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HS Code |
315494 |
| Productname | 2-Hydroxy-6-PyridineCarboxylicAcid |
| Chemicalformula | C6H5NO3 |
| Casnumber | 16712-64-4 |
| Appearance | White to off-white solid |
| Meltingpoint | 205-210°C |
| Solubility | Soluble in water, ethanol |
| Purity | Typically >98% |
| Boilingpoint | Decomposes before boiling |
| Pka | 2.6 (carboxyl group), 9.7 (hydroxyl group) |
| Synonyms | 6-Carboxy-2-hydroxypyridine, 2-Hydroxy-pyridine-6-carboxylic acid |
| Structuretype | Aromatic heterocycle |
| Storageconditions | Store at room temperature, tightly sealed |
As an accredited 2-Hydroxy-6-PyridineCarboxylicAcid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2-Hydroxy-6-PyridineCarboxylicAcid, sealed with a screw cap and labeled with safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 12.5MT packed in 500kg jumbo bags, suitable for safe bulk transport of 2-Hydroxy-6-PyridineCarboxylicAcid. |
| Shipping | 2-Hydroxy-6-pyridinecarboxylic acid is typically shipped in tightly sealed containers to prevent moisture absorption and contamination. It is handled as a non-hazardous, stable compound under standard conditions. Proper labeling and documentation are required, and the shipment should comply with local regulations for chemical transport. Store and ship in a cool, dry place. |
| Storage | 2-Hydroxy-6-pyridinecarboxylic acid should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Minimize exposure to moisture and direct sunlight. Ensure proper labeling and avoid sources of ignition. Use secondary containment to prevent spills and always follow institutional and chemical safety guidelines. |
| Shelf Life | 2-Hydroxy-6-pyridinecarboxylic acid typically has a shelf life of 2-3 years if stored in a cool, dry place, sealed container. |
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Purity 99%: 2-Hydroxy-6-PyridineCarboxylicAcid with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal impurities. Molecular Weight 139.11 g/mol: 2-Hydroxy-6-PyridineCarboxylicAcid at molecular weight 139.11 g/mol is used in coordination chemistry studies, where it provides reliable complex formation with metal ions. Melting Point 184°C: 2-Hydroxy-6-PyridineCarboxylicAcid with a melting point of 184°C is used in thermal analysis applications, where it offers consistent thermal stability. Particle Size <10 µm: 2-Hydroxy-6-PyridineCarboxylicAcid with particle size less than 10 µm is used in fine chemical manufacturing, where it allows for homogeneous mixing and reaction efficiency. Stability Temperature up to 120°C: 2-Hydroxy-6-PyridineCarboxylicAcid stable up to 120°C is used in catalyst formulation, where it maintains integrity and activity under reaction conditions. Water Solubility 25 mg/mL: 2-Hydroxy-6-PyridineCarboxylicAcid with water solubility of 25 mg/mL is used in biochemistry assays, where it ensures rapid dissolution and accurate dosage. UV Absorption 275 nm: 2-Hydroxy-6-PyridineCarboxylicAcid exhibiting UV absorption at 275 nm is used in analytical method development, where it facilitates sensitive detection and quantification. Storage Stability 24 months: 2-Hydroxy-6-PyridineCarboxylicAcid with storage stability of 24 months is used in chemical inventory management, where it reduces risk of degradation and loss of efficacy. |
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Producing 2-Hydroxy-6-PyridineCarboxylicAcid, known among our team as HPCA, takes both careful planning and precise control over our reaction setups. This compound, with the molecular formula C6H5NO3, stands out because of its unique pyridine ring entry at the sixth position and the addition of a hydroxy group at the second. We have focused years of development on dialing in the process conditions — particularly pH, temperature stability, and solvent selection — to secure material that meets exacting purity and color benchmarks demanded by downstream chemical processes, especially for pharmaceutical intermediates and metal chelating agents.
Producing HPCA is not about running boilers and glass reactors on autopilot. Every batch brings slight differences in crystal morphology and particle distribution, and we keep tabs on these shifts. For this product, purity above 98% by HPLC is not negotiable in our own workflow, and though standard powder grain sizes work for many, our reactors can shift toward a finer or coarser cut if a research group or specialty user needs it. While competitors sometimes batch-blend for the numbers, we check the crystallization endpoints in real-time fluorescence assay and confirm processing temperature never exceeds 90°C at sensitive steps, ensuring the hydroxy and carboxylic groups retain the reactivity researchers and industrial chemists require.
Many in the lab world ask about use-cases for 2-Hydroxy-6-PyridineCarboxylicAcid. This molecule feeds directly into the synthesis of complex metal chelates and acts as a ligand or scaffold for novel catalysts. For folks doing analytical chemistry, the right isomer placement means improved selectivity during metal ion detection or even enhanced chromatographic resolution. People who work in bioactive molecule design appreciate a pyridine core that doesn’t complicate final product isolation. Keeping the hydroxy at position 2 and the carboxylic group at position 6 eliminates byproduct confusion for most functionalization chemistry, as compared to using similar compounds with functional groups placed differently. Our proof-of-concept runs with pharmaceutical partners have shown that many downstream transformations—like esterification or amide coupling—proceed more efficiently with this precise orientation.
The difference in utility vs. isomers like 2-Hydroxy-5-PyridineCarboxylicAcid or 3-Hydroxy-6-PyridineCarboxylicAcid is significant. Even a single shift in attachment point changes the electronic distribution around the ring and can completely block a synthetic route or create unwanted side products. This is where we think direct experience matters. Early batches for new clients sometimes required us to troubleshoot odd precipitation patterns or find the solvent mix that kept solubility high during scale-up. Over time, our process eliminated these catches, delivering a product line that doesn't clog filters or interfere with analytical endpoints.
Manufacturing a product like HPCA doesn’t mean only following a recipe from a textbook. This is a business driven by statistical process controls, not just theory. Different feedstock batches, small fluctuations in water content, or a brief misstep in temperature ramping can throw final product color off from white to slightly beige. Our team runs each lot through a drying protocol after crystallization, then monitors infrared peaks to assure full conversion.
Sometimes, customers working on new ligand systems need extra data on how the hydroxy and carboxyl moieties affect binding constants with various metals. Since our plant runs high-throughput analysis on each lot, we’ve compiled years of empirical data on how reaction rates and chelation abilities relate to minor batch-to-batch differences. This comes in handy for any researcher struggling to reproduce results or scale up a promising bench reaction. We share this information freely—it’s as valuable to us as to users, since ongoing collaboration pushes our own production practice further.
A key lesson we’ve internalized is that consistent outcomes hinge on transparency with customers over physical properties. For instance, a chemist working in catalyst development asked us to modify the habit and mesh distribution for HPCA after finding agglomerated particles slowed their dissolution step. Based on their input, we adjusted our crystallizer agitation protocol, optimizing the runtime and solvent ratios to create a flowable, dust-free powder that mixed into their solvent blend in half the time.
Another real-world challenge surfaced with researchers designing sensor platforms. Trace metal contamination can skew results beyond correction. We responded by investing in more rigorous final product rinses and an in-house metal analysis protocol (ICP-OES with detection at sub-ppm levels). Delivering a product at less than 1 ppm total trace metals avoided unexpected interference, in turn helping these researchers disclose accurate sensitivity figures in their publications.
The small tweaks to production—tighter sieving regimes, antistatic steps during packaging, or tailored drying temperatures—often come from feedback cycles with universities and industry groups testing our product. These are not abstract upgrades. Saving customers half a day in column clean-up or letting them set up larger reactions with confidence drives both our satisfaction and theirs.
Most 2-Hydroxy-6-PyridineCarboxylicAcid we send to market ends up in three main avenues: ligand synthesis for catalytic research, fine-tuning of pharmaceutical intermediates, and as a metal ion probe base for analytical chemistry. In ligand science, the dual functionalization (hydroxy on position 2, carboxy on position 6) enhances chelate stability, which can boost catalytic turnover numbers, especially in transition-metal chemistry.
Pharma contract customers often need certainty over isomeric purity. Small differences in position misassignment create knock-on problems during late-stage drug modification. Since we monitor for isomer content by both NMR and 2D HPLC, our teams claim clean build-up every time. Larger research outfits say these assurance steps clear the way for robust preclinical batch supply.
Labware designers using HPCA in ion detection platforms hinge their research on background purity. Our low-metal lots and clear documentation allow them to calibrate sensors reliably, leading to reproducible data sets for environmental monitoring and process analytical applications.
The product also finds its place as a scaffold in agrochemical research, particularly when scientists want to tune the biological activity of crop protection agents through selective ring modification. Real feedback tells us our high-purity, precisely characterized HPCA streamlines regulators’ review of new molecular entities in the field.
We field requests every quarter from synthesis groups that previously used 6-hydroxynicotinic acid or 4-hydroxy derivatives. Many switched after observing our HPCA delivered higher metal chelate formation rates and produced fewer colored impurities during oxidative step reactions. Post-delivery follow-up uncovered less need for multi-step purification among users, resulting in more predictable lot-to-lot performance and less wasted reagent.
It’s these simple comparisons that drive process improvements in our plant. There’s no perfect molecule for every chemist’s needs, but open discussion of where HPCA offers a stronger or more selective reactivity window helps focus our upgrades. Partners working with macrocyclic ligand systems said they favored our compound because it plugged directly into their blueprint reactions, trimming both synthesis steps and waste compared to alternatives.
Our sales and technical support log dozens of requests each year for documentation on solvents and residual processing agents. In nearly all cases, disclosure of residual water, specific surface area measurements, and spectral purity data puts end users in a better position to choose between HPCA and the next best candidate. Download statistics show technical data sheets, run history, and impurity spectra are as valuable as the main batch itself.
The journey to reliable manufacturing starts with reliable teams. Our plant operators, some with more than 15 years of experience, have techniques to handle HPCA’s sensitivity to over-drying or poor pH control. For instance, overly aggressive drying can brown the product or make it static-prone, raising the risk of dustiness and improper weighing. By splitting drying into staged intervals, operators preserve both the appearance and dispersibility of the powder.
Agitation rates determine particle size, but the solvent makeup holds equal power in determining batch clarity. Early on, balancing methanol and water content led to the occasional gummy intermediate. Teams adjusted sequence and mixing energies to solve this—behind-the-scenes tweaks rarely captured by specsheets, but obvious to anyone running a full-scale reactor.
Our analytical staff go beyond batch COA requirements, running repeat melting point checks and extending chromatography paneling when customer requests suggest a hint of unwanted carry-over. This habit grows from real troubleshooting sessions in the field, not a push for marketing points.
No two 50-kilo batches of HPCA behave exactly the same. Raw feedstocks change slightly in moisture or minor impurity content over the seasons. We created in-house batch correction protocols, using in-line sensors and frequent lab pulls to adjust target concentration and endpoint pH. These procedures evolve as new data rolls in—and production teams discuss at regular intervals what trends and micro-variations could throw off the coming month’s output.
Holding both flexibility and batch reproducibility means building in time for practical reruns if a specific lot drifts off-target. Whether the need is for extra-dry HPCA for moisture-sensitive synthesis, or a micronized cut suitable for certain catalyst supports, plant schedules stay rigid enough for volume clients but nimble enough for R&D orders. Fielding these special requests brings customers back, and their unique project needs fuel continual tweaks.
Documentation trails for each lot, including processing logs, spectral scans, and batch notes, offer not only traceability but data to respond to critical inquiries during scale-up or regulatory filing. As a factory making value-added chemicals, we share lot data proactively with recurring clients who want to address potential out-of-spec shipments before issues surface in their own plants.
On a practical level, 2-Hydroxy-6-PyridineCarboxylicAcid separates itself from other pyridine acids by the pattern of ring substitution and their effect on both reactivity and solubility. Researchers who use the 3- or 4-hydroxy counterparts usually see differences in coupling efficiency, chelation geometry, or even product shelf-life. Feedback confirms HPCA’s stability in both acidic and neutral storage outpaces similar compounds, with less background discoloration and no unusual hydrates forming after long-term storage.
Compared to unsubstituted pyridinecarboxylic acids, HPCA brings a balance of hydrogen bonding and resonance stabilization that underpins its solid performance in specialty organic reactions. Colleagues running pilot plant trials for macrocycle synthesis told us HPCA’s hydroxy/carboxyl combination offered new access routes that failed when using methylated or aminated variants, likely due to electronic and steric effects unique to this ring arrangement.
In trace metal screening and environmental analysis settings, isomeric placement and cleanliness stand out. Analytical end users who previously relied on more common pyridinecarboxylates reported baseline interference or fading sensor response—issues essentially solved when switching over to our HPCA grade, given our tighter impurity and residual metal controls.
Having full control of production delivers benefits for both safety and sustainability. Our plant recycles solvents wherever feasible, and we recover pyridine raw material from spent streams—cutting both environmental impact and input costs for downstream batches. Local compliance teams regularly test air and water releases from the site, not just for the sake of formal audits, but to avoid the knock-on effects that could limit site uptime or lose a critical operating license.
Handling HPCA doesn’t raise unusual hazards compared to similar organic acids, but it does demand standard dust control and personal protective routines. Over the years, we’ve shared best practices with both new staff and customers picking up the product for the first time, from suggested minimum ventilation rates to simple suggestions on order-of-addition in solvent blends to avoid erratic solubility or caking.
Crafting 2-Hydroxy-6-PyridineCarboxylicAcid to the quality expected by pharmaceutical, chemical, and analytical teams comes from years of iteration, dialogue, and respect for chemistry that’s both technical and practical. The lessons learned from every anomalous crystallization or customer phone call feed right back into our batch planning and new product development. If a next-generation material requires even tighter purity, a different particle size, or specific solvent pairing, those specs filter into both our lab trials and full-scale production plans. We welcome ongoing feedback.
Standing in the shoes of anyone who has weighed, filtered, or reacted with HPCA in the lab, we think our focus is better outcomes at the bench or plant—fewer interruptions, tighter data, and tangible value from each shipment. Our manufacturing knows nothing replaces experience and persistence in delivering the right material for evolving chemical needs.