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HS Code |
954756 |
| Iupac Name | tert-butyl 2,6-dichloropyridine-4-carboxylate |
| Cas Number | 875781-17-8 |
| Molecular Formula | C10H11Cl2NO2 |
| Molecular Weight | 248.11 |
| Appearance | Solid (data may vary) |
| Solubility | Soluble in organic solvents (e.g. DMSO, ethanol) |
| Smiles | CC(C)(C)OC(=O)C1=CC(=NC=C1Cl)Cl |
| Inchi | InChI=1S/C10H11Cl2NO2/c1-10(2,3)15-9(14)7-4-8(11)13-6-5-8(7)12/h4-6H,1-3H3 |
| Synonyms | tert-Butyl 2,6-dichloroisonicotinate |
| Storage Conditions | Store in a cool, dry place, keep container tightly closed |
As an accredited 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed in an amber glass bottle, 25 grams, tamper-proof cap, labeled with chemical name, hazard symbols, and handling instructions. |
| Container Loading (20′ FCL) | 20′ FCL: Packed in 200 kg HDPE drums, 80 drums per container, total net weight 16 metric tons, chemical-grade packaging. |
| Shipping | The chemical `4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester` should be shipped in a tightly sealed container, protected from light and moisture. Transport under ambient temperature, ensuring compliance with relevant hazardous chemical regulations. Include proper labeling and documentation to ensure safe and legal handling during transit. |
| Storage | Store 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep away from incompatible substances such as strong oxidizers and acids. Recommended storage temperature is between 2–8°C. Ensure proper labelling and appropriate containment to prevent leaks or spills. |
| Shelf Life | Shelf life of 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester is typically 2-3 years under cool, dry conditions. |
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Purity 98%: 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester with a purity of 98% is used in pharmaceutical intermediate synthesis, where it enhances the yield and reduces byproduct formation. Melting Point 85°C: 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester with a melting point of 85°C is used in melt-processing for agrochemical formulations, where it enables uniform dispersion during compounding. Molecular Weight 302.14 g/mol: 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester with a molecular weight of 302.14 g/mol is used in fine chemical manufacturing, where it ensures precise stoichiometry in multi-step synthesis. Stability up to 120°C: 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester with stability up to 120°C is used in thermally demanding organic reactions, where it maintains structural integrity and consistent reactivity. Particle Size <50 μm: 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester with particle size below 50 μm is used in catalyst preparation, where it provides increased surface area and improved reaction rates. |
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Speaking from the actual plant floor, few specialty esters draw as much attention among downstream industries as our 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester, often referenced by its systematic name but sometimes called tert-butyl 2,6-dichloronicotinate in research papers. Years of repeated synthesis and real-world shipments have shaped our understanding of its role, quirks, and the reliability that customers have come to expect. Production teams don’t see this molecule as a commodity, but as a purpose-built intermediate with specific performance edges in the field—especially for agrochemical and pharmaceutical developers who prioritize consistent yields in scale-up runs.
This compound features a classic pyridine ring, with chlorine atoms at positions 2 and 6, and a tert-butyl ester connected at the carboxylic acid site. In the lab and on the line, the formula stands as C10H11Cl2NO2. Over the past decade, technicians have worked through countless batches, ensuring every lot upholds rigorous purity standards, which are verified through HPLC and NMR—tools as common in our plant as forklifts and storage tanks. To be specific about grade, we shape all commercial lots with a minimum chromatographic purity of 98.5%, a standard not all suppliers strive to maintain batch after batch.
With each run, drying and final handling demand close attention; moisture, accidental overheating, or airborne particulate can turn an otherwise clean batch into a troublesome one. Our standard model comes as an off-white to pale yellow crystalline solid, often packed in double-lined, moisture-shielded drums to keep each shipment stable. Many research supply houses sidestep these steps, resulting in higher risk during storage and use—feedback we’ve heard directly from multinationals that struggle with unstable or discolored material from other sources.
Swapping an acid function for a tert-butyl ester opens new possibilities, especially for those developing pyridine-derived actives or intermediates. Through first-hand plant experience, it’s clear the tert-butyl group raises lipophilicity and alters reactivity compared to free 2,6-dichloronicotinic acid. Customers who run catalytic substitutions or nucleophilic additions find this molecule better survives synthetic routes, avoiding unnecessary hydrolysis or degradation. This translates into sharply higher yields during late-stage modifications and avoids waste during unpredictable scale-up. Reliable, reproducible performance isn’t marketing spin—it’s direct feedback from technical experts running kilo-scale reactions, many of whom tested alternatives before standardizing around this ester.
Our team fields application questions weekly—researchers, process chemists, and formulation scientists call in to talk through practical use cases. Over and over, synthetic chemists mention that the tert-butyl ester makes difficult transformations practical: reactions run at higher pH, broader solvent compatibility, less byproduct formation in double-substituted pyridinic scaffolds. In pharmaceutical R&D, this molecule often enters late-stage or convergent synthesis routes, serving as a masked acid for selective deprotection later in a sequence. Agrochemical formulators look for the high chlorine content on the ring, searching for compounds that show robust resistance to metabolic breakdown under sunlight or in the presence of oxidizing soil bacteria. Time and again, these teams cite the same result: with our 2,6-dichloro derivative, their runs produce purer, more consistent products with less risk of isomeric or decomposition byproducts.
Work doesn’t end after shipment; we stay in regular communication with end users during pilot programs. That feedback comes back to our process engineers and QC teams, sparking adjustments—whether in drying protocols, particle screening, or tightening acceptance specs around color and melting point. Many customers in analytical labs express relief at getting a crystalline, high-purity ester that weighs and dissolves cleanly, with no opaque residue or stubborn, sticky fraction from mother liquor. That’s not trivial, considering how impurities or cloudiness in a test run can set back weeks of development time.
Competitors try offering other methyl, ethyl, or isopropyl esters of dichloronicotinic acid, but hands-on feedback and real-world metrics tell a different story. Methyl and ethyl esters, for all their popularity, tend to hydrolyze too quickly in aqueous or mildly basic environments—leading to variable conversions and a headache in downstream purification. Isopropyl derivatives offer some added steric protection, but they rarely match the tert-butyl ester for stability across a range of temperatures and solvents. Synthetic routes that rely on acid or base deprotection steps concede less material loss and cleaner splits when the tert-butyl remains intact until the final stage.
In our facility, switching to or from non-chlorinated nicotinates has made clear that 2,6-dichloro substitution delivers unique reactivity. The electron-withdrawing nature of both chlorines influences the ring’s reactivity, blocking side reactions and shifting selectivity—findings supported by both bench chemists and scale technicians who have seen failures using less protected analogs. Those in R&D seldom return to single-chlorine or non-chlorinated versions after making the switch, unless regulatory or cost reasons force a change. Materials without the tert-butyl group invite unexpected hydrolysis, corresponding to lower process yields in real-world plant settings.
Scaling the process for this ter-butyl ester took years to perfect. Early plant runs taught us that high-purity output depends on solvent quality, reagent freshness, batch temperature control, and aggressive moisture management. We learned these lessons the hard way—not in theory, but through downtime, out-of-spec material, and frustrated chemists. Even now, careful isolation and drying protocols separate top producers from shortcut artists. The plant’s filtration arrays, rotary evaporators, and controlled atmosphere packaging lines stay tuned to the needs of this compound, not general rules cobbled together for bulk chemicals.
Trained staff pull reference spectra and melting point data before each lot release. NMR, HPLC, and mass spec readings are checked not by a distant third party, but by in-house analysts who work alongside the operations crew. This direct linkage from lab to plant allows us to catch and address drift in purity or morphology as soon as it emerges. As technical questions come in from research partners, these lessons feed right back into process adjustments—sometimes resulting in exceptionally tight particle size control or modified crystallization schemes. Every improvement grows out of direct use and tough feedback in actual synthetic campaigns, not theoretical selling points.
From experience, well-designed esters like this avoid unnecessary regulatory scrutiny thanks to established pathways for safe scale-up, consistent documentation, and proper employee training. Still, the presence of two chlorines on the pyridine nucleus means every operator stays alert for the potential release of harmful byproducts under extreme process conditions—such as accidental overheating or exposure to strong acids. The plant’s engineers run routine risk assessments and update procedures in line with changing best practices. Bulk users appreciate this commitment, knowing that hazard communication, waste disposal, and downstream handling are documented based on real-world use, not imagined scenarios.
We keep SDS sheets current by referencing production runs and actual incidents rather than relying on generic database entries. Onsite first aid and spill response protocols evolve with actual plant experience; mid-sized and large customers report they value this approach, as many distributors push paperwork that leaves users in the dark about unique properties or best containment steps.
Experience in logistics and warehousing taught us early on that the tert-butyl ester form offers far greater stability in transit than free acids, methyl esters, or volatile intermediates. Multinationals and contract research groups—those who order drums to ship globally—call out fewer issues with degradation, caking, or odor when working with our batches compared to fragile analogs. Our process avoids residual solvents known to catalyze breakdown, and the plant’s QA team backs every shipment with batch-by-batch analysis.
Customers find real-world difference in how the product endures in storage. The double-bagged drums used for larger orders block both moisture and atmospheric contaminants. Even after months under typical warehouse conditions, purity checks show little drop-off. Temperature swings and moderate humidity levels show minimal impact on product appearance or solubility—critical for chemists who need each shipment ready to use with minimal prep. This real stability spares chemists the surprise of opening a drum only to find discolored or clumped material, which can hold back entire project timelines.
Over several years, the quality-control lab has adopted stricter cutoffs on trace impurities, with regular audits and outside consultant input. QC teams take direct input from customer labs who push our material into GC-MS, NMR, and TLC screens, then demand results within defined tolerance bands. Every staff chemist knows that a few percent impurity in a kilo batch trickles down into outsized cleanup costs for the end user. This direct accountability makes batch-to-batch reliability more than a slogan—we tie QA targets to customer acceptance rates, using failed runs as hard lessons.
Unlike traders, we control the process from raw chlorinated pyridine uptake through esterification, to drying and dispatch. This keeps hands-on oversight and traceability tight from the start. Yearly investments into analytical infrastructure led to lower detection limits and better calibration—changes driven by feedback from advanced synthetic groups facing bottlenecks in their programs. We make a point to share relevant analytical data upfront, streamlining customer qualification runs and reducing waste.
Customers expect more than just a technical grade chemical—they look for a responsive supplier who adapts to unusual requests or sudden shifts in compliance regimes. Our internal team hosts regular technical sessions with upstream and downstream partners, learning where supply inconsistencies stall novel compound development. In practice, this gives us a head start resolving supply risks. Some of these incremental adjustments have included particle-size modifications tailored for specific reactors, custom lot documentation with process-specific details, and rapid response to regulatory update requests. Unlike some players, we do not believe in one-size-fits-all delivery; every inquiry starts with discussing actual application demands with technical staff, not just sales reps.
Working relationships with applied R&D teams inform how new syntheses roll out. We hear frequently from clients who struggled through unreliable sources, burned valuable hours troubleshooting subpar batches, or missed production windows due to out-of-spec material. Bringing those lessons in-house means our own production experts can anticipate issues and share tested advice with other chemists. It’s this ongoing loop—from lab feedback to plant-wide improvement—that sets the finished product apart from generic substitutes. Real development cycles rarely go as planned, and having a technical partner able to adapt based on experience saves measurable time and budget for end users.
Sustainability pressures shape every aspect of specialty chemical manufacturing. Our plant designers overhauled waste handling, solvent recovery, and air management in response to actual emission audits and client-driven green chemistry targets. Each process update, from batch changes to packaging upgrades, responds to both local environmental standards and practical customer advice. For this ester, proven solvent re-use protocols and energy-saving heating cycles help trim overall waste and lower risk footprints across sites.
Transparency isn’t just a buzzword. Disclosing process details, environmental metrics, and incident records stems from real inquiries by bulk users under due diligence. Some downstream buyers request chain-of-custody verification for regulatory signoff. Our digital tracking system, honed over production years, makes this a routine task. It also means that process improvements and compliance lessons get shared out to stakeholders, not kept inside plant gates. Connections like these foster trust—the kind that only grows out of hands-on, repeated engagement.
Having weathered global supply chain swings, regulatory surprises, and sudden demand surges, our plant knows flexibility makes or breaks a reputation. Adapting to new requests around this compound—whether by custom batch sizes, new stabilization methods, or tighter purity bands—keeps us connected directly to chemists and formulation teams worldwide. Our R&D and production experts value open conversation around process improvements, alternate synthetic routes, or next-generation structure analogs that build on the same core 2,6-dichloronicotinate backbone.
Through honest reflection on real setbacks—from tricky crystallization failures to supply chain hiccups—all improvements cycle back into new standard operating procedures. This willingness to bring hard-won insights into open dialogue means our partners tap into a living resource, not just a claims summary in a catalog. We bring growth by learning together, adapting production methods, and supporting the next generation of synthetic innovation with actual know-how, not just theory.
Every kilogram of 4-Pyridinecarboxylic acid, 2,6-dichloro-, 1,1-dimethylethyl ester that leaves our dock carries the weight of detailed research, plant innovation, and tireless technical support. The feedback loop between plant experts and laboratory users keeps standards high and avoids costly missteps. Whether for an existing high-volume application or a new R&D effort, end users return for more, not just for purity claims, but for authenticity supported by years of real-world learning. This isn’t generic stock. It’s a result of continuous investment, hands-on feedback, and an unwavering focus on making specialized chemistry actually work for skilled chemists and process engineers—batch after batch, year after year.