our floor chemists commit to feedback cycles with every user request, making it possible to adjust grind size, dryness, or repackage for air/moisture-sensitive research presses or pilot-scale lines. We don’t view fit-for-purpose service as optional—it’s the baseline expectation for any partner hoping to help clients outpace their competition’s synthesis efforts.

    Cost-motivated shortcuts have little place in the market for research intermediates. Stocking extra material with uncertain shelf life, or getting locked into a single pack size, can create hidden costs. That’s why we offer customized solutions—from breaking bulk for specialized runs to preparing strictly QC-documented aliquots for screening campaigns—shaped by years of seeing what works and what disrupts research timelines. Not every request meets a strict catalog description; balancing production loads, maintaining material in ideal storage conditions, and prepping shipments to align with customer inventory schedules defends both timelines and budgets. Each detail, from labeling granularity to support for non-standard analytical requests, arose because research teams in the field demanded more from their suppliers and made their voices heard after every project cycle.

    Real-World Use: Bringing Practical Insight to Every Batch

    End users—sitting at the research bench or navigating the scale-up plant—encounter real challenges with complex intermediates like this pyridine derivative. Solubility swings, minor by-product shoulders, or difficulty in removing extraneous salts can upend weeks of project work. Drawing from years of feedback, we equip our support team with both the chemical expertise and institutional memory to recognize early warning signs. If a partner flags a yield drop or cropping issue on their end, odds are we have batch data or analogous user experience to cross-reference. This hands-on, no-ego approach shapes our improvement ideas. For instance, after a client detailed filtration headaches due to crystal clumping in a specific solvent system, we adjusted our drying cycle and shift packing protocols for future lots aimed at that application segment.

    Every chemist faces the push for cleaner, faster routes, and finding the ideal intermediate alignment means understanding subtle differences in reactivity between seemingly similar compounds. Compared with neighboring analogs—such as methyl-only or hydroxy-only substituted pyridines—our core offering empowers a more targeted approach to both functionalization and selective catalysis. Avoiding side-conversion or excess by-product formation translates to smoother scale-up, higher overall project yields, and faster path to a successful patent or registration. These are real gains, not just paper improvements, rooted in staff experience across thousands of kilo runs and a relentless drive to pair product with process improvements every cycle.

    Transparency, Adaptation, and Continual Learning

    Modern markets don’t reward stubbornness or slow response. The feedback cycle from world-class R&D and manufacturing teams presses us all to improve or risk irrelevance. Past failures and customer frustrations raised our bar for transparency. Now, every lot comes with robust documentation, QC batch history, and open lines for further support—not just generic phone numbers but real chemists who understand where a typical problem might emerge. We track regulatory shifts not as a forced exercise, but as a proactive guardrail; if an impurity or process change will matter for downstream registration or patent claims, our documentation is ready to support both scientific and compliance justifications.

    The pursuit of improvement never stops. Each project stretches our capabilities, demanding more from both synthesis and analytics. More than that, it gives our operators and support chemists tangible lessons, sparking dialogue, debate, and collaborative fixes. Transparency and detail-orientation turn small improvements into big gains, visible in happier project managers, fewer deviations, and smoother pilot-to-plant transitions at client sites. By tying each production cycle directly to end-user goals, the journey from kilo-scale specialty batch to commercial rollout grows both our expertise and the value we contribute to every team who relies on 3-cyano-4,6-dimethyl-2-hydroxypyridine to push their research forward.

    Conclusion: Chemical Manufacturing as a Trust-Based Endeavor

    Years working with high-value pyridine intermediates reveal the truth: trust forms the core of every successful supplier-researcher partnership. We built our process not just on technical training or financial calculation, but on the field-tested lessons from countless scale-ups, failed pilot runs, and fixes born out of researcher frustration. Meeting evolving real-world demands has shaped our approach to 3-cyano-4,6-dimethyl-2-hydroxypyridine, making us both more accountable and more in touch with what our partners actually need. Every batch, every purify step, every detail in documentation sits on a foundation of lived experience and commitment. That’s not just technical excellence—it’s the difference between hoping for repeatability and building it into the workflow with every shipment we release. For those who count on this critical intermediate, every detail counts, and we stand ready, batch after batch, to prove it.