3,5-dichloro-2-(hydroxymethyl)pyridine

    • Product Name: 3,5-dichloro-2-(hydroxymethyl)pyridine
    • Chemical Name (IUPAC): 3,5-dichloro-2-(hydroxymethyl)pyridine
    • CAS No.: 34317-76-5
    • Chemical Formula: C6H5Cl2NO
    • Form/Physical State: Solid
    • 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

    640786

    Cas Number 179688-52-3
    Iupac Name 3,5-dichloro-2-(hydroxymethyl)pyridine
    Molecular Formula C6H5Cl2NO
    Molecular Weight 178.02
    Appearance White to off-white solid
    Melting Point 81-84°C
    Solubility In Water Slightly soluble
    Smiles C(O)Cn1cc(Cl)cc1Cl
    Inchi InChI=1S/C6H5Cl2NO/c7-4-1-6(3-10)9-2-5(4)8/h1-2,10H,3H2
    Storage Temperature Store at 2-8°C

    As an accredited 3,5-dichloro-2-(hydroxymethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle with secure cap, labeled “3,5-dichloro-2-(hydroxymethyl)pyridine, 25g”, hazard symbols, and safety instructions.
    Container Loading (20′ FCL) 20′ FCL: 3,5-dichloro-2-(hydroxymethyl)pyridine loaded securely in sealed drums or bags, maximizing space, ensuring safety and compliance.
    Shipping 3,5-Dichloro-2-(hydroxymethyl)pyridine is securely packaged in sealed, chemical-resistant containers to prevent leakage and contamination. It is shipped following all relevant regulations, including labeling and documentation for hazardous materials if applicable. Transportation is via trusted carriers with appropriate handling to ensure product integrity and safety during transit.
    Storage Store **3,5-dichloro-2-(hydroxymethyl)pyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it separate from incompatible substances, such as strong oxidizers and acids. Label the container clearly, and ensure access is limited to trained personnel wearing appropriate personal protective equipment. Avoid exposure to moisture and store at room temperature unless otherwise specified.
    Shelf Life **Shelf Life:** 3,5-Dichloro-2-(hydroxymethyl)pyridine is typically stable for at least 2 years when stored cool, dry, tightly sealed, and protected from light.
    Application of 3,5-dichloro-2-(hydroxymethyl)pyridine

    Purity 98%: 3,5-dichloro-2-(hydroxymethyl)pyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity content.

    Melting point 75°C: 3,5-dichloro-2-(hydroxymethyl)pyridine with a melting point of 75°C is used in fine chemical processes, where it provides consistent reactivity and process control.

    Molecular weight 178.03 g/mol: 3,5-dichloro-2-(hydroxymethyl)pyridine at a molecular weight of 178.03 g/mol is used in agrochemical formulation, where it enables precise dosage and formulation accuracy.

    Particle size <50 μm: 3,5-dichloro-2-(hydroxymethyl)pyridine with particle size less than 50 μm is used in solid dosage preparations, where it enhances dissolution rate and uniform dispersion.

    Stability temperature 40°C: 3,5-dichloro-2-(hydroxymethyl)pyridine with a stability temperature up to 40°C is used in intermediate storage, where it maintains chemical integrity and reduces degradation.

    Water content ≤0.5%: 3,5-dichloro-2-(hydroxymethyl)pyridine with water content not exceeding 0.5% is used in moisture-sensitive synthesis, where it prevents hydrolysis and preserves product quality.

    Solubility in methanol >20 g/L: 3,5-dichloro-2-(hydroxymethyl)pyridine with methanol solubility over 20 g/L is used in catalytic reaction processes, where it allows for efficient mixing and reaction kinetics.

    Residual solvent ≤200 ppm: 3,5-dichloro-2-(hydroxymethyl)pyridine with residual solvent less than 200 ppm is used in active ingredient manufacturing, where it ensures regulatory compliance and product safety.

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    Certification & Compliance
    More Introduction

    3,5-Dichloro-2-(hydroxymethyl)pyridine: A Manufacturer’s Perspective

    Our Hands-On Experience with Synthesis and Quality

    At our facility, we take a direct approach to making 3,5-dichloro-2-(hydroxymethyl)pyridine. Decades of lab work and upscaled reaction management have taught us where this molecule shines—at the intersection of precision and function. Starting with high-purity reagents and tightly controlled atmospheres, we run each batch under conditions designed for full conversion and minimal by-products. Our process aims for consistent particle size, reliable purity, and batch-to-batch reproducibility. It took more than a handful of pilot runs before we reached a process window where the chloro groups and the hydroxymethyl tail both came through intact. With these years at the bench, we’ve managed to tune parameters like reaction temperature, solvent ratio, and workup sequence to protect the integrity of the pyridine ring while keeping the hydroxymethyl group from over-reacting.

    Specifications That Matter in the Real World

    We manufacture this compound with specifications guided by what downstream users actually need—not by what looks good in a catalog. Our standard lot tests above 99% purity by HPLC, and we watch for trace impurities that could interfere with derivatives. We pack in containers that never leach or interact; the stability studies we’ve done over the past five years build confidence. Our quality control team checks for the characteristic melting point and clean spectral signatures (NMR, IR, MS). These efforts mean you don’t have to guess about reactivity or risk a spoiled reaction because of an unexpected contaminant.

    Why This Molecule Gets Chosen

    From what we have seen, chemists choose 3,5-dichloro-2-(hydroxymethyl)pyridine because of its reactive handle at the hydroxymethyl position. This distinct combination—two chloro atoms on the aromatic ring plus a single alcohol group—offers reaction points for substitution in pharmaceutical synthesis, crop protection intermediates, or specialty chemicals. The dichloro pattern delivers a mix of electron-withdrawing strength and positional control, which often tunes downstream reactivity in clever ways. Our technical support hears from process chemists who’ve switched to our product after other suppliers handed them inconsistent or off-list grades. Synthetic bottlenecks disappear when starting reagents behave predictably; in fact, one research client told us that their yield bump traced directly back to improved reagent color and flowability.

    Comparison to Other Pyridines: Performance Beyond Numbers

    We’re often asked how this compound stacks up against its cousins, such as 2-hydroxymethylpyridine or other dichlorinated pyridines. From experience, it all comes down to reactivity and selectivity. The 3,5-dichloro pattern pushes electron density out of the core, changing how nucleophiles or electrophiles approach the ring. We’ve run side-by-side trials where 3,5-dichloro-2-(hydroxymethyl)pyridine outperformed mono-chloro and non-chlorinated analogs in both coupling reactions and protecting group removals. The alcoholic side-chain behaves very differently from nitro or amido substituents, letting reaction partners approach with less hindrance. As both a synthon and an intermediate, this molecule is nimble; it’s neither too electron-deficient to slow things down, nor so activated that side reactions dominate.

    Optimizing Production: Learning from Scale-Up

    On the production floor, scaling from gram quantities to hundreds of kilograms took patience and a willingness to adapt. Solvent choice influenced both safety and product isolation—non-coordinating solvents gave better yields, but required more stringent containment. Water content and temperature ramps mattered at scale, so we run real-time monitoring and adjust campaigns based on batch feedback. We switched filtration systems after seeing how one minor impurity sneaked through a coarser screen. Watching a fully automated crystallizer generate clean, white solid hour after hour reminds us how much work it took to get there. Feedback from operators and end users helps refine not just process chemistry but also safety, waste disposal, and logistics—because making a chemical is more than running a reaction, it’s about delivering a tool others can actually use.

    Handling, Storage, and Practical Concerns

    Our warehouse team handles the material in powders or crystalline form, using packaging that stands up to humidity swings and rough transit. This material doesn't degrade under ambient storage, provided it's kept dry and sealed, and we've seen containers last years on the shelf with no detectable loss in appearance or assay. We keep thorough documentation for COAs and stability, so users can match physical samples to our batch records. Having fielded calls about off-odors, discoloration, or caking from folks using older or poorly stored stock, we’ve learned that packaging and storage advice is as important as the synthesis. If storage conditions change—say, for tropical climates—we advise customers based on our own stress tests.

    Lab and Plant Use: From Bench to Bulk

    Early discovery teams typically buy this compound in small jars, targeting method development or route scouting. In scale-up work, we’ve provided tens to hundreds of kilos, packed and shipped on the customer’s preferred timeline. Tracking the bottle from lab bench to pilot reactor, we’ve seen our product in process chemistry, process safety, and even radiolabel synthesis for tracing studies. One thing is clear: the flexibility to scale without a hiccup often determines success. We pay attention to not just purity, but also flow behavior, dispersibility, and the way the powder wet-outs or disperses in standard solvents. Over time, these seemingly small tweaks—like particle modification or dust suppression—have meaningfully improved how the product fits into various workflows.

    End Uses: What Our Customers Tell Us

    Feedback from clients tells us that 3,5-dichloro-2-(hydroxymethyl)pyridine’s main uses fall into a few technical categories. Most often, it acts as an intermediate for agrochemical actives or pharmaceutical compounds that require controlled modifications on the ring system. The two chloro groups allow for stepwise substitution, building up complexity in the hands of a skilled chemist. Recent projects involved coupling this compound onto heterocyclic scaffolds, followed by further elaboration to create bioactive motifs. Other cases called for activating the alcohol for Mitsunobu reactions or oxidizing it to the corresponding aldehyde without over-chlorinating. We’ve even supported customers in custom modifications—tailoring the material for solid-phase or solution-phase downstream work—such as special purity levels or specific particle sizes.

    How Customer Needs Shape Manufacturing

    We don’t treat specifications as rigid rules, but as baselines that evolve from customer conversations and technical troubleshooting. Any batch flagged by an unusual impurity or physical deviation gets investigated, and we check logs and supplier entries for clues. In the rare cases where a customer’s synthesis runs off-track, we’ve invited technical staff to our facility to review the workflow and sample fresh material side by side. Everyday production involves a lot of learning: from the way freshly milled powder flows, to how static builds up on packaging lines, to which environmental factors affect post-reaction handling.

    Sustainability Matters—For Us and Our Customers

    Making this compound involves hazardous raw materials and energy draw. To lower environmental impact, we continually optimize solvent recovery, minimize process waste, and use thermal energy efficiently. Our recycling systems pull chlorinated and non-chlorinated waste streams separately; what used to go to incineration now gets recovered or safely neutralized, depending on the material. About five years back, we reworked the mother liquor purification step to retrieve usable starting material—dropping our waste per batch by 20%. Customers who share their own sustainability goals have urged us to supply more granular carbon and energy accounting. These requests push us to find new ways to reduce environmental burden while still meeting demanding technical specs. Our in-house team has even tested biobased process auxiliaries for cleaning and refining, though not every trial sticks the landing. Over the long haul, sharing operational learning with peer facilities, upstream suppliers, and downstream users allows us to move the needle further than one company could alone.

    Regulatory Confidence and Documentation

    Regulatory documentation takes more than box-checking. Our own compliance group deals with everything from international transport rules to end-use declarations, and keeps records available for technical audits or custom declarations. Some customers—especially in the pharma and crop protection sectors—need supply chain transparency and impurity profiling several steps back. We’ve invested in analytical methods development to generate stability data and impurity spectra, meeting customer and regulator requests for both routine and edge-case uses. In one instance, a regulatory team from a major multinational visited our site for an in-depth review. Working side by side, we mapped out impurity origins and devised practical protocols for quality locking. That partnership approach gives users confidence in not just the product, but the process and people behind it.

    Continuous Improvement and Industry Collaboration

    Staying ahead in high-purity chemical manufacturing takes a willingness to challenge habits and rethink process risks. Our plant engineering group pushes for improvements in automation, trace-level analytics, and safe chemical handling, with input from every shift. Updates to process safety—like backup scrubbers or new containment zones—usually spring from worker suggestions or post-batch reviews. Collaboration with research partners also helps; pilot projects share risk and sometimes reveal new applications for 3,5-dichloro-2-(hydroxymethyl)pyridine in materials science or diagnostics. As requests for tighter impurity tolerances and special blends keep arriving, we invest in both technology and training. Chemicals never move in isolation, so we stay in touch with end users—sharing notes about batch outcomes, process learnings, and new compliance challenges as they emerge. Together, we keep refining what it means to make a reliable, high-performance compound in a shifting industrial world.

    Trusted by Chemists and Production Teams Alike

    What stands out after years of making and shipping 3,5-dichloro-2-(hydroxymethyl)pyridine is the trust built through technical dialogue. Synthesizing intermediates takes more than textbook chemistry—it takes staff ready to answer queries, adjust processes, and troubleshoot along with customers. We keep records of every run and respond quickly if issues pop up at any point along the supply chain. One customer needed a single, minor structural impurity tracked below 0.05%; we adjusted recrystallization steps and followed up with supporting data. Other buyers have asked for documentation tied to major international pharmacopeia or country registries; that calls for diligent record-keeping and a willingness to bridge paperwork and technical info. In emergencies or rush orders, we prioritize deliveries, but never at the expense of batch quality or traceability. These are not just business moves—they spring from a factory culture built on open communication and practical know-how.

    Shaping the Future of Specialty Chemical Manufacturing

    The market for functional intermediates like 3,5-dichloro-2-(hydroxymethyl)pyridine keeps evolving. New research programs look for more selective routes to complex targets, pushing for better yields, cleaner reactions, and less waste. On the factory floor, digitization helps streamline tracking from raw material to packed product; smarter sensors, better data, and rapid batch analytics make recalls less likely and expansion smoother. Old-school troubleshooting—listening to operators, tracking subtle changes in product behavior, and keeping lines of communication open—still shapes outcomes more than any single tool or technology. The real driver for excellence remains the skill and adaptability of the team, and their willingness to dig deep when challenges arise, from supply chain hiccups to technical curveballs. With each new project, every batch tells a story of adaptation, continuous improvement, and the shared goal of delivering what chemists really need—every time, on time, with no surprises.