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HS Code |
531805 |
| Product Name | 3-Pyridylacetic Acid |
| Cas Number | 501-81-5 |
| Molecular Formula | C7H7NO2 |
| Molecular Weight | 137.14 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 140-144°C |
| Boiling Point | 338.2°C at 760 mmHg |
| Density | 1.273 g/cm3 |
| Solubility | Soluble in water, ethanol, and methanol |
| Pka | 3.95 |
| Iupac Name | 2-(pyridin-3-yl)acetic acid |
| Structural Formula | C5H4N-CH2-COOH |
| Synonyms | 3-Pyridineacetic acid; β-(3-Pyridyl)acetic acid |
| Refractive Index | 1.567 |
| Storage Conditions | Store at room temperature, keep container tightly closed |
As an accredited 3-Pyridylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Pyridylacetic Acid, 25g, is packaged in an amber glass bottle with a white screw cap, featuring a hazard label. |
| Shipping | 3-Pyridylacetic Acid is shipped in securely sealed containers to prevent contamination and moisture exposure. Packaging complies with relevant chemical safety regulations, including appropriate labeling and documentation. During transit, measures are taken to avoid extreme temperatures and physical damage. Handle with care upon receipt, following standard procedures for chemical storage and use. |
| Storage | 3-Pyridylacetic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature or as specified on the manufacturer's label. Handle with appropriate personal protective equipment to avoid contact and inhalation. |
Applications of 3-Pyridylacetic Acid in Industrial ManufacturingAs an established producer of 3-Pyridylacetic Acid, we serve a range of specialized industries leveraging the unique reactivity of this pyridine derivative. Our technical guidance supports downstream manufacturers with precise material application and integration for improved process yield and regulatory compliance. 1. Active Pharmaceutical Ingredient (API) Synthesis for Antihypertensive AgentsPharmaceutical manufacturers employ 3-Pyridylacetic Acid as a pyridine building block in the multi-step synthesis of antihypertensive APIs, notably those containing a pyridine moiety in their core structure. Strict control over contaminant profiles and residual solvents aligns with global pharmacopoeias. Material enters amidation or condensation reactions after being dissolved in appropriate solvents, reacting under controlled pH and temperature with defined coupling reagents. Final APIs then advance to purification, crystallization, and subsequent formulation as tablets or capsules. Industry compliance standards
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2. Agrochemical Intermediate ProductionSpecialty agrochemical synthesis plants utilize 3-Pyridylacetic Acid to construct herbicide and fungicide actives with improved environmental profiles and selective crop safety. The acid integrates into chlorination, esterification, or coupling steps that build target molecules. Formulators manage precursor ratios based on crop target and regulatory residue limits, processing material in closed-loop reactors to maintain product integrity prior to downstream formulation and dispersal as wettable powders or suspension concentrates. Industry compliance standards
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3. Fine Chemical Building Block for Dye Intermediate SynthesisFine chemical operations use 3-Pyridylacetic Acid as a precursor to synthesize pyridine-based dye intermediates, where electronic modification of chromophores is required for custom textile and leather application. The acid is introduced during the condensation phase with aldehydes or ketones, and further processed through subsequent cyclization or sulfonation units. Quality assurance teams monitor purity and residual pyridine content against textile and environmental standards before blending into dye formulations. Industry compliance standards
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4. Ligand Precursor in Custom Catalysts for Organic SynthesisIn the catalyst manufacturing sector, 3-Pyridylacetic Acid acts as a scaffold for tailored chelating ligands needed in transition metal catalyst complexes. Type and molar incorporation depend on metal center specification and desired electronic characteristics for downstream customer reactions. Operators dissolve and react the acid under inert atmosphere, attachment to metal or co-ligand structure occurring in temperature-controlled flasks. Finished catalysts undergo thorough QC prior to shipment to pharmaceutical and specialty chemical customers. Industry compliance standards
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With decades invested in fine chemical production, we never approach a new batch of 3-Pyridylacetic acid as routine. The molecule—often appearing as a white to off-white crystalline powder—holds a unique role in both pharmaceutical and agrochemical research. Unlike many general-purpose building blocks, its structure, featuring a pyridine ring linked to acetic acid, delivers more than just a functional group. Researchers in our facility recognize its versatility during amine coupling and heterocycle synthesis, which opens up distinct possibilities during medicinal chemistry projects.
Each batch, processed using carefully controlled parameters, consistently meets a minimum purity level of 98% (HPLC), catering to customers who expect a meticulous adherence to analytic performance. In our experience, pushing for higher purity lays the groundwork for dependable reactions and eliminates headaches further downstream—whether teams pursue small molecule API development or crop protection agents. The chemical’s CAS number (picolinic acid derivatives generally) distinguishes it firmly from pyridinecarboxylic acids, which behave differently under reaction conditions, especially in terms of solubility and side-reaction profiles.
Chemists gravitate toward this compound for its ability to serve as a practical scaffold. Several clients, from both academic and industrial labs, share direct feedback with our technical team after integrating our material into their workflows. We’ve observed teams use it to assemble pyridine-containing ligands, via direct amide or ester coupling. The carboxymethyl group activates the molecule for further transformations, providing an avenue to introduce new functionality efficiently.
In pharmaceutical research, we often field inquiries about making heterocycles that resemble natural alkaloids or electron-rich intermediates for bioactive compound screening. The specific substitution pattern on the pyridine ring in 3-pyridylacetic acid brings distinct reactivity, which we track with batch-to-batch analytical data. Compared to simple pyridine derivatives like picolinic acid or niacin, this acid offers improved synthetic accessibility, especially during condensation reactions or Grignard additions. Our facility uses modern glass-lined reactors with real-time monitoring to guard against off-spec batches; this attention to technical detail stems from years of collaborating with teams needing reliable starting materials under any project deadline.
Quality starts with precise raw material qualification, then strict handling protocols. We receive most raw pyridine feedstock under inert atmosphere, never exposing it to conditions that might trigger unwanted hydrolysis. Downstream, we store finished 3-Pyridylacetic acid in airtight drums, in climate-controlled spaces to maintain integrity above 98% purity for long intervals. Several technical managers in our team have seen overlooked humidity triggers leading to clumps or even discoloration with pyridine derivatives. To avoid such issues, we schedule quarterly stability testing and restrict the use of recycled drums.
Scale matters. Small batches allow us to experiment with temperature and crystallization parameters; large batches, which some biotech and pharma clients demand, require more rigorous controls to prevent trace impurities. Over years of scaling up, our standardized filtration and drying processes have been optimized to limit by-product formation, especially during acetic acid coupling. Less experienced operations sometimes overlook how residual solvents alter melting points or impact downstream purification, and our own chemists have used this learning to streamline cleanup steps, reducing solvent waste and increasing throughput.
In university spin-offs, our 3-Pyridylacetic acid often initiates exploratory reactions—testing how various catalysts behave as they seek efficient C–N coupling partners. We’ve seen demand spike for this compound within target-oriented synthesis, especially in early drug discovery. Larger fine chemical manufacturers ask for detailed impurity profiles, even for what appears to be “standard” white powder. Their downstream partners, often located in regulated markets, impose reproducibility standards that tolerate no variation from one drum to the next.
Project managers on our line track each shipment, confirming that each request—be it for a pilot or multi-kilo campaign—matches the project’s solubility, moisture, and trace metal specifications. We get questions about whether our material stands up to the demands of flow chemistry rigs or auto-sampler processes in high-throughput labs. Our QC experts draw on years of troubleshooting similar heterocyclic acids, sharing detailed notes with suppliers and clients alike. Reliable product characteristics become especially crucial during scale-ups, as teams must avoid unforeseen process changes due to minor impurities or hidden incompatibilities.
Researchers occasionally reach out for advice on differences among pyridine-based acids. The main distinction between 3-pyridylacetic acid and isomeric compounds—such as 2- or 4-pyridylacetic acid—lies in electronic and steric effects. From our own comparative batch tests, syntheses using 3-pyridylacetic acid as an acyl donor often proceed with smoother purification and less tendency for ring-opening byproducts. These isomers might share some application areas, but during pilot trials we traced improved overall yields and simpler workup procedures with the 3-substituted acid, particularly across HPLC purification runs.
Other commonly asked comparisons touch on price and availability. 3-Pyridylacetic acid requires a multi-step synthetic route with challenging controls over regioselectivity. Some vendors, cutting corners, supply material with off-target isomers—a practice we avoid by implementing multi-point NMR checks throughout production. The outcome is a product that saves our clients time during quality control and lets them focus on pushing science forward, not troubleshooting supply chain issues.
Every chemist knows that raw material variability torpedoes project timelines. Several of our largest pharmaceutical clients—many collaborating with us over a decade—point to our lot-to-lot reproducibility. Regular GC-MS and HPLC fingerprinting, including the reporting of trace impurity levels and residual solvents, drives confidence in downstream process qualification. We’ve invested heavily in this practice because, early in our manufacturing journey, we experienced headaches caused by inconsistent external suppliers. A collaborative effort between our QA and R&D teams led to the introduction of custom retention-time markers and internal controls, which allows for easier product qualification by advanced users.
Smaller biotech firms often ask for format flexibility. Besides the standard kilogram drums, we provide smaller packages suitable for bench-scale work—always with full analytic documentation. We avoid the temptation to cut corners with packaging, knowing from past recalls that moisture and trace oxidation can build up quickly in sub-optimal containers. Trust, for us, sits in these exact details: a stable product that behaves as expected, month after month, across any storage regime used by our partners.
Most end-users deploy 3-pyridylacetic acid as a synthetic intermediate, but we’ve helped clients adapt it for specialized ligand libraries and in radiolabeling protocols. The carboxylic group opens up further conjugation to peptides, dyes, and other pharmaceutical scaffolds. Over the last several years, our technical team supported joint development efforts with crop science companies pursuing safer and more effective treatments—applications where the unique electronic structure of the molecule leads to improved selectivity and performance.
Veteran process engineers, including those who have overseen hundreds of scale-ups, repeatedly cite the same advantage: predictable reactivity and minimal by-product formation compared to simpler pyridine acids. The practical outcome lands in higher yields per cycle, quicker chromatography runs, and less solvent waste—a trio of improvements that directly benefit both R&D budgets and production throughput.
Operating as a manufacturer means taking ownership of safety at each production step. With all pyridine derivatives, including 3-pyridylacetic acid, our plant team adheres to rigorous solvent recovery and waste handling protocols. Over the years, we’ve updated SOPs after observing tendencies for slow evaporation losses, especially during warm, humid weather. These seemingly minor tweaks—such as updated filter media and improved airlock controls—drastically reduce both product loss and occupational exposure risks.
Our relationship with local environmental groups, along with regular audits, keeps our disposal standards high. Unlike some firms operating with older venting systems, we chose to retrofit all acid lines with real-time VOC monitors. This choice increased upfront expenses, but led to safer work environments and more reliable supply to end-users within regulated industries. Our experience continues to show that responsible handling, not blind cost-cutting, supports stronger relationships and long-term business stability.
Real-world feedback from formulation scientists drives ongoing improvements in our production process. The distinct solubility profile of 3-pyridylacetic acid—freely soluble in polar aprotic solvents, moderately in water—matches its intended synthetic uses. Most teams using it in amide coupling reactions appreciate its low tendency to form emulsions during aqueous workups. Early batches, prior to refining our crystallization steps, sometimes left behind trace oily residues; today’s material, recrystallized to higher purity, streamlines both isolation and downstream conversion.
In cases where process changes have proven necessary, our chemists are available for troubleshooting: improvements such as modulating pH during coupling, or recommending drying agents to clients in high-humidity zones, often save a full day of lab work. Having manufactured diverse pyridine derivatives, we saw that some analogs with similar melting ranges behave unpredictably, forming stubborn by-products or showing low solubility under the same conditions. Our technical archive includes side-by-side reaction profiles compiled during method scale-up, and clients undertaking similar reactions frequently consult these archives to optimize their process.
Chemical production never remains static. Regulatory frameworks tighten, new performing agents crop up, and operational obstacles challenge established methods. Facing requests for custom modifications—higher purity, new solvent profiles, alternative counter-ions—forces us to stay flexible. For 3-pyridylacetic acid, we keep a small fraction of production lines ready for rapid adaptation, drawing upon lessons learned from both late-stage failures and early success stories. One ongoing lesson: continuous communication with end-users brings the clearest picture of emerging requirements.
Product traceability, paired with strong relationships between technical teams and customers, heads off most troubleshooting. During a recent scale-up requested by a pharmaceutical group, subtle shifts in temperature tolerance surfaced. Our in-house troubleshooting uncovered a reaction with batch-specific microimpurities, prompting a review and modification of precursor filtration. The corrected protocol became a new standard—an approach reflecting the kind of adaptive, experience-driven quality our partners have come to expect.
Price pressures mount across the specialty chemical industry, driven by global fluctuations in raw material costs and transport bottlenecks. Our choice to source directly from trusted feedstock partners, rather than generic commodity markets, shields our operations from some turbulence seen by others. Periodic raw material shortages prompt us to offer clients transparent lead time forecasts, and our in-house logistics team monitors each lot from synthesis through to shipping. Producing 3-pyridylacetic acid often means absorbing short-term supply swings on our end—not passing unexpected cutbacks or lapses in quality on to downstream users.
We continue working with customers to develop annual supply contracts, which address both volume discounts and stable lead times. Such arrangements have historically proven most resilient during periods of market volatility. Our clients, both large and small, reference the reassurance that their work won’t be derailed by out-of-spec materials or batch delays. Ongoing conversations with procurement teams across drug, agrochemical, and academic fields provide the clearest sign that reliability outpaces cost-cutting in real-world research environments.
When reviewing the journey of 3-pyridylacetic acid from lab-scale curiosity to industrial mainstay, hands-on manufacturing experience makes the difference. It’s more than just technical know-how—it’s a deep familiarity with process challenges, a willingness to adapt equipment and procedures, and an investment in analytic rigor that gives our customers an edge. This knowledge translates into fewer surprises, better yields, and a product that regularly exceeds expectations wherever precision, repeatability, and time-saving matter.
Our conversations with chemists, process engineers, and formulators—both local and international—reveal similar stories: a reliable feedstock triggers innovation, supports cleaner syntheses, and frees creative energy within the laboratory. For 3-pyridylacetic acid, this commitment to hands-on precision, supported by strong analytic backing, forms the foundation behind each shipment we send out. For anyone building tomorrow’s drug molecules, crop treatments, or specialty catalysts, the real value emerges in knowing exactly what’s in the drum, every single lot. That trust, built over years, sets our manufacturing approach apart, and drives us to constantly improve with each campaign.