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2-Methyl-1,3-Dithiane

    • Product Name 2-Methyl-1,3-Dithiane
    • Alias 2-Methyldithiane
    • Einecs EINECS 222-589-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 2-Methyl-1,3-Dithiane

    Applications of 2-Methyl-1,3-Dithiane in Industrial Manufacturing

    We 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 Synthesis

    Contract 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 (Finished Pharmaceuticals GMPs)
    • European Pharmacopoeia raw material monograph compliance (where applicable)
    • Chinese Pharmacopoeia (ChP) reference for locally filed APIs

    Typical usage ratio

    • 0.8–3.5 molar equivalents relative to the carbonyl substrate, adjusted according to the target structure and reaction route

    Downstream process integration

    • Charged in protection or formation stage reactors during the synthesis of β-ketoesters, diketones, or in mask-unmask cycles, then isolated and purified prior to further transformation

    Final product types

    • Thiol-containing drug substance intermediates
    • Beta-lactam antibiotic building blocks
    • Synthetic opioid precursors
    • Orphan drug candidate scaffolds (research scale)

    2. Agrochemical Intermediate Manufacturing

    Major 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

    • FAO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for Agchem Ingredients
    • REACH registration (EU 1907/2006) for intermediary chemicals
    • China Ministry of Agriculture NY/T 1978-2010 (pesticide raw materials)

    Typical usage ratio

    • 1.2–2.7 mole equivalents based on target agrochemical precursor; rate varies with ring size and desired substitution level

    Downstream process integration

    • Fed into reaction vessels before sulfur cyclization during the synthesis of thiazolyl and thiadiazole derivatives, followed by intermediate isolation and downstream functionalization

    Final product types

    • Precursors for triazole fungicides
    • Sulfur-bridged herbicidal intermediates
    • Thiadiazole-based insecticide components
    • Patent-pending experimental agricultural actives

    3. Flavors and Fragrances Synthesis

    Authorized 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

    • IFRA Code of Practice for Fragrance Ingredients
    • FCC (Food Chemicals Codex) additive grade requirements
    • US FDA 21 CFR Part 172 (Food Additives Permitted for Direct Addition to Food for Human Consumption)
    • ISO 22000:2018 Food Safety Management Systems

    Typical usage ratio

    • 0.15–0.45% w/w in aroma synthesis batches; concentration optimized to balance odor strength and residual solvent levels

    Downstream process integration

    • Dosed during the condensation or protection steps in sulfur flavorant production, downstream purification via vacuum distillation, finally diluted into bulk perfumery or flavor blends

    Final product types

    • Sulfurous flavor agents (e.g., for savory/bouillon bases)
    • Fragrance compositions with earthy or alliaceous notes
    • Ready-to-use flavor blends for processed food
    • Specialty essence concentrates for sauces or condiments

    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

    • SEMI C85 Specification for Electronic Chemical Purity
    • IPC-CH-65B Guidelines for Cleanroom Chemical Control
    • ISO 9001:2015 for electronic-grade chemical manufacturers
    • IEC 62474 (Material Declaration for Electronics Industry)

    Typical usage ratio

    • 0.05–0.15 mole fraction within precursor syntheses; adapted based on resin backbone requirements and masking group efficiency

    Downstream process integration

    • Introduced during the construction of photoresist precursor molecules, proceeding through deprotection and resin coupling, then purified to sub-ppb contaminant levels for semiconductor fab delivery

    Final product types

    • Photoresist monomer intermediates
    • Advanced lithography resin additives
    • Custom electronic-grade masking agents
    • Semiconductor dielectric material modifiers

    5. Specialty Polymer Additives Production

    2-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

    • ISO 14001:2015 Environmental Management for Polymer Processing
    • ANSI/SOCMA ChemStewards for specialty chemicals safety
    • UL Yellow Card Chemistry Certification (as required in certain applications)
    • ASTM D4000 Classification System for Polymers

    Typical usage ratio

    • 0.2–1.0 phr (parts per hundred resin) depending on base polymer type and crosslinking pathway; dosage adjusted for required mechanical properties

    Downstream process integration

    • Added during reactive extrusion or batch polymerization, followed by compounding, pelletizing, and potential blending with further functional additives

    Final product types

    • Sulfur-modified engineering plastics
    • Crosslinked specialty elastomers
    • Thermoplastic vulcanizate masterbatches
    • Custom-application additive concentrates
    Free Quote

    Competitive 2-Methyl-1,3-Dithiane prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2-Methyl-1,3-Dithiane: Our Direct Experience with a Key Synthesis Reagent

    Introducing 2-Methyl-1,3-Dithiane Inside the Plant

    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.

    A Closer Look: Synthesis and Control Points

    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.

    Specification and Real-World Usability

    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.

    Comparing 2-Methyl-1,3-Dithiane to Other Sulfur Heterocycles

    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.

    Industrial Usage: Facts from Real Orders

    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.

    Addressing Common Problems and Pitfalls in the Supply Chain

    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.

    Continuous Product Evolution, Informed by End-User Feedback

    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.

    Why Consistency and Experience Matter

    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.