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(2-Chloro-Pyridin-4-Yl)-Methanol

    • Product Name (2-Chloro-Pyridin-4-Yl)-Methanol
    • Alias (2-chloropyridin-4-yl)methanol
    • Einecs EINECS 607-093-6
    • 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

    622436

    Chemical Name (2-Chloro-pyridin-4-yl)-methanol
    Molecular Formula C6H6ClNO
    Molecular Weight 143.57 g/mol
    Cas Number 876718-47-1
    Appearance White to off-white solid
    Melting Point 86-90 °C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, tightly sealed
    Smiles C1=CC(=NC=C1CO)Cl
    Synonyms 2-Chloro-4-pyridylmethanol

    As an accredited (2-Chloro-Pyridin-4-Yl)-Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging consists of a sealed amber glass bottle containing 25 grams of (2-Chloro-Pyridin-4-Yl)-Methanol, labeled with safety and handling instructions.
    Shipping (2-Chloro-Pyridin-4-Yl)-Methanol is shipped in secure, sealed containers to prevent leaks or contamination, typically under ambient conditions. Proper labeling and documentation, including hazard identification, are ensured to comply with chemical safety regulations. Packaging adheres to international standards for the transport of laboratory chemicals, minimizing risks during handling and transit.
    Storage (2-Chloro-pyridin-4-yl)-methanol should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition and direct sunlight. It should be kept separate from incompatible materials such as oxidizing agents. Proper chemical storage procedures, including secondary containment and appropriate labeling, are recommended to prevent leaks, spills, and accidental exposure.
    Application of (2-Chloro-Pyridin-4-Yl)-Methanol

    Applications of (2-Chloro-Pyridin-4-Yl)-Methanol in Industrial Manufacturing

    (2-Chloro-Pyridin-4-Yl)-Methanol is a specialized intermediate applied in the synthesis of advanced functional materials. We manufacture this compound to address critical performance demands across several high-end industrial sectors, supporting customers with reliable supply and consistent quality on a large scale.

    1. Agrochemical Intermediates for Pyridine-Based Herbicides

    Large agriscience producers utilize this material as a primary building block in manufacturing selective herbicides targeting broadleaf and grassy weeds. Synthetic routes incorporate the molecule at early coupling stages where the pyridine ring substitution and hydroxymethyl group enable further halogenation or etherification steps, which are necessary for preparing active herbicide moieties such as chlorpyridine derivatives. Regulatory authorities closely monitor agricultural applications, necessitating adherence to recognized agrochemical standards and low residual solvent content controls.

    Industry compliance standards

    • ISO 9001:2015 certified production systems
    • EU REACH registration for agrochemicals
    • Food and Agriculture Organization (FAO) specifications for technical-grade inputs
    • Maximum residue limits set by U.S. EPA, EU SANCO, and China NDRC

    Typical usage ratio

    • 5–20% by mass of intermediate batches, with adjustments according to targeted molecular structure and downstream halogenation stage

    Downstream process integration

    • Added to condensation or coupling phases under controlled pH and temperature, followed by derivatization or chlorination in multi-step synthesis lines

    Final product types

    • Broad-spectrum post-emergence herbicides (e.g., pyridine-type active ingredients)
    • Grass and weed control agents for corn, wheat, rice cultivation
    • Technical herbicidal concentrates
    • Formulated crop protection granules

    2. Pharmaceutical Intermediate for Antiviral and Neurological Actives

    Originator and generic pharmaceutical manufacturers leverage this material for constructing API scaffolds where functionalized pyridines are critical for biological activity, notably in antiviral and central nervous system therapeutics. The compound participates in methylation and nucleophilic substitution steps where precise steric and electronic configuration is crucial. Each lot is produced under controlled conditions with full traceability and robust impurity profiling to satisfy regulatory pre-approval.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and EP reference quality control methods (where relevant for process intermediates)
    • FDA DMF (Drug Master File) submission support
    • Pharmaceutical cGMP traceability (including batch records and impurity profiles)

    Typical usage ratio

    • 0.2–5 molar equivalents per core synthetic step, with process optimization performed during route scouting and scale-up

    Downstream process integration

    • Introduced at pyridyl methylation, amination, or cyclization steps, serving as a precursor to API backbone assembly with full in-process analytics

    Final product types

    • Pyridine-derived antiviral APIs
    • Neurological disorder treatment actives under clinical development
    • Research-stage lead compounds
    • Regulatory reference standards

    3. Custom Synthesis for Fine Chemical and Material Science Applications

    Advanced material producers and contract R&D labs require this intermediate for heterocyclic core modifications, especially within optical, electronic, and functional monomer synthesis. Specialized applications include photoactive molecules, charge-transport agents, and ligand frameworks for catalysis. Our supply supports stringent project-specific specifications such as high-purity, low metal content, and batch-for-batch reproducibility vital for downstream polymerization and material assembly.

    Industry compliance standards

    • ISO 14001 Environmental Management System for specialty fine chemical plants
    • Chemical hazard classification and labeling in compliance with GHS and local regulations
    • RoHS (Restriction of Hazardous Substances) for electronic chemical supply
    • Internal QA/QC protocols tailored for specialty chemical handling

    Typical usage ratio

    • 0.5–10% by mass depending on design of the molecular framework and degree of functionalization required by customer project

    Downstream process integration

    • Incorporated during nucleophilic or electrophilic aromatic substitution reactions for oligomer, polymer, or ligand synthesis carried out under inert-atmosphere conditions

    Final product types

    • Specialty optical monomers and copolymers
    • OLED charge-transfer matrices
    • Photoinitiators for UV curing
    • Custom ligands for metal-catalyzed reactions

    4. Active Ingredient Synthesis for Veterinary Drug Products

    Veterinary pharmaceutical manufacturers demand this compound as a precursor for halogenated pyridine APIs intended for antiparasitic and anti-inflammatory veterinary drugs. These applications require high-purity material subjected to residual solvent and impurity controls, matching the requirements of major veterinary pharmacopoeias. Our plant maintains segregated production lines for vet pharma grades, ensuring compliance with zoonotic safety regulations and traceability for global export.

    Industry compliance standards

    • VICH GL (Veterinary International Conference on Harmonization) guidelines
    • European Pharmacopoeia (monographs for pyridine derivatives)
    • US FDA Guidance for Industry #205 (veterinary APIs)
    • Import/export clearances for veterinary actives (USDA, CFDA)

    Typical usage ratio

    • 2–15% by mass in active ingredient synthesis, ratio controlled based on target pyridine substitution pattern and desired API pharmacological profile

    Downstream process integration

    • Engaged at either initial halogenation or oxidative coupling steps during API precursor preparation, monitored via in-process HPLC and GC

    Final product types

    • Finished veterinary antiparasitic drug substances
    • Veterinary anti-inflammatory actives
    • Pre-mixes for oral or injectable animal health formulations
    • Veterinary finished dosage forms
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    Certification & Compliance
    More Introduction

    Meeting Complex Chemistry Needs with (2-Chloro-Pyridin-4-Yl)-Methanol: Our Experience and Perspective

    Introduction: Reliable Building Blocks from the Manufacturer’s View

    At our facility, we have watched the demand for fine chemicals shift steadily toward more specialized, high-value building blocks. (2-Chloro-Pyridin-4-Yl)-Methanol stands out in this space. Our experience manufacturing this compound has often delivered insights across both chemistry and project management. The process, starting from raw material selection through crystallization and purification, reflects a relationship to every batch: nothing leaves our doors without extensive analysis, traceable documentation, and a close eye on both physical and chemical properties.

    Why (2-Chloro-Pyridin-4-Yl)-Methanol Matters in Modern Synthesis

    Conversations with customers in medicinal and agrochemical research remind us daily that molecules like (2-Chloro-Pyridin-4-Yl)-Methanol are not just theoretical lab tools. They’re irreplaceable in the real-world pursuit of new actives. Its balance of reactivity and selectivity provides researchers options that make downstream chemistry more reliable. Chemists prize its pyridine ring—altered with a chloro at position 2 and capped by a primary alcohol—for diversity in functionalization.

    Our scale ranges from kilo-lab to hundreds of kilo capacity. Each batch aligns itself with the evolving needs of product development—seasonal fluctuations on the customer side often mean we keep strategic stock. We have found that consistency, more than anything, keeps our reputation intact. In chromatographic analysis, the sharpness of each peak reflects our surveillance on side reactions and impurity carryover.

    Technical Particulars and User Feedback

    Chemists tend to ask about melting point, moisture content, and overall impurity profile. Reactions tend to run smoother when the compound’s water content holds below 0.2% and heavy metal levels are measured in parts per million, monitored batch-to-batch. The method we use to introduce the chloropyridine motif demands tight process conditions. It takes repeated trials to dial in temperature and mixing speeds that keep content uniform without excessive byproduct formation.

    Clients from drug discovery programs tell us that our crystals dissolve easily in standard organic solvents. The hydroxy group at the side chain allows for versatile use, feeding smoothly into either oxidation or protection steps. Physical stability in ambient storage conditions has been another reported plus—the compound’s robust lattice structure fends off decomposition and ensures it stands up to longer project timelines.

    Application Insights: What Makes This Molecule Distinct

    Direct input from synthetic chemists speaks volumes compared to technical data sheets. (2-Chloro-Pyridin-4-Yl)-Methanol brings a particular edge to sequences involving nucleophilic substitution, and often slots into Suzuki coupling or Mitsunobu reactions. The presence of the alcohol group changes the game in comparison to its close cousin, 2-chloro-4-pyridine—a substrate that lacks the flexibility for further derivatization. Attaching the methanol to the pyridine nucleus broadens its utility in core-building and late-stage functionalization. Scientists push for functional groups that facilitate both reactivity and handle-ability; this molecule delivers on both.

    Some older analogs—pyridines without halogen substitution or with different alkyl groups—showed higher volatility or decreased shelf-life. Our QC team’s records indicate that (2-Chloro-Pyridin-4-Yl)-Methanol holds up better in storage, with consistently low peroxide formation compared to secondary alcohol alternatives. That stability means less troubleshooting for analysts and fewer reruns for downstream chemists.

    Manufacturing Practices: Daily Lessons from the Bench

    Mornings at the plant usually start with a review of prior batch results. Our chemists and production team analyze HPLC, NMR, and GC data from the previous twenty-four hours. A successful process centers on continuous improvement—input from the floor shapes decisions. Formulators and operators working side-by-side, drawing on years spent in both pilot and large-scale production, have taught us that slight tweaks in base addition or timing mean the difference between side-product suppression and an off-spec batch.

    We take nothing for granted in purification. Solvent choice changes not just the efficiency but the physical appearance, from colorless prisms to sometimes slightly off-white powders. Trend analysis on yield and particle size points to ways we can minimize clumping during drum filling and reduce scattering in subsequent particle analysis. There are always new solvents to trial, but we stick by protocols proven to drive down impurity content over the long haul.

    Much of our reliability comes from batch record transparency. Each step feeds into our data history, which our customers ask to review. We frequently invite partners for on-site audits; a walk through the packing line often garners specific questions. Some focus on labeling, others hone in on in-line monitoring. From early feedback, we learned that small points—whether it’s anti-static handling or lot traceability—often prevent bigger problems downstream.

    Safety, Packaging, and Traceability—Frontline Concerns

    Speaking honestly, chemicals like (2-Chloro-Pyridin-4-Yl)-Methanol demand more than just routine attention. Some years back, we faced a customer complaint over residue noticed after transfer from our drums to lab glassware—a detail easily missed in visual checks, traced to a sealant compatibility issue. Since then, nothing passes without a dual sign-off between warehouse and quality control. New shipping methods—lining drums with inert barriers, sealed inside nitrogen—now standard procedure. Oversight becomes personal when you watch engineers on your team working with these chemicals every day.

    End users come from across Europe, North America, and Asia. Regulatory documentation for each lot ties back to raw material origin, batch conditions, and in-process monitoring. More than certification alone, end users expect transparency—auditable records, step-by-step, and regular updates. Familiarity with international transport requirements results in tailored outer drum and package materials that survive variable shipping climates without degradation.

    User Experience: A Dialogue, Not a Transaction

    Nearly every inquiry—whether for a 200g sample or a metric ton—turns into a technical dialogue. Users ask about best practices to dissolve or derivatize in unpredictable reaction mixtures. We’ve found that advice grounded in lab experience helps: pre-wetting with a chosen solvent, gentle heating, or specific order of addition cuts down on surprises. Shared process notes often avoid bottlenecks in application: uneven mixing, unexpected color changes, or crystallization in cold storage.

    We have seen labs leverage (2-Chloro-Pyridin-4-Yl)-Methanol in heterocycle construction and directed metalation protocols, areas where its profile matches modern efficiency standards. Feedback cycles with process chemists highlight the small wins—days saved, side reactions tamed—showing us the ripple effect one small molecule can have on a multi-year R&D program.

    Where (2-Chloro-Pyridin-4-Yl)-Methanol Sits in the Product Ecosystem

    It stands apart from its close neighbors, such as unsubstituted pyridinyl-methanols and dichloro analogs. Comparative trials—run by both client and in-house teams—point out the practical impacts: stronger resistance to hydrolysis, more predictable response under basic and acidic conditions, and safer handling profiles due to reduced volatility. Less hazard in bench-scale and pilot operations relaxes containment requirements, opening up usage for a broader group of researchers and project timelines.

    In the earlier days, reliance on certain chloropyridine derivatives meant higher amounts of hazardous byproducts and longer purification cycles. The arrival of (2-Chloro-Pyridin-4-Yl)-Methanol meant projects reached milestone syntheses sooner. Its specialized structure creates fewer unwanted side products—a property repeatedly proven in column-processing runs and analytical records. Such impacts go beyond lab procedure; they show up in the rushed tempo of a launch schedule or in the consistent quality of a new formulation.

    Continuous Improvement Driven by Partnership

    Every batch test brings a fresh lesson. Our R&D crew keeps a reserve of previous production samples for side-by-side comparison in both stress testing and method development. The pursuit of improved yields finds us reevaluating catalyst screening and considering solvent swaps in response to real-world feedback.

    On occasion, process engineers join clients for joint troubleshooting sessions, adjusting reaction conditions or reformulating isolation strategies. Whether discussing filtration times or observing polymer formation at trace levels, the best solutions surface when both parties bring credible data and a willingness to adapt. These collaborations reshape both our workflow and the compound’s trajectory as a research staple.

    Sustainability: Balancing Performance and Environmental Responsibility

    Not all process enhancements are about speed or yield. Recent initiatives pivot toward solvent recycling, improved waste stream management, and a fundamental drop in hazardous intermediates. We have introduced closed-loop systems to reduce losses and continual emissions monitoring—steps that challenge earlier habits but pay off in cleaner operations. Chemistry for the modern world goes hand-in-hand with responsible sourcing, minimized carbon footprint, and a move away from legacy practices that put employees or the surrounding community at risk.

    Many conversations now turn to regulatory standards, from the EU’s REACH to evolving U.S. requirements for chemical tracking and documentation. End users expect more than just technical data—they expect a path to environmentally managed, reproducible, and enduring supply. Updates in our internal workflow, from upstream audit of precursor suppliers to energy efficiency in plant utilities, reflect these new priorities. Each commitment, large or small, bends the arc toward an industry that doesn’t sacrifice responsibility for productivity.

    Beyond the Data Sheet—Day-to-Day Realities

    Product data sheets cover solubility, appearance, and basic storage—a baseline but far short of what partners need in high-pressure development cycles. Our production and development teams draw daily insight from stories shared across industries. For instance, pharmaceutical teams prioritize clarity over ambiguity in impurity profiles and timeline certainty, while agricultural chemistry specialists may confront scale-up bottlenecks tied directly to reaction reproducibility.

    The nuts and bolts of delivering (2-Chloro-Pyridin-4-Yl)-Methanol involve communication that goes beyond formal documentation. Our technical staff occasionally face queries about unforeseen reaction outcomes, pressure concerns during distillation, or unexpected contaminants in delivered lots. We share what we know, document what we don’t, and stay open to process tweaks that benefit all stakeholders. This ongoing feedback loop—not just regulatory compliance—sustains our long-term partnerships.

    Looking Ahead: Challenges and Guiding Values

    The biggest challenge remains keeping ahead of the curve—responding to the shifting needs of both lab-scale innovators and industrial expansion projects. Experience shows us the world rarely rewards standing still. Changes in regulatory landscapes, equipment upgrades, and supply volatility force continual revision of best practices. We lean on operational flexibility, a data-driven approach to troubleshooting, and a willingness to invest in improved analytical tech.

    Real-world chemistry never unfolds in a vacuum. Chemical manufacturers must balance production targets with a responsibility to both customer and environment. Our commitment to open communication, clear documentation, and reliable delivery shapes every day’s work—creating a role for (2-Chloro-Pyridin-4-Yl)-Methanol that endures beyond its chemistry.

    Final Reflections: Experience Shapes Deliverables

    Reflecting on years spent at the intersection of product manufacture and customer expectation, we have learned that every lot represents more than a transaction. It’s a testament to practical know-how, transparent process, and a shared investment in research success. By engaging with end users, refining plant operations, and anticipating where innovation intersects with compliance, we have positioned (2-Chloro-Pyridin-4-Yl)-Methanol as more than a chemical; it marks a strategic tool trusted by scientists pursuing the next breakthrough.

    As markets evolve, demand surges, and technical hurdles arise, the principles guiding our work remain grounded in personal accountability and the ongoing pursuit of better science. The story of (2-Chloro-Pyridin-4-Yl)-Methanol—shaped not in abstracts, but in results—continues to unfold, drawing on shared lessons, everyday problems solved, and a commitment extending from our plant floor to your laboratory bench.