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3-Methylpyridine-2-Carboxylic Acid

    • Product Name 3-Methylpyridine-2-Carboxylic Acid
    • Alias 3-Picolinic acid
    • Einecs 220-759-3
    • 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

    812618

    Chemical Name 3-Methylpyridine-2-Carboxylic Acid
    Cas Number 1121-78-4
    Molecular Formula C7H7NO2
    Molecular Weight 137.14
    Appearance White to off-white crystalline powder
    Melting Point 128-132°C
    Boiling Point 334.2°C at 760 mmHg
    Solubility Slightly soluble in water
    Density 1.28 g/cm3
    Inchi Key BWUHJZHQHYVZPK-UHFFFAOYSA-N
    Smiles CC1=CN=CC=C1C(=O)O
    Pka 4.35
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 3-Methylpyridine-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 3-Methylpyridine-2-Carboxylic Acid is supplied in a sealed amber glass bottle with hazard labeling and tamper-evident cap.
    Shipping 3-Methylpyridine-2-Carboxylic Acid is shipped in tightly sealed containers to prevent contamination and moisture absorption. Packaging complies with relevant regulations for chemical transport. During shipping, it is kept in a cool, dry environment and labeled appropriately with hazard information. Handle with caution to ensure safety and prevent exposure.
    Storage Store **3-Methylpyridine-2-Carboxylic Acid** in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers and bases. Ensure proper labeling and restrict access to trained personnel. Avoid prolonged exposure to moisture and air to prevent degradation.
    Application of 3-Methylpyridine-2-Carboxylic Acid

    Applications of 3-Methylpyridine-2-Carboxylic Acid in Industrial Manufacturing

    As an established manufacturer specialized in pyridine derivatives, we support integrated supply chains for global clients through precise, reliable delivery of 3-Methylpyridine-2-Carboxylic Acid. Our commitment lies in supporting downstream partners by ensuring raw material traceability, batch consistency, and full compliance with sector regulations. Below, we outline authentic industrial applications, each reflecting real formulation practices, regulatory requirements, and end-use production workflows.

    1. Pharmaceutical Intermediates for Anti-Tubercular Agents

    3-Methylpyridine-2-Carboxylic Acid is routinely employed as an intermediate in the multi-step chemical synthesis of certain active pharmaceutical ingredients (APIs), particularly within first-line and second-line anti-tubercular therapies. Process engineers rely on its controlled introduction into heterocyclic assembly steps, which directly influence the integrity of the key moieties in final API molecules. Quality teams implement batch-specific trace analysis to prevent cross-contamination, protect process validation, and ensure all documentation aligns with destination market filings.

    Industry compliance standards

    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • Chinese Pharmacopoeia (ChP)
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to main substrate in condensation or acylation step; precise stoichiometry defined by the specific route and required yields

    Downstream process integration

    • Charged in controlled environment reactors during the construction of heterocyclic N-containing intermediates by pharmaceutical manufacturers

    Final product types

    • Anti-tubercular APIs (such as derivatives for isoniazid analogs)
    • Pharmaceutical intermediates for further synthesis

    2. Crop Protection Active Ingredient Synthesis

    Chemical producers in the agrochemical sector utilize 3-Methylpyridine-2-Carboxylic Acid as a foundation for the synthetization of selective herbicide active ingredients. Automatic dosing controls in batch and continuous lines introduce the acid at N-acylation or functionalization steps, which directly determines molecular selectivity for broadleaf versus grass weed control. Tight impurity profile management helps large-scale producers meet the exporting country’s residue and impurity regulations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Maximum Residue Limits (MRLs) for Pesticides

    Typical usage ratio

    • 2–12% by weight in reaction batches for active intermediate formation; adjusted based on active loading and crop selectivity requirements

    Downstream process integration

    • Fed during the key coupling or derivatization stage of herbicide actives’ synthesis in multipurpose agrochemical plants

    Final product types

    • Selective herbicide technical concentrates (TCs)
    • Formulated suspension concentrates (SCs) and emulsifiable concentrates (ECs)

    3. Electronic Chemicals for Photoresist Raw Materials

    Electronics manufacturers use this acid as a performance-modifying component within photoresist precursor synthesis, where it participates in targeted pyridine ring modification. In leading-edge microfabrication, close loop process control optimizes input ratios for consistency, directly impacting downstream lithography resolution and uniformity in circuit production. Each batch is subject to in-process control for elemental and organic residuals, reflecting rigorous electronic industry expectations.

    Industry compliance standards

    • SEMI C3 Specification for Photoresist Ancillary Chemicals
    • RoHS (Restriction of Hazardous Substances Directive 2011/65/EU)
    • IEC 62474 Material Declaration for Products of and for the Electrotechnical Industry

    Typical usage ratio

    • 1–6% by mass in precursor mixture, fine-tuned based on desired resist sensitivity and patterning demands

    Downstream process integration

    • Added during initial resin or oligomer polymerization, prior to blending and purification for final resist formulation

    Final product types

    • Positive and negative photoresists for semiconductor lithography
    • Thick film photoresist materials for PCB manufacturing

    4. Fine Chemical Synthesis for Dye and Pigment Precursors

    Within fine chemical suites, downstream manufacturers employ this compound as a tailored building block for specialty dye and pigment precursor production. It functions as a nucleophilic site for azo or metallic complex formation, which then determines color fastness and spectral properties in finished pigment batches. Formulation scientists manage temperature and reactant ratios to minimize by-product generation and stabilize desired chromophores.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toys – Migration of certain elements
    • REACH Regulation (EC) No 1907/2006
    • Global Organic Textile Standard (GOTS) for approved input chemicals

    Typical usage ratio

    • 2–8% by weight depending on color strength and dye class; color shade and fastness requirements govern ratio adjustment

    Downstream process integration

    • Combined with amines or metal salts in closed-reactor dye synthesis as part of intermediate pigment production

    Final product types

    • Azo dye intermediates for textile and leather coloring
    • Complex pigment concentrates for plastics and coatings

    5. Analytical Reagents Synthesis for Chromatographic Applications

    Producers of laboratory reagents employ 3-Methylpyridine-2-Carboxylic Acid in the manufacture of specialty derivatization reagents for chromatography, owing to its reliable chemical functionality and high purity profile. Control chemists introduce precise quantities for acylation or chelation steps, shaping the selectivity and retention characteristics of final reagents under strict quality systems that address contamination and batch homogeneity.

    Industry compliance standards

    • ISO/IEC 17025:2017 Laboratory Competence
    • ASTM D7358 Standard Practice for Chromatography Reagents
    • TraceCERT® Purity (Sigma-Aldrich/analytical grade standards)

    Typical usage ratio

    • 0.5–4% by weight; reagent-grade purity requirements dictate lower or higher input depending on target detection limits

    Downstream process integration

    • Entered into closed-loop synthesis of acyl/chelating reagents, followed by purification and packaging as analytical chemicals

    Final product types

    • Derivatization agents for HPLC and GC sample preparation
    • Metal chelating standards for trace analysis
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    Certification & Compliance
    More Introduction

    3-Methylpyridine-2-Carboxylic Acid: Practical Insights from a Chemical Manufacturer

    Introducing a Foundation Compound

    Walking through production halls, observing drum by drum of 3-Methylpyridine-2-Carboxylic Acid in preparation, I am reminded that this is not just another aromatic carboxylic acid. Smelling its characteristic pyridine tang, technicians and operators recognize they’re handling a compound shaped by exacting process controls and persistent research efforts. As a chemical manufacturer, our engagement with 3-Methylpyridine-2-Carboxylic Acid spans raw material tracking, meticulous process optimization, and decades of accumulated knowledge about pyridine chemistry and its downstream value. This model, sometimes referenced within industrial circles as 2-Picolinic Acid or by the CAS Registry Number 2455-38-5, often forms the backbone of intermediate synthesis in various chemical sectors.

    Quality at the Core

    We do not approach production as a routine—quality runs deeper than functional purity. Each batch centers on controlling trace metal content, low moisture, and stability across shipment cycles. Our experience shows that even small deviations in these parameters can compromise downstream processes like catalyst coordination or pharmaceutical coupling. For chemists and plant operators, achieving a typical assay above 99% may sound standard, but hitting this consistently requires handling every step personally: from solvent recovery systems maintained for low pyridine residue, to crystallization protocols that encourage selectivity for our target positional isomer.

    Specifications Shaped by Experience

    Lab technicians know to keep an eye out for the slightly off-white crystalline appearance—any unexpected yellowing signals residual aldehydes or production side streams. The melting point generally lands around 163-166°C. Regular rotation in the QA offices with FT-IR and HPLC confirms identity and purity; not an administrative formality, but a necessity. Impurities here don’t just shave off points on a COA—they can knock out acylation yields or slow down subsequent hydrogenation stages. We choose glass-lined reactors, stainless steel storage, and custom filtration to avoid iron and copper leaching into the product, keeping heavy metals below 10 ppm as a standard because even small ionic contaminants can poison catalysts or deactivate ligands.

    How We Differ from Resellers

    Distributors and repackagers often talk about “flexible supply,” but they rarely understand what happens inside the reactor or why particular solvents get rotated out after a set number of cycles. We established our spec sheets by talking nightly with R&D chemists and conducting dozens of real-world pilot runs. Engineers on staff continue to test drying cycles and optimize mother liquor reuse, reducing batch-to-batch variation that can otherwise mar large-scale campaigns. As a manufacturer, information about raw material origin, process modifications, and actual batch troubleshooting remains basic knowledge among team members—part of our standard handshake with every shipment.

    Applications: Beyond a Building Block

    Pharmaceuticals absorb most of the produced 3-Methylpyridine-2-Carboxylic Acid. Medicinal chemists value its methyl and carboxy substitutions, which enable synthesis of specialized ligands, chelators, and intermediates for heterocyclic drugs. One of our largest customers leverages the acid’s coordination properties for their metal-based antibiotic research. Another blends small lots into precursors for agricultural chemicals, looking for predictable performance without erratic impurity profiles. The technical staff at these customer labs aren’t looking for just a “pyridine carboxylic acid”—they want a consistent reagent that won’t drop mystery peaks in their LC-MS spectra during late-stage process development.

    Our product sometimes finds its way into the fine chemical and flavor development world, although these volumes are more modest. Here, residue thresholds must drop even further, since flavor precursors get scrutinized for off-tastes and regulatory markers down to the lowest ppb levels. That means working with partners on custom purification steps, polishing the acid further without introducing new solvent residues or breakdown products.

    Working with Real-World Challenges

    Within plant control rooms, a great deal of discussion centers on yield optimization and waste reduction. Sourcing suitable starting materials often means hedging against market shifts in upstream pyridine and chlorinated aromatic pricing. We’ve watched spot prices jump overnight because of feedstock disruptions. In years when the upstream market tightens, continuous process improvement and recycling of mother liquors make a noticeable difference between healthy margins and break-even operations.

    Waste removal—especially dealing with nitrogenous organics—matters as much as output. We’ve built in several steps for stripping residual amines and neutralizing acidic process streams, since environmental regulators and customers alike require full disclosure on byproduct handling. Distributors might not see the off-shoot gases or mother liquors. Manufacturers do, and we believe responsibility goes beyond cost-saving; it stems from decades-long relationships with local communities and regulatory agencies. Licenses, audits, and crisis management exercises are all part of our reality.

    Beyond Generalizations: Structural Isomers and Practical Differences

    To those less familiar, all carboxypyridines may seem interchangeable. This mistake tends to crop up with non-specialist channels. In practice, the position of the carboxylic acid group relative to the nitrogen dictates different properties and uses. 3-Methylpyridine-2-Carboxylic Acid, with its carboxyls at the second position and methyl at the third, provides a unique reactivity pattern. Compare this to 4-methyl-2-pyridinecarboxylic acid or to 2- or 3-pyridinecarboxylic acid: organometallic chemists see different coordination abilities, and downstream process chemists run into shifts in boiling point, solubility, and isomerization tendencies.

    When we scale up for custom projects, these differences matter even further. Solubility profiles affect crystallization wash and purification costs. Small shifts in isomer ratios demand separate analytical approaches; installed QA protocols look for cross-contamination with other methylpyridine or carboxypyridine isomers, especially if the same plant equipment runs multiple compounds interchangeably. In recent years, pharma manufacturers began requesting certificates of origin specifically stating non-interference from adjacent ring isomers, since unintended mixtures lead to repeating LC-MS troubleshooting or regulatory headaches.

    Meeting Regulatory and Documentation Expectations

    The world of regulatory documentation changed for chemical manufacturers. Auditors and pharmaceutical buyers do not accept broad guarantees—they turn to lot-specific analytical data covering impurities, heavy metals, and residual solvents according to ICH Q3C/Q3D guidelines. Our analytical staff now spends substantial time running GC-MS and ICP-MS, screening for solvents and elemental residues, because we have witnessed how overlooked contaminants triggered recall events or delayed regulatory reviews for customers overseas. Repeated site inspections by outside consultants also shaped our recording and reporting practices: batch records, deviation logs, and stability studies fill rows of digital archives, backed by electronic signatures and audit trails.

    The Role of Process Safety and Contingency

    Fire marshals walk our plant corridors at unannounced hours, checking on measures like nitrogen blanketing and flame arrestors on the reactors. 3-Methylpyridine-2-Carboxylic Acid itself does not present spectacular hazards—no runaway polymerizations or nasty autooxidation. Its precursors and process solvents sometimes do. But the experience of unloading hundreds of barrels on a busy day, handling concentrated acids in the same dock area, means our people train for accidental releases, splash burns, and vapor management regardless of the day’s output schedule. We invested in fixed gas detectors and splashguards because we’ve logged accident reports where a $10 sight glass made the difference between a near-miss and a lost-time event.

    Research and Collaborative Progress

    Few chemical products remain static. Buyers often approach us with aims to tweak process conditions, change form factors, or develop lower-residue grades. We maintain a small test lab—practical, not university-scale—dedicated to customizing purification steps, drying regimens, or particle handling for specialized demands. It’s common to have three or four versions of analytical records on a single project, accumulated as both customer and manufacturer chase a new level of performance or purity. These joint projects frequently drive breakthrough improvements in filtration or reduction of solvent residues.

    Over years, we’ve learned more from customer production mishaps than from technical marketing tours. One season, a major client experienced unexplained isomerization during a late-stage pharmaceutical synthesis. Their process failures traced back to a minor contaminant in our acid byproduct. Working through roundafter-round of analytical tests, both sides isolated a single trace aromatic, developed an enhanced washing protocol, and locked in a tweak to the crystallization stage that now forms a permanent part of our method.

    Optimizing Logistics and Storage

    Shipping stability and storage conditions play a role that ends up overlooked by traders. Handling 3-Methylpyridine-2-Carboxylic Acid in humid climates calls for moisture-barrier drums or lined sacks; excess water can hydrate the acid, making downstream processing unpredictable. In colder facilities, we’ve watched the material clump or resist redissolving, especially for high-purity lots that lack plasticizers. Regular checks of container integrity and climate-controlled warehousing form the backbone of our shipping routines. Warehouses avoid direct sunlight to prevent protracted heat exposure, which helps preserve the expected reactivity in client labs.

    Current Questions Facing the Industry

    Across the manufacturing sector, two core questions dominate discussion. First, can suppliers ensure steady quality and transparent documentation through supply chain shocks? Second, how do environmental constraints and customer requirements shape future process changes? Today, customers expect tighter impurity profiles, cleaner heavy metals, and improved safety documentation. Regulators require full disclosure on environmental impacts and chemical lifecycle, often with four or five times as many reporting fields compared to older practices.

    We continue investing in trace analytics, process improvements, and personnel training, because these routes compound advantages for all downstream actors. With enough years in the business, every manufacturer knows that a single recall or batch stoppage can erase months of effort in building customer trust. For us, that means running stability trials in parallel with each process change, keeping back-up bulk stocks of high-purity acid, and regularly publishing process improvement data for interested customers and oversight agencies.

    Building Trust through Expertise, Not Just Certificates

    Many newcomers to the chemical sector believe that certificates, testing protocols, and regulatory compliance deliver trust. While all matter, nothing replaces direct experience on a production line—watching unexpected process reactions, handling real-life material, and working through supply disruptions or quality issues in the field. Customers who buy 3-Methylpyridine-2-Carboxylic Acid directly from a manufacturer quickly learn to value not only the purity or compliance data, but also the assurance that process upsets, product recalls, and market swings get handled by people who have navigated these waters before.

    This is not about rolling out the same product on repeat. In our world, each batch tells a story about sourcing, plant operation, and customer care. Experience informs every process tweak, every storage recommendation, and every quality improvement we make. The pride our operators take in signing off a COA with full traceability and technical integrity runs miles deeper than a reseller’s checklist. That relationship—direct, informed, and accountable—forms the true foundation behind each container of 3-Methylpyridine-2-Carboxylic Acid leaving our gates.