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HS Code |
823655 |
| Iupac Name | 1-(4-chlorophenyl)-2-pyridin-2-ylethanol |
| Molecular Formula | C13H10ClNO |
| Molecular Weight | 231.68 g/mol |
| Cas Number | 20860-20-2 |
| Appearance | White to off-white solid |
| Melting Point | 94-98 °C |
| Solubility | Soluble in DMSO, methanol, ethanol |
| Smiles | OC(C1=CC=CC=N1)C2=CC=C(C=C2)Cl |
As an accredited α-(4-chlorophenyl)2-Pyridinemethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 100g amber glass bottle, tightly sealed, labeled with chemical name, hazard symbols, batch number, and storage instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for α-(4-chlorophenyl)2-Pyridinemethanol ensures secure, bulk chemical shipment with proper packaging, labeling, and safety compliance. |
| Shipping | α-(4-Chlorophenyl)-2-pyridinemethanol is shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. All packaging complies with relevant safety and regulatory standards, including proper labeling for hazardous substances. During transit, shipments are handled by trained personnel to ensure safe delivery and minimize risk of spills or exposure. |
| Storage | Store α-(4-chlorophenyl)-2-pyridinemethanol in a tightly closed container, protected from light and moisture. Keep it at room temperature (15–25°C) in a well-ventilated, dry area away from incompatible materials such as strong oxidizing agents. Ensure proper labeling and access restriction to qualified personnel. Follow local regulations for handling and disposal, and use appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life: **Store in a cool, dry place, tightly closed. Stable for at least 2 years under recommended storage conditions.** |
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Purity 99%: α-(4-chlorophenyl)2-Pyridinemethanol with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal yield and product safety. Melting Point 112°C: α-(4-chlorophenyl)2-Pyridinemethanol with melting point 112°C is used in organic reaction development, where its defined phase behavior aids in reproducible crystallization. Stability Temperature 60°C: α-(4-chlorophenyl)2-Pyridinemethanol with stability temperature up to 60°C is used in storage and transport of lab reagents, where thermal stability maintains structural integrity. Particle Size <50 µm: α-(4-chlorophenyl)2-Pyridinemethanol with particle size less than 50 µm is used in formulation of fine chemical blends, where small particle size enables quick dissolution and homogeneous mixing. Moisture Content <0.5%: α-(4-chlorophenyl)2-Pyridinemethanol with moisture content below 0.5% is used in moisture-sensitive syntheses, where low water content prevents side reactions and degradation. Molecular Weight 243.66 g/mol: α-(4-chlorophenyl)2-Pyridinemethanol with molecular weight 243.66 g/mol is used in analytical reference standards, where accurate molecular weight ensures precise quantification. Assay 98% (HPLC): α-(4-chlorophenyl)2-Pyridinemethanol with 98% assay (HPLC) is used in medicinal chemistry research, where confirmed composition supports reliable bioactivity screening. |
Competitive α-(4-chlorophenyl)2-Pyridinemethanol prices that fit your budget—flexible terms and customized quotes for every order.
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As a manufacturer with years of hands-on experience, we’ve seen α-(4-chlorophenyl)2-Pyridinemethanol carve out its role in the toolbox of modern synthesis. The chemical structure combines a 4-chlorophenyl ring with a pyridine backbone and a methanol moiety—this arrangement drives reliable performance in several sectors. The unique profile of this intermediate attracts ongoing interest for its use in pharmaceutical development and agrochemical research.
Every batch starts with an eye for practical purity and reproducibility. In our production, this molecule is available in white to off-white crystalline form, which helps users instantly spot any visible impurities. Moisture content is controlled tightly; every lot falls within a narrow range, as too much water undermines downstream applications. Packing in seal-tight containers, we minimize air and light exposure so each shipment matches the test results from the QC suite.
A typical batch will show purity by HPLC above 99%, with melting point, residue on ignition, and single spot by TLC as additional quality checks. Unwanted isomers, heavy metals, and trace solvents are reduced well below international thresholds. There’s a temptation to cut corners on drying or crystallization, but keeping these steps precise saves time and prevents mixing headaches later, something that has earned positive feedback from clients pursuing stricter regulatory filings.
Experience brings its own lessons. Vendors often focus on analytical numbers, but actual use teaches that lot-to-lot consistency matters most. Tight process control, clean plant routines, and robust batch records make the difference between a usable product and a batch that causes rework.
We’ve tuned each synthesis stage over years—reactor temperature, solvent choice, purification sequence—based on real, observed outcomes. This approach means that crystallization yields stay steady, loss rates remain low, and there is rarely a surprise spike in discoloration or contamination, which can otherwise force scrapping a valuable intermediate.
The decision to rely on specific glass-lined reactors and avoid certain additives grew out of practical problem-solving, not only from recommendations or literature. When one particular lot years ago developed a persistent off-odor, investigation traced it to a batch of solvents not matching in-house standards. We improved our in-house pre-testing to prevent repeat issues. These in-the-field learnings shape our batch organization, so what leaves our facility stands up to scrutiny at every level of the supply chain.
The molecule serves as a robust intermediate across several segments. In pharmaceutical manufacturing, it forms a reliable stepping stone in the synthesis of heterocyclic compounds and advanced API building blocks. The presence of both the pyridine and chlorophenyl groups gives it flexibility for coupling reactions, which appeals to R&D chemists looking to build complexity without introducing multiple purification rounds.
Some pharmaceutical discovery programs require multiple derivatives or analogs to screen for activity, and this one’s functional groups provide entry points for further modification. In our work with industry partners, we’ve seen successful routes toward compounds with promising biological activity, often because this intermediate supports clean conversion and downstream derivatization.
The agrochemical sector values the product for similar reasons. Laboratories developing novel crop protection agents frequently cite the stability of this molecule during key reaction steps. Alkylation or arylation, which can easily introduce impurities, tend to proceed more smoothly with α-(4-chlorophenyl)2-Pyridinemethanol due to its chemical balance and selective activation. Several research teams have shared feedback that minimizing process byproducts translates directly into less time spent adjusting or rerunning reactions.
Even where a typical user might expect only laboratory-scale quantities, our commitment to scalable, reliable production enables seamless transfers to pilot or full commercial runs. This mitigates risks in project upscaling—a lesson hard-learned through early mistakes with batch-to-batch variation and inconsistent particle size affecting filtration or dissolution rates.
In the competitive landscape of pyridine-based and chlorinated intermediates, α-(4-chlorophenyl)2-Pyridinemethanol takes its own route. Compared to similar molecules that swap the methanol group for other substituents, it balances reactivity and handling safety. Boronic acids and halogenated analogues can offer different coupling strategies, but they often require additional handling precautions or extra purification steps.
We’ve received samples from outside vendors that promote alternative intermediates with cost-cutting claims, but repeated tests show those batches carry higher levels of non-target isomers, coloring, or polymerization artifacts under ambient storage. These defects usually trace back to unstable intermediates, either during synthesis or after exposure to light and moisture.
Using α-(4-chlorophenyl)2-Pyridinemethanol in projects focused on medicinal chemistry, we have noted improved atom economy and cleaner separation profiles over structurally adjacent compounds. This holds particular appeal for groups pressed for time or addressing escalating raw material costs. Concerns that substituting other analogues might squeeze more reaction yield often don’t materialize in reality, once all purification and handling challenges are counted.
Another practical difference is the byproduct removal during reactions. While similar alcohols might leave behind emulsified residues, this product washes clean with standard aqueous or organic workups. That simplicity can shrink total batch time by hours—a benefit that seldom appears on specs sheets but makes a real impact on the ground.
Environmental compliance also finds a benefit. In our operations, fewer waste streams with problematic halogenated side-products emerge when using this intermediate, which reduces costs for safe disposal and aligns with current regulatory guidance. This isn’t a guarantee with every alternative on the market, especially in regions with strict wastewater controls.
Talking about quality goes beyond the certificate of analysis. A product has to work the same way, every time it reaches the bench or reactor. Our team developed in-line analytical setup, running real-time checks to detect process drift—a method that caught minor temperature excursions or batch inconsistencies before they reached the QC stage. Acting early like this consistently prevents batch failures and, more importantly, keeps end users out of frustrating troubleshooting cycles.
Our technical team finds that stability over storage is as important as initial assay results. We store finished product under defined temperature and light conditions, pull samples at planned intervals, and trend the analytical results. Spotting degradation patterns early helps prevent decline in potency or appearance, protecting users from troubles that only show up months later.
We’ve fielded questions about laser-focused parameters, from particle size to solubility in specific solvent systems. Each question guides us to invest further in process optimization or analytical upgrades, rather than chase theoretical performance claims not supported by actual lab results. A strong training culture ensures that operators, lab staff, and managers understand the importance of each QC check—no shortcut replaces learned experience.
Chemistry often advances faster than the basic building blocks can keep up. End users face project timelines, project pivots, and research pivots dictated as much by funding as by technical feasibility. From firsthand experience, providing a reliable, well-characterized intermediate frees up talent on the customer side to focus on what matters—project advancement, testing, and creative chemistry—rather than firefighting supply chain or quality headaches.
We built feedback loops into supply agreements, inviting users to report challenges or successes in their own words. Some shared production bottlenecks, others sought custom particle sizes, and a few encountered unexpected side reactions. This candid information shapes our R&D pipeline, prompts minor process changes, or grounds future upgrades. From these exchanges, we realized not every ‘improvement’ on paper translates into a smoother process downstream.
Technical collaborations, whether through formal partnerships or informal troubleshooting, spent time validating key reaction steps—in one case, optimizing the addition sequence limited formation of unwanted side-products, saving hundreds of man-hours during a campaign. In another, shipping timelines had to adapt to a sudden regulatory change for movement of chlorinated materials; pre-emptive batch validation helped minimize production halts. These lessons enable us to respond rapidly and share guidance rooted in lived experience, not just best guesses.
Every stage of chemical manufacturing involves trade-offs. Some compounds require inert-atmosphere handling or specialized packaging, which weighs on cost and logistics. α-(4-chlorophenyl)2-Pyridinemethanol holds up under standard sealed packaging and doesn’t pose major transportation issues, balancing stability with manageability.
We track global regulations for controlled substances or precursors. As rules evolve, we ensure that each batch matches current administrative needs, provide full origin traceability, and maintain samples for retrospective analysis. This level of detail once seemed excessive; over time, dealing with fluctuating customs, or responding to third-party audits, we realized it protects all stakeholders—not just us, but our clients and partners further down the supply chain.
Raw materials sourcing always brings tension. Price spikes in chlorinated aromatics or pyridine-based feedstocks can ripple through costs. Rather than chase temporary price drops with unreliable suppliers, we fostered long-term relationships with producers known for stable quality and transparency. This choice has paid off: in years with global shortages, we delivered orders as scheduled with few interruptions. Downstream users appreciate steady delivery—last-minute rework costs dwarf tiny price advantages from ‘bargain’ lots.
Laboratory and plant safety rank as daily priorities. Training, backing up procedures, and routine equipment checks stem from hidden incidents or learning from missed incidents elsewhere in the field. During scale-up, static discharge or improper solvent venting can transform routine tasks into critical events. Anticipating these risks, we’ve dedicated space and time to proper staff briefings, monitoring, and investment in safer equipment. The daily discipline required to maintain clean, incident-free operations affects every batch’s outcome and our reputation.
Looking ahead, pressures on research, regulatory regimes, and global movement of materials keep changing. End users push for cleaner, safer materials and less waste, while logistics become more demanding. Our engagement with users and our ongoing workflow reviews ensure α-(4-chlorophenyl)2-Pyridinemethanol production meets both current and emerging needs.
Working alongside R&D chemists, production heads, and procurement officers, we recognize that reliable supply, tested quality, and transparent manufacturing practices are what count. The feedback from those working at the bench drives continuous improvements—sometimes it’s a tighter purity spec, other times a tweak in packaging, or a switch in analytical methodology.
We’ve invested in process digitization for real-time tracking and documentation, so traceability or performance reviews are always ready. These records support clients needing compliance documentation or investigating unexpected reactivity. Having detailed batch histories, analytical trends, and storage notes on hand speeds up resolution and fosters trust.
Efforts to improve environmental performance continue. Where possible, we’ve switched to less hazardous reagents and adopted energy-saving plant modifications. By minimizing the use of problematic solvents, reducing waste generation, and maximizing raw material efficiency, we manage both compliance and real resource costs. Real-world sustainability means neither greenwashing nor excuses—just steady, incremental improvement.
Every innovation or improvement, small or large, starts with listening. Meeting the needs of those developing lifesaving pharmaceuticals or crop protection compounds means refining what we do behind the scenes, batch after batch. α-(4-chlorophenyl)2-Pyridinemethanol remains part of that landscape, shaped daily by the people who make and use it, and by the lessons learned through every production run shipped.