|
HS Code |
317043 |
| Chemicalname | 2-Chloro-3-Fluoropyridine |
| Casnumber | 261953-36-6 |
| Molecularformula | C5H3ClFN |
| Molecularweight | 131.54 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 179-181°C |
| Meltingpoint | -18°C |
| Density | 1.381 g/cm3 |
| Purity | ≥98% |
| Refractiveindex | 1.517 |
| Flashpoint | 62°C |
| Solubility | Slightly soluble in water |
| Smiles | C1=CC(=NC=C1Cl)F |
| Inchi | InChI=1S/C5H3ClFN/c6-5-4(7)2-1-3-8-5/h1-3H |
As an accredited 2-Chloro-3-Fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Chloro-3-Fluoropyridine is supplied in a 100g amber glass bottle, tightly sealed and clearly labeled with hazard warnings. |
| Shipping | 2-Chloro-3-Fluoropyridine is shipped in tightly sealed containers, compliant with applicable safety and hazardous materials regulations. Packaging ensures protection from moisture and physical damage. During transit, the chemical is labeled according to relevant transportation guidelines. It is recommended to store and ship this compound in a cool, dry, and well-ventilated environment. |
| Storage | 2-Chloro-3-Fluoropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Proper labeling and secure storage are essential to prevent accidental exposure or environmental contamination. Always follow relevant safety and regulatory guidelines during storage. |
Applications of 2-Chloro-3-Fluoropyridine in Industrial Manufacturing2-Chloro-3-Fluoropyridine plays a crucial role as an intermediate in multiple industrial sectors due to its unique halogenated pyridine structure. Our direct manufacturing expertise provides consistent supply and traceability, supporting advanced synthesis in several high-value downstream applications where this compound’s reactivity and selectivity are essential. 1. Pharmaceutical API Synthesis: Anti-Infective and Oncology IntermediatesAs a building block in the pharmaceutical sector, 2-Chloro-3-Fluoropyridine is utilized in manufacturing critical intermediates for both anti-infective and oncology active pharmaceutical ingredients. Medicinal chemistry teams specify this raw material for creating fluorinated pyridine cores, which enhance molecular stability and bioavailability. It enters multi-step synthesis processes at an early stage, providing the framework for heterocyclic scaffold construction required by several registered drug substances, especially in quinolone and kinase inhibitor classes. Industry compliance standards
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2. Agrochemical Synthesis: Herbicide and Insecticide IntermediatesThis compound serves as a key intermediate for synthesizing advanced agrochemical actives. Leading crop protection formulators use it to construct fluorinated pyridine backbones required in next-generation herbicides and insecticides. It becomes integrated during early reaction stages, enabling site-specific modification for regulatory-approved actives targeting weed and pest resistance in various crop systems. Industry compliance standards
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3. Advanced Material Precursors: Electronic and Liquid Crystal IndustriesManufacturers of specialty electronic materials and liquid crystal compounds utilize 2-Chloro-3-Fluoropyridine as a precursor for high-performance functional monomers. The halogenated pyridine ring enables tight control over dielectric and refractive properties in specialty polymers and display panel films. It is fed into advanced organic synthesis operations focused on delivering materials with defined molecular orientation and high thermal stability. Industry compliance standards
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4. Fine Chemical Synthesis: Custom Fluorinated Building BlocksCustom synthesis providers develop specialized pyridine derivatives incorporating both chloro and fluoro groups by utilizing this intermediate. Laboratories and industrial process chemists value precise lot-to-lot consistency to achieve selective halogen substitution or cross-coupling for downstream synthesis of fluorinated ligands, advanced reagents, and analytical standards, which are supplied to diverse chemical and biological R&D environments. Industry compliance standards
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Making specialty intermediates for the pharmaceutical and agrochemical sectors often feels like a balancing act between efficiency, purity, and reliability. Over the years, our team has earned experience in chlorinated and fluorinated pyridines—compounds prized for their selectivity and reactivity. We take pride in producing 2-Chloro-3-Fluoropyridine, one of the more versatile building blocks in organofluorine chemistry, and we’d like to share our hands-on view on how this compound fits into research and manufacturing settings.
2-Chloro-3-Fluoropyridine is a pale to colorless liquid or crystalline solid, depending on storage temperature. Its compact molecular structure features a chlorine atom at the second position of the pyridine ring and a fluorine atom at the third. Chemical formula: C5H3ClFN. CAS Number: 39890-95-4. Typical purity of our batches exceeds 99.5%, achieved by rigorous distillation and precise control over synthesis pathways. We focus on maintaining consistency—every drum and flask should meet or beat spec, so our end-users, whether in pharma or crop protection research, stay confident about their results.
Not all fluoropyridines behave the same in a reactor or under scale-up conditions. In our experience, minor differences in substitution patterns affect not only reactivity but also handling and storage. Compared to analogues like 2-chloropyridine or 3-fluoropyridine, this molecule exhibits a distinctive mix of electron-withdrawing effects from two substituents. That makes it more reactive for nucleophilic aromatic substitution (SNAr) at the fourth or fifth positions, which is a quality many synthetic chemists value when building up more complex molecules. Our observations show that, under standard conditions, it resists hydrolysis—unlike some chloro-only derivatives, which tend to degrade unless carefully handled.
Choosing a synthetic route for 2-Chloro-3-Fluoropyridine means juggling raw material availability, yield, and downstream hazard minimization. In our plant, we select fluorination agents and chlorination steps based on efficiency, atom economy, and whether the process fits with environmental controls. Over the last decade, we invested in closed-loop venting, improved handling of hydrogen fluoride residues, and replaced some batch methods with continuous-flow reactors to control exotherms better and maximize throughput. Regular monitoring at every step checks for isomeric impurities, such as 2-chloro-5-fluoropyridine, since even trace-level deviations impact how our customers’ own syntheses perform.
Dealing with highly reactive halopyridines poses special logistical challenges, especially over long transit. We realized some years ago that standard steel drums weren’t suitable—the compound can react with traces of moisture and corrode untreated surfaces. For this reason, we pack product in polyethylene-lined containers or HDPE bottles and store them under an inert nitrogen blanket. This way, both high-volume and laboratory-scale users receive material as we shipped it, not degraded by transit or time on a warehouse shelf.
Feedback from formulation chemists and process R&D teams guides how we run our plant. 2-Chloro-3-Fluoropyridine plays a key role as a building block for medicinal chemists, agrochemical researchers, and polymer scientists alike. Its pattern of halogenation unlocks coupling reactions leading to kinase inhibitors, novel herbicide backbones, or fluorinated electronic materials.
In life sciences, medicinal chemists appreciate this compound’s clean reaction with phenol or amine nucleophiles, allowing rapid screening and optimization cycles. Our contacts in herbicide research tell us that 2-chloro-3-fluoropyridine enables synthesis of photostable, potent scaffolds where single-halogen analogues failed. Over time, requests have involved gram-scale samples for structure-activity studies and multi-metric-tonne lots for pilot plant validation.
We also see steadily growing interest from materials science labs exploring new pathways for high-performance coatings and specialty polymers. The presence of both chlorine and fluorine in such a small, stable core makes this molecule a rare and valuable intermediate—small enough to flow through automated systems, reactive enough to enable further derivatization without major side-product challenges.
We’ve worked with nearly every chlorinated or fluorinated pyridine that sees industrial use, so we notice small advantages that aren’t always obvious to someone only reading a catalog. In our direct work-up and purification steps, we noticed higher thermal stability compared to 2-chloropyridine. This means less loss to distillation columns even when running 24/7 during peak season.
Comparing it to 2-fluoropyridine, you trade slightly higher reactivity at the pyridine ring for a material that resists breakdown in the presence of strong bases. We have seen that certain catalysts and ligands tolerate this molecule better—resulting in fewer side reactions and higher yields for cross-couplings, especially when making C–N or C–S bonds. For process engineers, this difference lessens downtimes for cleaning equipment fouled by polymeric byproducts, which arise more often with mono-halogenated precursors.
Moving from grams in a lab flask to metric tonnes in a chemical reactor poses big challenges. Our own journey scaling up 2-chloro-3-fluoropyridine started in small, jacketed vessels. Temperature control and mixing were the first obstacles—chlorinated and fluorinated aromatics react quickly, so exotherm management takes priority. We tuned agitation speeds, feeding rates, and surveillance with real-time analytics, learning that stable conversion requires attention to every variable.
Purification must balance cost and purity. Simple distillation doesn’t always separate the close-boiling point isomers and byproducts. Adoption of in-line GC-mass detection and fractional, high-efficiency columns allowed us to achieve high-purity levels at commercial scale. Our continual improvement programs review any off-spec batch, feeding those lessons back into both the batch and continuous production lines.
Our operators know this process inside out. Over countless batches, we reduced solvent usage, improved vent scrubbing, and developed protocols for waste minimization. We’ve fine-tuned crystallization from mixed solvents to boost recovery and match target crystal habits needed by our pharmaceutical partners for fast dissolution and reactivity profiles.
Safety lies at the heart of halogenated heterocycle production. Chlorine and fluorine reactions risk forming hazardous intermediates. We developed and enforce rigorous PPE usage, emergency drill schedules, and automated gas detection throughout the facility. Regular training ensures even temporary workers understand the risks. We maintain documentation and change control for every modification to reactor settings, housekeeping routines, or new equipment. Continuous monitoring for leaks or contamination prevents minor issues from growing. Over the years, investments in on-site waste treatment—scrubbers, neutralization pits, and thermal oxidation—cut our emissions well below local regulatory limits, reflecting what responsible manufacturing means to us.
Transport requirements for halopyridines grow stricter, and rightfully so. Customers appreciate our strict adherence to international shipping and storage protocols. We regularly audit our logistics partners for compliance and temperature traceability. Downtime or spoilage costs everyone more—and keeping the product within specification throughout the journey remains a point of pride.
We notice our best process improvement ideas come from regular talks with formulators, scientists, and safety officers using our material. Some request special particle size or non-standard solvents; others need assays traceable to particular reference standards. Our approach doesn’t rely on a one-size-fits-all mentality. While the core chemistry stays the same, we’re open to packaging adjustments, tailored documentation, or shared process validation. Every time we support a new regulatory submission or tech transfer, we gain insight into evolving needs and future trends in this field.
Demand for 2-chloro-3-fluoropyridine has surged due to increased research into fluorinated pharmaceuticals and advanced crop protection products. Sector after sector seeks tailored halopyridines for rapid lead discovery or enhanced residue profiles. With this backdrop, our investment leans toward faster synthesis cycles, tighter impurity profiling, and larger production runs to meet both small development and large commercial demands.
Emerging synthetic strategies—such as direct C–H activation or biocatalysis—are starting to reshape how we approach manufacturing. We monitor these developments, collaborating with academic and industry partners. If new methods make sense for scale and safety, we adapt. Keeping production local enables closer relationships with both buyers and regulators, something globalized supply chains seldom replicate.
Stringent expectations around regulatory data, especially for pharmaceutical intermediates, direct much of our effort. We compile full analytical profiles from multiple techniques, support REACH registration where required, and maintain a standardized batch retaining system for retrospective testing. Testing extends beyond bulk material—storage studies examine changes in both product and container, and findings flow into our packaging and transport recommendations. We follow evolving best practices for toxicology and environmental impact, partnering with third-party labs when external data improves confidence.
Handling and disposing of halogenated waste presents ongoing hurdles for us and for the industry. We face tighter discharge and waste disposal rules every year but believe chemical manufacturing must keep pace or set examples for sustainable practices. Our engineers continually experiment with solvent recovery, catalyst reuse, and non-aqueous quenching to draw down energy, water, and raw material use. Partnerships with local recycling firms help close the loop, returning cleaned barrels and drums to production lines.
Global events sometimes crimp supply of precursor chemicals or new regulatory interpretations alter classification, so our business continuity plan maintains dual-source suppliers and contingency stock. Each year we review disaster recovery plans on site and with freight partners, stress testing systems to uncover new vulnerabilities and keep customers supplied through uncertainty.
Close connection to process, people, and product runs through everything we do. We know from experience what small contaminant peaks or temperature swings mean downstream and don’t treat production as a black box. We believe this transparency and hands-on involvement offers reassurance and confidence for researchers building new molecules or engineers running batch syntheses at scale.
We find value not only in process optimization, but also in customer collaboration. Whether advising on compatible solvents, troubleshooting reaction profiles, or co-developing analytical methods, we support partners throughout the R&D cycle. This approach helps tackle real-world problems, from controlling trace impurities to fine-tuning selectivity in scale-up.
We welcome inquiry and conversation on the chemistry, performance, and future applications of 2-chloro-3-fluoropyridine. Decades of combined lab and plant floor experience shape both our process and our relationships. Those working at the bench or in pilot plants can rely on our attention to detail and desire to share what we’ve learned—a continuous cycle of adaptation, improvement, and support for discovery.