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HS Code |
516396 |
| Cas Number | 67843-74-7 |
| Molecular Formula | C6H11ClO |
| Molecular Weight | 134.60 |
| Iupac Name | 2-(Chloromethyl)oxane |
| Appearance | Colorless to yellowish liquid |
| Boiling Point | 180-182 °C |
| Density | 1.082 g/mL at 25 °C |
| Refractive Index | 1.458-1.461 |
| Flash Point | 68 °C |
| Pubchem Id | 24373679 |
| Melting Point | -10 °C (approximate) |
| Solubility In Water | Slightly soluble |
| Synonyms | 2-(Chloromethyl)tetrahydro-2H-pyran |
| Smiles | C1CC(OC1)CCl |
| Inchi | InChI=1S/C6H11ClO/c7-5-6-3-1-2-4-8-6/h6H,1-5H2 |
As an accredited 2-(Chloromethyl)Tetrahydropyran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100g of 2-(Chloromethyl)tetrahydropyran, tightly sealed with a screw cap and hazard labeling. |
| Shipping | 2-(Chloromethyl)Tetrahydropyran should be shipped in tightly sealed containers, protected from moisture and light. Transport according to local, national, and international regulations for hazardous chemicals. Ensure proper labeling with hazard identification. Use appropriate secondary containment and cushioning to prevent breakage or leaks during transit. Temperature control is not typically required. |
| Storage | 2-(Chloromethyl)Tetrahydropyran should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Use appropriate chemical-resistant containers. Store in a chemical storage cabinet, preferably in a flammable materials or corrosives section, clearly labeled, and away from moisture and direct sunlight. |
Applications of 2-(Chloromethyl)Tetrahydropyran in Industrial Manufacturing2-(Chloromethyl)Tetrahydropyran serves as a key intermediate for several specialized chemical synthesis pathways. As the original manufacturer, we supply this compound to global clients in tightly defined downstream sectors where unique reactive profiles, strict compliance, and integrated processes drive demand. 1. Pharmaceutical Intermediate for Protected Nucleoside SynthesisFor advanced pharmaceutical manufacturing, our material functions as a tetrahydropyranyl (THP) etherifying agent during the protection of alcohol groups on nucleosides and carbohydrates. The selectivity and reactivity make it critical in multi-step API synthesis, especially for antiviral and oncology drugs where stability and protecting group removal yield influence overall efficiency. Our compound enables consistent process yields and purity profiles demanded by regulated markets. Industry compliance standards
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2. Fine Chemical Synthesis of Specialty Agrochemical Building BlocksWithin advanced agrochemical synthesis, 2-(Chloromethyl)Tetrahydropyran is utilized as an alkylation and protecting group agent to modify precursor molecules. Its role ensures stability of sensitive functionalities throughout multi-step processes, supporting stringent quality demands for crop protection active ingredient manufacturing. Integration within these synthesis routes contributes to selectivity and downstream hydrolysis performance. Industry compliance standards
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3. Production of Fine Fragrance Ingredients and FlavorsIn the flavors and fragrance industry, our product is leveraged as a masked aldehyde precursor and protected functionality provider. It enables stepwise synthesis of target aroma compounds—especially those containing sensitive aldehyde or alcohol groups—protecting against unwanted side reactions during oxidation, esterification, or acetal hydrolysis required for final note release. Its use under strictly monitored food-grade conditions supports batch reproducibility and regulatory acceptance for direct and indirect contact products. Industry compliance standards
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4. Advanced Materials Synthesis for Performance PolymersIn polymer and specialty resin manufacturing, 2-(Chloromethyl)Tetrahydropyran serves as a reactive intermediate for introducing functionalized pyran rings or as a monomer modifying agent. Its addition imparts controlled hydrophobicity, flexibility, and chemical stability in advanced polymer matrices, supporting the development of custom-engineered films, coatings, and high-performance adhesives. The process integration directly impacts end-use characteristics, especially for electronics, automotive, and specialty packaging sectors. Industry compliance standards
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Experience on the plant floor and in the laboratory shapes our approach every day, especially with products like 2-(Chloromethyl)Tetrahydropyran. This compound does not show up in textbooks as a star chemical, but its significance becomes obvious in specialized syntheses and pharmaceutical pipelines. Long before it makes its way downstream, its journey starts with a careful balance between chemical science and hands-on engineering.
The molecule itself comes from a straightforward family—tetrahydropyrans—but with a chloromethyl group snugged onto the ring. This configuration isn’t just for show. That extra chlorine atom increases its reactivity, opening doors for further functionalization in fine chemical and pharmaceutical synthesis. Unlike basic tetrahydropyran, the chloromethyl variant doesn’t just serve as a solvent or mild reactant; it actively participates as a key building block, especially for more advanced molecules where selective introduction of a chloromethyl group saves both time and cost.
2-(Chloromethyl)Tetrahydropyran, sometimes abbreviated as CMTHP in laboratory shorthand, lands in a specific category: it acts as an intermediate—not a final ingredient. During multi-step syntheses, the molecule often gets deployed where selectivity and stability matter. The placement of the chloromethyl group allows chemists to build out longer carbon chains, introduce nitrogen by substitution, or attach protected fragments to the ring without fussing over side reactions common with less stable chlorinated building blocks.
Looking at practical manufacturing, purity lends weight to the reliability of any reactive chloro-compound. Most synthesis flows demand a minimum purity of 98 percent, often pushing higher for sensitive processes. To get there, attention has to go not just to the starting material, but to every phase—from solvent selection, to temperature control, to the tight containment of hydrochloric acid off-gas during the chloromethylation step. Even storage requirements put their own demands on the plant.
Tetrahydropyran derivatives, once chlorinated, do not tolerate moisture and prolonged air exposure, or their quality quickly declines. Each batch must be sealed right away in containers designed for minimal headspace and tested for both water content and residual solvents. Over the years, we’ve seen Rudimentary fume hoods replaced by closed-loop scrubbing systems, not just for worker safety but also to scrub every last trace of acid that might degrade the product. Operators require a hands-on understanding of these nuances, built by monitoring real outcomes batch after batch.
2-(Chloromethyl)Tetrahydropyran seems to have found its real utility in pharmaceutical discovery and custom synthesis. Here, researchers look to it as a building block for protected alcohols, specialized heterocycles, and modified sugars that often become key fragments in active molecules. Unlike more basic alkyl chlorides, the tetrahydropyran ring forms a stable platform that resists hydrolysis, which helps the molecule survive under the harsh conditions sometimes necessary later in synthesis.
In the course of scaling from milligrams to kilograms, we’ve worked closely with chemists requiring even tighter tolerances—for example, reducing any by-products like the bis-chlorinated tetrahydropyran or recovering the ring structure if unwanted isomerization crops up. Every tweak, from changes in catalyst loading to adjustments in agitation speed during the chloromethylation step, makes a measurable difference at scale. These aren’t changes you read in journal articles; they are discoveries aged through direct contact with hundreds of process runs.
Specifications aren’t just about hitting a number on a certificate of analysis. Real-class operations test for trace impurities—down to single-digit parts per million—because once this molecule enters further reactions, impurities can catalyze side reactions or poison metal catalysts, leading to dropped yields or sticky downstream purification. One experience comes to mind: a client’s process yielded stubborn by-products, traced back to trace levels of formate left from a poorly neutralized batch. Cases like this inform why each process change goes through months of verification, not just for compliance, but for long-term stability.
Every batch release gets treated as a final statement of integrity. Even a simple moisture test or residual solvent exam can reveal a bigger story about upstream controls. Our own process control data show that slightly extended reaction times tend to boost selectivity, while overly aggressive chlorination generates hard-to-remove by-products. Transferring that knowledge into robust manufacturing protocols gives our partners confidence that the product will perform exactly as intended, no surprises mid-project.
Similar molecules sometimes create confusion for end-users. For instance, 2-(Bromomethyl)Tetrahydropyran or 2-HydroxymethylTetrahydropyran enter the same conversations. The bromide brings even higher reactivity, making it more suitable for certain nucleophilic substitutions but at the cost of lower stability and higher cost of both raw materials and waste treatment. The hydroxymethyl cousin gives a milder, less reactive platform, often favored in situations needing slow release or where environmental stability counts more.
In the real world, chemists seek a tradeoff between selectivity and reaction rate. The chloro version finds a sweet spot—easier to handle and store safely than the bromide, more reactive than the hydroxy or methoxy analogs, and less prone to nasty side reactions or decomposition during scale-up production. This gives it a practical edge, especially for complicated syntheses where stray halide ions or unwanted free radicals can slow everything down.
Experience teaches that 2-(Chloromethyl)Tetrahydropyran can demand respect during both production and use. Chlorinated intermediates require conscious control of emissions, containment, and worker exposure. Overlooking these safeguards quickly leads to corrosion issues or off-target contamination in both plant equipment and finished goods.
We use specialty linings on reactor internals and stainless valves where ordinary steel would fail within a few cycles. In our own startup phase, we learned the hard way that all process seals and bare metal must resist not only chlorinated solvents, but also trace HCl—and these headaches rarely appear in academic write-ups. Downtime and wasted batches rack up much faster in production reality than on the lab bench.
Training on in-plant handling goes well beyond standard safety lectures. Technicians work through scenarios where leaks might crop up, so containment and air monitoring systems back up every process run. Additional exhaust scrubbers and strategically placed drain points address the inevitable drips and off-gassing without creating unnecessary shutdowns. All these practices stem from running dozens of cycles, learning where procedures needed to tighten, and sometimes taking corrective actions after the fact. At this level of specialty chemistry, equipment engineering and chemistry knowledge blend seamlessly.
Few products offer such a clear window into the value of incremental change. Over the years, switching to more precise feed systems and updating reaction monitoring equipment allowed us to dial in temperature and stir rates—just enough to outpace side reactions by a few percentage points. Many improvements echo what we hear from downstream partners: clearer isolation procedures, improved rotary evaporator technique, and double-verified analytical protocols with both HPLC and GC-MS.
Another improvement has come in logistics and storage. Transporting chlorinated heterocycles adds extra complexity because improper packaging or delays make for real risk: hydrolysis, container deformation, or traces of acidic leaching. Speciality UN-rated packaging and lined drums are now a standard response to long transit times or wide fluctuations in warehouse temperature. We routinely perform stability checks—retesting for purity and reactivity every three months—to keep real-world feedback in sync with product shelf-life claims.
The cycle of feedback is not just encouraged—it’s necessary. Consistent reports from long-term clients shape both batch protocols and packaging upgrades. For example, several years back, a pharma partner noticed trace yellowing in a stored batch. It didn’t show up in routine QA, but post-release storage under humid conditions kicked off a color-forming reaction. The lesson prompted both us and the client to re-examine humidity controls in warehousing—ending with us introducing new silica-packed liners and a stricter cutoff for field replacements.
Most modifications like this originate from the intersection of plant experience, technical feedback, and willingness to act. In one project, researchers flagged minor losses in yield attributed to a buildup of halogenated residues late in their synthesis. By tracking it back to our wetting agent and shifting to a cleaner grade, we closed the yield gap. Such changes do not always appear on official paperwork but significantly affect downstream outcomes—timelines, costs, and operator trust.
Sourcing the right raw materials for specialty chlorinated products requires keeping one eye on regulatory changes and another on global supply. Early in our own journey, volatility in commodity solvents caused disruptions. Since then, we’ve adopted just-in-time supplies for critical feedstocks and built up relationships with two or more qualified vendors for high-risk inputs. Downstream, customers benefit from that stability—on-schedule deliveries mean no last-minute project delays due to chemical shortages.
With the increasing focus on sustainable chemistry, environmental compliance applies not only through all stages of production but also to emissions, effluent, and waste transport. We log every emission and run annual audits. These processes lead to cleaner operations and fewer surprises—both for regulators and clients with their own corporate sustainability standards.
Compared to bulk chlorinated solvents or simple alkyl chlorides, 2-(Chloromethyl)Tetrahydropyran’s true value lies in its tailored functionality. General-purpose chlorinated chemicals aim for cost-effectiveness on giant scales, but in our experience, the tetrahydropyran variant addresses far more targeted problems for pharmaceutical, agrochemical, or specialty material developers.
Bulk chloro compounds, such as dichloromethane or chloroform, concern themselves mainly with volatility and extraction capability, lacking opportunities for subsequent molecular elaboration. The six-membered oxygen-containing ring in 2-(Chloromethyl)Tetrahydropyran presents a scaffold for greater diversity in synthetic design—with practical results in everything from prodrug masking to flavor and fragrance engineering. These differences alter how clients think about process timing, functional group installation, and downstream purification.
Specialty intermediates push up against challenges not always visible on day one—reacting to evolving regulations, increased environmental scrutiny, and demand spikes caused by emerging drug targets. Our method answers those signals by combining operational discipline with hands-on flexibility. Real-world cases underline the importance of batch traceability, accurate record-keeping, and proactive communication with downstream users.
In practice, this translates to sample retention, robust deviation reporting, and periodic reviews of both old and new production data to spot trends. Reliable supply in this class of chemistry is forged not just in the reaction flask but through every stage—sourcing, process control, quality assurance, and transparent client dialogue. Small mistakes cascade quickly, so staying three steps ahead defines the difference between a reliable manufacturing partner and one who simply fills orders.
Today’s pharmaceutical and fine chemical sectors expect both flexibility and reliability. Given current trends toward more complex, highly functionalized molecules, demand for building blocks like 2-(Chloromethyl)Tetrahydropyran continues to grow. At the same time, tolerance for process upset—caused by out-of-spec input—decreases every year.
We’ve witnessed the migration of many partners from bulk analogs to specialty reagents to gain that last increment of stability, selectivity, or reactivity. The fine line between academic research and commercial production continues to narrow, yet field experience still provides the anchor. Many initial inquiries come from researchers running protocols published years before; the reality of scale, regulatory hurdles, and stringent impurity control rarely matches textbook expectations. Product stewardship combines a respect for the science with a respect for the uncertain—meaning continual investment in both process and partnership.
We carry forward a commitment to this balancing act—keeping work practical, rooted in direct experience, and constantly evolving based on both chemistry and customer realities.