2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI)

    • Product Name: 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI)
    • Chemical Name (IUPAC): 5-hydroxy-3-methylpyridine-2-carbonitrile
    • CAS No.: 6654-57-5
    • Chemical Formula: C7H6N2O
    • Form/Physical State: Crystalline Powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    475819

    Iupac Name 5-hydroxy-3-methylpyridine-2-carbonitrile
    Cas Number 4318-19-2
    Molecular Formula C7H6N2O
    Molecular Weight 134.14
    Smiles CC1=CN=C(C=C1O)C#N
    Inchi InChI=1S/C7H6N2O/c1-5-2-6(8)9-4-7(5)10/h2,4,10H,1H3
    Appearance Solid (may vary: white to off-white powder)
    Melting Point 134-138 °C (literature value)
    Solubility In Water Slightly soluble
    Pubchem Cid 256894

    As an accredited 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 100g amber glass bottle, featuring a secure screw cap and clear hazard and identification labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 12 metric tons packed in 25 kg fiber drums, securely palletized, suitable for international chemical shipments.
    Shipping 2-Pyridinecarbonitrile, 5-hydroxy-3-methyl- (9CI) should be shipped in a tightly sealed container, protected from light, moisture, and incompatible substances. Transport in accordance with chemical safety regulations, with appropriate labeling and documentation. Use secondary containment and temperature control if recommended. Handle only by trained personnel using proper personal protective equipment (PPE).
    Storage 2-Pyridinecarbonitrile, 5-hydroxy-3-methyl-(9CI) should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Ensure proper chemical labeling, and avoid exposure to heat or flame. Store at room temperature unless otherwise specified by the manufacturer or Safety Data Sheet (SDS).
    Shelf Life 2-Pyridinecarbonitrile, 5-hydroxy-3-methyl-(9CI) should be stored tightly sealed; typical shelf life is 2-3 years under proper conditions.
    Application of 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI)

    Purity 98%: 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) with a purity of 98% is used in pharmaceutical intermediate synthesis, where high purity ensures selective reaction yields.

    Melting Point 158°C: 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) with a melting point of 158°C is used in solid-state formulation processes, where its defined phase transition enables precise compound integration.

    Molecular Weight 146.15 g/mol: 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) at a molecular weight of 146.15 g/mol is used in chemical research applications, where accurate molecular mass contributes to formulation calculations.

    Stability Temperature up to 120°C: 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) stable up to 120°C is used in high-temperature reaction environments, where thermal stability avoids decomposition.

    Particle Size <20 μm: 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) with particle size below 20 μm is used in fine chemical dispersion, where small particles enhance uniform mixing and reactivity.

    Solubility in Ethanol 15 mg/mL: 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) with solubility in ethanol at 15 mg/mL is used in solution-based synthesis, where adequate solubility facilitates homogeneous reactions.

    UV Absorbance 320 nm: 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) featuring UV absorbance at 320 nm is used in analytical studies, where distinct absorbance allows for quantitative UV monitoring.

    Assay by HPLC ≥99%: 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) assayed by HPLC at or above 99% is used in quality control laboratories, where high assay purity guarantees analytical reliability.

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    Certification & Compliance
    More Introduction

    Introducing 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI): A Manufacturer’s Perspective

    Insight from Daily Practice: What Sets This Compound Apart

    At our manufacturing facility, the story of 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) always begins at the reactor, with careful monitoring of reagents, temperatures, and reaction times. Watching this compound form is a reminder that not every pyridine derivative behaves the same way. The 5-hydroxy and 3-methyl groups matter. Their positions on the aromatic ring influence reactivity in ways that alter not just theoretical yield, but real-world outcomes—purity, crystallinity, handling during isolation.

    Some chemists who have spent years with more basic pyridinecarbonitriles may assume switching to a hydroxy-methyl substituted variant brings no surprises. In practice, subtle changes in solubility and reactivity determine the choice of solvents for recrystallization, or the best temperatures for controlling side reactions. The 9CI configuration is more than a catalog number; it’s a recipe for productive synthesis and fewer headaches during scale-up.

    Production Integrity: From Lab to Kilo Scale

    Scaling up this compound requires a steady hand and a clear mind. Batch consistency rarely comes from automatic processes alone. We monitor batch parameters as much for the minor fluctuations as for the expected endpoints. It becomes clear that moisture and airborne contaminants can undermine the hydroxy position, leading to unwanted byproducts, especially when chasing high assay requirements. We’ve learned that purging all traces of residual acid or base at every stage can preserve the integrity of the molecule far better than any imprecise downstream purification.

    Our approach puts as much effort into the upstream stage as the so-called finishing steps. For 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI), controlling heat ramps and agitation speeds during the ring closure step can be the difference between a bright white product and a discolored one needing extra cleanup. Over time, we’ve customized reactor interiors to minimize product adherence and improved filtration methods to recover every last gram. These optimizations improve environmental impact—less waste, lower solvent use—while also serving our core goal: reliably homogenous product that feels the same in the hand whether it’s the first kilo or the hundredth.

    Meeting User Demands: Real Uses, Real Outcomes

    End users bring their own needs, shaped by real-world applications. Many come from pharmaceutical research, where the 5-hydroxy-3-methyl substitution has proven relevant in lead generation for heterocyclic scaffolds. The goal isn’t just to add another building block. Researchers choose this compound because the added hydroxy group can anchor a wide range of downstream modifications—esterification, ether formation, or conversion into more complex pharmacophores. The methyl group at the 3-position modulates electronic effects in the pyridine ring, which in turn impacts yield in sequential reactions.

    Customers working in agrochemicals tell us they appreciate the compound’s slightly increased polarity compared to strictly methyl-substituted variants. Their feedback traces back to improved dissolution profiles in pre-emergent herbicide studies. The result? More reproducible field trial data, especially when soil absorption plays a big role in product performance. We supply analytical support to help researchers map out the metabolite profiles following application, and these data often support regulatory filings.

    For those in material science, the presence of both hydroxy and nitrile groups introduces new hydrogen bonding possibilities. Researchers have documented stronger interactions in copolymer blends, and there’s growing interest in this variant as a modifier in specialty coatings where thermal stability is needed without sacrificing processability.

    How 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI) Differs from Other Pyridinecarbonitriles

    Side-by-side with standard pyridinecarbonitrile, this compound exhibits a higher melting point, an expected result given the added hydrogen bonding from the hydroxy group. But it’s not just the physical data: during purification, we noticed the compound retains less residual solvent following vacuum drying. This carries through to downstream users, who report fewer complications during formulation, especially with sensitive enzyme screens and LC-MS protocols.

    More common derivatives might cut corners in price, but we’ve observed that too much focus on cost strips away value. We take special care verifying the position of the methyl and hydroxy groups using multiple analytical techniques—NMR, HPLC, and IR. We maintain LC-MS data for every lot, since a shift in peak retention or fragmentation can reveal an unnoticed isomer. Some might not bother; our chemists do, and our QC logs show the long-term payoff: fewer complaints and returns.

    Standard nitrile-bearing pyridines without the hydroxy substitution lack the chemical windows that unlock further value. The hydroxy group acts as a chemical handle, which has opened the door to unique chemical transformations not possible with methyl or nitrile lone pairs alone. The versatility shows up in both literature references and customer case studies—faster route optimization, fewer steps needed to introduce other functional groups.

    Ensuring Safety, Reliability, and Traceability

    In our plant, every batch gets its own history. There’s no shortcut for recordkeeping or for ensuring batch-to-batch consistency. We equip our team with the best tools and training, and every operator understands the link between daily lab tests and customer outcomes. Moisture analysis, residual solvent tests, and standard melting point checks become routine before we ever approve a shipment.

    Some clients request tighter purity specifications, and the discussion always returns to trace impurities. The biggest challenge with this molecule is the control of metal residues after synthesis. Our purification techniques—especially chelating resin columns and extra polishing steps—address these directly. We log findings so we can give transparent reporting, which makes conversations with highly regulated industries much smoother.

    On the rare occasion that a technical inquiry arises, we open our process records and share not just specs, but the reality of how we achieved them. Open communication with users is how we’ve solved unexpected hurdles, like occasional sensitivity in downstream coupling reactions due to microtrace amine contamination. With every instance, solutions come from fast feedback and immediate corrective action—tighter filtration, additional quality checks, changes to packing materials.

    Crafting a Product Born from Experience, Not Guesswork

    Years spent developing this compound means we’ve made mistakes and learned lessons that don’t show up in literature articles. For instance, some tried flash chromatography to purify this molecule. After running expensive columns and lengthy solvent gradients, the answer turned out to be much simpler. Crystallization from ethanol-water mixtures, with careful temperature control, gives cleaner material at larger scale. This saves time, environmental impact, and labor.

    Worker safety influences material choices as much as chemical efficiency. The presence of the nitrile group means this compound doesn’t emit strong odors or volatiles under routine handling, making it easier to manage in plant operations. This improves the atmosphere not just for workers, but for the environment around our facilities.

    From container choices to outer packaging, feedback from receivers has shaped our delivery process. We switched container linings after a small group of long-term customers in a humid climate showed us how the compound picked up trace moisture from ambient air. By adding extra foil liners and checking desiccant packs before shipping, our returns due to caking or loss of free-flowing powder have dropped sharply. These may sound like small tweaks, but for every end user, consistency in the bag can mean consistency in the beaker. It’s not just what’s produced in the reactor; it’s what arrives safely at the bench.

    Environmental Responsibility at Scale

    Manufacturing at scale means keeping one eye on process efficiency and another on environmental responsibility. Solvent choice during synthesis has a direct impact on waste streams, especially for compounds featuring active functional groups like 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI). Over several campaigns, we’ve shifted away from chlorinated solvents in favor of greener alternatives without sacrificing yield or purity. Waste minimization stands alongside product quality as the measure of good manufacturing.

    Energy management also shapes our process. The hydroxy methyl substitution pattern calls for different crystallization and drying conditions than standard nitrile derivatives. We optimize for lower-temperature drying cycles to reduce total energy usage during the final step. Facility monitoring includes solvent recovery and distillation for reuse, which adds practical cost savings and lessens environmental impact.

    We keep regional regulations in mind and collaborate directly with local authorities to ensure our emissions stay within accepted boundaries. Clear records, periodic audits, cooperative partnerships—these matter as much as any lab protocol, because the cost of compliance pales next to the value of trust from local communities and customers.

    Continuous Feedback: Innovating to Improve

    Listening to users has driven unexpected process changes. Pharmasynthesists who experienced sticking during tablet blending taught us how ambient humidity during packaging could affect downstream processability. We learned to run moisture checks not just on the batch but on the actual packaged goods before sealing them for transit.

    Academic groups provided feedback on solubility. Some research groups found solubility in acetonitrile better than anticipated, inviting us to do side-by-side solubility studies with related compounds. This led to improved recommendations for use in high-throughput screening, and the feedback even led us to update FAQ documents shared with collaborative partners. In return, we’ve received compelling application notes showing success in Suzuki couplings, where the functional group orientation impacted reaction times.

    Technical feedback has driven equipment upgrades. Our crystallization tanks now include automated cooling ramps, not just because it looks impressive, but because data from user feedback loops suggest improved particle size control gives smoother downstream formulation—a difference users measured themselves during filtration and drying steps.

    Supporting Technical Transparency

    We recognize the importance of technical data for our clients, but equally important is the openness about batch information. We run reference standards from every batch through our in-house NMR and HPLC facilities. This data gets shared with established accounts, not out of legal requirement, but as part of fostering trust. A researcher who spots a minor impurity peak can talk directly with our technical team for real discussion, not just customer service platitudes.

    In our experience, transparency shortens project timelines for users. If a reaction fails or behaves poorly, researchers do not waste time second-guessing the raw material. Our investment in product characterization means their QC teams spend less time on raw material investigations. We see this in repeat orders, as well as in the long-term partnerships we’ve built with small and large labs alike.

    Conclusion from the Production Floor: What Users Can Expect

    If you’ve worked with 2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI), you know it isn’t an off-the-shelf pyridine knockoff. Producing a consistent, pure compound in quantity takes more than following a published procedure—real-world differences in reactivity and handling become clear outside the lab notebook. The features that make this molecule unique—the hydroxy and methyl arrangement, the reactivity patterns, the compatibility across synthetic, agrochemical, and material science fields—have guided our process improvements and daily working practices.

    We’ve learned that supporting users isn’t about offering the lowest price or rushing pallets out the door. It’s about providing material that performs exactly as expected, supported by all the information needed for seamless integration into demanding workflows. Our direct communication, investment in quality systems, and a willingness to take feedback and turn it into action all define our role as a partner, not just a supplier. This is the standard we hold for every batch, every day.