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1,2-Butanedithiol

    • Product Name 1,2-Butanedithiol
    • Alias 1,2-BDithiol
    • Einecs 217-844-1
    • 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

    227460

    Cas Number 110-64-5
    Molecular Formula C4H10S2
    Molar Mass 122.25 g/mol
    Appearance Colorless to pale yellow liquid
    Odor Strong, unpleasant (mercaptan-like)
    Boiling Point 195 °C
    Melting Point -58 °C
    Density 1.055 g/cm³ at 25 °C
    Solubility In Water Slightly soluble
    Flash Point 81 °C (closed cup)
    Refractive Index 1.525 at 20 °C
    Vapor Pressure 1 mmHg at 43 °C

    As an accredited 1,2-Butanedithiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 mL of 1,2-Butanedithiol, tightly sealed with a screw cap and chemical hazard labeling.
    Shipping 1,2-Butanedithiol is typically shipped in tightly sealed, chemical-resistant containers, protected from light and incompatible substances. It must be handled with proper labeling and safety documentation, in accordance with hazardous material regulations. During transit, temperature control and ventilation are maintained to minimize the risk of vapor release or accidental spills.
    Storage 1,2-Butanedithiol should be stored in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as oxidizing agents. Keep the container tightly closed and protected from light. Store in a secondary containment to prevent leaks or spills. Use only containers made from materials compatible with thiols to avoid container degradation or chemical reactions.
    Application of 1,2-Butanedithiol

    Applications of 1,2-Butanedithiol in Industrial Manufacturing

    1,2-Butanedithiol is an aliphatic dithiol compound widely recognized for its unique chemical properties, particularly as a chain transfer and crosslinking agent. Direct end-user industries rely on its thiol functionality for structural and performance enhancements in several niche but critical production pipelines, as detailed below.

    1. Polymeric Additives and Curing Agents in Specialty Elastomers

    Manufacturers in the specialty rubber and elastomer sector incorporate 1,2-butanedithiol as a multifunctional crosslinker to achieve specific mechanical properties and chemical resistance in products such as hydrogenated nitrile butadiene rubber (HNBR) and fluorinated elastomers. By leveraging the two terminal thiol groups, processors can efficiently increase network density during peroxide or sulfur vulcanization stages. The compound’s integration directly modifies cure rate, elasticity, and solvent resistance, making it indispensable in O-ring, gasket, and automotive seal production where stability and performance under harsh fluids and high temperatures are critical. Polymer scientists adjust addition levels to optimize cure profile while preventing over-crosslinking and related property loss.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for elastomeric manufacturing
    • ASTM D2000 for automotive rubber products
    • RoHS Directive 2011/65/EU for restricted use of hazardous substances
    • REACH Regulation (EC) No. 1907/2006 compliance for chemical safety

    Typical usage ratio

    • 0.5–2.0 phr (parts per hundred rubber), adjusted to polymer type, sulfur/peroxide cure system, and target hardness/performance

    Downstream process integration

    • Added in the internal mixer or open mill during rubber compounding, prior to vulcanization or molding cycle

    Final product types

    • Seals, gaskets, fuel system O-rings, valve cover gaskets, oil-resistant hoses

    2. Odorant Precursors for Natural Gas and LPG Detection

    Gas utility companies and odorant formulators select 1,2-butanedithiol for use as a sulfurous component in blends that impart a distinct warning smell to otherwise odorless natural gas and liquefied petroleum gas (LPG). The compound’s persistent, low-threshold odor profile enables reliable leak detection in residential and industrial gas distribution. Formulators blend it with additives such as tert-butyl mercaptan or tetrahydrothiophene, controlling ratios to balance volatility, detectability, and safety without compromising product purity or stability during storage and pipeline transport. Routine batch-quality assessments ensure consistency across regional codes and end-user requirements.

    Industry compliance standards

    • EN 13725:2003 for olfactometric testing
    • 49 CFR Part 192.625 (U.S. Department of Transportation) for natural gas odorization
    • CSA B149.1-15 Natural Gas and Propane Installation Code (Canada)
    • Internal company specifications for detection thresholds and purity

    Typical usage ratio

    • 5–30 ppm by volume in final odorant blends, calibrated per pipeline length, ambient temperature, and regional detection limits

    Downstream process integration

    • Introduced at regulated injection points within gas distribution systems or at odorant blending facilities before bottling or pipeline entry

    Final product types

    • Natural gas odorant mixtures, propane odorant blends, safety warning markers for industrial gases

    3. Organic Synthesis Building Block for Dithiol-Containing Pharmaceutical Intermediates

    Pharmaceutical manufacturers and custom synthesis firms use this dithiol as a key intermediate in the preparation of dithiol-bridged heterocycles including chelating agents, enzyme inhibitors, and thiol-functionalized API precursors. Synthetic chemists use its bifunctional thiol groups for nucleophilic substitution, cyclization, or coupling reactions. During fine chemical manufacturing, strict control of stoichiometry and reaction conditions ensures high-purity intermediate output, supporting downstream multistep synthesis of biologically active compounds that require traceability and full compliance with regulatory filings.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF monographs for pharmaceutical grade intermediates
    • 21 CFR Part 211 Current Good Manufacturing Practice (cGMP) for finished pharmaceuticals
    • ISO 13485 for medical device intermediates where relevant

    Typical usage ratio

    • Equimolar to limiting reactant in condensation or cyclization; typically 1–1.2 equivalents depending on desired conversion and downstream purification method

    Downstream process integration

    • Charged into the reaction vessel during thiol-alkylation, Michael addition, or as a dithiol linker for API intermediate synthesis; subsequent distillation or crystallization yields target compound

    Final product types

    • Dithiol-containing building blocks for APIs, chelating agents, synthetic enzyme cofactors, specialty drug intermediates

    4. Metal Surface Treatment and Corrosion Inhibitor Formulations

    Producers of metalworking fluids and corrosion inhibitors employ 1,2-butanedithiol to create formulations that actively prevent oxidation and sulfide stress cracking on ferrous and non-ferrous metals. The compound’s ability to form strong metal–sulfur bonds provides long-lasting passivation layers in closed-loop cooling, oilfield, and high-humidity storage applications. Its dual thiol moieties enable improved adhesion to substrate surfaces compared to mono-thiols, resulting in superior film formation and durability. Technicians calibrate dosage according to system volume, operating environment, and type of metal treated, as part of broader anti-corrosion treatment programs.

    Industry compliance standards

    • ASTM D1384 Standard Test Method for Corrosion Test of Engine Coolants in Glassware
    • ASTM D4627 Standard Test Method for Iron Corrosion in Diesel Fuels
    • ISO 8044:2020 Corrosion of metals and alloys
    • OSHA 29 CFR 1910.1200 for chemical hazard communication in inhibitor blending

    Typical usage ratio

    • 0.1–1.0% by weight in finished corrosion inhibitor blends; precise amount determined by severity of conditions, metal type, and exposure duration

    Downstream process integration

    • Blended with carrier solvents and other protective additive packages during inhibitor concentrate manufacturing; batch-tested prior to bulk packaging for industrial end-users

    Final product types

    • Engine coolant additives, oilfield brine inhibitors, closed-system metal protection fluids, storage compound protective sprays

    5. Chemical Modification Agents in Silver Recovery and Refining

    Precious metals refiners introduce 1,2-butanedithiol during hydrometallurgical processes to selectively precipitate silver as dithiolate complexes or to facilitate downstream recovery via solvent extraction. The compound’s chelating action allows process engineers to target silver ions while minimizing interference from other metals, improving product yield and purity. Addition rates depend on feedstock composition and target recovery efficiency, with strict analytical monitoring performed throughout precipitation and extraction cycles to ensure compliance with environmental and product quality regulations before effluent discharge or metal recovery.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for refining operations
    • EPA 40 CFR Part 261 for hazardous waste determination and disposal (U.S.)
    • OECD Environment, Health and Safety Publications for chemical use in extractive metallurgy
    • Local water quality discharge permits

    Typical usage ratio

    • Variable, typically 1.05–1.15 stoichiometric equivalents per silver present, adjusted by assay results and targeted recovery percentage

    Downstream process integration

    • Added to aqueous leachates or electrolytes following ore digestion; silver-dithiolate complexes then collected by filtration, solvent extraction, or electro-deposition

    Final product types

    • Recovered elemental silver, silver chemical products, silver for electronics and jewelry, high-purity silver bullion

    6. Sulfur Crosslinking Agent in Chemical Resistance Coatings

    Coating manufacturers incorporate 1,2-butanedithiol into two-component epoxy and vinyl ester coatings designed for aggressive chemical exposure, such as in tank linings and secondary containment. The dual thiol functions enable covalent bonding with unsaturated polymer backbones, improving crosslink density and increasing protection against acids and aggressive solvents. Plant technical teams conduct pilot testing to set loading levels that maximize cure completeness, minimize VOCs, and meet field-applied QC analytics, directly impacting in-service performance and lifespan for the finished coating system.

    Industry compliance standards

    • ISO 12944-6:2018 Paints and varnishes - Corrosion protection of steel structures by protective paint systems
    • ASTM D5227 for testing of chemical protective coatings
    • EU Regulation (EC) No. 1935/2004 for coatings on food-contact tanks
    • OSHA 29 CFR 1910.1200 for workplace chemical safety

    Typical usage ratio

    • 0.3–1.2% by weight of liquid resin, with adjustments based on target thickness, base resin type, solvent composition, and final cure requirements

    Downstream process integration

    • Introduced as part of the hardener or crosslinker module at the blending/mixing station before packaging as a ready-to-use, two-component kit

    Final product types

    • Chemical-resistant tank coatings, secondary containment sealants, pipe linings, acid storage protective membranes
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    Certification & Compliance
    More Introduction

    1,2-Butanedithiol: Our Experience as Producers

    A Look Into 1,2-Butanedithiol

    In our daily production cycle, 1,2-Butanedithiol stands out among our organosulfur offerings. This clear, strong-smelling liquid, sometimes labeled as BDT or 1,2-dimercaptoethane, pulls its weight well beyond its sharp odor. Generations of technicians have handled thiol chemicals, but BDT often pushes its own set of advantages in the lab and on the shop floor. Born from the careful alkylation of ethylene dibromide with sodium hydrosulfide, its chemistry is surprisingly straightforward—two thiol groups flanking a butane backbone. Yet, with such a structure, the molecule evolves into a reactive, versatile building block.

    We see plenty of requests for BDT each month, especially from polymer manufacturers, flavor and fragrance houses, and metallurgy labs. Each customer values the way its two sulfur groups stretch their reach across various transformations. For example, producing crosslinked polymers calls for strong, flexible linkages. BDT supplies the dual reactivity needed to bind polymer chains, outshining other dithiols like 1,4-butanedithiol or dithiolane in situations where chain flexibility and shorter backbone spacing are crucial. Compared to mono-thiol products, BDT simply opens more doors—two handles for reaction instead of one.

    Experience With Purity and Handling

    Handling BDT is a daily task for our crew, so we don’t rely on secondhand hearsay about its quirks. The pungent, mercaptan odor is notorious—ventilation matters, and so does PPE. We deliver BDT above 98% purity, colorless and free of the oxygen or water content that can compromise reactivity. Operations start by ensuring storage tanks are dry and oxygen-excluded, as the compound loves to oxidize to disulfides, especially if left exposed to air over time. Unlike many simple ethers or alcohols, the active thiol groups beg for prompt, clean handling right off the point of manufacture. Our real-world process, from synthesis to drum filling, never loses sight of how sensitive the molecule is—freshness means higher reactivity, lower contamination risk, and better results in end products.

    We track each batch with full-spectrum GC analysis, confirming thiol content and looking for trace disulfide levels. On the ground, we source high-purity feedstocks and never cut corners with reagent quality. If anyone’s ever dealt with batch-to-batch inconsistency, they know the headaches raw materials can bring. Our own plant learned the hard way how contaminants—be it from a leaky flange or inconsistent catalyst charge—can grind downstream production to a halt. We’ve found that regular maintenance on steel lines and real-time monitoring with HPLC help us catch deviations before they snowball.

    Suitability For Different Applications

    Our experience shows BDT turns up in places many don’t expect. In the rubber industry, it supports vulcanization, helping to cure diene elastomers through efficient crosslinking. Tire and industrial rubber manufacturers prefer the shorter butane chain of BDT over bulkier dithiols because it grants tighter, more flexible crosslinks. In PVC stabilization, BDT acts as a potent scavenger for heavy-metal residues—its twin thiol groups grab metals like lead or cadmium far more efficiently than mono-functional analogs. No one enjoys chasing after off-spec batches due to misbehaving stabilizers, and BDT’s reactivity narrows that risk.

    High-purity BDT brings added value in the electronic chemicals market. Here, its dual thiol interface creates stable linkages on gold or silver surfaces for advanced molecular electronics, printable circuitry, and sensor construction. Over the years, academic groups and R&D departments have cited BDT’s ability to form reliable self-assembled monolayers. Its shorter butane linker, compared to classic 1,6-hexanedithiol, offers different spacing and orientation—sometimes the difference between a successful sensor and a failed experiment. Factories fabricating miniature circuits or testing new sensor platforms are quick to notice if their dithiol is contaminated. Here, we make sure our shipping drums stay nitrogen padded right to the dock.

    Differences in Dithiol Structures

    A common debate in the R&D teams—should the project use 1,2-butanedithiol or another dithiol variant? Commercial pressures aside, technical merit settles the question. With BDT, the sulfur groups sit terminally on a four-carbon chain, closer together than in hexane or longer analogs. This affects flexibility, steric hindrance, and how effectively the crosslink forms. In polymer networks where material strength and flexibility need careful balancing, making the leap from mono-thiols or 1,6-hexanedithiol to BDT can deliver measurable benefits. We’ve watched rubber-modified plastics shift in their tear and elongation characteristics solely due to changing the backbone of a dithiol crosslink.

    Classic dithiols like 1,4-butanedithiol or 1,2-ethanedithiol differ in reactivity profiles. The two central atoms in ethanedithiol put the sulfurs impossibly close, fostering higher crosslink density at the expense of flexibility. BDT strikes a compromise between density and chain mobility, hitting a sweet spot in certain elastomer and polymer blends. Our technical sales staff routinely review test data comparing tensile strength, modulus, and final product clarity when different dithiols swap in the formulation. Results support that BDT often improves performance in applications like adhesives, coatings, and wire insulation. The sulfur spacing is more than just a chemical curiosity—it shapes the real feel and usage of the end material.

    Production Insights and Practical Realities

    Running a plant that regularly produces 1,2-butanedithiol brings home the daily challenge of odor management. Anyone nearby would know production launched by the smell alone. The exhaust system, scrubber maintenance, and double-checked seals matter just as much as instrument calibration and analytical verification of purity. If you’ve never dealt with large-scale mercaptan synthesis, it’s hard to appreciate the persistence of this odor—and how important it is that we keep it where it belongs. Proper PPE, continuous leak monitoring, and thorough staff training mean two things: staff safety and zero complaints from neighboring businesses.

    Each campaign brings its own learning curves. We’ve optimized our reactor temperatures to minimize byproduct formation, especially unwanted disulfides or overalkylation. Overcooling leads to incomplete reactions, wasted feedstock, and higher purification costs. Overheating accelerates degradation, pushing yields down and fouling equipment. A sweet spot exists, and reaching it translates into consistently pure product, fewer shutdowns, and less chemical waste. Decades working with dithiol chemistry have taught us that the difference in process yields comes down to temperature precision and feed mixing.

    There’s never a “standard run” with BDT. Even minor adjustments in raw material purity or process stability echo through the whole batch. Our crew reviews analytical results every shift. One time, a miscalibrated feed pump nudged the reaction off-spec; catching it in real time kept the bad batch from going downstream. That mindset—don’t just trust the numbers, verify everything—is what maintains our reputation for purity and reliability.

    BDT in Research and Industrial Collaboration

    Research partners, from university groups to major specialty chemical labs, choose our BDT for custom syntheses and novel material development. They value a production partner willing to tweak quantities or packaging and give real-time analytical support. When a research chemist calls asking for a batch with ultra-low residual carbonyls, we engage our QC team to run detailed TGA and Karl Fischer analysis before signoff. Our years working with these demanding clients have reinforced the need for direct dialogue—no third-party misunderstandings or hesitance about revealing batch performance data.

    On the industrial end, our large-volume customers in paint, adhesives, and coatings consistently report tighter quality control for viscosity and curing speed when using our material. They have shared real metrics from their own lines; switching to our BDT cut batch adjustments and reduced variable waste in curing cycles, compared to alternate suppliers’ material. This data doesn’t just serve marketing; it drives our own continuous improvement. Repeated feedback from mixers and process engineers pointed us toward packaging improvements: robust drums with tamper-evident seals and nitrogen headspace to maintain freshness until the last drop.

    Sustainability, Health, and Future Outlook

    Sustainable chemical production is not a distant target—it’s the reality of our daily operation. Working with chemicals as pungent and potent as 1,2-butanedithiol, we hold ourselves to strict environmental compliance. Feedstock traceability, closed-loop waste handling, and stack scrubber upgrades have made a measurable difference in reducing environmental impact. We don’t ship off spent product or byproduct streams for anonymous disposal either. Instead, we refine reclaimable streams and ensure our waste partners provide the same documented chain-of-custody we expect from our own suppliers.

    Working with volatile thiols, health and safety can never be an afterthought. Even low concentrations in air can irritate, so we monitor levels well below published exposure limits. Staff are trained not just to work around hazardous materials, but to recognize when a process might pose unforeseen risks. Our incident reporting and continuous improvement loop—combining real experience in the plant with updated best practices—means that we expect emerging risks before regulations catch up.

    On the horizon, new applications for 1,2-butanedithiol are cropping up in bio-based materials and next-generation electronics. Several of our partners are experimenting with BDT-derived crosslinkers for biodegradable rubbers and tough hydrogel systems meant for medical devices. Lab-scale data suggests the unique reactivity profile of BDT could help engineer selective degradability without compromising functional stability. The difference comes from BDT’s balanced flexibility and crosslinking efficiency. While some competitors promote longer-chain dithiols for higher flexibility, their compounds tend to reduce ultimate strength or don’t degrade as predictably. BDT’s short chain and dual sulfur groups hit the mark for these next-gen challenges.

    Comparisons With Related Chemical Products

    Among all the dithiols our catalog offers, 1,2-butanedithiol occupies a middle ground. Its backbone is longer than ethanedithiol, shorter than 1,6-hexanedithiol, and far more reactive than the cyclic dithiols like dithiolane. We often field technical calls from clients questioning whether “just any dithiol” will work in their process. Our direct experience says otherwise. The choice affects not just final product performance, but also how easily the intermediate reactions run in real conditions—time, temperature, side-product risk, ease of purification all depend on getting the chemistry right. For example, 1,2-ethanedithiol can crosslink faster, but results in brittle, tightly networked matrices that don’t flex, which renders them poorly suited for elastomer products.

    Our production chemists have compared BDT to 1,3-propanedithiol and 1,4-butanedithiol across several synthesis pathways. In flavor chemistry, where trace differences in precursor structure change the final aroma, customers prefer BDT for its cleaner thiol release profile and less tendency to form sulfurous side products under higher temperature operations. In electroplating and gold recovery, BDT’s chain enables stronger, more selective chelation. Drilling down to basic chemistry, the spacing of the thiol groups sets up different chelation angles; BDT latches onto precious metals without grabbing calcium, magnesium, or other background cations as aggressively as some longer alternatives.

    Downstream, users appreciate that our BDT blends cleanly into both polar and nonpolar solvents. We’ve tested it ourselves in house, routinely confirming miscibility and monitoring how minor process tweaks affect phase separation during scale-up. Our records show that, unlike some competitors’ dithiols, our batches don’t leave cloudy residues or introduce untested mineral content. This becomes especially important in electronics and food-flavor production, where every contaminant matters. We don’t rely on “standard market grade” as an excuse, either—our outgoing product gets a full impurity panel and purity report, which our buyers have come to expect from each delivery.

    Shipping, Storage, and Reliability Lessons Learned

    Shipping BDT has its own set of lessons. The compound’s volatility and strong smell make leak-tight packaging critical. In our own trucks, a faulty drum seal once led to a project delay while flooring, racks, and handling equipment went through complete decontamination. The takeaway—never compromise on drum quality or pressure testing. Nitrogen overlay, secondary containering, and just-in-time scheduling have protected customer confidence and kept punitive delays at bay. We learned early on to invest in drum handling safety and digital tracking, so that every order reaches the customer just as fresh and pure as it left the plant.

    Storage at end-user sites gets the same attention. Many of our clients operate just-in-time or batch-by-batch. For them, large-scale bulk storage of BDT rarely makes sense. We offer a wide range of drum sizes, but always encourage our customers to monitor warehouse inventories carefully. Freshness in BDT isn’t marketing fluff—over time, sulfur groups inch toward oxidation, reducing desirable reactivity right where the customer needs it most. We share what we’ve learned about optimizing storage—dry, cool, oxygen-free. These may sound like small points, but the downstream costs of using an oxidized or contaminated batch are anything but minor.

    Continuous Improvement From Production Floor to Application Lab

    The story of producing and supplying 1,2-butanedithiol is an ongoing one—full of practical challenges, real feedback, and steady improvement. In thirty years of batch records, shift logs, and customer reports, we’ve built a library of what works—and just as importantly, what hasn’t. The knowledge gained from every batch means we don’t just supply a commodity, we solve real-world problems with our customers. Whether it is selecting the best dithiol for a given crosslinking step, adapting to impurity specifications, or working through the headaches of industrial odor management, we back every delivery with everything our crew has learned on the floor and in the lab.

    For those evaluating 1,2-butanedithiol for new research, novel industrial synthesis, or simply seeking more reliable performance and cleaner application results, our perspective comes not from a catalog description but from thousands of tons of real product moved safely, responsibly, and with an eye to future demand. Our commitment stretches from the first raw material inspection through every filled drum to the end use that shapes tomorrow’s technology.