|
HS Code |
305309 |
| Cas Number | 87120-72-7 |
| Molecular Formula | C11H8ClN |
| Molecular Weight | 189.64 |
| Iupac Name | 4-chloro-2-phenylpyridine |
| Appearance | solid (off-white to light yellow) |
| Melting Point | 67-70°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CC=C(C=C1)C2=NC=CC(Cl)=2 |
| Inchi | InChI=1S/C11H8ClN/c12-10-7-8-13-11(9-10)6-4-2-1-3-5-6/h1-9H |
| Purity | Typically >98% (commercial sample) |
| Synonyms | 2-Phenyl-4-chloropyridine |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited pyridine, 4-chloro-2-phenyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 4-chloro-2-phenylpyridine is a 25-gram amber glass bottle, clearly labeled with chemical name, hazard symbols, and batch number. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for pyridine, 4-chloro-2-phenyl-: Securely packed in drums or bags, ensuring safe, efficient chemical transport. |
| Shipping | Pyridine, 4-chloro-2-phenyl-, should be shipped in tightly sealed containers, protected from light and moisture. It must comply with all relevant hazardous material regulations, including appropriate labeling and documentation. Transport should occur via approved carriers, following UN and DOT guidelines, as the compound is typically classified as a flammable liquid and may pose health hazards. |
| Storage | Pyridine, 4-choro-2-phenyl- should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers and acids. Keep the container protected from light and moisture. Use proper personal protective equipment when handling. Store in accordance with local, state, or national chemical safety regulations. |
| Shelf Life | The typical shelf life of 4-chloro-2-phenylpyridine is 2-3 years if stored in a cool, dry, tightly sealed container. |
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Purity 98%: pyridine, 4-chloro-2-phenyl- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield reactions and product consistency. Melting point 60°C: pyridine, 4-chloro-2-phenyl- with melting point 60°C is used in agrochemical formulation, where it facilitates efficient compound blending and process control. Molecular weight 219.67 g/mol: pyridine, 4-chloro-2-phenyl- with molecular weight 219.67 g/mol is used in organic synthesis research, where it enables accurate stoichiometric calculations and reproducibility. Stability temperature up to 120°C: pyridine, 4-chloro-2-phenyl- with stability temperature up to 120°C is used in high-temperature reaction protocols, where it maintains structural integrity and limits decomposition. Particle size <10 µm: pyridine, 4-chloro-2-phenyl- with particle size <10 µm is used in solid formulation development, where it improves dissolution rate and homogeneity in the final blend. Chromatographic purity 99%: pyridine, 4-chloro-2-phenyl- with chromatographic purity 99% is used in analytical reference standards, where it delivers reliable calibration and quantification accuracy. |
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There’s no mistaking the shift in chemistry labs and manufacturing spaces over the past decade: precision compounds are in high demand, and their selection shapes success in everything from pharmaceuticals to crafted materials. Pyridine, 4-chloro-2-phenyl-, with a well-defined molecular structure and targeted performance attributes, stands out for sound reasons. The arrangement of the chlorine and phenyl groups on the pyridine ring gives this compound a unique edge, offering results both in the yield and reliability columns that chemists and engineers value.
People working at the bench or behind a computer modeling reactions see the difference first-hand. Classic pyridine derivatives have always served as pillars in synthetic routes, but swapping in a chlorine at the 4-position and a phenyl group at the 2-position opens up distinct reactivity. The 4-chloro group subtly rearranges electron density on the ring, tweaking both the nucleophilicity and the aromaticity of the molecule. Add in the large, stable phenyl moiety, and you’re looking at a compound that navigates distinct lanes in catalysis, drug discovery, and dye synthesis.
Synthesizing pyridine, 4-chloro-2-phenyl-, whether in modest research batches or scaled-up for commercial operations, is not a one-size-fits-all operation. Chemists are sticklers for purity because even a trace contaminant can derail synthesis or throw analytical results into doubt. This specific pyridine derivative usually comes in a crystalline or powdered form, with producers reporting purity levels of 97% or higher. Moisture levels, melting point range, and spectral fingerprints play into evaluations, too. In my experience, overlooked specs cause headaches, and chasing them down eats up time and money—so starting with robust, transparent quality checks pays off.
Having spent long hours poring over NMR and GC-MS traces, I can say that spectral clarity is far more than a box to tick; it safeguards every downstream application. With 4-chloro-2-phenyl-pyridine, the signature peaks—the aromatic hydrogens, the distinctive chloro-induced shifts—offer solid confirmation you’re working with the right material. That kind of verification matters, especially for anyone optimizing multi-step syntheses or preparing new pharmacophores.
Those who’ve worked on complex syntheses can vouch for the frustration that comes with an unreliable intermediate. Pyridine, 4-chloro-2-phenyl- solves plenty of those problems, acting as a springboard for more elaborate molecules. In fine chemicals and agrochemistry, it serves as an anchor, making the leap from benchtop curiosity to scalable input. Grad students once dreaded batch inconsistencies, but with today’s rigorous production controls, this compound now delivers repeatable outcomes for gram-scale reactions and pilot runs.
It’s not only about reaction yields; safety and environmental impact come into the spotlight, too. Working with certain pyridine derivatives used to mean chasing down foul odors and tackling waste handling nightmares. The 4-chloro-2-phenyl modification, though, often reduces volatility and sharpens selectivity, cutting down both loss and exposure risk. Material management in the lab feels smoother, and scaling up to production lines or kilo labs usually brings fewer surprises.
Traditional pyridine compounds built many foundational tools for the life sciences, but not every derivative wears the same hat. Adding a phenyl group at the 2-position adds bulk and a degree of rigidity, while chlorine at the 4-position subtly alters physical and electronic character. These small variations shift the way molecules interact in a reaction vessel and guide the paths chemists can take. With 4-chloro-2-phenyl-pyridine, you’re usually looking at higher thermal stability compared to simpler alkyl-substituted pyridines, as well as improved shelf life.
In catalytic coupling reactions, some pyridines fade under harsh conditions, while the phenyl-chloro version keeps its cool. Medicinal chemists spot new binding profiles when this compound comes into play. Dyes, pigments, and specialty polymers also depend on subtle shifts in structure for color or material strength. Anyone who’s swapped out a methyl group for a phenyl in a synthesis can tell you it isn’t just academic—the product’s performance and the way the process scales up both change.
Pharmaceutical researchers often gravitate to compounds like pyridine, 4-chloro-2-phenyl- for their versatility. Those working on kinase inhibitors, for example, appreciate its ability to anchor a range of side chains while standing up to tough deprotection steps. Patent filings from drug developers tell the story: more teams are looking for molecular scaffolds that behave consistently under variety of coupling and cyclization conditions. In my own project history, compounds built from this pyridine startpoint consistently outperformed those relying on less substituted rings.
Outside pharma, it plays a growing role in electronic materials, chiral ligands, and even as a probe molecule in analytical chemistry. The blend of lipophilicity from the phenyl group and tunable electron density from the chloro means the compound doesn’t just disappear in a mix. It adds sticking power and guides selectivity, which has practical upshots in separations, sensors, and ink formulations. Dye chemists, in particular, lean on it for stability and richness of color.
Like every specialized reagent, pyridine, 4-chloro-2-phenyl- comes with a learning curve. It doesn’t behave like standard pyridine; technicians must calibrate for changes in polarity and reactivity. Storage deserves respect—keeping it dry and away from strong acids or oxidizers extends shelf life and prevents breakdown. Those who’ve lost batches to rogue moisture will testify to the costs involved in careless handling. Chemical suppliers often seal the product in amber glass or specialized polymers to keep it stable between delivery and use, a practice I’ve personally seen cut waste by a large margin.
Waste disposal practices follow the same scrutiny as with other specialty reagents. While advancing regulations tighten up disposal options, responsible labs work ahead with efficient quench protocols and pre-approved waste streams. Peer-reviewed studies increasingly point to greener synthesis routes for this and related compounds, replacing harsh solvents and minimizing heavy-metal byproducts. As a chemist who has watched the shift toward greener alternatives, I recognize how compounds like pyridine, 4-chloro-2-phenyl- can slot neatly into new methods built around sustainability.
No matter where a team picks up its supply—whether from large global suppliers or niche specialty manufacturers—batch consistency becomes a make-or-break factor. One false step can throw off multi-kilogram synthesis, force unplanned purification, or even void product registrations. From my own experience collaborating with both commercial and academic partners, I’ve learned that robust quality documentation and transparent supply chains mean fewer headaches later. That’s especially true when sourcing for regulated markets, where audit trails matter as much as the molecule itself.
Feedback from users in the field regularly highlights the need for clear handling data and updated safety advice. Manufacturers aware of these needs have started including QR-coded links to lab-scale handling protocols or even video guides showing common troubleshooting steps. That kind of practical support feels far more useful than dry data sheets, particularly for junior staff or new researchers onboarding to a project for the first time.
Market shifts can hit raw material pricing hard, and specialty chemicals like pyridine, 4-chloro-2-phenyl- often ride the rollercoaster. Supply bottlenecks, changes in upstream chlorination processes, or even temporary trade restrictions put budgets under pressure. Those managing budgets in R&D or production can’t ignore cost when planning new methods, so substitutability becomes a key consideration. Discussions between procurement and laboratory teams get to the heart of balancing price with performance when deciding which intermediates to stock.
One notable trend has been cooperative bulk purchasing and closer relationships between reputable suppliers and end users. This reduces risk and locks in stable pricing, instead of leaving labs exposed to last-minute price surges. Teams managing inventory wisely, predicting runs and aligning batch sizes, see fewer workflow interruptions and less cash trapped in unplanned overstocks. The chemistry might be cutting-edge, but the supply chain side is about clear communication and mutual trust.
With hands-on work comes an awareness of health and safety. Pyridine, 4-chloro-2-phenyl- doesn’t call for full hazmat gear, but it’s no household cleaner, either. Reasonable ventilation, gloves, and goggles form the front line of defense. Most experienced chemists follow checklists, but the real lessons hit during incident debriefs or safety audits—things that get missed with even the best procedures on paper. Consistent labeling, proper segregated storage, and clarity on emergency actions make daily work safer for teams of all skill levels.
People who’ve spent time in teaching labs appreciate the subtle difference between textbook safety and the pulse of a busy workday. The best-run programs set aside time for hands-on drills and refresher briefings, not because regulation demands it but because long-term safety culture depends on lived experience. Mentoring new staff into good habits makes for smoother lab runs and safer workplaces overall.
Companies and academic groups can’t overlook the environmental angle. As laboratory and industrial protocols adapt to tighter waste control and lifecycle reporting, compounds like this pyridine derivative play crucial roles in safer, less toxic syntheses. Published literature has begun documenting greener preparation paths: swapping out hazardous reagents, recycling solvents, and stepping away from heavy metals. While not every project can go green overnight, the increasing uptake of greener alternatives shows a clear direction.
By sharing tips and lessons learned across the community—whether that means using less solvent, avoiding toxic byproducts, or designing shorter synthetic routes—the bar moves higher for everyone. Even small changes in how a common intermediate gets produced echo down the chain, improving the sustainability profile of the finished product. Based on my own time in collaborative consortia, I’ve noticed that success stories spread quickly and influence supply decisions for similar compounds.
There’s no substitute for experience in the lab or on the production line, but good products build lasting trust over time. Pyridine, 4-chloro-2-phenyl- has earned its place in the toolkit of research groups, development chemists, and manufacturing teams by standing up to rigorous testing, day after day. Teams who share their data openly—whether on purity, handling, or environmental footprint—make a clear case for sticking with a reliable source. This transparency lines up with global trends in evidence-based decision making and traceable supply.
Practical details—clear lot-level traceability, informed tech support, and honest sharing of both strengths and limitations—allow buyers and users to make informed choices based on genuine experience rather than second-hand reports or marketing gloss. That’s how robust products build reputations, not just as a number in a catalog, but as trusted components of discovery and production pipelines.
What’s sometimes missed in industry overviews is the degree of hands-on expertise driving every step, from raw material selection to final delivery. Behind every drum or vial stands a team—synthetic chemists fine-tuning reaction times, analytical chemists confirming purity, and packaging staff safeguarding integrity through distribution. Practical wisdom flows from one generation to the next as younger staff pick up not only technical skills but also a sense of pride over getting the little things right.
Chemistry, at its heart, depends on both data and intuition. Teams juggling schedules, weathering market swings, and chasing the perfect batch know how much can go wrong without close attention. The best operations combine seasoned perspective with a willingness to adapt, using both automation and hands-on troubleshooting. It’s that blend of reliable product and reliable people that lets pyridine, 4-chloro-2-phenyl-, and compounds like it, serve as more than just another reagent on the shelf.
This compound speaks to larger trends in research and technology: the push for better building blocks, smarter syntheses, and more robust products. As AI and advanced analytics transform the route-planning and troubleshooting sides of the chemical business, the tangible properties of molecules like pyridine, 4-chloro-2-phenyl- become more valuable than ever. Data from high-throughput experimentation and detailed molecular modeling reinforce practical outcomes, ensuring each new generation of chemists builds on proven results rather than reinventing worn paths.
Collaborative projects, particularly those crossing boundaries between academic curiosity and industrial pragmatism, have begun using this compound as a reference point for new reaction classes and breakthrough materials. That’s the kind of progress students, postdocs, and team leads alike get excited about: working from a well-defined, high-performing intermediate lets research move past the stumbling blocks of unreliable starting material.
The impact of well-characterized, reliably sourced intermediates radiates outward. Pyridine, 4-chloro-2-phenyl- plays direct roles in developing new therapeutics, safer agrochemicals, and longer-lasting materials—all areas shaping how societies face future challenges, from health to climate to manufacturing resilience. The ability to source, handle, and put this compound to use with confidence shelters teams from risk, encouraging bold science grounded in practical safeguards.
For many scientists, trustworthy intermediates underpin a culture of openness and innovation. It’s these connections between hard data, proven materials, and the daily work of researchers that unlock progress not just in one institution or company, but across an entire field. The story of pyridine, 4-chloro-2-phenyl-, stands as a testament to the care, experience, and commitment behind every successful experiment or scalable process.