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HS Code |
878693 |
| Chemical Name | 2,3-dichloro-6-pyridinecarboxylic acid |
| Molecular Formula | C6H3Cl2NO2 |
| Molecular Weight | 192.00 g/mol |
| Cas Number | 15128-56-2 |
| Appearance | white to off-white solid |
| Melting Point | 235-240°C |
| Solubility In Water | Slightly soluble |
| Density | 1.67 g/cm3 (approximate) |
| Pka | 2.2 (carboxylic acid group) |
| Logp | 1.93 |
| Smiles | C1=C(C(=NC=C1Cl)Cl)C(=O)O |
As an accredited 2,3-dichloro-6-pyridinecarboxylicacid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package features a sealed amber glass bottle, labeled “2,3-dichloro-6-pyridinecarboxylic acid,” with CAS number and hazard symbols. |
| Container Loading (20′ FCL) | 20′ FCL can load about 10 metric tons of 2,3-dichloro-6-pyridinecarboxylic acid, packed in secure export-grade drums. |
| Shipping | 2,3-Dichloro-6-pyridinecarboxylic acid is shipped in tightly sealed containers, protected from moisture and light. It must be handled according to standard chemical shipping regulations, including proper labeling and documentation. Transportation follows applicable local, national, and international hazardous material guidelines to ensure safety and prevent leaks, spills, or contamination during transit. |
| Storage | **Storage of 2,3-dichloro-6-pyridinecarboxylic acid:** Store in a tightly sealed container in a cool, dry, and well-ventilated area, away from moisture, incompatible substances, and sources of ignition. Protect from direct sunlight. Store separately from strong oxidizers, bases, and reducing agents. Avoid inhalation, ingestion, or contact with skin and eyes; always use appropriate personal protective equipment when handling the chemical. |
| Shelf Life | 2,3-Dichloro-6-pyridinecarboxylic acid is stable under recommended storage conditions; store tightly sealed, protected from moisture, and light. |
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Purity 98%: 2,3-dichloro-6-pyridinecarboxylicacid with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal side products. Molecular weight 192.01 g/mol: 2,3-dichloro-6-pyridinecarboxylicacid of molecular weight 192.01 g/mol is used in agrochemical formulation, where it provides consistent compound reactivity. Melting point 180°C: 2,3-dichloro-6-pyridinecarboxylicacid with melting point 180°C is used in specialty chemical manufacturing, where it facilitates stable processing conditions. Particle size <50 µm: 2,3-dichloro-6-pyridinecarboxylicacid with particle size less than 50 µm is used in catalyst preparation, where it enables optimal surface area interaction. Stability temperature up to 120°C: 2,3-dichloro-6-pyridinecarboxylicacid with stability temperature up to 120°C is used in polymer additive blends, where it maintains chemical integrity under process heat. Water solubility 0.5 g/L: 2,3-dichloro-6-pyridinecarboxylicacid with water solubility 0.5 g/L is used in aqueous dispersion systems, where it enables controlled solubilization rates. Low residue on ignition: 2,3-dichloro-6-pyridinecarboxylicacid with low residue on ignition is used in electronics materials synthesis, where it reduces inorganic contamination levels. |
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Every batch of 2,3-dichloro-6-pyridinecarboxylic acid starts with the same principles that have guided fine chemical synthesis for decades: attention to purity, careful selection of raw materials, and tracking each reaction step to ensure a consistent product. Our process favors minimal waste streams, using high-purity chlorinated intermediates and pyridine ring precursors that allow precise substitutions in key positions. We invest in containment and ventilation to keep exposure to chlorinated byproducts at bay for both our team and the environment.
Reactions are monitored for byproduct formation that can complicate purification, making our jobs both demanding and rewarding. The distinctive molecular signature of 2,3-dichloro-6-pyridinecarboxylic acid—a dichloro-substituted pyridine ring linked to a carboxylic acid at the 6-position—offers synthetic chemists a versatile scaffold. We see daily how a carefully controlled ring chlorination and carboxylation open new versions for further chlorination, esterification, or cross-coupling downstream.
Long days in the plant have taught us that appearance and purity aren’t just academic numbers, they represent the discipline and care our operators put into every batch. The most sought-after form of this acid is a solid crystalline powder, ranging from pale yellow to near-white—often dictated by trace impurities or even the drying conditions post-filtration. Our standard product ships at a minimum purity of 98 percent by HPLC, with a small amount of permissible water picked up during filtration and drying. Experienced eyes catch the subtle cues that point to off-spec product—unusual lumpiness, tinting, or residual solvent smell all lead to additional drying or purification.
Packing and storing are never taken for granted. The carboxylic acid moiety absorbs moisture out of the air. So, drums and polyester-lined bags are sealed tight before heading to customers. Decisions on granulation, particle size, or surface area all trace back to practical concerns: ease of weighing, dissolving, and handling for large-scale applications.
Plant operators, batch chemists, and application engineers know this acid best as a building block. In agrochemical production, 2,3-dichloro-6-pyridinecarboxylic acid forms key skeletons for fast-evolving herbicide structures. Carboxyl and chloro substituents unlock targeted derivatization, essential for tuning biological activity.
Pharmaceutical chemists tap this molecule’s core to branch into fluorinated derivatives and pyridine-based drugs. We have seen many start with direct amidation or amidoxime couplings to introduce new linkages off the 6-position carboxyl group. The double chloro pattern supports direct nucleophilic substitution and is a backbone for coupling reactions pivotal in modern medicinal chemistry.
In the dye and pigment world, careful substitution patterns mean new shades, improved lightfastness, and unique application profiles. 2,3-dichloro-6-pyridinecarboxylic acid gives access to a group of chlorinated pyridine derivatives that behave predictably under high-heat and UV exposure.
A chemist might glance at the catalog and see many pyridinecarboxylic acids or even several dichlorinated pyridines. What separates ours from the crowd comes down to experience in managing the interplay between molecular structure and process reliability.
Working with dichloro isomers, position specificity is crucial. For many applications, only 2,3-dichloro-6-pyridinecarboxylic acid delivers the combination of reactivity and selectivity needed. Isomers with similar formulas fail to match the downstream transformation rates or purity profiles in advanced syntheses. The tendency for unwanted side-chain formation during handling is minimized thanks to the stringent in-house controls we maintain on reaction kinetics and isolation procedures.
A good share of customers once purchased non-specific “chloropyridinecarboxylic acids” from broad trading houses. What arrives is often a complex isomer blend, leading to inconsistent process yields or tricky isolation steps. In contrast, we devote resources to targeted regioselectivity, using custom reagents and timed additions, so every kilogram contains a tightly defined isomer.
Beyond structural control, our team faces ongoing demands to eliminate trace impurities: residual starting materials, colored side products, or extraneous chloride that could poison catalysts further down the line. Laboratory assay methods get regular upgrades to catch micro-impurities that might escape the usual checks.
Bringing 2,3-dichloro-6-pyridinecarboxylic acid to the market takes more than just following textbook reactions. We have learned that stepwise chlorination demands controlled temperatures and well-chosen solvents. Excessive heat or rapid reagent dumping introduces tarry byproducts. So, we monitor exotherms with jacketed glass reactors and restrict scale-up with batch-to-batch learning. The acid’s sensitivity to base and high humidity means we must keep tight handling protocols—without them, decomposition or hydrolysis creeps in.
Troubleshooting goes well beyond the reaction flask. If we spot off-tests on the final batch, our team retraces each step: from the water content in the starting pyridine, to ambient air quality on the crystallization floor. Tiny operational variables, like the dew point during drying or the seal integrity on a reaction vessel, can nudge impurities above warning levels. Experience tells us that there’s no shortcut to tight process analytics and careful monitoring.
We have seen mounting scrutiny on halogenated intermediates, especially those headed for agricultural and pharmaceutical markets. Waste minimization is not just a regulatory concern, but a day-to-day part of our site operations. Our process team has worked over several years to close solvent loops, reclaim spent reagents, and power energy-intensive chlorination steps through low-carbon sources.
Handling chlorinated pyridines demands extra safety. Team members follow strict PPE, splash protection, and closed-system sampling. We eliminate open-system transfers, and solvent tanks are nitrogen-blanketed against accidental vapor exposure. Each chemical operator completes hands-on training in spot-cleaning and spill management, so releases stay well within safety limits. The result: barely any chemical escapes beyond the site barrier, and air, water, and ground testing backs it up.
Field engineers and technical purchasers push us to keep improving. No datasheet can match the value of hearing from a plant chemist troubleshooting a blocked filter or a researcher dealing with poor dissolution. Through these relationships, we test new drying cycles and packaging types, always looking for incremental gains.
On more than one occasion, customer partners asked us to halve trace impurity limits or offer a new particle size distribution. Rather than standardize a one-size-fits-all model, we keep batch logs open for post-shipment discussion. Process tweaks and recipe adjustments grow directly from this feedback. Staff from R&D often visit customer plants to observe first-hand how our product performs in real production environments, giving us insights well beyond the bench.
We hear plenty about regulatory shifts. Buyers come to us with inquiries about batch traceability or inquiries about REACH and EPA compliance. Our answer comes from the confidence that good records go back years, and each drum links back to a controlled operation with verifiable analysis data on file.
Hard-won knowledge lets us scale up productively. Unlike general-purpose traders, we control each step from raw ingredient reception through to final drum sealing. Decisions about solvent purity, drying times, and batch splits all trace back to accumulated know-how. We avoid cross-contamination by devoting equipment and line-clearance protocols specific to pyridinecarboxylic acids, so batch-to-batch variation stays minimal.
Customers introducing new synthetic routes get more than a molecule—they get access to our technical team’s troubleshooting. We field direct questions about reactivity profiles, solubility in non-standard solvents, and compatibility with novel reagents in pilot-plant experiments. Our scale-up engineers help bridge the gap between research and full production, flagging any technical hurdles at the earliest stage. This partnership has proven its worth in sustained supply, quick turnaround on analytical questions, and fine-tuning order logistics.
Each year brings customer-driven changes. Pesticide innovators look for ever-finer control over substitution patterns. Custom synthesis clients chase downstream modifications that test the limits of purity and isomeric control. We support their work by maintaining a well-benchmarked trace impurity profile—every dataset guides us to a tighter, cleaner product.
As green chemistry principles push for milder, less hazardous conditions, our research group explores new ways to achieve the same dichloro substitution without legacy reagents. This includes enzyme-catalyzed steps, more selective catalysts, or greener oxidants for ring activation. Some ideas prove out, some stall, but all move us closer to a product portfolio in line with the best global practices.
Over years of manufacturing 2,3-dichloro-6-pyridinecarboxylic acid, we have learned that repeatable quality never comes by accident. Each operator carries the company’s track record in their gloved hands. From the chemistry bench to the warehouse loading dock, the people behind each drum of acid make the difference between a product that performs in the field and one that disappoints.
We see our role as selling more than just a reagent—we offer tangible proof that process discipline, investment in analytics, and close customer partnerships lead to real-world results. In chemistry as in other fields, direct manufacturing experience gives substance and reliability that traders can’t supply. Customers tell us that the consistency of our acid, backed by direct application support, lets them run tighter processes and achieve higher-value outcomes.
Working here has reinforced that small details—choice of a filtration aid, timing of extraction, how tightly a drum gets sealed for shipment—compound into real improvements for those relying on our product downstream. We measure our success by the ongoing trust of customers who ask for our name on the label, and by our continued ability to support new ideas as they move out of the lab and into production.