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HS Code |
313292 |
| Compound Name | 1-Boc-1,2,3,6-tetrahydro-pyridine |
| Iupac Name | tert-butyl 1,2,3,6-tetrahydropyridine-1-carboxylate |
| Molecular Formula | C10H17NO2 |
| Molecular Weight | 183.25 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Cas Number | 146705-99-1 |
| Boiling Point | 110-112°C at 10 mmHg |
| Density | 1.03 g/cm3 |
| Purity | Typically ≥97% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Solubility | Soluble in organic solvents (e.g., dichloromethane, ethyl acetate) |
| Smiles | CC(C)(C)OC(=O)N1CCC=CC1 |
| Inchi | InChI=1S/C10H17NO2/c1-10(2,3)13-9(12)11-7-5-4-6-8-11/h4,7H,5-6,8H2,1-3H3 |
As an accredited 1-Boc-1,2,3,6-tetrahydro-pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25g of 1-Boc-1,2,3,6-tetrahydro-pyridine; sealed with a screw cap and labeled with hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely loaded 1-Boc-1,2,3,6-tetrahydro-pyridine in sealed drums, ensuring stability and compliance with safety regulations. |
| Shipping | **1-Boc-1,2,3,6-tetrahydro-pyridine** is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It is transported in accordance with all relevant regulations for hazardous chemicals, typically under ambient conditions, unless specified otherwise. Proper labeling and documentation accompany the shipment to ensure safe handling and regulatory compliance. |
| Storage | Store **1-Boc-1,2,3,6-tetrahydro-pyridine** in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, in a cool, dry, and well-ventilated area. Protect from light, moisture, and sources of ignition. Refrigeration (2–8°C) is recommended to minimize degradation. Ensure proper chemical labeling and follow all relevant safety protocols for handling organic compounds. |
| Shelf Life | 1-Boc-1,2,3,6-tetrahydro-pyridine is stable for up to 2 years when stored tightly sealed at 2–8°C, protected from moisture. |
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Purity 98%: 1-Boc-1,2,3,6-tetrahydro-pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures reproducible yield and high final product quality. Melting Point 38-42°C: 1-Boc-1,2,3,6-tetrahydro-pyridine with a melting point of 38-42°C is utilized in solid-phase peptide synthesis, where controlled phase transition enhances coupling efficiency. Stability Temperature up to 60°C: 1-Boc-1,2,3,6-tetrahydro-pyridine with stability temperature up to 60°C is deployed in multi-step organic transformations, where it maintains structural integrity under rigorous conditions. Molecular Weight 198.28 g/mol: 1-Boc-1,2,3,6-tetrahydro-pyridine with molecular weight 198.28 g/mol is applied in quantitative NMR analysis, where precise mass contributes to accurate quantification. Low Moisture Content <0.5%: 1-Boc-1,2,3,6-tetrahydro-pyridine with low moisture content (<0.5%) is employed in moisture-sensitive couplings, where minimized water content prevents hydrolysis side reactions. Colorless Oil Form: 1-Boc-1,2,3,6-tetrahydro-pyridine in colorless oil form is used in automated synthesis workflows, where clear appearance facilitates visual inspection and purity control. Single Isomeric Form: 1-Boc-1,2,3,6-tetrahydro-pyridine in single isomeric form is used in enantioselective catalysis experiments, where isomeric purity ensures stereochemical predictability. |
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Organic chemistry keeps moving forward because of great tools and fresh approaches. One compound making a real difference for researchers and industrial chemists these days is 1-Boc-1,2,3,6-tetrahydro-pyridine. Over the years, new protecting groups and functional building blocks have reshaped what’s possible, especially in pharmaceutical development. Looking at this product, there’s a reason it’s become a staple in both start-up labs and big facilities.
On paper, the structure of 1-Boc-1,2,3,6-tetrahydro-pyridine looks simple. It’s a nitrogen-containing heterocycle with a tert-butoxycarbonyl (Boc) protecting group at the first position. In the real world, this structure addresses pain-points that chemists have had for years. For example, any synthesis needing a nitrogen atom without the headache of unwanted side reactions gets a big boost. I’ve met chemists who lost entire batches because similar compounds didn’t give enough stability or clean reactivity.
The Boc group offers clear benefits. Out of the available protecting groups, Boc shows up more and more because it handles a range of reaction environments, sitting firm against both acid and base under moderate conditions. Take an amine without protection—one stray acid wash, and things go south. So that simple Boc shield keeps work on track, saving hours or days.
Some vendors and catalogs stock a long list of protected tetrahydropyridines, but only a few options work across scales without unexpected surprises. I’ve seen the slow frustration when a compound breaks down halfway through a run, leaving teams scrambling for a fix. Consistency counts for a lot, especially when scaling from milligram quantities in a discovery project to kilograms in process development. Here, 1-Boc-1,2,3,6-tetrahydro-pyridine keeps its promise. Reactions tend to run smooth, batch to batch, even when swapping solvents or changing temperatures within normal lab ranges.
Compared to simple tetrahydropyridine or straight 1,2,3,6-tetrahydropyridine hydrochloride, the Boc-protected form simplifies downstream steps. Purification gets easier. Isolation leaves less mess, which matters when deadlines are tight. Fewer byproducts mean less column time, so scale-ups can stay lean. In a world where everyone watches the bottom line, that’s real value.
Almost every medicinal chemist I’ve met has a story about nitrogen heterocycles. These rings appear across treatments for depression, Parkinson’s, hypertension, and beyond. The 1-Boc-1,2,3,6-tetrahydro-pyridine core matches several targets in both small molecule drug research and agrochemical pipelines. Instead of starting from scratch, teams reach for this intermediate and use it as a launchpad for further transformations—alkylation, acylation, ring expansions, and even selective oxidations.
Adding a Boc group makes a world of difference at the planning table. Most synthesis projects try to keep options open. With this compound, after removing the Boc group under simple acid conditions, the underlying amine stands ready for final modifications. That means start-ups don’t risk a pile-up of failed projects, and late-stage research dodges wasted effort. Instead of getting boxed in, the route stays flexible, boosting success rates.
Work in agriculture, material science, or specialty chemical sectors usually needs efficient, cost-effective intermediates. I’ve seen this firsthand in polymer modification projects and pesticide synthesis planning. Here, 1-Boc-1,2,3,6-tetrahydro-pyridine shines because it resists breakdown under conditions that would ruin similar amines, letting teams introduce new functionality or connect to advanced scaffolds.
In polymer science, nitrogen building blocks have opened up new types of conductive materials and coatings. The Boc-protected ring allows gentle incorporation into existing polymer chains, sidestepping uncontrolled crosslinking that can make films brittle or uneven. This isn’t theoretical—it’s what lets advanced films and membranes work in everything from batteries to next-gen drug delivery vehicles.
Talking about a raw material, people often worry about handling risks and stability in storage. Over the years, the field moved away from corrosive, unstable nitrogen reagents toward milder, safer options. 1-Boc-1,2,3,6-tetrahydro-pyridine offers solid shelf-life. As long as it stays dry, workers can weigh, transfer, and dissolve it into standard solvents without a mess or dangerous fumes. In my own work, reducing the number of hazardous steps made the project run smoother, and everyone felt safer.
Long-term storage studies publish solid numbers. This compound resists oxidation in sealed containers and doesn’t need cooling as aggressively as old-fashioned alternatives. For operations managing tight space, every cubic meter of storage counts. Not having to reserve deep-freezer slots lightens the load for both bench chemists and logistics staff.
Research and manufacturing often run into roadblocks at the compliance or documentation stages. Complex mixtures, impurity profiles, and non-standard chemistry slow down release or trigger longer review cycles. Because 1-Boc-1,2,3,6-tetrahydro-pyridine sits in clean territory with strong characterization (think NMR, LCMS, and FTIR), it stands up well to scrutiny. That helps regulatory packagers in pharma and agrochemical fields tick another box—no ambiguity about structure, traceability, or identification testing.
This isn’t trivial. For teams trying to move forward on synthetic routes, every ambiguous analytical result means delays and potentially more costs. Building a route around well-characterized building blocks pays off down the line. I’ve seen projects lose months waiting for a supplier to resolve batch inconsistencies, and frequently, simply choosing a compound like 1-Boc-1,2,3,6-tetrahydro-pyridine would have spared headaches.
Every chemist faces decisions about efficiency and reliability. If a non-protected tetrahydropyridine works, why bother with the extra protection group? Over time, experience shows that protection isn’t just a theoretical precaution—it shapes yield, controls selectivity, and sometimes makes the difference between a project hitting its milestone or going back to the drawing board. By avoiding uncontrolled reactions at the amine site, this Boc-protected option keeps the rest of the molecule open for bolder chemistry.
Other protecting groups compete, such as benzyl or fluorenylmethyloxycarbonyl (Fmoc). Still, Boc treatments balance the need for stability and ease of removal. Acidic work-ups are routine in most labs, and this compound cleans up nicely without exotic reagents. With Fmoc, you need basic conditions and extra purification. Anyone who’s spent time optimizing deprotection workflows knows every extra wash or step introduces another place for things to go wrong.
In early research, most compounds behave. As projects scale up, differences come to light. I’ve run into intermediates that only play nice at gram scale, then produce problematic residues on kilogram runs. With 1-Boc-1,2,3,6-tetrahydro-pyridine, the simple handling gets appreciated more as the stakes get higher. Larger systems forgive fewer mistakes. Handling, solubility, thermal stability, and clean reactions with alkyl or acyl halides matter at scale. The more I talk with process chemists, the more they want tools that stay reliable all the way from discovery to manufacturing floor.
Cost also steps into the picture. For a protected intermediate, affordable access in bulk lots is key. Vendors keep improving on this front for Boc-protected heterocycles, and investment in route optimization has made this compound more widely available. Start-ups and large firms alike appreciate a stable supply without sharp price swings. In one case, a team kept their project afloat during a vendor shutdown because another source offered consistent supply of 1-Boc-1,2,3,6-tetrahydro-pyridine—something that didn’t happen with more specialized options.
High-purity intermediates matter for the final product. Impurities, especially nitrogen-based ones, sometimes sneak through even the most thorough monitoring but get flagged in downstream bioassays or toxicology screens. In my years of talking to quality teams, this is where Boc-protected intermediates pay for themselves. The steric bulk and predictable reactivity profile mean unwanted rearrangements and byproducts show up less often—saving development timelines and supporting safer medicines and chemicals.
This matters for public trust, too. Drug recalls or delays eat up headlines, cost millions, and can erode confidence across a whole sector. By choosing intermediates with fewer chances for odd byproducts, companies reduce the risk of late-stage surprises. In chemical manufacturing, successful teams build their decks with high-quality, reliable inputs, and this compound checks every box.
Waste management, sustainable sourcing, and energy usage matter more each year. Green chemistry isn’t a token phrase—it’s become central to decision-making. Several case studies show that Boc protection routes for tetrahydropyridine derivatives produce less hazardous waste and allow for recycling of solvents and simple work-up. The lighter environmental footprint helps both compliance officers and company sustainability pledges.
Switching to a product like 1-Boc-1,2,3,6-tetrahydro-pyridine also opens the door to shorter reaction sequences. Less steps, less waste, and less exposure to high-risk chemistries. Colleagues in contract research tell me that using this compound early lets them trim entire days off project timelines, which in itself saves hundreds of liters of solvent and reduces energy bills. Every time these improvements happen, research budgets breathe easier and teams sidestep regulatory headaches over chemical waste.
Current research trends show demand rising for intermediates that combine clean performance with easy modification. I see it every year at conferences—teams showcasing shorter, more efficient routes to complex products, often enabled by careful choice of starting building blocks. 1-Boc-1,2,3,6-tetrahydro-pyridine ticks key boxes: solid chemical stability, simple protection/deprotection, clear analytical signatures, and ready up-scaling. These factors push the field forward and let innovative ideas get off the ground faster.
What’s most interesting: feedback keeps cycling from manufacturing to discovery. Large-scale groups value consistent yields and simple purification, while discovery teams need flexibility and speed. This building block, used across both settings, keeps the community moving. Lessons from one camp inform improvements for the other.
Nothing’s perfect. Some synthesis protocols still favor older protecting groups, mostly out of habit or because in rare cases, Boc protection complicates highly acid-sensitive functional groups elsewhere in the molecule. The call is clear: keep the toolkit flexible. Plenty of labs experiment with combinations, moving between Fmoc-, Cbz-, and Boc-protected variants to squeeze every bit of efficiency from routes. Staying open to switching up strategies keeps teams competitive.
Supply chain reliability often gets overlooked until a batch runs dry or geopolitical shifts disrupt import patterns. More vendors entering the space for this particular intermediate help blunt that risk. I always tell project managers to keep at least two independent sources lined up. Sharing that experience saves headaches—since even strong intermediates amount to little if logistics falters.
Keeping chemistry projects on time and within budget means more than just choosing good raw materials. It’s about anticipating hiccups and building in robustness. Over time, practices have shifted to favor intermediates that offer both chemical track records and practical handling—the sort of “set and forget” reliability that only shows its real power in the toughest projects. 1-Boc-1,2,3,6-tetrahydro-pyridine fits this profile because it brings together straightforward storage, clarity under the microscope, and versatility under reaction conditions.
More companies invest in automation for synthesis, running high-throughput procedures to screen new reactions. Here, batch consistency shines. Technicians and algorithms alike benefit from intermediates that deliver predictable outcomes. I’ve watched more than one lab team swap in this Boc-protected tetrahydropyridine and see yield bumps or process cycle times shrunk, making a difference for both large firms chasing patents and academics chasing tenure.
Looking forward, the push for even greener, more sustainable methods continues. This calls for deeper partnerships between suppliers and researchers, so supply chains stay nimble and quality remains high. Transparent documentation and regular independent testing matter just as much as up-front savings. Choosing intermediates with solid scientific backing, demonstrated across the literature, makes success less a matter of luck and more a matter of planning.
In the end, chemistry success stories rarely come from a single miracle discovery. They build on a foundation of countless smaller wins—like swapping a tricky starting material for something cleaner and safer, or choosing an intermediate that removes worry from process scale-up. 1-Boc-1,2,3,6-tetrahydro-pyridine sits at this intersection. By offering stability, clarity, and flexibility where it counts, it’s powering innovations ranging from smarter medicines to tougher, greener materials, and keeps the field pressing forward.