|
HS Code |
862226 |
| Chemical Name | 2,6-Pyridinedicarboxylic acid chloride |
| Synonyms | Dipicolinic acid chloride, Pyridine-2,6-dicarbonyl dichloride |
| Molecular Formula | C7H3Cl2NO2 |
| Molecular Weight | 204.01 g/mol |
| Cas Number | 499-84-3 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 87-89°C |
| Boiling Point | 340°C (decomposes) |
| Solubility | Reacts with water, soluble in organic solvents like dichloromethane |
| Purity | Typically ≥97% |
| Storage Conditions | Store in a cool, dry place under inert atmosphere |
| Smiles | C1=CC(=NC(=C1)C(=O)Cl)C(=O)Cl |
As an accredited 2,6-Pyridinedicarboxylic Acid Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,6-Pyridinedicarboxylic Acid Chloride is packaged in a sealed amber glass bottle containing 25 grams, labeled with hazard symbols. |
| Shipping | 2,6-Pyridinedicarboxylic Acid Chloride is shipped in tightly sealed containers, under cool, dry conditions, away from moisture and incompatible substances. Appropriate hazard labeling is applied, and shipments usually comply with regulations for corrosive materials. Ensure containers are handled with care, using protective gloves and eye protection during transit and handling. |
| Storage | 2,6-Pyridinedicarboxylic Acid Chloride should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong bases and oxidizers. Keep container tightly closed and protected from light. Use corrosion-resistant containers, and store under an inert atmosphere such as nitrogen if possible, due to its reactivity with water. Handle with appropriate personal protective equipment. |
Applications of 2,6-Pyridinedicarboxylic Acid Chloride in Industrial ManufacturingAs a direct manufacturer, we support international industrial clients with 2,6-Pyridinedicarboxylic Acid Chloride for use in advanced specialty chemical synthesis. This intermediate plays a key role in the development of functional materials and value-added compounds in several high-performance sectors. Here, we detail its primary downstream applications based on actual industry practices, technical requirements, and compliance demands. 1. Polyimide Film and Resin Monomer SynthesisPolyimide producers utilize this diacid chloride as a critical monomer for high-heat-resistant polyimide resins and films. Reaction with diamines or diols at controlled temperatures leads to premium-class aromatic polyimides widely used in electronics and aerospace sectors. Manufacturers select this material for its consistent reactivity, supporting tight molecular weight control and enhanced mechanical properties in the end product. Plant safety and emissions management demand strict control of chlorinated byproducts throughout the process. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical API Intermediate ManufactureOur material is a cornerstone in multi-step organic synthesis for active pharmaceutical ingredient (API) manufacturing, particularly in molecules requiring pyridine-2,6-dicarboxamide or -diimide motifs. Pharmaceutical companies employ this acid chloride under GMP-controlled environments for amide coupling with amines, facilitating complex molecular constructs found in anticancer and antiviral drug candidates. Careful process design ensures complete reaction and minimal genotoxic impurity carryover. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Polymer Crosslinking AgentProducers of high-durability, chemically resistant polymers incorporate this compound as a crosslinking agent, leveraging its bifunctional reactivity in step-growth polymerizations. It is used to introduce rigid pyridine ring structures into coating, adhesive, and elastomer matrices, enhancing thermal stability and solvent resistance. Quality control teams monitor residual monomer levels and molecular structure integration according to supplier specifications and industry test methods. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Ligand Synthesis for Metal Organic Frameworks (MOFs)Research labs and advanced materials companies select 2,6-pyridinedicarboxylic acid chloride as a precursor for ligand synthesis in MOF production, especially for materials targeting gas absorption, separation, or catalysis. Reacting the acid chloride with specific functionalized amines yields tailored carboxamide- or imide-modified pyridines, which then serve as chelating ligands offering consistent geometry and reactivity with metal ions. Synthesis methods require careful atmospheric and solvent control to achieve ligand purity as dictated by end-use demands in energy storage or environmental remediation projects. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,6-Pyridinedicarboxylic Acid Chloride prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Through decades of chemical manufacturing experience, it’s easy to tell how certain intermediates quietly make all the difference in fine chemical synthesis. 2,6-Pyridinedicarboxylic acid chloride (model: PDC-C106) is one of those compounds. Its molecular structure, built on a pyridine ring with acid chloride groups at the 2 and 6 positions, creates a platform for transformations that many other aromatic acid chlorides simply can’t match. This isn’t just a small tweak in a formula—the two reactive acid chloride handles open plenty of options for more complex chemistry. Over the years, our technical team has seen this product forge essential links in pharmaceutical intermediates, specialty polymers, and agrochemical synthesis because of its precise reactivity and the way it lets chemists control molecular architecture.
While plenty of acid chlorides are designed for single acylation, the symmetric diacid chloride structure of 2,6-Pyridinedicarboxylic acid chloride lets users build bridges between two other molecules, such as diamines for polyamide chains or diols for polyesters. In the early days of production scale-up, our process engineers had to tackle some hard-won lessons about hydrolytic sensitivity—the compound reacts instantly with water, so strictly anhydrous handling and storage became part of daily routines in our plant. The result is a consistently reliable batch-to-batch product trusted by advanced material scientists and pharma process chemists alike.
From bench chemistry to commercial synthesis, 2,6-Pyridinedicarboxylic acid chloride supports innovations that stem from its dual reactivity and aromatic stability. In the drug development space, this intermediate steps into the role of linker for conjugated pharmaceutical agents, where its reactivity toward amines and alcohols allows medicinal chemists to tether drugs to carriers or modify solubility profiles. Our partners in the agrochemical industry pursue efficient couplings for advanced crop protection agents. The acid chloride groups react swiftly, often at mild conditions, cutting down synthesis times and streamlining purification steps.
Anyone who’s spent years in a chemical plant knows the critical job safety and purity standards play. Our PDC-C106 grade emerges free from high-boiling pyridine tar byproducts and traces of lower chlorides—these have always threatened color stability and downstream reactivity in other commercial samples. We adopted extra distillation steps and proprietary drying techniques so our customers waste less time troubleshooting impurities. This attention to purity made a difference not just for the end-user, but in our own lab work, keeping side-product formation at bay even in multi-step syntheses.
Comparisons with benzene diacid chlorides or single ring-based acid chlorides reveal stark variations. 2,6-Pyridinedicarboxylic acid chloride’s pyridine core serves more than structural variety; it offers increased solubility in polar aprotic solvents and sometimes even alters the electronic behavior during reaction with nucleophiles. The nitrogen atom in the ring encourages distinct hydrogen bonding and electronic effects, sometimes changing the rate or selectivity of coupling. Our own QC teams track batch outcomes and have recorded lower formation of N-acylated byproducts compared to isophthaloyl chloride reactions under similar conditions.
Working with buyers from both large pharma and material science innovators, we’ve seen how the differentiated structure pays dividends during upscaling. The symmetry of the molecule allows construction of highly regular polymers and crystalline linkers, leading to devices or coatings with improved performance. Researchers in the electronics sector, for example, reported fewer low-molecular-weight tars after switching from phthaloyl to pyridinedicarboxylic acid chlorides in semiconducting polymer projects. The difference grows with scale—by the kiloton, even minor improvements in thermal behavior or decreased fouling during processing mean lower maintenance shutdowns and smoother production runs.
It’s common to hear talk about trace contaminants and batch variability from industry newcomers, but seasoned chemical plant operators see how the smallest trace of pyridine N-oxide or moisture triggers chain reactions of headaches. From the earliest stages, we standardized our procurement of raw pyridine and enforced downstream controls, such as real-time FTIR monitoring during the chlorination phase. This lets our teams catch anomalies before they become a problem in a client’s reactor. Every drum holds a barcode traceable to its exact batch—and over years, this level of documentation has proven essential for multinational partners needing full compliance for their end-use audits.
We don’t just look at quality assurance after a drum is filled. Our operators spent months designing the current closed-system transfer method for PDC-C106, preventing ambient moisture uptake which leads to hydrolysis during loading at customer facilities. Stories from the field showed us too many spills and ruined lots from makeshift pumps or open transfer, so we equipped every container leaving our plant with integrated PTFE-lined valves. This slight increase in operational overhead cut in-field product complaints to near zero.
In practical use, 2,6-Pyridinedicarboxylic acid chloride replaces multi-step reagent setups involving pre-activated carboxyl derivatives. Researchers who previously resorted to coupling reagents like DCC or carbodiimides in combination with diacids now sidestep those additional hazards, as PDC-C106 reacts directly. We regularly receive feedback from contract research organizations—not only does this save time, it lowers the overall exposure to toxic byproducts created by older conjugation approaches.
Our own R&D teams discovered the dual benefit of this reagent in polymer modification projects. Similar diacid chlorides often leave polymer ends inadequately capped or introduce unwanted coloration, particularly at elevated reaction temperatures. In contrast, aromaticity and electron distribution in pyridine-based diacid chloride reduce yellowing, and our proprietary control of isomeric purity eliminates off-odors in end-use coatings. These differences may seem minor from a desk, but for those standing next to a 5,000-liter reactor or troubleshooting a wonky quality batch, this product offers real, tangible advantages.
We make it a point to study environmental regulation shifts closely. Chlorinated intermediates, especially acid chlorides, face scrutiny worldwide. Years ago, our operations department moved to closed-waste solvent recovery and established real-time monitoring for atmospheric venting. This foresight coached us through updated discharge guidelines in the EU and North America. By prioritizing these steps, we’ve kept insurance premiums reasonable and can provide solvent-handling documentation on request during transportation or customs review. Our clients trust us to anticipate—not just react to—compliance headwinds.
Beyond direct emissions, we promote processes that cut down on extraneous reagents downstream. 2,6-Pyridinedicarboxylic acid chloride’s efficient reactivity leaves fewer residual reagents for hazardous waste streams, which matters for plants working to minimize incineration volumes. Collaborations with end-users showed the final reduction in byproduct waste tied directly to the intermediate’s clean conversion. Those small advantages add up in both cost savings and regulatory safety nets. Our technical liaison staff always stay engaged with changing national and local guidelines, and partners profit from periodic updates on compliance-related modifications to packaging and labeling requirements.
We’ve heard plenty of war stories—delayed deliveries, unexpected clogging, off-color product shipments—from purchasing managers and process chemists caught relying on unproven suppliers. In our own transition from pilot to full-scale production, we learned that robust pre-shipment screening isn’t a bonus; it’s table stakes for global chemical supply. Each tonne we ship passes through three phases of analytical review, including HPLC, Karl Fischer moisture analysis, and titration checks on acid chloride content. This rigor isn’t just about checking a box—it saves labs and factories thousands of dollars in re-runs and failed synthesis steps. Feedback loops between our lab, plant, and customer tech support strengthen the product at every step.
Specialty batch sizes for new product development or scale-up pilots are regular requests we fulfill. Once, our team worked side-by-side with a new-pharma partner transitioning from glassware-based route scouting to a 1,000-liter batch. We adapted our batch planning to their unusual solvent system and proved that a dedicated batch train not only meets specs but shaves weeks off their tech transfer timeline. These hands-on experiences taught us to ask better questions about downstream needs, whether that’s focusing on particle size distribution, custom packaging, or modified purity specs for an exacting end-use.
We’ve handled our share of moisture issues, as 2,6-Pyridinedicarboxylic acid chloride hydrolizes rapidly if given the chance. Decades of process optimization distilled into rigorous humidity controls and dedicated dryers in the packaging hall. Rather than cutting corners, we invest in extra personnel training to ensure airtight seals every time—so users don’t open a fresh drum to find caked material or diminished reactivity. Trouble-shooting in our own facility led us to supply desiccant-packed drums for sites in seasonally humid climates, a move that cut re-order complaints by more than half in Southeast Asia and South America.
Working with strong acid chlorides requires respect for corrosive vapors and allergic reactions—not just lab gloves and fume hoods, but properly designed air handling in bulk rooms and safe waste neutralization protocols. We’ve run multi-day workshops with in-house EHS experts to build effective product-specific MSDS training for customer sites, so users know how to handle spills or exposure. Years of direct engagement with industrial hygiene teams worldwide led to product handling tips, ranging from best decontamination practices to first aid essentials that now accompany every major export shipment.
Academic and industry collaborations fuel ongoing improvements in our product. Customers from materials science labs regularly request modifications—unique morphology for membrane fabrication, tailored particle size for catalyst supports, or lower-odor grades for sensitive device work. We welcome such challenges. In fact, our laboratory developed a microcrystalline version of PDC-C106 for a next-generation polymer lab, dramatically improving their processability and final product transparency. The project drove us to revamp grinding and drying equipment fleet-wide, so now all clients benefit from tightly controlled particle characteristics.
On the pharmaceutical side, a client brought us granular feedback on improved ligand construction when using our high-purity grade. Armed with real-world data from batch comparisons, we iterated new purification cycles for contaminant control that allowed even tighter identification of trace non-pyridinic byproducts. Our technical support lines stay busy, not just solving emergencies but supporting customers with time-saving reaction protocols, equipment design advice, and scalable process recommendations.
One big lesson we’ve learned is that reliable chemical manufacturing isn’t just about what happens inside our plant gate. Success happens when customer and producer share feedback and shape the product pipeline together. Overhauling logistics for better cold-weather shipping, developing new container linings to cut down on off-gassing, or working through regulatory documentation for specific end-use certifications—each challenge gives us a new chance to improve.
Some clients buy a few kilograms a month; others receive metric tonnes by ocean container. No matter the size, consistency matters more than any single product feature. We understand that a delay or quality slip on a critical intermediate like 2,6-Pyridinedicarboxylic acid chloride has cascading effects on timelines, costs, and product launches down the line. Every new complication we solve adds another layer of trust with our customers, and we treat each collaboration as a building block for the next production cycle.
Few intermediates span as broad an application spectrum as 2,6-Pyridinedicarboxylic acid chloride. Every day, R&D and production teams count on the dependability of its reactivity for high-performance materials, smarter pharmaceuticals, and breakthrough agricultural compounds. Our legacy as a direct manufacturer means these benefits flow straight from our shop floor to the end-users’ bench or reactor, backed by problem-solving experience and a culture of continual improvement. Each new project, every course-correction in process engineering, gives us more reasons to refine and elevate our PDC-C106, supporting both current needs and the unknown challenges tomorrow may bring.