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2-Methyltetrahydrofuran-3-Thiol

    • Product Name 2-Methyltetrahydrofuran-3-Thiol
    • Alias 2-Methyl-3-mercaptotetrahydrofuran
    • Einecs 690-714-9
    • 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

    967212

    Cas Number 31786-29-1
    Molecular Formula C5H10OS
    Molecular Weight 118.20 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 130-133 °C
    Density 1.019 g/mL at 25 °C
    Refractive Index 1.4860
    Flash Point 31 °C
    Solubility Slightly soluble in water
    Odor Strong, sulfurous odor

    As an accredited 2-Methyltetrahydrofuran-3-Thiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 2-Methyltetrahydrofuran-3-Thiol arrives in an amber glass container with a secure screw cap and hazard labeling.
    Shipping 2-Methyltetrahydrofuran-3-thiol should be shipped in tightly sealed, chemically resistant containers under cool, dry conditions. It is typically transported as a liquid and should be protected from heat, moisture, and incompatible materials. Shipping must comply with relevant hazardous material regulations due to its flammability and potential health hazards.
    Storage 2-Methyltetrahydrofuran-3-thiol should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as oxidizers and acids. Keep the container tightly closed and clearly labeled. Store under an inert atmosphere, such as nitrogen, if possible, to prevent oxidation. Avoid prolonged exposure to air and moisture. Use only in chemical fume hoods.
    Application of 2-Methyltetrahydrofuran-3-Thiol

    Applications of 2-Methyltetrahydrofuran-3-Thiol in Industrial Manufacturing

    2-Methyltetrahydrofuran-3-thiol is a specialty sulfur-containing heterocycle used in several advanced chemical manufacturing sectors. As a direct manufacturer, we serve established downstream industries where this compound provides unique functional properties. Below, we detail primary application segments, highlighting compliance, formulation, production workflow, and representative finished goods.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize this compound as a thiol building block for synthesis of custom molecules in targeted drug development. Especially in thiolated drug candidates and as a masked thiol group precursor, it enables modifications in late-stage functionalization during active pharmaceutical ingredient (API) synthesis. Customers employ controlled reaction conditions to convert or protect thiol groups in high value small molecules, maintaining traceability from raw material to API batch manufacturing.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 210/211 (US cGMP regulations)
    • EU GMP Guidelines (EudraLex Volume 4)
    • USP <1092> Pharmaceutical Ingredients

    Typical usage ratio

    • 0.01–0.5 molar equivalents, adjusted based on target API’s synthetic path and downstream conversion efficiency

    Downstream process integration

    • Integrated in multi-step API synthesis at the stage requiring addition or transformation of thiol-containing functional groups, often after key carbon–carbon bond formation

    Final product types

    • Thiol-functionalized APIs
    • Drug development intermediates
    • Proprietary clinical trial candidates
    • Generic pharmaceutical products

    2. Aroma and Flavor Ingredient Manufacturing

    Flavor and fragrance producers use this thiol structure in creating sulfur notes for savory and roasted aroma profiles. It can act as a direct precursor or as a reactant in Maillard-type flavor systems. Industrial blending must monitor both concentration and off-odor control, since sulfur compounds influence profile at low ppb to ppm levels. End-users apply compositional traceability according to food ingredient supply chain requirements and analytical methods for thiol quantification.

    Industry compliance standards

    • FEMA GRAS (Flavor and Extract Manufacturers Association)
    • EU Regulation (EC) No 1334/2008 (Flavourings regulation)
    • 21 CFR § 172.515 (Flavoring agents and related substances)
    • ISO 22000 (Food safety management systems)

    Typical usage ratio

    • 0.1–10 ppm in final flavor concentrate, with dilution to ppb range in finished food or beverage products; exact dosage depends on sensory panel evaluation and regulatory threshold

    Downstream process integration

    • Added during top note creation or base flavor building in closed mixing reactors, typically after solvents and major volatile ingredients are dosed, under nitrogen to limit oxidation

    Final product types

    • Savory flavor concentrates
    • Prepared seasonings
    • Instant food flavor systems
    • Roasted and meat analog aromas

    3. Agrochemical Compound Synthesis

    Manufacturers in the crop protection sector incorporate this thiol as a specialty functional group in developing novel pesticides and herbicide molecules. The methylated furan ring and sulfur atom allow structural tuning for biological activity, stability, and target specificity. QC protocols track impurity profiles tightly, as thiol intermediates require segregation from general chemical storage and controlled venting during formulation.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Good Laboratory Practice (GLP)
    • ISO 17025 (Testing & calibration laboratories)
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products)

    Typical usage ratio

    • 0.5–2.5% by mole in active ingredient synthesis steps, scalable according to targeted final API structure and yield optimization in pilot or commercial lots

    Downstream process integration

    • Charged into reactor vessel after initial core scaffold synthesis, introducing sulfur functionality via substitution or ring modification; further processed through purification, crystallization, and formulation for field testing

    Final product types

    • Herbicide intermediates
    • Custom pesticidal actives
    • Seed treatment compounds
    • Chemical probes for agronomic research

    4. Advanced Polymer Crosslinker Sourcing

    Polymer producers value this compound’s thiol group as a chain-transfer or crosslinking agent, particularly in specialty elastomers and networked functional polymers. Its structure facilitates precise control over network density and enables post-polymerization modifications. Operators must manage monomer-to-crosslinker ratios tightly to ensure mechanical property targets and avoid excessive brittleness or undercure in final materials.

    Industry compliance standards

    • ISO 9001 (Quality management systems for polymer production)
    • REACH Regulation (EC) No 1907/2006 (EU Chemicals registration and safety)
    • ASTM D2000 (Standard classification for rubber products)
    • ISO 14001 (Environmental management for chemical synthesis)

    Typical usage ratio

    • 0.05–1.0 wt% as crosslinker or chain transfer agent, ratio adjusted for targeted molecular weight distribution and crosslink density in each polymer batch

    Downstream process integration

    • Metered into polymerization vessel post-initiation, either in bulk, solution or emulsion processes; followed by curing steps under controlled temperature and inert atmosphere to minimize side-reactions

    Final product types

    • Functionalized synthetic rubbers
    • Thermoset elastomers
    • Adhesive and sealant matrices
    • Conductive polymeric coatings
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    Certification & Compliance
    More Introduction

    2-Methyltetrahydrofuran-3-Thiol: A Practical Chemical for Complex Organic Synthesis

    Direct from the Manufacturer: Our Perspective on 2-Methyltetrahydrofuran-3-Thiol

    Working hands-on every day with 2-Methyltetrahydrofuran-3-Thiol gives us a unique sense for the subtle differences and core qualities that define this compound. Unlike the usual bulk chemicals, this fine specialty material doesn’t have an off-the-shelf identity. Every drum and bottle carries a precise profile, shaped by the way we handle and produce it. Over the years in our plant, we've seen it find its place as a distinctive tool in organic synthesis and the advanced flavors sector, carving a niche that straight-base thiols and regular tetrahydrofuran derivatives can’t fill.

    Consistent Quality from Our Facility

    We base our work on getting the chemistry right every time—because even the smallest shift in process will show up in the color, odor, and purity. This is not an anonymous commodity. Our teams run multiple checks on each batch, confirming tight specification on parameters like refractive index, thiol content, and chromatographic purity. By working with our equipment directly, performing fractional distillations under controlled temperature and pressure, we keep contaminants like water, peroxides, and oxidized by-products far below typical acceptance limits. Years ago, we learned that skipping a step or hurrying a purge introduced sulfur traces that could throw off critical syntheses. These lessons stick with us and shape each day’s production.

    Functionality and Appeal in Chemical Synthesis

    2-Methyltetrahydrofuran-3-Thiol isn’t just a name on a label. It’s a functional building block in organosulfur chemistry—one with a specific three-dimensional arrangement that lets it act as a precursor, ligand, or mild nucleophile. Chemists and process engineers know this compound for its role in introducing a methyl group alongside the thiol, offering more selectivity in transformations than basic tetrahydrothiophene or linear alkanethiols. We've found that, through iterative improvements in our process, a product free from by-products like 2-Methyltetrahydrofuran or 3-mercapto derivatives creates more reliable results in high-stakes R&D labs.

    Working on pilot-scale syntheses, we see 2-Methyltetrahydrofuran-3-Thiol often deployed when a customer wants to tune flavor ingredients, pharmaceutical intermediates, or functionalized materials with a recognizable, persistent sulfur note. Its moderate volatility and moderate water solubility mean easy handling and phase transfer without the hazards posed by heavier or more reactive thiols. Customers report that the compound integrates into reaction sequences smoothly, rarely introducing unexpected reactivity or off-odors that complicate downstream isolation.

    Our Experience with Customer Applications

    Our close connections with clients have shown us a broad range of uses. Flavor and fragrance formulators appreciate the precise, green-vegetal nuance given by this molecule. Chemists working on new ligands or catalysts draw on its ability to impart a mixed ether-thiol functionality to their compounds, granting a balance of air stability and powerful sulfur coordination. Pharmaceutical teams testing novel analogs need consistency batch to batch because even a minor variation in thiol concentration affects final biological activity and safety testing.

    From our production site, we have often prepared this thiol for custom projects with tailored impurity profiles. In synthetic work, success hinges on minimizing background sulfur and controlling the exact position of methyl and thiol groups. Over the years, we've observed that the compact structure of 2-Methyltetrahydrofuran-3-Thiol enables formation of cyclic intermediates and cross-linkers that wouldn't work with open-chain thiols. Its relatively lower odor profile, compared to straight-chain thiols, can be a boon in process labs with limited ventilation.

    Standing Apart from Alternative Products

    In the world of organic intermediates, pattern and structure matter. 2-Methyltetrahydrofuran-3-Thiol brings unique reactivity to the lab bench. Compared to tetrahydrothiophene, the introduction of a methyl unit at the 2-position alters the electron distribution and shifts boiling and melting points. For the synthesis chemist, this difference means gentler reactivity, tighter selectivity, and better tolerance for temperature-sensitive reactions. Standard 1-alkanethiols—such as 1-octanethiol—lack the cyclic ether backbone and this removes the ability to perform certain cyclizations or asymmetric syntheses.

    Customers who have tried substituting basic tetrahydrofurans or other thiols soon realize that the '3-Thiol' motif changes everything. Working with the actual material, we notice that presence or absence of a single methyl group influences how fast a reaction goes, what by-products form, and how easily a product can be purified. Typically, our experience tells us that switching to straight-chain analogues increases the risk of forming off-odors or unstable intermediates.

    Specification Control in Real Factory Settings

    Specification sheets tell part of the story, but as chemical manufacturers, the hands-on details matter more. Our facility runs regular GC-MS and NMR analyses on every batch, cross-referencing against historical data to catch trends in impurity drift before they become problems at customer sites. Our teams are quick to pick up on batch variations, whether in color, clarity, or the presence of foreign odors. Years of tracking analysis results alongside actual application feedback let us fine-tune our process so that each kilogram of 2-Methyltetrahydrofuran-3-Thiol matches the core needs of advanced chemical synthesis.

    We don't outsource final production; keeping it in-house gives us control over everything from raw material quality to packaging. Our investment in closed-system transfer and inert atmosphere filling lines didn’t come cheap, but minimizes air oxidation and gives a longer storage life once the product arrives at a client’s facility. Regular feedback from users pushing the boundaries in pilot plants and research benches brings us solid, actionable data we use to adjust each production run.

    Safety and Environmental Handling Out in the Real World

    Working directly with thiols, our operators are no strangers to the occasional pungency and the need for careful containment. Compared to heavier alkylthiols, 2-Methyltetrahydrofuran-3-Thiol tends toward less persistent odor and lower skin irritation, provided standard PPE and fume extraction are in place. Over the years, we’ve refined our spill response protocols and air monitoring to keep shop-floor exposure levels well below regulatory limits. We know how a leak affects a whole wing of the plant, so our filling lines are engineered for tightness, and our waste protocols are modeled on decades of in-house experience managing organosulfur residues.

    From an environmental standpoint, the compound doesn’t persist once incinerated or when run through active carbon scrubbing. Our production waste stream is routed through our dedicated sulfur recovery and treatment unit, minimizing the load on municipal treatment and reducing odors around our site. These are not textbook procedures but the product of real-world troubleshooting and root-cause investigation over many years. Our understanding grows with every batch, every refill, every report from our shipping and safety teams.

    Solving Challenges Unique to 2-Methyltetrahydrofuran-3-Thiol

    Experience has taught us that certain challenges arise more often with this compound than with standard thiols or furans. Packing and transport present logistical puzzles, especially in warm climates where vapor pressure bumps up and sealed drums risk bulging. We've solved this by switching to vented closures and double-sealed liners, eliminating drum failures and customer complaints about seepage or fumes at delivery docks.

    Preventing discoloration over shelf life requires active oxygen scavenging, so we incorporate trace copper chelators in our drum coatings and use nitrogen headspace on every fill. Despite these extra steps, customers receive a bright, clear product, not the darkened, heavy-smelling material that sometimes comes from rushed commercial production. Close attention to these details means downstream users won’t be thrown off by odd hues or shifts in reactivity as the product ages.

    The Role of Traceability and Transparency

    Traceability sits at the core of our operations. We engrain it in our batch labeling and chain-of-custody documentation. From every run, we keep micro-samples archived under refrigerated, light-tight conditions for long-term stability monitoring. When a customer calls with a question about a batch’s odor, color, or any perceived off-spec result, we can pull up the run’s data, analytic profile, and formulation log on the spot.

    Transparency with clients builds trust and keeps us grounded in the realities they face. Laboratories come to us for clear answers about contaminants, potential reaction by-products, and the best way to store or dispose of spent material. This dialogue informs our engineering and helps us tweak our process, packaging, and logistics.

    What Makes Our Product Different—Insights from Day-to-Day Production

    Every production run, our crews work right alongside high-precision instrumentation. Over the years, we’ve learned the specifics: how a subtle shift in reactor temperature alters the balance between 3-Thiol and unwanted side products; how agitation speed and distillation sequence impact residual moisture or subtle co-distilled impurities. These aren’t academic concerns but hard-won factors that shape what a customer receives in each shipment.

    In process-intensive applications—especially multi-step syntheses—our 2-Methyltetrahydrofuran-3-Thiol consistently offers higher yields and less workup hassle versus bulk suppliers’ material. Chemists appreciate that each bottle and drum opens to the same characteristic, mild thiol note, not the overpowering sulfur stink that complicates lab ventilation and downstream blending. Customers regularly report fewer surprises in isolating their products, thanks to our dedication to minimizing secondary sulfur by-products.

    Building Long-Term Partnerships

    We view each supply relationship as long-term, centered on reliability, dialogue, and mutual problem-solving. It’s common for our technical staff to trade notes with a customer’s chemists, dissecting unexpected analytical findings or working through a process hiccup step by step. These close relationships drive innovation—for instance, a process tweak we introduced after a Japanese client flagged a recurring odor issue, or our move to redesigned packaging after multiple labs cited premature product aging.

    Our reach isn’t just in shipping a box or sending a certificate. Continuous feedback loops and honest evaluation with our partners mean our 2-Methyltetrahydrofuran-3-Thiol evolves as their process needs expand, whether in fine fragrances, advanced materials, or in the search for novel active ingredients in the pharmaceutical sector.

    Looking Ahead: Meeting Future Needs in Applied Chemistry

    As the fields of flavors, fragrances, and specialty pharmaceuticals move toward ever more specific and exotic compounds, the demand for tightly specified intermediates like 2-Methyltetrahydrofuran-3-Thiol is on the rise. The complexity of modern synthesis routes places a premium on predictable behavior, low impurity background, and documentation that tracks every stage of manufacture. We take pride in our ability not just to meet current technical requirements, but to anticipate the next set of challenges, whether it lies in regulatory scrutiny on trace residuals, or the call for greener, cleaner production routes.

    We invest in the skills of our production teams and the reliability of our plant infrastructure to keep pace with this evolution. As new analytical methods emerge, like high-throughput LC-MS screening or advanced gas-phase odor analysis, we incorporate them straight into our QC pipeline. This forward-focused stance doesn’t just benefit our process, it directly supports our customers building high-value products at the cutting edge. Each improvement we make is a real, material change for those clients who depend on reproducibility at every stage of their operations.

    Summing Up: The Manufacturer’s Direct View

    In the end, the value of 2-Methyltetrahydrofuran-3-Thiol boils down to reliable chemistry, transparent supply, and hands-on know-how. We know every nuance of making, analyzing, and shipping this molecule. Our product stands apart because we live and work in the details—tweaking process conditions, scrutinizing analytics, and serving as technical partners to some of the world’s most exacting chemists. Over time, this direct connection to the reality of manufacturing makes all the difference. In laboratories and factories worldwide, the unique properties of our material solve problems and open new possibilities every day.