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HS Code |
962339 |
| Cas Number | 528-48-3 |
| Molecular Formula | C4H10O2S2 |
| Molecular Weight | 154.25 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | -2 °C |
| Boiling Point | 210-213 °C |
| Density | 1.294 g/mL at 25 °C |
| Solubility In Water | Miscible |
| Refractive Index | 1.601 (20 °C) |
| Flash Point | 109 °C (closed cup) |
As an accredited 2,2'-Dithiodiethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,2'-Dithiodiethanol is packaged in a 500 mL amber glass bottle with a secure screw cap and clear hazard labeling. |
| Shipping | 2,2'-Dithiodiethanol is shipped in tightly sealed containers to prevent leakage and protect against moisture and air exposure. The chemical is classified as hazardous for transport, requiring proper labeling and handling according to regulations. It should be kept away from heat, sparks, and incompatible substances, and transported by authorized carriers only. |
| Storage | 2,2'-Dithiodiethanol should be stored tightly sealed in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Store in a corrosion-resistant container, protected from moisture and incompatible substances such as strong oxidizers. Proper labeling and secondary containment are recommended to prevent spills and environmental contamination. Always follow safety regulations and institutional guidelines. |
Applications of 2,2'-Dithiodiethanol in Industrial Manufacturing2,2'-Dithiodiethanol plays a critical role as a functional intermediate, process modifier, and molecular building block in chemical manufacturing. The following sectors extensively adopt this raw material for its controlled reactivity, high purity profile, and reliable performance throughout demanding process environments. 1. Pharmaceutical Active Ingredient SynthesisGlobal pharmaceutical producers utilize 2,2'-dithiodiethanol for thiol protection, disulfide introduction, and controlled reduction steps during the synthesis of APIs, particularly in peptide and small molecule drug production. Its compatibility with GMP and multiple pharmacopeias supports use in regulated settings. Manufacturers fine-tune the reagent feed to balance product purity, batch reproducibility, and process safety from pre-clinical R&D through to commercial batch scale. Integration occurs in solid-phase synthesis cycles and post-reaction modification steps, enabling the precise construction of disulfide bonds for structural stability in peptide drug candidates. Industry compliance standards
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2. Rubber Vulcanization and Processing ChemicalsMajor rubber goods and elastomer manufacturers use 2,2'-dithiodiethanol as a vulcanizing agent and sulfur donor for tailoring crosslink densities in both natural and synthetic rubber systems. Its disulfide bridge structure provides flexible yet stable crosslinking points, tuning mechanical properties such as elasticity and heat resistance. Integration into rubber compounding lines requires precise weighing and feed monitoring to achieve desired network structure and cure characteristics. Industry compliance standards
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3. Electroplating and Metal Surface TreatmentSurface treatment plants and electronics manufacturers leverage 2,2'-dithiodiethanol as a grain refiner, brightener, and leveling agent during copper and other metal electroplating work. Its sulfur-containing backbone enhances deposit grain structure, smoothens surface finish, and prevents dendritic growth—ensuring quality coatings for circuit boards and connector components. Implementation involves tank-side feed and real-time process control to manage bath composition, current efficiency, and plating uniformity. Industry compliance standards
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4. Polymerization Chain Transfer for Specialty PolymersProducers of engineered resins and functional polymers employ 2,2'-dithiodiethanol as a chain transfer agent in radical polymerization systems. The compound moderates polymer molecular weight and end-group functionality, enabling the design of polymers with pre-defined mechanical strength, flexibility, or reactive handle introduction. Its diol functionality further supports subsequent crosslinking or grafting processes for tailored polymer architectures. Industry compliance standards
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5. Photographic Chemical FormulationHigh-end imaging and film manufacturers integrate 2,2'-dithiodiethanol in photographic developer and fixer formulations as a mild reducing and stabilizing agent. Its use allows the modulation of development kinetics while maintaining uniformity and minimizing fog formation during silver halide development. Batch-to-batch consistency depends on precise dosing and tight control of solution composition, which is essential for industrial-scale film coating and processing lines. Industry compliance standards
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6. Biochemical Research and Protein ChemistryLaboratory-scale and industrial bioreagent suppliers use 2,2'-dithiodiethanol as a controlled disulfide bond cleaving agent for protein denaturation, folding, and stabilization studies. Its action enables specific reduction of protein or peptide disulfide bridges, facilitating downstream structural analysis, enzymatic digestion, or site-specific labeling. Integration requires carefully validated procedures for reagent concentration and buffer compatibility. Industry compliance standards
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For years, we have been refining and producing high-purity 2,2'-Dithiodiethanol—not just from chemical blueprints, but from repeated hands-on runs and continuous feedback from industrial users. Known chemically as Bis(2-hydroxyethyl) disulfide, this colorless-to-pale yellow liquid with molecular formula C4H10O2S2 stands out in research and manufacturing for its functional groups and the kind of consistency that only comes from technique honed by real-world practice. No matter how many years pass, our focus hasn't wavered: tight control on synthesis, reliable batch output, and a willingness to talk straight about why 2,2'-Dithiodiethanol matters to those who use it.
We craft 2,2'-Dithiodiethanol with purity levels tailored for both demanding biochemical applications and broader industrial needs. Out of the reactor, our typical pharmaceutical/intermediate grade comes out at ≥99% purity (by GC), while specialty orders across research sectors sometimes require custom stabilization and moisture controls. This liquid brings a distinct odor, moderate viscosity, and high miscibility in water and polar organic solvents. Each liter ships dense with promise: a clear, low-ash, sulfur-rich compound ready for reduction, modification, and further synthesis.
Packaging never feels casual here. Whether bulk drums or cleanroom-sealed bottles, our own experience in scale-up lines means the product reaches users uncontaminated and safely handled, minimizing exposure to air or light where oxidative instability could degrade quality. From pilot scale to >1,000-kilogram annual runs, our operators treat 2,2'-Dithiodiethanol production as a meticulous, high-responsibility craft. Records show traceability back to source reagents, test logs, and production times—a full lifecycle understood from top to bottom.
Our chemists didn’t choose this molecule just for a spot in the catalog. Work in fine chemicals and specialty manufacturing keeps uncovering new uses: cleaving agent in peptide synthesis, reduction of disulfide bonds in proteins, anti-oxidant function in polymer processing, and cross-linking in advanced coatings. This isn’t theoretical. Decades of bench and plant work prove that the–S–S– bridge linking two hydroxyethanol units brings unique blend of reactivity to the table, especially where standard 1,2-alkanediols or other thiols fall short.
Protein chemists, for instance, often rely on 2,2'-Dithiodiethanol as a low-odor, stable alternative to β-mercaptoethanol. Not all reducing agents perform the same: high volatility and toxicity issues with smaller thiols frequently force researchers to search for something less hazardous in air and less harsh on their samples. This product fills that role ably, providing effective reduction without offensive odors or rapid evaporation. The structure, with its spaced-out ethanol handles and central disulfide, reacts controllably compared to other sulfur reagents.
By making 2,2'-Dithiodiethanol ourselves, every decision—from reactor pressure profiles to the rate of acid addition—comes down to more than just cost. We’ve learned that the slightest inconsistency in temperature ramp or inert gas flushing can introduce byproducts like mono-thio analogues, or cause unwanted oxidation. Such impurities might not be flagged in a casual analysis, but they wreak havoc on sensitive peptide reactions or downstream syntheses.
This isn’t armchair talk. Our labs ran side-by-side comparisons against outside-sourced material and saw the differences play out in real analytic runs. Low-level sulfur contaminants, excess water, and off-spec byproducts drive up purification costs for end users and put published research at risk. We adopted a triple-filtration protocol and continuous monitoring not out of habit, but from real problems encountered. A run ruined by poor reducing agent costs more than just money—it erodes trust.
We build cycles of improvement into every batch. Recovered solvents go through extra distillation where possible, and we supply full analytical data so customers can assess compatibility with their own protocols. If peptide synthesis purity drops or HPLC forensics finger a trace oxidant, we pull the full batch history for review and learn from it. Manufacturing never stands still, and neither does our method for making 2,2'-Dithiodiethanol.
The most frequent calls about 2,2'-Dithiodiethanol come from researchers needing gentle, thiol-based reduction without extreme volatility. In protein denaturation and renaturation protocols, our customers substitute in this compound as both a storable reducing agent and as a component compatible with downstream mass spectrometry. Unlike β-mercaptoethanol, it sports a molecular bulk that discourages significant off-gassing, keeping it safer for repeated handling and more stable on the shelf.
In specialty coatings and resins, manufacturers appreciate how its disulfide bridge adds reactivity points—allowing cross-linking and post-cure modifications that plain glycols can’t achieve. Polymer blends modified with 2,2'-Dithiodiethanol often show increased sulfur content, leading to enhanced abrasion resistance or chemical resilience. That’s feedback we’ve validated in both our in-house materials lab and through outside customer case studies. Some agrochemical formulators use it to graft functional groups or build more complex thiol-ester architectures—another demand our production team meets with regular supply.
We’ve even assisted companies working in battery electrolyte research. Here, the careful balance of redox activity and solvency delivered by 2,2'-Dithiodiethanol’s twin hydroxy ends proves valuable in prototype electrolytes. They report more consistent performance and longer shelf life versus common alternative diols, a storyline we’ve followed closely in the pilot stage.
Years in chemical production taught us that sulfur-rich reagents can test patience if not managed carefully. 2,2'-Dithiodiethanol, while less malodorous and volatile than smaller thiols, shouldn’t be left to sit unprotected, especially under sunlight or in unlined containers. We package under inert gas, use tested HDPE or amber glass, and ship with field-tested seals—details supported not by specification, but by seeing what happens over months in real-world warehouses.
Customers sometimes struggle with oxidized residue or slow yellowing during long-term storage. As producers, we keep a line of communication open: shipment logs, test data, and support for requalification if needed. Some biochemists reached out after spotting sample degradation in open containers or delayed reactions due to subtle oxidation. Our advice comes from on-the-ground troubleshooting, not theory: minimize air access, use dispensed aliquots, and keep containers tightly closed in cool, shaded storage.
Operational technicians in resin plants have flagged the occasional gelation if exposure to heat or moisture rises during drum transfers. A decade ago, we upped moisture controls and tracked batch performance, improving product reliability and supporting smoother plant operation for our partners. Feedback loops like this happen because we produce—and care about—what leaves our doors.
Most competitors distribute or relabel imported stocks of 2,2'-Dithiodiethanol. We do the synthesis work ourselves, choosing the precursors, monitoring exotherms, and managing the entire chain. This direct control allows improvements based on customer trends—say, a request for tighter chloride specs for electronics applications, or low-metal content for catalysis trials.
A recent year saw us reduce metallic residue by a full order of magnitude after several electronics industry clients linked minor failures to trace contaminants. Not content to simply pass off certified material, we changed reagent grade, revamped reactor clean-in-place systems, and instituted blind batch testing to ensure our claims matched user expectations, not just existing standards.
We know that documentation matters, but experience trumps paper. More than once, we’ve been called by process chemists struggling with unexplained yield loss, only to discover that off-brand 2,2'-Dithiodiethanol suffered from partial hydrolysis or instability during transit. Because we produce every lot, we cross-reference problems back to process logs and raw material batches, making targeted improvements. Customers using our material in continuous flow setups report fewer shutdowns due to unplanned variability.
From early days, our approach to compliance hasn’t just been about passing audits. We’ve watched regulations shift around sulfur chemistry and workplace exposure; reactive chemicals demand respect, and we invested in employee protection and environmental controls before external mandates hit. Automated fume extraction, scrubbed emissions, and solvent recovery all emerged out of necessity for a sustainable operation, not from compliance checklists.
Every step of our 2,2'-Dithiodiethanol production, from sourcing to shipment, includes built-in safeguards because people up and down the line rely on us for repeatable, quality output. Our traceability runs deep—each drum connects to lot and sublot, and we back up our assurances with in-lab test data. If a new application (say, a medical investigation or a specialty electronics assembly) requires expanded impurity profiles, we rise to the occasion and evolve our documentation transparently.
We maintain open lines with academia, industry, and testing labs around the world, learning with each collaborative troubleshooting call or unexpected result. More than a decade in sulfur chemistry has taught us that raw adherence to a standard never outperforms hands-on quality built up over time, backed by people who understand both the product and its many uses.
Many scientists encounter reducing agents like dithiothreitol (DTT), 2-mercaptoethanol, or glutathione long before handling 2,2'-Dithiodiethanol. Differences go far deeper than catalogs suggest. DTT, for example, shows greater reducing strength thanks to a dithiol structure, but lacks the liquid handling and shelf stability of our product—a major win if users require bulk quantities or extended storage in variable lab conditions.
Mercaptoethanol’s volatility and potent smell make it a poor candidate for scale-up or field use. In contrast, 2,2'-Dithiodiethanol offers nearly the same reactivity toward disulfide bonds, but produces less vapor and fewer workplace complaints about odor. Glutathione comes up often in biochemical circles, but its higher cost, solid form, and variable water compatibility limit use outside small-scale research. Our molecule wins out in process chemistry where bulk delivery and liquid-handling matter.
Practical polymer synthesis calls for molecules with both reactivity and dual alcohol ends—just the setup found in 2,2'-Dithiodiethanol. The chemical handles let users fine-tune properties of emerging polymers or specialized surface coatings, tying sulfur-based performance into base polyol chains. This is something standard mono-thiols or glycols simply cannot provide, no matter the synthetic route.
For users investigating alternatives due to regulatory or process changes, it pays to assess not only the nominal sulfur content, but also real-world batch purity, reactivity profile, and ease of handling. Batch after batch, direct-from-source material with full analytical tracking outperforms resale-type supply options, and the difference emerges clearly as end users report fewer delays and less batch-to-batch surprise.
Research reproducibility remains a hot topic for good reason. Take protein sequencing or diagnostic panel development—every minute contamination in a reduction step distorts outcome or clouds a new result. We go beyond the catalog to talk directly with our research customers, double checking that our 2,2'-Dithiodiethanol doesn’t just meet, but exceeds, practical purity requirements. If a protein aggregation step goes wrong, we want feedback to refine the next batch.
Our process chemists track repeat runs over years. Consistent product means that new process development or scale-up seldom stalls due to changing chemical input. This builds confidence among users in both R&D and scaled manufacturing; it removes the hassle of troubleshooting unwanted side reactions that arise when material varies unpredictable.
Quality in this context comes from patient, long-term investment—not from periodic certification but from data and repeatable field experience. The product remains the same at scale as it does at research scale, so a process developed in the lab can transfer to the plant with full reliability.
Producing 2,2'-Dithiodiethanol at quality levels demanded today means facing down day-to-day hurdles. Sulfur chemistry never grants a dull moment; the risks of over-oxidation, side reactions with water, and batch contamination stick around for anyone not watching the details. Low purity at the input stage often results in waste at the output. After several years of seeing how minor solvent impurities disrupt both synthesis and final product stability, we shifted to stricter precursor specification and added extra water-removal steps at the end. This made a measurable impact in both product shelf life and downstream reaction reliability for our customers.
Waste and environmental management matter. Sulfur compounds, left unchecked, threaten air and water quality; we built up a dedicated effluent treatment setup that recovers solvents and neutralizes outflow before safe disposal. We count this among our core responsibilities, as no product success justifies the risk of local environmental damage. Years of practical operations equipped us to implement these measures economically and effectively as part of routine production.
Perhaps most importantly, we have developed a culture of responsiveness. That means troubleshooting rare events, shipping reference samples for parallel testing, and keeping our team engaged with actual user results instead of cloistering away in isolated process engineering. A team that takes pride in manufacturing brings authenticity and consistent output to the table.
Users who rely on consistent results look for experience as much as they do purity numbers. Our years spent building and refining the 2,2'-Dithiodiethanol process have taught us that quality rests on more than test reports—it comes from dedicated production, user feedback, and relentless improvement with every batch. This is what we offer to every lab, pilot plant, or full-scale customer who chooses to work directly with a source that stands behind the product in both word and practice.