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HS Code |
813934 |
| Name | 2-Methyl-1,3-dithiane |
| Cas Number | 4251-35-2 |
| Molecular Formula | C5H10S2 |
| Molecular Weight | 134.26 |
| Appearance | Colorless to yellow liquid |
| Boiling Point | 184-186°C |
| Melting Point | -17°C |
| Density | 1.101 g/cm3 at 25°C |
| Refractive Index | 1.552 |
| Flash Point | 76°C |
| Solubility In Water | Insoluble |
| Smiles | CC1CSC(S1)C |
| Pubchem Cid | 10496 |
As an accredited 2-Methyl-1,3-Dithiane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle with a secure screw cap, labeled "2-Methyl-1,3-Dithiane" and detailed hazard/safety information. |
| Shipping | 2-Methyl-1,3-Dithiane is shipped in tightly sealed, clearly labeled containers to prevent leaks and contamination. It should be transported in compliance with local and international chemical shipping regulations, typically using cool, dry conditions. Handle with care, and ensure proper documentation, hazard identification, and emergency contact information are included with each shipment. |
| Storage | 2-Methyl-1,3-dithiane should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Proper labeling and segregation from food and drink are essential. Use appropriate personal protective equipment when handling to prevent exposure. |
Applications of 2-Methyl-1,3-Dithiane in Industrial ManufacturingWe supply 2-Methyl-1,3-Dithiane to original equipment manufacturers and contracted processors requiring a high-purity sulfur-containing reagent for strictly defined organic synthesis workflows. The following sectors actively incorporate this material in tightly controlled routes, governing exact formulation and process integration to achieve consistent product quality and compliance with international industry regulations. Detailed below are the principal industrial application scenarios, with specific compliance, dosage, process, and end product references based on actual downstream usage. 1. Pharmaceutical Intermediate SynthesisContract API manufacturers and pharmaceutical fine chemical plants use 2-Methyl-1,3-Dithiane as a key intermediate or masked thiocarbonyl equivalent in multi-step active pharmaceutical ingredient development, especially for molecules requiring selective carbonyl protection or introduction of sulfur heterocycles. The formulated intermediate typically proceeds through protection-deprotection strategies or offers a controlled sulfur source when constructing thiol-containing drug structures. Facilities operate under validated protocols, with strict batch traceability and impurity profiling. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingMajor crop protection synthesis facilities employ 2-Methyl-1,3-Dithiane as a masked carbonyl reagent or sulfur donor for the preparation of selective herbicides, fungicides, or insecticidal active ingredient precursors. The intermediate typically enters into catalyst- or base-promoted condensation sequences, facilitating the production of sulfur-substituted ring systems essential in modern agrochemical structures. Producers document batch-wise material control and downstream process validation under sector-specific regulatory guidelines. Industry compliance standards
Typical usage ratio
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3. Flavors and Fragrances SynthesisAuthorized aroma chemical producers introduce the compound in the synthesis of sulfur-containing flavor or fragrance ingredients where specific odorant notes are required, such as truffle, garlic, or meaty undertones. 2-Methyl-1,3-Dithiane is engaged as a protected sulfur precursor, facilitating the construction of target molecules with exacting sensory profiles while maintaining food-grade process control. Production runs must demonstrate full traceability, with batch records and organoleptic profiles secured for audit. Industry compliance standards
Typical usage ratio
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4. Electronic Chemical Synthesis (Photoresist Component Precursor)Specialty chemical plants serving the microelectronics sector integrate 2-Methyl-1,3-Dithiane into the closed-loop synthesis of sulfur-containing intermediates used in advanced photoresist systems. The material acts as a precursor for custom protecting groups and bridging ligands required in photolithography resin engineering. Tight control over metal content, trace impurities, and batch documentation is mandatory to ensure semiconductor process compatibility and adherence to industry reliability specifications. Industry compliance standards
Typical usage ratio
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5. Specialty Polymer Additives Production2-Methyl-1,3-Dithiane is incorporated by polymer compounders as a specialty sulfur donor or protected monomeric unit in controlled-rheology polymers or crosslinker synthesis. The compound modifies polymer backbone functionality, introduces targeted chain branching, or facilitates post-polymerization chemical modification. Facilities ensure raw material traceability with batch-wise QC to validate sulfur incorporation and final property profile against performance standards or customer-specified formulation protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
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Over the years, our manufacturing line has handled hundreds of organosulfur compounds, but anyone who’s run a synthetic chemistry operation knows that not every dithiane behaves the same. 2-Methyl-1,3-dithiane carries its own specific set of traits that make it well suited as a building block in fine chemical synthesis. Unlike its parent, 1,3-dithiane, the introduction of the methyl group at the 2-position gives the molecule a different shape and reactivity profile. This change unlocks new possibilities for our partners working at the cutting edge of fragrance, pharmaceuticals, and materials science.
Our product, recognized by the CAS number 505-29-3 and molecular formula C5H10S2, crystalizes as white to off-white needles—a form that reduces dusting and makes precise weighing much more practical in a full-scale synthesis bay. While some products have a tendency to retain impurities from the raw thiodiglycol feedstock, our process targets batch-to-batch consistency. Years of incremental improvement have minimized off-smells and secondary cyclic sulfur compounds, which carry over easily in poorly controlled batches. No amount of paperwork or certification can match the confidence a sharp-eyed operator gets from seeing consistent visual and olfactory cues—details experienced shippers and warehouse managers never discount.
In the organosulfur world, byproducts occur fast, especially when you run a process involving hydrogen sulfide gas or formaldehyde. For 2-methyl-1,3-dithiane, each run starts with methyl mercaptan in strictly measured concentrations. We monitor the temperature curves tightly. Lab teams, often skeptical of minor changes, have seen clear spikes in minor thioaldehyde impurities when shortcuts are taken. Our hands-on experience says straight out: keeping reaction temperatures within several degrees of the optimum delivers both yield and purity. Older literature misses much of the nuance that today’s real-world operators face. For example, moisture content, even in trace amounts, will impact shelf life and the product’s practical use in enolate chemistry.
The chemistry here gets more interesting. Adding the methyl group at the 2-position nudges the electron density around both sulfur atoms. This seemingly subtle change enables more selective lithiation. In the lab, customers often tell us that they reach greater yield in alkylation steps using 2-methyl-1,3-dithiane compared to the unsubstituted parent. We keep a small sample from each batch for in-house reaction tests before shipments ever leave our facility—no third-party intermediary determines acceptance criteria for us. At this point, we’ve tracked outcomes for years, not months. Failures and surprises never stay hidden for long when the performance in the end use is tracked so closely.
In a world driven by high-throughput labs, every minute saved matters. 2-Methyl-1,3-dithiane’s melting point sits between 43-45°C, which means operators dealing with low-temperature crystallization or distillation simply do not face the same challenges found in more volatile cyclic thioethers. In practice, this helps keep process equipment clean and free of persistent residues. Chemists running alkylation or condensation reactions send us feedback on how easier it is to recover product during workup, as compared to more polar or less crystalline alternatives.
Specific gravity, refractive index, and GC purity still lead global standards for chemical trade, but our experience shows that trace impurities and decomposition behavior deserve as much day-to-day attention. Our long-term warehouse tests confirm that our packaging—the result of several rounds of feedback from both our logistics team and frontline customers—prevents oxygen and moisture ingress. This keeps the crystallinity sharp for months, outperforming traditional glass and most plastics. Temperature swings in transport across continents never result in caking or unwanted polymorphs, due to the careful moisture control at the fill stage.
Lab and process chemists regularly compare different dithianes, thianes, and even dithiolane analogs. It’s not a theoretical exercise. 1,3-dithiane itself remains common as a carbonyl protecting group, but its unsubstituted nature can lead to less selectivity and, sometimes, side products that lengthen post-reaction clean up. Our product’s extra methyl group changes reactivity in an essential way for lithium-halogen exchange and for alkylation regioselectivity. Several development teams working on fragrance intermediates have achieved higher chiral control—less wasted solvent, reduced purification time, and lower cost per kilogram in active ingredient development.
In gas phase or high vacuum work, other dithio-analogs like 1,3-dithiolane sublime more easily, causing product loss and potentially problematic accumulation in cold traps. 2-Methyl-1,3-dithiane presents a more robust option under these conditions. Its higher molecular weight and boiling point protect against volatile emissions during handling. From frontline technical operators to QA inspectors, the actual difference shows up in better safety records and increased reliability for the same budget.
Over several years and hundreds of shipments, 2-methyl-1,3-dithiane finds a home in dozens of application segments. The pharmaceutical industry draws heavily on its consistent lithiation for carbonyl umpolung chemistry. Several clients in peptides and small-molecule API production report higher batch-to-batch reproducibility compared to less substituted dithianes. Aromatic aldehyde and acetaldehyde masking goes more cleanly, with better overall recovery after deprotection.
Beyond pharma, the flavor and fragrance sectors have shifted toward custom derivatives, where a methylated dithiane can serve as an essential precursor for sulfur-containing aromatic compounds. We work with R&D labs that need kilogram-scale runs for pilot fragrance molecules. These groups rely on products that withstand extended storage, repeated opening, and repackaging. In these cycles, some dithiane analogs oxidize or polymerize far too easily; the stability of 2-methyl-1,3-dithiane, paired with the inert packing, delivers less product waste—a simple, measurable advantage.
Materials researchers experimenting with advanced polymers, particularly those exploring high-index or sulfur-rich matrices, often require a dithiane that doesn’t interfere with radical initiators or crosslinking agents. Our internal tests show that subtle changes in impurity levels—sometimes a variance of just 0.2%—draw the line between clean polymerization and gelling failures. These lessons aren’t found in standard handbooks or online datasheets; they come from daily troubleshooting, missed shifts, and direct feedback from crews handling both small-scale and tonne-lot orders.
Many down-the-line users underestimate the challenges inherent in the dithiane family. For example, purity on a certificate can mask persistent low-level contaminants. Over time, poorly controlled batches with incomplete reaction or insufficient purification turn up as trial failures in the customer’s lab, not during internal QC. Our solution combines incremental changes across the line: more refined reaction monitoring, periodic retraining in both the lab and on the shop floor, and process audits anchored in both yield numbers and real shipment feedback. We put as much focus into mid-batch sampling as we do the end test. The most valuable insights come from data trend tracking—seeing where, over 50 or 100 batches, a small drift appears and catching it before it becomes a cost-center issue.
Shipping and storage rarely receive enough attention from outside observers. In practice, dithianes can pick up odors or yellowing from air exposure, especially under suboptimal logistics. As a matter of course, we’ve adapted our fill process around high-barrier liners and inert gas blanketing for all major shipments. Extended shelf-life studies—often dismissed as nice-to-have—uncovered that the difference between a minor visual change and out-of-spec product can float just above modern analytical detection. Through practical, real-world QA, not just paperwork, we’ve prevented lost inventory for both ourselves and downstream users. Our internal waste reduction, since shifting to these methods, has climbed by more than ten percent, freeing up space, cash flow, and workflow time on our own site and for our customers.
Long-term success in chemical manufacturing never depends solely on initial process optimization or technical capability. Direct, unfiltered feedback from chemists, scale-up leads, and even maintenance engineers feeds into our day-to-day adjustments. When one partner reported occasional glassware fouling during large-scale extractions, our technical group traced it back to trace sulfur species evolving above the melting point. Minor tweaks in post-reaction purification solved the problem—and the customer’s yield returned to spec with no new capital expense.
In sectors where the requirements evolve at the pace of regulation, we use real data—failure rates, off-spec flags, and outlier batches—to drive each process upgrade. By keeping the manufacturing line directly connected to usage case results, we react quickly to small shifts in demand for custom specifications. In a year where solvent trace limits dropped for export into the EU, our line had already adapted, reducing solvent carryover below the new threshold ahead of schedule. Years of experience cutting solvent levels, swapping suppliers, and trialing new packing media made the transition fast and trouble-free for all parties downstream.
We’ve also built out data archives that go beyond standard batch tracking. Instead of only referencing lot numbers, our records include production conditions, operator logs, shipment routes, and customer QC reports spanning years. This helps us spot trends and anticipate possible issues tied to season, transport, or supplier changes. These archives, which began as a tool for in-house QA, have become valuable for consulting on process improvements with both new and long-term customers, many of whom rely on the subtle screening insights that only repeated, high-frequency experience delivers.
On every metric beyond raw material spec, the industry wins or loses on consistency—something only achieved through repetition, observation, and an unwillingness to let minor issues slide. Products like 2-methyl-1,3-dithiane succeed on scale because of continuous attention to details, not high-level descriptors or marketing speak. Our product joins a category many view as commodity but, in our experience, every improvement, every tiny tweak, makes a measurable difference for the user.
We know from many conversations and site visits that clients want more than an acceptable spec sheet. They need a product that does not introduce surprises in the middle of a critical campaign, that captures opportunity in throughput, and that reduces downtime in reaction setup. With our investment in analytic infrastructure and process reliability, feedback loops close fast. A customer reporting a minor off-odor or drop in visual quality will see that result tracked, traced, and mitigated at the source—no finger-pointing, no run-around through intermediaries.
We see, batch after batch, that diligence in process, combined with flexibility and speed of response, keep both the chemical and the business strong. For those out in the field, running late-stage process validation or driving R&D lines for new fragrance or pharma intermediates, such reliability means deadlines met and value captured. While it’s rare for end users to see all the steps behind a product like 2-methyl-1,3-dithiane, each bottle moving out our door carries years of hard-won knowledge, measured and improved through every shipment, every customer call, and every returned lot analyzed in our onsite lab. This is the story behind our product, and the experience guiding every batch forward.