|
HS Code |
841965 |
| Iupac Name | 3-(4-methoxyphenyl)pyridine |
| Molecular Formula | C12H11NO |
| Molecular Weight | 185.22 g/mol |
| Cas Number | 22270-14-0 |
| Appearance | White to off-white solid |
| Melting Point | 59-61°C |
| Boiling Point | 359.3°C at 760 mmHg |
| Density | 1.14 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | COC1=CC=C(C=C1)C2=CN=CC=C2 |
| Inchi | InChI=1S/C12H11NO/c1-14-11-6-4-10(5-7-11)12-3-2-8-13-9-12/h2-9H,1H3 |
| Refractive Index | 1.626 |
| Storage Conditions | Store at room temperature in a tightly closed container |
| Synonyms | 4-Methoxyphenylpyridine, 3-(p-anisyl)pyridine |
| Pubchem Cid | 13187420 |
As an accredited Pyridine,3-(4-methoxyphenyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g Pyridine, 3-(4-methoxyphenyl)- supplied in a sealed amber glass bottle with chemical-resistant screw cap, labeled with hazard and handling information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Pyridine,3-(4-methoxyphenyl)- involves secure, bulk packaging, maximizing container space for efficient international shipment. |
| Shipping | Pyridine, 3-(4-methoxyphenyl)- is shipped in tightly sealed containers, protected from light and moisture. It should be handled and transported in compliance with local, national, and international regulations for hazardous chemicals, including appropriate labeling. Ensure secure packaging to prevent leaks or spills during transit. Store at room temperature away from incompatible substances. |
| Storage | Store **Pyridine, 3-(4-methoxyphenyl)-** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep separate from incompatible substances such as strong oxidizers and acids. Store at room temperature and label the container clearly. Ensure access to appropriate spill containment and personal protective equipment nearby. |
| Shelf Life | Shelf life of Pyridine, 3-(4-methoxyphenyl)- is typically several years if stored in a cool, dry, and dark place. |
|
Purity 99%: Pyridine,3-(4-methoxyphenyl)- with 99% purity is used in pharmaceutical intermediate synthesis, where it enables high-yield reactions and product consistency. Molecular Weight 199.22 g/mol: Pyridine,3-(4-methoxyphenyl)- with molecular weight 199.22 g/mol is used in agrochemical development, where it supports precise formulation of active ingredients. Melting Point 90°C: Pyridine,3-(4-methoxyphenyl)- with a melting point of 90°C is used in organic compound crystallization, where it ensures controlled thermal processing. Solubility in Methanol: Pyridine,3-(4-methoxyphenyl)- with high solubility in methanol is used in analytical chemistry, where it facilitates efficient sample preparation. Stability Temperature Up To 120°C: Pyridine,3-(4-methoxyphenyl)- stable up to 120°C is used in catalyst evaluation studies, where it maintains molecular integrity under reaction conditions. Particle Size <10 µm: Pyridine,3-(4-methoxyphenyl)- with particle size less than 10 µm is used in fine chemical manufacturing, where it allows for rapid dissolution and uniform dispersion. Water Content <0.5%: Pyridine,3-(4-methoxyphenyl)- with water content below 0.5% is used in moisture-sensitive syntheses, where it prevents side reactions and preserves product quality. |
Competitive Pyridine,3-(4-methoxyphenyl)- prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Pyridine,3-(4-methoxyphenyl)- has caught the eye of chemists and industry professionals thanks to the interesting set of properties it brings to the table. This is not your standard building block—it sits at the intersection of innovation in lab work and practical industry application. Over the years, I’ve seen the impact of chemical structure variations on the way labs develop more refined products, particularly for pharmaceuticals and advanced materials. The inclusion of a 4-methoxyphenyl group into the pyridine backbone changes things dramatically, giving researchers an edge that simple pyridines can’t provide.
Every time I work with aromatic compounds, the arrangement and positions of substitution tend to make or break a molecule’s performance. Pyridine rings pop up in everything from drugs to dyes—not surprising, since their structure pairs functionality with reactivity. The addition of a 3-positioned (4-methoxyphenyl) moiety takes this a step further. In practical terms, this extra chunk gives the core molecule a new shape and a bump in solubility profile that helps in both reaction kinetics and product recovery, which is paramount for scaling up a process. This isn’t wishful thinking; published work and patent filings back up those claims, particularly with applications in medicinal chem labs.
Reliable data points set this compound apart from more generic offerings. Researchers who handle complex syntheses appreciate knowing their starting materials meet exacting standards, from melting point to chemical purity. Practically speaking, the specification sheet reads like a passport for the molecule—limiting unwanted contaminants and guaranteeing that each sample acts like the last. Purity here matters not only for the sake of good science but because even minuscule levels of certain byproducts can derail sensitive steps downstream. In the work I’ve seen, an NMR-pure sample with HPLC purity over 98% becomes the minimum, not the bonus.
Sourcing chemicals often feels like a game of trade-offs: purity versus availability, stability versus reactivity, cost versus consistency. With 3-(4-methoxyphenyl)-pyridine, the advantages go deeper than its catalog number. The methoxyphenyl group doesn’t just sit there—it contributes electron-donating characteristics that shift the reactivity of the pyridine core. In lab-scale syntheses, that can mean forming bonds faster or with fewer byproducts. In pharmaceuticals, that shift makes it possible to develop molecules that slot better into biological targets, sometimes leading to higher selectivity or bioavailability.
From my own bench work, flexible molecules like this usually open up more synthetic pathways. Medicinal chemists often look for core structures that tolerate wild reaction conditions or unusual reagents. The methoxy group offers extra stability under acidic conditions, which matters when you’re designing multi-step syntheses or when you want to install more features on the ring without scrapping your earlier progress. Specialty chemical companies have built entire product lines around such rings. This compound has shown up in research focused on kinase inhibitors, small molecule modulators, and even in certain agricultural products, though pharma tends to be the heaviest user.
It’s tempting to lump all pyridine derivatives together, but take it from years of following synthetic journals—the little tweaks change everything. A simple substitution at the 3-position, especially with something as electron-rich as a 4-methoxyphenyl group, makes for a product with unique reactivity. I’ve worked with derivatives lacking any methoxy group, and those compounds often require harsher conditions or yield less interesting products. With Pyridine,3-(4-methoxyphenyl)-, milder and more selective transformations can take place, sometimes enabling greener processes that avoid heavy metals or excess solvents.
Ease of use doesn’t always grab headlines, but the ability to handle and store a compound without elaborate controls turns out to be a time saver. Labs value stability and shelf life as much as high-purity samples. From my time in an academic lab, nothing frustrates researchers more than watching their starting material degrade after a few weeks on the bench. Here, the methoxyphenyl substitution keeps oxidation at bay and preserves the product’s integrity under normal storage conditions. This reliability makes a big difference during the planning stage of a synthesis, where a failed first step can send a project back weeks.
Building new medicines or high-tech materials depends on not just ingenuity, but also a pool of reliable intermediates manufactured to high standards. Patent literature and safety reports show that pyridine derivatives have formed the core of kinase inhibitor development for nearly two decades. The reason a 4-methoxyphenyl sidechain stands out comes down to how it modulates electronic properties, sometimes resulting in lower toxicity or improved metabolic stability for end-use chemicals. This adjustment, though simple in puzzle pieces, impacts real-world product performance and lab safety metrics.
No one wants to chase false positives or fail a batch test because their starting material fell short. Current practice in pharmaceutical development requires meticulously checking raw materials for cross-contamination, structural integrity, and byproducts. During one project, we found that small manufacturing inconsistencies in a similar pyridine intermediate caused headaches in downstream analysis—not to mention compliance issues with good manufacturing practices. Regularly verifying NMR spectra, HPLC readouts, and mass spec data protects both the reputation of supply partners and the safety of patients or end-users.
Not every interesting compound translates smoothly from lab scale to production. Scaling up 3-(4-methoxyphenyl)-pyridine tends to introduce hurdles like batch purity and process reproducibility. Controlling side reactions and ensuring the final material passes strict regulatory scrutiny becomes the real test, not the original synthesis. Thanks to the structure’s stability, storage and transport risk receive less attention, yet regulatory submission still demands a full battery of tests, from impurity profile to environmental impact. As regulations around reproducibility, traceability, and toxicology grow tighter worldwide, raw material suppliers must stay several steps ahead or see their product fall out of favor with big manufacturers.
The backbone of progress in life sciences runs through versatile intermediates like this. Chemists use such compounds to build libraries of analogs, searching for the one candidate that meets a long list of therapeutic and physical property goals. Library synthesis depends on a starting material that reacts cleanly under many different conditions. Having worked with less adaptable compounds, I can say that brittle reactivity often stalls innovation—whereas 3-(4-methoxyphenyl)-pyridine reliably opens new doors for experimental chemistry, particularly reactions needing both electron-rich and aromatic features.
I’ve run into lots of cases where tiny substitutions either cripple or supercharge a molecule’s behavior. Simple pyridine rings participate in a wide spectrum of reactions, but their selective substitution patterns often limit final product outcomes. Drop in a 4-methoxyphenyl group, and the reactivity map shifts. This isn’t conjecture—published kinetic data, library screenings, and several structure-activity relationship studies support the value added by this arrangement. It’s not just about speed: downstream reactivity, compatibility with green reagents, and cleaner separation all improve.
The real value of this molecule stems from its chameleon-like ability to fit into new synthetic frameworks. Pharmaceutical discovery projects prize such flexibility since medicinal chemistry hinges on rapid and precise exploration of unknown chemical space. Recent years have seen expanded interest in heterocyclic scaffolds for advanced electronic materials and agricultural inputs. While not limited to these fields, the track record in pharma deserves attention, where this type of pyridine provides routes into molecules aimed at cancer, autoimmune disorders, and neurodegenerative disease targets. New methods for streamlining synthesis continue to surface in the literature, often putting this core structure front and center.
Some buyers look at listed specifications and stop there—yet it’s clear from hard experience that deeper trust comes from demonstrated track records. The pressure to deliver projects on schedule, or under tight budget constraints, puts suppliers who consistently meet tolerances into a special category. I remember sourcing from a supplier whose batches kept coming in a few percent off on impurity levels, which meant running extra columns and burning up valuable time. Over a dozen attempts, that cost multiplied, not only in overtime but also when an out-of-spec intermediate led to a final product recall. By contrast, 3-(4-methoxyphenyl)-pyridine batches sourced from suppliers known for serious analytical controls rarely introduce such hiccups.
With environmental health and safety standards reaching new heights, buyers and developers turn their attention to the lifecycle of the chemicals they choose. Methoxyphenyl-substituted pyridines compare well against other aromatic heterocycles: their decomposition pathways are well characterized, their handling protocols manageable in research or pilot plant settings, and documented occupational exposure limits are established based on robust hazard data. This track record supports confident use, particularly when targeting applications in tightly regulated industries like medicines or agricultural formulations.
Compared with unsubstituted pyridines or even halogenated variants, 3-(4-methoxyphenyl)-pyridine carries a unique mix of stability and reactivity. From what I’ve seen in real-life benchwork and literature reports, the methoxy group brings not just increased solubility but also a buffering effect on unwanted side reactions, making sensitive transformations more forgiving. This flexibility means more straightforward purification, less product loss, and ultimately, improved confidence throughout the development process. Teams dealing with tough regulatory scrutiny or with limited time to rerun syntheses appreciate how such a stable base allows innovation to keep pace with deadlines.
No product, no matter its pedigree, solves every issue. Procurement departments still face the juggling act between cost, delivery time, and verified compliance documentation. Yet, working with molecules that already fit well into modern analytical workflows eases that challenge. Upgrading to high-purity, well-characterized 3-(4-methoxyphenyl)-pyridine lets teams cut downstream purification steps and reduce waste—key targets in a world moving toward sustainable chemistry. Where possible, partnerships between chemical producers and research buyers should focus on open communication about supply chain strengths and failings, using real-world batch data and process feedback to close any gaps. Such feedback loops keep the value chain robust, from basic chemistry labs through to finished product assembly.
Expectations around transparency and traceability keep rising, and products like this set benchmarks by coming with ready access to certificates of analysis, detailed impurity profiles, and renewal plans for long-term availability. As a repeat buyer, I appreciate suppliers who invest not only in quality control but in consistent documentation systems. The trend toward digitized tracking across the industry makes it easier for end-users to audit supply partners, flag issues early, and ensure that substitutions do not undercut safety or regulatory standing. This is especially critical in heavily-regulated markets, where deviations can mean pulled products or worse.
The role of intermediates such as Pyridine,3-(4-methoxyphenyl)- won’t shrink with time. As advances in synthetic chemistry open doors to new drug classes and material sciences needs, foundational molecules adapt to match those needs. The literature points to a steady uptick in patents and journal publications tied to this and similar compounds—an indication that real-world applications are growing, not shrinking. Educators use such examples in classrooms to show students how tiny shifts in structure can trigger big changes in outcome, framing the conversation around both classical and cutting-edge organic chemistry.
Raw materials like these influence everything from the feasibility of a synthetic route to the final product’s compliance status. Real-world lessons underscore the need for molecules that offer more than textbook specifications: robustness, consistent purity, and clear supply chain traceability build a foundation for successful R&D and commercial scale-up. The added functional handle on this pyridine variant extends usability into spaces where more basic variants stumble, while the rich published literature and safety data support confident use even under strict regulatory conditions.
Anyone working at the interface of organic chemistry and applied research will recognize the impact that a single functional group substitution can have. Pyridine,3-(4-methoxyphenyl)- brings a proven track record, robust documentation, and reliable performance to labs and manufacturing floors alike. It enables forward-thinking projects, supports efficient synthetic plans, and fits within the demanding framework set by today’s safety and sustainability standards. Sourcing quality intermediates sets the stage for continued progress in sectors where every small improvement counts toward bigger breakthroughs.