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HS Code |
253919 |
| Product Name | 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride |
| Cas Number | 3564-41-6 |
| Molecular Formula | C11H15N · HCl |
| Molecular Weight | 197.71 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 244-249 °C (dec.) |
| Solubility | Soluble in water and methanol |
| Synonyms | 4-Phenyl-1,2,3,6-tetrahydropyridine hydrochloride |
| Storage Conditions | Store at 2-8 °C, keep container tightly closed |
| Purity | ≥98% (typical) |
| Iupac Name | 4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride |
As an accredited 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 25 grams of 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride, labeled with hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL loaded with securely packed drums of 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride, ensuring safe, moisture-free chemical transportation. |
| Shipping | 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride is shipped in tightly sealed, chemical-resistant containers. It should be protected from moisture and light, and transported under ambient conditions unless otherwise specified. Compliant with relevant safety and regulatory guidelines, the package is clearly labeled as per hazardous material standards, ensuring safe and secure delivery. |
| Storage | Store **1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride** in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Use proper labeling and secondary containment to prevent spills. Follow all safety guidelines and local regulations for storage of laboratory chemicals. |
| Shelf Life | **Shelf Life:** 1,2,3,6-Tetrahydro-4-phenylpyridine hydrochloride is stable for at least two years when stored tightly sealed and protected from light and moisture. |
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Purity 99%: 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride with 99% purity is used in pharmaceutical intermediate synthesis, where high purity ensures optimal yield and minimal by-product formation. Melting Point 218°C: 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride with a melting point of 218°C is used in controlled crystallization processes, where thermal stability supports process robustness. Molecular Weight 211.72 g/mol: 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride with a molecular weight of 211.72 g/mol is used in medicinal chemistry research, where precise dosing and reproducible results are required. Stability Temperature 40°C: 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride with stability up to 40°C is used in ambient storage conditions, where material integrity is maintained during handling and transport. Water Content ≤0.5%: 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride with water content below 0.5% is employed in anhydrous organic synthesis protocols, where low moisture prevents hydrolysis of sensitive intermediates. Particle Size D90 ≤100 µm: 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride with particle size D90 below 100 µm is used in tablet formulation, where fine particle distribution enhances homogeneous mixing and bioavailability. |
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Stepping into any research lab, you quickly see the shelves lined with bottles labeled in meticulous detail. Some names carry more weight than others, thanks to unique properties or critical uses. 1,2,3,6-Tetrahydro-4-phenylpyridine Hydrochloride holds a place among compounds that persistently draw attention for both its molecular structure and what it contributes to synthesis. Though it looks like a mouthful, anyone who’s spent time in synthetic organic chemistry likely remembers its role in developing new catalysts or producing intermediates for pharmaceuticals. This compound stands out due not only to its reactivity but also for the practicality it brings to chemical processes.
Talking about 1,2,3,6-tetrahydro-4-phenylpyridine hydrochloride means recognizing what gives it a competitive edge. This compound features a phenyl group attached to a partially saturated pyridine ring, with a hydrochloride salt counterion—details that aren’t just textbook notations, but real working distinctions chemists rely on daily. Pairing that with its crystalline nature and solid stability makes it easier to measure and handle than some of the more volatile options often used in similar syntheses. I’ve yet to see it give as much trouble as more hygroscopic alternatives or those moisture-prone reagents that clump up on humid days.
Specifications always matter, especially once scale moves beyond milligrams. Pure 1,2,3,6-tetrahydro-4-phenylpyridine hydrochloride offers a fine white to off-white appearance and a consistent melting point, which usually sits around the 220-225°C range. That might sound like a footnote, but this window helps definitively confirm the substance on hand, which spares rework and headaches when preparing it for further use. Levels of detection using nuclear magnetic resonance and infrared spectroscopy line up with the structural formula, giving extra peace of mind on quality. The hydrochloride salt form allows for improved solubility in polar solvents such as water and ethanol, opening multiple doors for reaction planning.
Unlike some of the wilder compounds, it doesn’t bring a strong odor, making bench work a bit less distracting. Though mild, it isn’t without caution—like any pyridine derivative, it deserves the usual gloves and ventilation setup that protects against accidental skin or respiratory exposure. Even after years around the lab, that kind of respect for chemistry’s hazards never fades, no matter how familiar the name on the label.
Use in pharmaceutical research has long put 1,2,3,6-tetrahydro-4-phenylpyridine hydrochloride on the map. Its role? Often acting as a building block for more advanced chemical entities, providing a stable foundation for further functionalization. In my early career days, working with this material sped up several synthetic routes, since its structure encourages nucleophilic addition and various coupling reactions with fewer unwanted byproducts. For those moving through early-stage drug development, fewer purification rounds translate directly into saved time—and often, money.
Continuing innovation keeps expanding uses for this compound. Some groups rely on it in creating dopamine-related pharmacophores, exploring central nervous system agents, or chasing after more selective enzyme inhibitors. While not every project ends up at clinical trial, plenty of promising candidates carry fragments from this simple starting material. If there’s a lesson in all this experimenting, it’s that reliable access to baseline molecules like this one speeds up not just experimental chemistry, but also innovation cycles on a larger scale.
It’s not just new drug development where this hydrochloride matters. Advanced materials chemistry taps it for the formation of functional polymers and ligands. These materials go on to support catalysis or even separation technologies, broadening the reach far outside the medicine cabinet. From personal experience, I’ve seen collaborative projects in my network use it to anchor custom ligands for metal complex formation, with results crossing over into green chemistry and cleaner manufacturing processes. Those broader applications often appear in journals a couple of years later, reshaping what seemed possible during the late hours at the bench.
Stepping back, it pays to look at what separates 1,2,3,6-tetrahydro-4-phenylpyridine hydrochloride from its close cousins. Alternative pyridine derivatives, such as 2,3,4,5-tetrahydropyridine or plain pyridinium compounds, sometimes see use in similar reactions. Still, they bring their own quirks—lower stabilities, higher reactivity that gets unpredictable, or less versatile solubility when shifting between solvents. To cite just one common frustration, rival compounds that lack the phenyl group don’t deliver the same conjugated character. That limits their effectiveness in reactions requiring strong pi-stacking or those where aromaticity bolsters material properties.
Compare ease of handling: the hydrochloride salt is much less finicky over time than the free base form of the same compound. I’ve seen free bases degenerate after a few mishandlings, introducing impurities just by sitting too long on the shelf. Being able to keep a hydrochloride salt stable under standard storage, deciding to scale up without a string of quality checks, gives this product a practical leg up.
Synthetic accessibility also matters—like many in the field, I’ve weighed time savings against cost more times than I can count. This tetrahydro-phenylpyridine doesn’t take elaborate steps to synthesize, compared to many other heterocyclic precursors. That helps bring costs in line, makes planning smoother, and saves precious calendar days in a development timeline. For teams trying to beat out patent cliffs or respond to competitive pressure, such an edge can be the deciding factor.
From personal experience, the single biggest difference happens in routine. A high-quality batch seldom disrupts workflow with unexpected inconsistencies in melts, IR data, or purity. If project timelines depend on scheduled delivery and reliable results, that kind of predictability is worth its weight in gold. Many labs—mine included—record lot numbers and crosscheck supplier data to keep tabs on any small shifts in physical properties. Most other tetrahydropyridines don’t deliver the same outcomes, which shows up when yields take a hit. Reliable consistency, over time and across suppliers, allows researchers to focus on discovery instead of troubleshooting.
Beyond lab scale, pilot plants and manufacturing lines value the same traits. Predictable crystallization and steady purity profiles keep downstream processes on track. One minor impurity can balloon into wasted effort during scale-up; a reliable starting point nips that risk early. If there’s anything I’ve learned from scale-up headaches, it’s never to take tight analytical controls for granted.
Current awareness of environmental impact continues to shape chemical choices, especially over the past decade. 1,2,3,6-Tetrahydro-4-phenylpyridine hydrochloride doesn’t pose the same waste disposal headaches or volatility issues present in older, more hazardous aromatic amines or polycyclic byproducts. We were able to integrate it into reaction streams that required minimal tweaks to existing waste management protocols. That doesn’t exempt it from standard safety data reviews or impose on compliance routines, but it simplifies the job.
For regulatory filings, knowing the provenance and purity of material speeds things up. This compound often ships with the necessary certificate of analysis—shaving time off the tedious repetition of in-house testing for every new lot. While every chemical involves paperwork, streamlined supply and quality checks count in highly regulated environments, easing the journey from benchtop to scaled production.
Research thrives on access to proven building blocks. The steady demand for 1,2,3,6-tetrahydro-4-phenylpyridine hydrochloride in both public and private research institutions shows just how integral it has become, especially with the appetite for rapid molecular diversification. Citing statistics from the past two decades, published studies have pointed time and again to its utility in producing tailored pharmaceutical agents. Use in creating dopamine analogs or exploring neuropharmacological agents demonstrates the real, measurable impact of having this material on hand.
Collaborative projects between academia and industry draw on these resources not just for one-off synthesis, but for iterative rounds of modification and structure-activity relationship studies. In conversations with colleagues at major research centers, access to this particular hydrochloride meant fewer failed syntheses, more reproducible results, and less troubleshooting waste mid-project. That’s a benefit that doesn’t show up in the catalog listings but shines through in publication records, patent filings, and review boards.
While the compound has roots in laboratory-scale processes, demand has moved sharply upward with the emergence of high-throughput screens and automated batch reactors. Projects that once took a postdoc months now finish in weeks, thanks to easy integration into robotic workflows. Having personally overseen such an automation ramp-up, ready availability of starting materials like this saved both money and project morale. It let teams focus on fine-tuning reactions and brainstorming new targets.
Many labs aim for safer, more ergonomic routines. When the compounds in use are less volatile or hazardous, safety training gets easier, and everyday use feels less fraught. The hydrochloride version of tetrahydro-4-phenylpyridine brings clear benefits by being less fussy about air and moisture exposure, and more predictable in solid form. No more scrambling to seal bottles between each sample or worrying about chemical clouds escaping. As anyone who’s spent hours in fume hoods knows, patient, thoughtful choices about materials add up in energy saved—and in reduced stress for early-career researchers.
Not all chemicals travel equally well. Substances that degrade, require refrigeration, or present fire risk often raise logistical hurdles on their way to the lab. This hydrochloride doesn’t call for special shipping restrictions. Common storage on a dry shelf suffices, meaning it can be incorporated easily into laboratory or even small-scale manufacturing stockrooms. Fewer delivery hiccups mean fewer delays overall. My own team faced fewer missing shipments and less spoilage as a direct result of switching to compounds with this kind of transport resilience.
Cross-disciplinary projects can put extra strain on chemical supplies, especially if organic chemists, medicinal chemists, and analytical scientists align on short notice. Working with a compound known for consistent structure and purity bridges those gaps, letting teams work in parallel with fewer surprises. Teams lean on such dependable materials to move ideas from conceptual stages through iterative design, synthesis, and analysis. Breaking down barriers between research areas starts to rely on everyday decisions about the chemicals called upon, and this one often appears as that bridge.
Broader uptake often reflects cost and availability more than mere technical performance. In the institutions where I trained, lab managers balanced budgets down to the last cent. The relatively straightforward synthesis of 1,2,3,6-tetrahydro-4-phenylpyridine hydrochloride brings down costs, meaning smaller teams aren’t priced out of ambitious projects. This democratizes research a step or two, fostering discovery regardless of the grant size backing a project.
Even a product with many strengths isn’t without its issues. This hydrochloride, while more manageable than precursor forms, still falls under controlled handling due to compound class. Stringent storage in secure areas ensures safety, which can slow down workflow or introduce paperwork. Chemical users need regular refresher training to keep health and safety compliance sharp, as even less toxic derivatives call for discipline and oversight. Keeping up with these requirements takes ongoing effort from teams and infrastructure.
Some users have noted batch-to-batch variability when switching suppliers, as not all production methods mirror each other exactly. These hiccups rarely halt a project outright, but they remind teams to double-check supplies well before key experiments or deadlines. Labs often adopt a policy of pre-testing new lots and maintaining communication with producers for transparency on synthesis and purification procedures. Such strategies help minimize downtime and keep project risk manageable.
The larger research community continues to press for improvements where small changes deliver wide gains. Broader access to analytical data for every lot produced builds trust across the supply chain. Open, regular dialogue between producers and lab teams shortens troubleshooting cycles, especially if minor changes in synthetic routes or purification methods introduce impurities. Some innovators suggest crowdsourced reporting of any new findings or impurities, which could help everyone recalibrate best practices in real time.
Reducing environmental and safety burdens through greener production methods feels within reach, given industry trends. Switching to cleaner solvents or minimizing waste during manufacturing not only drops disposal costs but also appeals to companies aiming for long-term sustainability. Pilot projects using continuous flow or less hazardous reagents show what’s possible—progress sometimes comes faster in new plant setups than in legacy facilities, but interest across the chemical industry remains strong.
Integration with real-time analytical systems supports tighter quality control, letting users spot outliers and defects before they enter the research cycle. Recent studies point toward automation in both process control and reporting, cutting down on tedious paperwork and improving transparency. For those juggling fast-moving projects, these improvements will likely play a big role in keeping teams focused on science, not administration.
Stepping out of my own experience and looking across the broader landscape of chemical research, the value of a thoughtfully engineered compound becomes clear. 1,2,3,6-Tetrahydro-4-phenylpyridine hydrochloride continues to make its mark by blending practical benefits with reliable performance. From lab novices just learning their trade to seasoned process chemists streaming up new products, this compound finds a spot not just on the shelf but in the daily problem solving that moves science forward. While there’s always room for improvement, and every innovation writes new stories into the fabric of research, dependable materials like this one help sharpen focus—letting teams keep their eyes on discovery, not distraction.