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2,5-Dimethylfuran-3-Thiol

    • Product Name 2,5-Dimethylfuran-3-Thiol
    • Alias 2,5-Dimethyl-3-thiolfuran
    • Einecs 474-090-0
    • 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

    965914

    Cas Number 13689-84-0
    Molecular Formula C6H8OS
    Molecular Weight 128.19
    Iupac Name 2,5-dimethylfuran-3-thiol
    Appearance Colorless to pale yellow liquid
    Smell Sulfurous, meaty, roasted aroma
    Synonyms 3-Mercapto-2,5-dimethylfuran
    Structure Description Furan ring with methyl groups at positions 2 and 5, thiol at position 3
    Pubchem Cid 25693759
    Safety Precautions Use gloves and work in well-ventilated area

    As an accredited 2,5-Dimethylfuran-3-Thiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, sealed with a screw cap. Labeled with chemical name, CAS number, hazard pictograms, and handling instructions.
    Shipping 2,5-Dimethylfuran-3-Thiol is shipped in secure, tightly sealed containers to prevent leakage and exposure. It is typically packaged under inert gas and kept in a cool, dry environment, clearly labeled in compliance with chemical safety regulations. Appropriate documentation and hazard warnings accompany each shipment to ensure safe transport and handling.
    Storage **2,5-Dimethylfuran-3-thiol** should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as oxidizers. Store in a cool, well-ventilated area, preferably under an inert atmosphere like nitrogen or argon to prevent oxidation or degradation. Proper labeling and secondary containment are recommended to avoid leaks or spills, ensuring safe chemical management.
    Application of 2,5-Dimethylfuran-3-Thiol

    Applications of 2,5-Dimethylfuran-3-Thiol in Industrial Manufacturing

    As a direct manufacturer, we support industrial partners with high-purity 2,5-Dimethylfuran-3-Thiol supplied under strict quality management systems. This specialty thiol offers unique performance in several established downstream sectors driven by high sensory specificity and targeted functionality. Below are key application scenarios, each featuring real-world process guidance and regulatory benchmarks.

    1. Savory Flavor Creation in Food Additive Formulation

    Flavor houses integrate this compound to mimic complex roasted, meaty, and onion notes required in flavor systems for packaged savory foods. The material enters compound fragrance formulations, contributing sulfuric depth within bouillon, snack seasoning, and prepared dish enhancements. Downstream users apply strict sensory QC to batch production and must comply with food safety framework for finished goods sent to consumer markets.

    Industry compliance standards

    • GB 2760-2024 (China National Standards for Food Additive Use)
    • FDA 21 CFR Part 172.515 (USA – FEMA GRAS Flavour Substances List, reference FEMA No. 4510)
    • EU Regulation (EC) No 1334/2008 – Food Flavouring Substances
    • ISO 22000:2018 – Food Safety Management within manufacturing facilities

    Typical usage ratio

    • 0.01 to 3 ppm in end product weight; formulators adjust between 0.5 to 1.5 ppm for broths, and up to 2.5 ppm in high-flavor-impact snack seasonings after bench testing for desired aroma intensity

    Downstream process integration

    • Compounders introduce the ingredient during premix blending of liquid or powder flavor formulations under nitrogen protection to prevent oxidative degradation

    Final product types

    • Instant noodle seasoning sachets
    • Dehydrated bouillon cubes
    • Potato chip and extruded snack flavor powders
    • Ready-to-use soup bases

    2. Aroma Chemical Synthesis for Fine Fragrance Markets

    Perfumery ingredient suppliers employ the compound as a unique sulfur bridge within complex aroma chemical synthesis, providing a characteristic roasted, sulfury profile useful in tobacco, leather, and luxury market perfumes. Process chemists utilize controlled micro-quantification to avoid overbearing notes, and maintain strict tracking of intermediate and by-product elimination for high-value olfactory blends.

    Industry compliance standards

    • IFRA Standards (The International Fragrance Association – amendment 51 restricting use levels for specific thiols)
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • ISO 9001:2015 for fragrance compound manufacturing
    • REACH (EC) No 1907/2006 substance dossier for CMRs and toxicology review

    Typical usage ratio

    • 0.001% to 0.02% of total fragrance concentrate batch; typically less than 0.005% in ‘top note’ focused compositions and up to 0.02% in base notes of complex leather or tobacco-type accords

    Downstream process integration

    • Introduced post-core aldehydic or citrus top note assembly, often as a pre-dilution with dipropylene glycol, in fragrance compounding rooms with segregated air handling

    Final product types

    • Fine fragrances and Eau de Parfum blends
    • Personal care perfume oils
    • Luxury scented candles
    • High-value aroma intermediates for custom market

    3. Process Flavor Generation for Culinary Ingredient Manufacturing

    Bulk food ingredient producers add this molecule in Maillard reaction systems, targeting authentic cooked, caramelized-allium flavor bases for use in industrial gravies and ready meal sauces. End-users control precursor balance to optimize thiol expression at critical heating stages, supporting formulation of high sensory-impact functional ingredients tailored for food service and further manufacturing.

    Industry compliance standards

    • FSMA (US Food Safety Modernization Act) requirements for food ingredient facilities
    • FSSC 22000 (Food Safety System Certification Scheme 22000)
    • Safe Quality Food (SQF) Code Edition 9
    • ISO 17025 laboratory validation for process control

    Typical usage ratio

    • 1 to 7 ppm in ingredient premix, adjusted for Maillard precursor content and heating parameters; custom formulations may range up to 10 ppm in development of high-browning sauces

    Downstream process integration

    • Added prior to thermal reaction stage with amino acids and sugars, then monitored for conversion yield and off-note suppression through in-line GC or sensory panel, prior to drying/concentrating

    Final product types

    • Spray-dried process flavor powders
    • Culinary allium concentrates
    • Shelf-stable soup paste bases
    • Umami flavor enhancers for further B2B sale

    4. Patent Synthesis Intermediate for Drug Discovery R&D

    In pharmaceutical research, R&D teams employ this thiol as a key sulfur-containing precursor in the synthesis of sulfur-heterocycle lead compounds and analog libraries, especially within antibacterials and CNS-active molecules. Synthetic route optimization hinges on sulfur reactivity, selectivity, and impurity removal in early-stage process development conforming to GMP indirect material controls.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for API
    • 21 CFR Parts 210 & 211 (cGMP for Finished Pharmaceuticals)
    • USP General Chapter <795> for compounding controls (when used in research)
    • ISO 13485:2016 Quality Management for Medical Device Development (if applicable to API intermediates)

    Typical usage ratio

    • Varies from 0.5 to 2 molar equivalents in synthetic step depending on substitution targets; initial screens use 1:1 stoichiometry, with final routes optimizing to lowest practical excess

    Downstream process integration

    • Introduced at protected or deprotection step, with nitrogen/argon glovebox handling and in-process HPLC/Purity analysis to monitor intermediate conversion before further ring closure or coupling

    Final product types

    • Pharmaceutical intermediates for lead optimization
    • Preclinical compound screening libraries
    • Specialty building blocks for advanced heterocyclic synthetic chemistry
    • Chemical reference standards for process development

    5. Specialty Sulfur Additive in Advanced Lubricant Formulations

    Lubricant manufacturers introduce this rare thiol as a specialty sulfur additive to enhance boundary lubrication performance and anti-wear features in select industrial greases, where its structure enables synergistic protection alongside phosphorus-based chemistries. Formulation chemists perform batch qualification blending and stability analysis under ISO-based lubricant QA protocols for finished goods dispatched to critical machine and automotive markets.

    Industry compliance standards

    • DIN 51517 (Industrial lubricants — Lubricating oils — Requirements and testing)
    • ASTM D4951 – Standard Test Method for Additive Elements in Lubricating Oils by ICP
    • ISO 9001:2015 for finished lubricant production
    • REACH (EC) No 1907/2006 material assessment for additives

    Typical usage ratio

    • 0.02% to 0.10% w/w (200–1,000 ppm), adjusted by base oil group and targeted friction performance; field-specific blends require R&D testing for sulfur/ash compatibility

    Downstream process integration

    • Metered dosing during post-blend additive convergence, with performance QC by four-ball wear and oxidation stability testing prior to packaging and dispatch

    Final product types

    • Heavy-duty industrial greases
    • Automotive gear oil formulations
    • High-load synthetic compressor lubricants
    • Specialty metalworking fluids
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    Certification & Compliance
    More Introduction

    Introducing 2,5-Dimethylfuran-3-Thiol: Practical Experience in Flavor Chemistry

    A Closer Look at Our Production Site

    Years spent behind reactors and distillation columns leave you with a particular sense for what matters in specialty chemical production. Among the many compounds we manufacture, 2,5-Dimethylfuran-3-Thiol stands out, not just because of the technical challenges, but for the value it creates for those who count on purity and character in flavor applications. Our team has worked with this molecule long enough to see its real-world impact, and that shapes our view of its place in the market.

    Understanding 2,5-Dimethylfuran-3-Thiol

    This compound, assigned CAS number 13678-51-8, features a furan backbone with two methyl groups at the 2 and 5 positions and a thiol group at the 3 position. It doesn’t appear on a general list of “commodity” thiols—you won’t see it stacked in a warehouse with tons of generic aroma chemicals. Its nuanced molecular structure brings out a distinct profile, particularly valuable in flavor formulations designed for roasted, nutty, or savory notes. Our routine covers production in lots ranging from pilot-scale to commercial volumes, using stainless equipment to maintain integrity. This hands-on approach means our team works directly with the technical aspects, monitoring parameters such as temperature and moisture, always focused on keeping impurity levels down to where they won’t interfere with performance.

    Purity and Consistency: Not Just Buzzwords

    Purity isn’t an abstract number. If the batch leaves residues of byproducts or contains too much water, downstream blending turns unpredictable. Our standard for 2,5-Dimethylfuran-3-Thiol emphasizes purity levels no less than 98%. Over years, the quality assurance process has evolved—GC and HPLC analysis with regular confirmation against NMR data. Because the stakes in flavor chemistry are real: one off-taste, and your customer’s finished product shifts. Rejection of out-of-spec material costs both money and trust, so investing in better purification, refined vacuum techniques, and ventilation safeguards has paid off.

    Sensory Contribution and Industry Use

    Maybe the word “impact” gets overused, but for this molecule, there isn’t a better descriptor for its flavor contribution. We’ve watched customers in food technology and beverage development bring this thiol into their systems to create roasted, sulfurous notes in coffee, roasted nuts, meat flavors, and even some specialty snack seasonings. Industrial food chemists tell us it builds complexity in formulations where plain methyl furans fall flat. The character delivered by that sulfur-functional group covers more than just aroma intensity; it bridges the dry, nutty, and sweet-sulfur nuances essential to modern savory flavor profiles.

    From early trial batches, we discovered that stability and handling must be top priorities. The active thiol group interacts quickly with oxygen and metal ions, so we package under inert conditions using nitrogen flushes, usually in amber glass bottles or certified HDPE containers fitted with PTFE liners. Storage protocols call for cool, dry environments, shielded from light and air. Over time, we’ve learned where to draw the line: avoid storing near basic reagents or metal catalysts, keep every transfer under protective atmosphere, and always test for off-odors before dispatch.

    Differences from Other Specialty Thiols

    Having synthesized a range of thiols for flavor work, the distinctiveness of 2,5-Dimethylfuran-3-Thiol becomes more evident the more you work with it. Unlike lower molecular weight thiols, which can veer into aggressive, unpleasant sulfur notes even at trace amounts, this molecule steers toward balance. It lends rounded, culinary roasted flavors at lower addition rates without overpowering lighter notes. We often compare it to 2-methyl-3-furanthiol—a classic for coffee and meat flavors. But while 2-methyl-3-furanthiol contributes a very piercing meaty aroma, the dimethyl variant reduces that sharpness and brings a mellow finish. Processors seeking a softer imprint in savory profiles increasingly turn to 2,5-Dimethylfuran-3-Thiol as a solution for flavor stability and integration.

    Crossover with non-thiol flavor chemicals proves rare because the thiol backbone confers a category of aroma that’s hard to replicate. As compared to regular methyl furans, which present sweet wood and caramel nuances, 2,5-Dimethylfuran-3-Thiol walks the line between nutty and freshly roasted coffee notes, adding versatility. It has carved out a place where complexity is necessary, particularly in broths, roasted meat analogs, instant soups, and high-end savory seasonings.

    Production Insights: What Sets Us Apart

    Standardization doesn’t come easy in the world of organosulfur compounds. Shelf-life, oxidation, and cross-contamination are constant risks. Our process begins with carefully sourced raw materials, controlled atmospheres during synthesis, and real-time monitoring during critical stages. Every cycle through our reactors sees live tracking: measuring sulfur release, pressure, temperature, and the cooling curve. Team members have encountered failed batches—abortive side-reactions or tainted by unseen impurities—which is how we know the value of hands-on oversight backed by reliable automation in data logging.

    We don’t shy from challenging batches. The odor threshold for impurities isn’t forgiving. Equipment maintenance and batch scheduling ensure no leftover contaminant from a previous run ends up in the final sample. Over years, incremental upgrades to distillation columns, improved gaskets, and validated cleaning cycles between runs allowed us to achieve steady yields above industry averages—without accepting convenience-driven shortcuts that threaten batch independence. The learning curve means meeting tough flavor house standards every time, no exceptions.

    Meeting Real-World Demands

    Flavor houses depend on trace-level consistency and predictable reactivity. Feedback from application chemists shapes how we package and QC-test each lot. On occasion, requests come through for tighter specification ranges or split lots for R&D versus production, especially for regional flavor priorities. We scale according to need—delivering pilot batches for developmental work or just-in-time shipments for large scale flavor operations. Working alongside customers with strict formulation targets, we’ve adapted our batch records and technical data to better support their verification procedures and traceability needs. Some prefer fully documented chain-of-custody and exhaustive impurity profiling to streamline their internal audits—our experience in offering transparent documentation continues to grow from these collaborations.

    Handling and Safety Observations

    It only takes a single incident of unwanted reactivity or an improperly sealed drum to set back a project and cause a safety incident. As a specialty thiol, 2,5-Dimethylfuran-3-Thiol deserves careful treatment. Vapors drift easily and carry odor far beyond the drum or flask, so proper PPE, good local ventilation, and immediate spill cleanup are essential. Spills left on benchtops produce a persistent sulfur aroma, stubborn to remove. Our team’s protocols favor smaller container sizes for easier handling and quicker turnover. Working at the production site, staff double-check fixtures, bottle seals, and labeling to prevent leaks and misidentification. The goal is to avoid accidents both in-house and down the distribution chain by operating with clear, simple, practiced routines involving only necessary personnel.

    Collaboration with Application Developers

    Research-focused partners seeking custom characteristics for aroma and flavor work closely with us in refining provision protocols. Over the years, we’ve participated in bench trials, offering not just a product but insight into practical solubility, shelf-life, and scaling challenges. Modest changes to feed ratios or solvent selection sometimes unlock significant improvements in both flavor yield and chemical stability, so we compare notes with R&D contacts on results, focusing on how our workflow aligns with theirs. Labs working on vegan roast flavors, meat alternatives, and health-oriented seasonings have explained their hurdles with masking unwanted bitterness and achieving rounded savory depth. Our site’s flexibility allows us to answer such insights with tailored approaches: adjusting temperature regimes, refining post-synthesis washes, and testing for any unforeseen solvent residues.

    Product development cycles increasingly reward manufacturers who talk less about theoretical capability and show more willingness to test ideas side by side with industrial-scale users. By sitting in on sensory panels or sending trained staff to discuss performance in pilot plants, we build mutual knowledge. This experience-driven collaboration helps establish confidence in 2,5-Dimethylfuran-3-Thiol, for both established profiles and fresh concepts still under wraps.

    Monitoring Regulatory Expectations

    Specialty thiols often come under more rigorous review in national and international food regulations. Regulators want evidence on both acute safety and cumulative exposure, especially for compounds with distinctive odor. Our documentation aligns with regionally accepted food grade regulations, leveraging third-party lab validation to cover purity and the absence of banned contaminants. No manufacturer in this segment avoids paperwork: traceability matters not just for quality reassurance, but also in keeping ingredients eligible for wider use. On our end, investment in data management, batch traceability, and QC archiving makes future audits and re-certifications smoother for our downstream partners. Consistent records permit rapid answers to technical questions at any stage in the product’s use.

    Market Changes: Perspective from the Floor

    Interest in savory, “umami” field flavors has risen in line with growth in prepared foods, meat analogues, and premium snacks. The complexity and naturalism that 2,5-Dimethylfuran-3-Thiol delivers supports the shift away from blunt, artificial flavor options. As a direct producer, we notice demand spikes that follow regional launches in plant-based and ethnic-inspired products. Taste test panels in various markets report preference for roasted and fully developed backgrounds, which this molecule helps achieve. In response, our process scheduling and raw material stock control remains robust to absorb unexpected upticks, minimizing lead times and missed deadlines. We track raw material costs, monitor supply forecasts, and remain ready to discuss realistic timelines with customers facing promotional surges or rollout changes.

    Technical Lending: Fielding Customer Questions

    Conversations with formulation chemists range from routine questions on stability to more challenging requests about minimizing metallic off-flavors or eliminating carryover solvent. We’ve developed technical guidance based on first-hand troubleshooting on our manufacturing floor—like managing trace oxygen with additional passivation treatments, or responding to lingering feedstock odor with lengthened distillation steps. Direct experience informs our advice: we don’t relay canned responses stitched from literature. Instead, teams lean on real QC outcomes, operational records, and a habit of cross-verifying advice with updated batch histories. Fielding these technical questions builds mutual reliability with users, many of whom depend on insights from those who have handled the product by hand.

    Quality Driven by Experience

    Stories accumulate as years go by in specialty manufacturing. Sometimes production challenges force “all hands” efforts—working through the night to turn around a threatened batch. Other times, a successful run rewards with the assurance that the process fits within limits tighter than catalog standards. These lessons shape every lot of 2,5-Dimethylfuran-3-Thiol we release to the market. For those seeking a molecule that offers more than a standard flavor boost, our production site delivers not just output, but the earned trust that comes from deliberate, experienced practice.

    Supporting Innovation: A Partnership Model

    Our involvement doesn’t end as the drum leaves our site. Newer applications—like those in next-generation coffee alternatives or advanced protein crisps—come from collaborations that challenge us to think differently about 2,5-Dimethylfuran-3-Thiol. Providing sample data, quick-turn small batch runs, and post-delivery troubleshooting keeps us tuned to both practical needs and innovation-driven projects. As the market for complex, authentic flavor solutions expands, our team brings operational experience to the partnership, making the process smoother from the blend tank to the consumer’s taste experience.

    Looking Forward in Flavor Chemistry

    Innovation in food science calls for molecules that do real sensory work. Standard offerings fall short for formulators chasing roasted, nutty, or complex meaty impressions. 2,5-Dimethylfuran-3-Thiol represents years of production tweaks, technical troubleshooting, and field experience, all contributing to a molecule that bridges the gap between chef-level artistry and large-batch consistency. Our commitment remains unchanged: reliable, high-quality batches grounded in genuine chemical manufacturing knowhow. Users count on these traits, whether developing the next generation of plant protein snacks or elevating the savory base in ready-made meals. By keeping one foot in the reactor room and another in the sensory lab, our process reflects a practical reality—the ongoing need for flavor ingredients made by those who know each step from raw input to aroma release in the finished food.