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HS Code |
569080 |
| Iupac Name | 5-hydroxy-6-propylpyridine-3,4-dicarboxylic acid |
| Molecular Formula | C10H11NO5 |
| Molar Mass | 225.20 g/mol |
| Cas Number | 2492-59-1 |
| Appearance | Solid |
| Melting Point | Approximately 210-214°C |
| Solubility In Water | Slightly soluble |
| Chemical Class | Pyridinedicarboxylic acid derivative |
| Functional Groups | Carboxylic acid, hydroxyl, propyl |
| Smiles | CCCc1ncc(C(=O)O)c(C(=O)O)c1O |
As an accredited 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a sealed amber glass bottle, labeled, containing 25 grams of 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl-. |
| Container Loading (20′ FCL) | 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl- is loaded in 20′ FCL drums, securely packaged to prevent contamination or leakage. |
| Shipping | The chemical **3,4-Pyridinedicarboxylic acid, 5-hydroxy-6-propyl-** should be shipped in tightly sealed containers, clearly labeled, and protected from moisture, light, and extreme temperatures. Ensure compliance with local and international regulations regarding the transport of laboratory chemicals. Appropriate safety documents and Material Safety Data Sheets (MSDS) must accompany the shipment. |
| Storage | 3,4-Pyridinedicarboxylic acid, 5-hydroxy-6-propyl- should be stored in a cool, dry, and well-ventilated area, away from sources of heat and direct sunlight. Keep the container tightly closed and protected from moisture and incompatible substances such as strong oxidizers. Store in a designated chemical storage cabinet with appropriate labeling to ensure safe handling and prevent contamination. |
| Shelf Life | Shelf life of 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl-: Typically stable for 2-3 years if stored dry, cool, and sealed. |
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Purity 98%: 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl- with purity 98% is used in pharmaceutical synthesis, where it ensures high yield and low impurity levels in active pharmaceutical ingredients. Molecular weight 211.2 g/mol: 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl- of molecular weight 211.2 g/mol is used in analytical chemistry research, where it enables precise calibration for quantitative analysis. Melting point 185°C: 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl- with a melting point of 185°C is used in high-temperature reaction protocols, where it maintains stability and prevents decomposition during synthesis. Stability at pH 7: 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl- stable at pH 7 is used in buffer formulation studies, where it preserves chemical integrity over extended storage periods. Particle size <50 microns: 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl- with particle size less than 50 microns is used in fine chemical compounding, where it enhances uniform dispersion and mixing efficiency. |
Competitive 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl- prices that fit your budget—flexible terms and customized quotes for every order.
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Inside our plant, where chemical syntheses meet practical applications, we work hard to supply advanced intermediates that let researchers, analysts, and formulation chemists push their boundaries further. 3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl-, known within our labs as a tailored pyridine carboxylic acid derivative, grew out of direct requests from pharmaceutical partners and agrochemical developers searching for high-purity, reliable starting materials. Its journey from bench-top reactions to commercial batches reflects more than a formula; it carries experience, troubleshooting, and trust in every bottle.
The batch we offer carries a model long tested by our QC team. Crystalline powders show up as off-white to pale yellow, sometimes trending to slightly tan with gentle oxidation on exposure to light—never pure white, owing to both the molecule’s structure and our avoidance of over-bleaching steps that cripple downstream reactivity. Melting points hover at consistent ranges, a direct result of monitored temperature ramps and staged recrystallizations. Every kilo processed under our roof passes repeat screening for moisture, residual solvents, and assay by HPLC, so specifications match the needs of kinetic studies, scale-ups, and pilot runs.
Research chemists tell us repeatedly: small modifications in pyridinedicarboxylic acids can drive entirely new behavior in their active molecules. The 5-hydroxy and 6-propyl substitutions turn what could have been another basic scaffold into a more functionally rich intermediate. Those extra groups set reactivity at precise points, letting enzymatic studies or cross-coupling chemistries proceed where the classical 3,4-pyridinedicarboxylic acid would have been silent. We have seen its role extend into heterocyclic ring formation, kinase inhibitor research, and crop protection agent development where specific ligand patterns hinge on the placement of a single hydroxy or alkyl arm.
Technical teams in our partner labs look for consistent reactions each time, not just at the five-gram scale. For them, a batch of 3,4-pyridinedicarboxylicacid, 5-hydroxy-6-propyl- that shows variable solubility or an odd impurity profile means weeks lost in troubleshooting. We have invested in parallel batch validation, so researchers are not stuck questioning their solvent system or protective groups every time the order arrives. Instead, they see matching TLC mobility and LC-MS profiles with every drum, a result of both recipe fidelity and instrument upgrades on our end.
Classical pyridinedicarboxylic acids see broad use in ligands, chelating agents, and polymer backbones. What sets 3,4-pyridinedicarboxylicacid, 5-hydroxy-6-propyl- apart is the direct impact of the hydroxy at 5 and the propyl at 6 on the electron density and steric profile. A straight-chain alkyl isn’t just a plug; it opens up opportunities for solubility tuning, pi-stacking disruption, and selective enzymatic oxidation. In our scale-up work, product managers traced a significant improvement in catalyst compatibility during Suzuki couplings when researchers replaced unsubstituted variants with our propylated version.
Synthetic routes for this product also allow for greater control over regioisomeric purity. Many competing materials, especially those from process routes not using mild oxidizing agents, carry double-migration errors or mixed substitution. We undertook in-depth NMR and chromatography work to confirm a sharp isolable main product—avoiding batch-to-batch drift that haunted the open-market material. Analytical transparency is something we train our production chemists in every day, from spot-checking the oxidation profile in mid-synthesis to cross-confirming the final crystalline product under polarized light and FTIR.
Every time we ship this specialty acid, project leads ask about the application tips. In our experience, the 5-hydroxy functionality lends itself well to etherification, acylation, or directed ortho-metalation, kicking off selective modifications that classic parent scaffolds refuse to permit. The propyl sidechain tolerates standard hydrogenations, Grignard additions, and even the presence of alkyl radicals—something not always true with bulkier or branched analogues. Whether you dissolve it in methanol, DMF, or a buffered aqueous solution, you get defined behavior when handled under dry or mild neutral conditions.
Where we’ve seen customers struggle is in fast-swap reactions (microwave or flow chem), where trace moisture or unexpected side reactivity can paint the product darker than the near-pale baseline. Our technical team responds by running compatibility panels in-house, alerting customers if their current solvent systems or heating profiles fall outside our tested safe zones. This level of guidance builds confidence for anyone running library syntheses, scale-up optimizations, or even regulatory filings for downstream actives.
We produce a range of pyridine derivatives—differences extend beyond a single substituent. Bench-scale users sometimes ask: “Why not just use the unsubstituted acid?” From our years in production, subtle modifications make or break compatibility with modern synthetic and biological targets. Other pyridinedicarboxylic acids in our range often miss the dual hydrophilicity and slight hydrophobicity this product demonstrates. The hydroxy-propyl combo carves out a workable space between full water solubility and retention in organics. This lets researchers dial up or down the polarity to suit new API precursors or polymer building blocks.
Compared to analogues with bulkier side chains, the 6-propyl avoids steric crowding, giving enzyme-mimetic chemistries more access to both carboxyls and avoiding inhibitor “dead ends.” Materials with halogens or branched chains elsewhere on the ring often build in rigidity, slowing down functional group exchange or binding. Our 5-hydroxy-6-propyl model keeps flexibility, essential for dynamic interactions in assay work or structure-activity relationship (SAR) mapping.
Problems with commercial pyridine carboxylic acids most often come down to unreliable production controls. We have learned that small deviations in reaction time, acidity, or even feedstock source corrupt the final product—and those errors sneak through bulk blending. Our plant design and batch record system emphasize stage-by-stage isolation with in-process checks, stopping poor batches before they hit the drum or warehouse.
Trace metals, residual solvents, and thermal decomposition products plague those sourcing from indirect or overseas routes. To avoid these risks, every lot faces a battery of analyses—ICP-MS for metals, GC for solvent traces, UV for byproduct comparison, and standard titrations for carboxylic acid content. Our investment in digital inventory controls and staff retraining pays off in clear transparency; customers see how we define and deliver each lot, not just a summary of “meets typical spec.”
Production chemists on our team take pride in measuring actual material output alongside commercial-grade paperwork. Inspectors confirm that every bottle shows the right crystallinity, expected melting behavior, and a distinct odor profile. Incoming customer QA staff often remark that sensory checks—feel, smell, easy handling—set our material apart before they ever run a lab-based test.
We’ve kept listening to feedback from synthesis leads and project managers at client research organizations. In one recent survey, over eighty percent noted downtime costs from inconsistent or underlabeled materials—a legacy of supply chain shortcuts. Their formulation work benefits directly from knowing every shipment lands with updates, run notes, and test lot archives. We hear about productivity gains whenever new batches integrate seamlessly without shaking up their SOPs.
Failures or setbacks in API intermediates often start with a mischaracterized input; by working directly as the manufacturer, our teams can quickly troubleshoot or replace material. In one pharmaceutical development project, a customer’s pilot run hit a roadblock due to impurity “spiking” that crept in from older, vendor-blended stock. Our technical support team initiated side-by-side analyzes and provided a fresh, in-house lot—tracing the issue to insufficient vacuum drying at their previous supplier. This field engagement sets us apart, as there’s no middleman downtime or vague accountability.
Some of our most significant improvements started with pain points from actual production runs. Standardized drying ovens brought better reproducibility, but small tweaks in airflow or rack tightness made a real difference in moisture content and crystal form. The transition from acetate-based extraction to salt-based workups provided better yields and sharper purities. These are changes you do not see on a typical specification sheet but show up in the lab, where less time spent recrystallizing equates to real savings.
Analytical surprises—unexpected isomer peaks or mild decomposition under UV—forced us to review steps from raw material vetting to packaging. Each year, our end-of-year review dives deep into field return data. If a single shipment shows color drift, solubility loss, or more than trace off-odors, we backtrack and revalidate the affected steps. This ongoing process means that we keep the product dependable through changing environmental regulations, new supplier checks, or seasonal climate shifts in shipping.
Trends in medicinal chemistry and advanced material science never rest. Biologists demand tighter controls on byproduct levels for in vivo studies; formulation teams want easier solubilization with fewer co-solvents. Our R&D and production arms collaborate in response, running small-lot process experiments and packing in feedback from early adopters.
Environmental and regulatory demands keep tightening. For us, this means not just filling out SDS sheets or hazard labels but proactively switching to greener solvents, implementing energy-efficient cooling for crystallization, and offering detailed traceability. Every kilogram of 3,4-pyridinedicarboxylicacid, 5-hydroxy-6-propyl- reflects these operational choices, from improved recycling to source verification. We take customer sustainability needs seriously, updating our process streams and communicating new certifications as soon as they arrive.
Evolving project needs often push us to pilot small-batch, high-purity runs or create alternate packaging that better suits handling in microgram and milligram scales. This feedback loop, direct from users, shapes our future batch offerings and keeps our product lineup both fresh and dependable for an industry that cannot afford surprises.
Our role as manufacturer includes helping customers handle material safely and effectively. Each outgoing batch comes with up-to-date usage and storage notes rooted in our own plant experience: keep containers tightly closed, avoid unnecessary exposure to open air or high humidity, and always use appropriate PPE in formulation spaces. Technical teams can request on-site demonstrations or remote walkthroughs if scaling from test tube to multi-kilo is new to their facility.
Case stories from client R&D labs show that properly handling this acid—from bench to production vessel—prevents losses and contamination. If a customer experiences sudden shifts in solubility or unexpected reactivity, our specialists are on hand to walk through protocols and double-check their workflow. We know firsthand that minor environmental differences—airflow, outdated desiccants, or solvent residues—result in unpredictable outcomes, and we help teams adjust to those real-world variables.
Success in specialty chemicals owes more to trust and performance than to paperwork or marketing. Our focus on hands-on, process-rooted manufacturing pays off where generic supply chains fail. By sharing our experience, documenting real changes, and keeping the conversation open between lab teams and production engineers, we keep improvement underway at every scale.
3,4-Pyridinedicarboxylicacid, 5-hydroxy-6-propyl- embodies this approach: precise chemistry, stable lots, transparent support lines, and honest admission of both strengths and learning curves. We welcome feedback—by phone, email, or site visit—so future production matches the tough, shifting realities of advanced chemical research and industry.
Chemical manufacturing is not a static tradition for us. Each success builds on troubleshooting, partnership, and ongoing learning—values that underpin our commitment to producing advanced pyridinedicarboxylic acids right, every time.