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HS Code |
194588 |
| Cas Number | 594-44-5 |
| Molecular Formula | C8H18S |
| Molar Mass | 146.29 g/mol |
| Iupac Name | 2,2,4,4-Tetramethyl-3-thiapentane |
| Synonyms | 1,1,3,3-Tetramethylbutyl mercaptan |
| Appearance | Colorless to pale yellow liquid |
| Density | 0.83 g/cm³ |
| Boiling Point | 163-165 °C |
| Flash Point | 49 °C |
| Solubility In Water | Insoluble |
| Odor | Strong, unpleasant (mercaptan-like) |
| Refractive Index | 1.461 |
As an accredited 1,1,3,3-Tetramethyl-1-Butanethiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL amber glass bottle with tamper-evident seal, labeled with hazard symbols and chemical details for 1,1,3,3-Tetramethyl-1-Butanethiol. |
| Shipping | 1,1,3,3-Tetramethyl-1-butanethiol should be shipped as a hazardous material in accordance with local, national, and international regulations. It must be packed in tightly sealed, chemically resistant containers, clearly labeled, and cushioned to prevent leaks. Transport only by authorized carriers, ensuring compatibility and proper documentation to minimize risks during transit. |
| Storage | **Storage of 1,1,3,3-Tetramethyl-1-Butanethiol:** Store in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as oxidizers and acids. Use secondary containment if possible. Keep away from direct sunlight. Ensure proper labeling and avoid inhalation or contact with skin and eyes by using appropriate protective equipment. |
Applications of 1,1,3,3-Tetramethyl-1-Butanethiol in Industrial Manufacturing1,1,3,3-Tetramethyl-1-Butanethiol plays a critical role in several specialized chemical manufacturing sectors where high-purity organosulfur compounds are essential for downstream synthesis, selective catalysis, and functionalization. Our factory-grade material consistently delivers the performance necessary in demanding industrial environments, with thorough batch documentation and quality controls aligned to relevant regulatory requirements. Below, we describe its established use-cases and detailed field deployment in global manufacturing supply chains. 1. Polymerization Chain Transfer Reagents in Specialty PolymersMajor polymer resin and elastomer manufacturers utilize 1,1,3,3-Tetramethyl-1-Butanethiol as an organosulfur chain transfer agent to control molecular weight distribution and end-group structure during free-radical emulsion and solution polymerization of acrylate copolymers, styrene-butadiene rubbers, and specialty latexes for adhesives and automotive coatings. Polymer engineers specify this thiol to achieve controlled branching and conversion rates, influencing both process efficiency and polymer performance. Industry compliance standards
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2. Sulfur-Based Vulcanization Accelerators in Synthetic Rubber FormulationTire and technical rubber compounders rely on this thiol as a functional component in proprietary accelerator blends. 1,1,3,3-Tetramethyl-1-Butanethiol contributes active sulfur species that fine-tune crosslink density and optimize elasticity in automotive, industrial hose, and sealing rubber composites. By regulating network structure in sulfur-cured elastomers, manufacturers meet both global and customer-specific durability standards, especially for high-stress and dynamic environments. Industry compliance standards
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3. Functional Intermediate in Organosulfur Synthesis for Agrochemical ActivesAgrochemical manufacturers engaged in the production of sulfur-containing fungicides, insecticides, and herbicide antidotes incorporate 1,1,3,3-Tetramethyl-1-Butanethiol as a specific thiolating agent. Its unique structure facilitates the introduction of highly branched thioalkyl moieties, enhancing bioactivity profiles and fine-tuning volatility for safe field application. Strict documentation, trace impurity control, and full batch traceability ensure alignment with local and international agrochemical regulations. Industry compliance standards
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4. Odorant Additive in Natural Gas and Industrial Fuel DistributionGas utilities and fuel blending plants make controlled use of this specialty thiol as an odorant component in gas odorization formulations. The compound provides a persistent warning smell in natural gas and LPG, which lack a native odor, thereby ensuring leak detection and meeting regional safety regulations. Its high volatility and distinct olfactory threshold support accurate dosimetry and minimize residue downstream, contributing to efficient system audits and occupational health compliance. Industry compliance standards
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5. Surface Functionalization in Electronic and Semiconductor ChemicalsProducers of electronic-grade specialty chemicals apply 1,1,3,3-Tetramethyl-1-Butanethiol as a unique surface modifier and ligand precursor in processes such as the fabrication of gold and silver nanoparticle inks, semiconductor etchant stabilization, and surface passivation solutions. The compound introduces compact, sterically shielded thiolate layers, controlling nanoparticle agglomeration and providing controlled functional group density at interfaces—both critical for electrical conductivity and long-term device reliability. Industry compliance standards
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From a manufacturer's perspective, every specialty thiol tells a story of refining, purification, and careful handling. Take 1,1,3,3-Tetramethyl-1-Butanethiol, for example. This compound—often recognized by chemists for its four methyl groups hugging a central thiol-bearing butane backbone—offers a specific set of properties shaped by that branching structure. Synthesizing it to high purity goes beyond technical data; it taps into decades of experience controlling impurities, managing sulfur reactivity, and responding to the precise needs that industrial users bring to our doors.
Back at our plant, every batch of 1,1,3,3-Tetramethyl-1-Butanethiol begins with raw material selection. Strict specifications govern the precursor alcohols, the thiolation agents, and every solvent in the process. The resulting thiol’s strong, characteristic odor means that containment isn't just a preference; it remains an operational necessity. Our teams check every transfer line, every reactor seal, and even secondary scrubbers. The sense of responsibility is real—not only for the end-use but also for co-workers and the surrounding community.
Demand comes in waves across the globe. Markets in lubricants, polymerization modifiers, pharmaceutical intermediates, and even specialty odorant blends rely on the unique branched structure that this molecule brings. Technicians in the application labs depend on its sharply defined boiling point and reactivity with specific transition metal catalysts. You won’t find the same level of steric hindrance, nor the same subtle tuning of nucleophilicity, in straight-chain analogs.
Chemists reach for 1,1,3,3-Tetramethyl-1-Butanethiol when they need a bulky mercaptan—the kind that resists easy oxidation, stands up to harsh processing conditions, or interrupts radical chains with less byproduct formation. This structure outdoes simpler mercaptans in scenarios where standard options run afoul of control or quality issues. The tetra-alkyl branching keeps the sulfur atom protected, offering a marked difference in reactivity compared with less hindered thiols. That makes all the difference in synthesizing sensitive intermediates or designing next-generation additives.
Every batch that leaves our reactors comes with a certificate anchored in data but shaped by human experience. Quality checkpoints exist well beyond the regulatory hurdles. In-line spectrometry traces batch-to-batch variations. A slight drift in gas chromatograph peak shapes sparks a roundtable discussion with R&D, not just a flagged lab report. Regulatory status matters, but so does the arc of feedback—hearing from a polymer chemist who found that our product allowed them to nudge conversion rates by half a percent without fouling downstream separations.
We’ve worked with engineers from several sectors who swore off straight-chain mercaptans due to poor odor stability or aggressive discoloration in their end-products. With 1,1,3,3-Tetramethyl-1-Butanethiol, the chemical stability measured under real processing temperatures means fewer headaches, less downtime, and an easier path to scaling up without a burdensome redesign.
It’s one thing to blend a kilogram in the lab. Scaling up to hundreds of metric tons places unique demands on plant infrastructure. This isn’t a molecule that gets slapped together. Controlling the thiolation reaction, quenching side products, scrubbing every last wisp of mercaptan vapor—all these are muscle memories for an experienced thiol manufacturer. Over the years, tweaks to thermal control and continuous process monitoring became critical. Too much heat or an off-pH moment, and you’ll spend days reprocessing waste.
Our operators learned early how mercaptan chemistry responds to small changes. Even a half-degree shift in distillation temperatures can let in excessive forerun or tail fractions, and those impurities wind up haunting the final downstream application. Careful column loading, a sharp eye on vacuum seals, hands-on training with every generation—these aren’t checkboxes. The result: a finished product meeting the spec not just in theory, but in the hands of customers running one-of-a-kind reactions.
The feedback loop is constant. Customers developing specialty polyolefins wanted a mercaptan that doesn’t act like an open invitation for chain scission, and our 1,1,3,3-Tetramethyl-1-Butanethiol filled that need. Others came to us looking for a thiol that survives in base-catalyzed processes, due to the molecular shielding from those four methyl branches. Without this protecting effect, they were left with attack on the sulfur atom and yields that simply failed to meet commercial benchmarks. Having this specific molecule on the shelf shortened their development timelines.
The manufacturing lines hardly slow down, but safe transport always rides along with process control. Packaging this thiol means more than drum sizes or standard labeling. It brings to bear years of working with resistant liners, checking every weld on bulk tankers, and ensuring our partners down the chain handle pallets with secure venting systems. Temperature controls keep product from degrading or picking up moisture. Training runs deep, right down to the warehouse, so that nobody treats thiol packaging casually.
Storage tells its own tale. Even small leaks aren’t tolerated—we’ve put in place multi-level detection and containment. Our approach evolved out of real-world challenges. Early on, we ran into trouble with gasket material compatibility, and instead of chalking it up to “industry standard,” our maintenance planners revised every fitting on dedicated lines. This is an operations-driven decision, rooted in the hands-on knowledge that 1,1,3,3-Tetramethyl-1-Butanethiol, given its volatility and strong odor, asks for double and triple containment and a response plan more robust than the regulations outline.
User safety moves beyond paperwork. We supply downstream partners with guidance for ventilation and decontamination. The product demands respect for its sulfur content, even if its steric bulk reduces reactivity compared to smaller mercaptans. Every technical call with a client engineer is grounded in our field experience—making sure gloves are right for the job, fume hoods are functional, and recovery systems don’t get overlooked on busy shift changes.
Performance in practice means more than purity. Engineering teams seek out 1,1,3,3-Tetramethyl-1-Butanethiol when they need consistent quality run after run. In the lab, the bottle stays sealed until ready for use, while on the plant floor, a bulk container might be pumped over several shifts. Temperature excursions, accidental mixing of off-spec loads, or cross-contamination incidents expose just how crucial cycle-to-cycle control really is.
Polymer scientists shared stories of inferior thiols fouling reactors or sending their product into non-compliance—a few ppm of the wrong impurity upended productivity targets for months. We worked together to optimize not only the supply but also the handling and feeding protocols. Sourcing directly from a manufacturer with documented control over the full process, not just a repacker downstream, helped them close those gaps.
Reaction chemists, formulating new catalysts and ligands, rely on lot-to-lot consistency. Thiols make up only a fraction of a formulation, but changes in backbone branching or impurity profiles throw off kinetics and lead to expensive troubleshooting. We’ve tracked those results—not just in our own QA labs but in sitting across from users and reviewing their batch sheets. The difference became clear: using a thiol manufactured with attention at every stage protects the reputation of the end-product and saves precious time in scale-up.
Lubricant formulators took a keen interest in 1,1,3,3-Tetramethyl-1-Butanethiol’s unique resistance to oxidation, aided by its methyl groups. Traditional thiols didn’t last through repeated heat cycles and turned up as foul-smelling contaminants, corroding sensitive components. Our bulk customers reduced changeovers, extended machinery uptime, and actually tracked measurable savings at the maintenance level—attributable not just to chemical specification, but to a close relationship with a supplier who listens and adapts.
The market knows plenty of mercaptans with simpler backbones. Straight-chain groups like 1-butanethiol or 1-hexanethiol offer easier synthesis routes. They tend to come cheaper, but they bring along drawbacks. Odor volatility, higher reactivity, and unwanted byproduct formation trouble both experienced handlers and new entrants alike.
Our observations, spanning years, show that 1,1,3,3-Tetramethyl-1-Butanethiol escapes many of these traps. Its robust molecular shielding means fewer oxidation and polymerization side reactions, which keeps downstream streams purer and makes downstream separation less burdensome. Handling improvements go beyond hard numbers: our shipping teams spend less time on deodorization and corrective action, allowing more focus on scaling and feedback with large industrial users.
Regulators also keep a close eye on sulfur specialty chemicals—both for safety and environmental reasons. Meeting compliance once isn’t a badge to rest on. For this thiol, emission control, odor management, and product declarations get baked in from the first stages of design. We have spent years refining emission abatement strategies to make sure no unnecessary costs land with our customers. Industry networks feed us early notice when new standards look likely, and our technical staff respond by innovating not just for our compliance, but for all those who deploy our product in sensitive applications.
Any chemical plant brings together a variety of experiences—operators, engineers, regulatory affairs, maintenance, logistics. Feedback from the shop floor shapes product and process more than any outside audit. In thiol production, it’s rarely the textbook reactions that mark progress—it’s the on-the-ground decisions and collaborative troubleshooting that set apart a specialty chemical manufacturer.
We built our approach around the understanding that every kilogram produced finds itself at the center of a complex value chain. Every batch record, every process improvement, speaks to the lessons learned through working hand-in-hand with customers. One year, small adjustments to agitation rates in our reactors cut impurity spikes that had long resisted standard analytical tuning. Another year, a partnership with downstream blenders led to packaging redesign, eliminating spillage during high-volume unloads.
The specialty thiol market rewards not just technical prowess, but empathy and adaptability. Customers with process lines in different countries shared how packaging, climate, and supply timing all affected their workflows. Responding to these stories, we adjusted supply windows and worked with logistics planners to avoid disruptions. When a partner in the polymer sector sought to introduce a new manufacturing technology, our team stood alongside theirs during pilot trials, sharing insights and adjusting product specifications in near-real-time. This kind of partnership isn’t just a nice-to-have; it has become essential for both progress and trust.
Analytical abilities define quality, too. Spectral fingerprints of each batch are checked against historical data. Variations in color, odor, or trace impurities catch a trained technician’s eye. Instead of shipping out “within spec” products by default, we revisit batches that seem subtly off—the small differences a seasoned chemist or engineer would actually notice in end-use. This kind of vigilance means fewer surprises for our own teams and for customers scaling up ambitious projects.
Discussions about specialty thiols increasingly include responsible sourcing and environmental footprint. While the feedstocks and industrial chemistry don’t change overnight, our purchasing teams prioritize reliable, certified suppliers, and our process development group looks for steps to minimize excess reagent use. This isn’t mere good publicity—it’s a reflection of the questions we hear from downstream users: “How do you guarantee consistency? Where do the raw materials originate? Are your transport channels robust enough for my production schedules?”
With 1,1,3,3-Tetramethyl-1-Butanethiol, supply assurance doesn’t just hinge on the product sitting in a warehouse. It comes from maintaining long-term partnerships up and down the chain. Regular audits, supplier engagement, and open discussion about shortages or surges flow back into our own process planning. Experience shows that fixing problems at the source beats chasing solutions at the delivery dock.
Our journey includes open reporting about waste streams, emission controls, and energy consumption—factors that, in the end, affect both the price and sustainability of every kilogram we produce. Customers have shared that this level of openness—backed by hard data—lets them put forward their own sustainability reports with more confidence, traceability, and actual numbers.
Looking at recent trends, demand for high-performance additives and modifiers has pushed manufacturers to raise the bar. In additive manufacturing, 1,1,3,3-Tetramethyl-1-Butanethiol’s stability and selectivity set it apart from traditional mercaptans. Research partners have highlighted how its controlled reactivity enables them to push formulations into new ranges, achieving finer control of properties like molecular weight and end-group functionality.
Polymer researchers embrace the predictable chain-transfer and termination profile delivered by the unique backbone. Integration into specific catalyst systems – those built around transition metals – has taken on new importance as regulatory frameworks tighten for catalyst residues. Early-stage projects have benefited from direct collaboration, shortening testing cycles, allowing more focus on innovative chemistry rather than off-target side reactions.
New applications continue to surface. In electronics, for example, process engineers need sulfur donors that walk the line between activity and benign behavior in delicate etching steps. Aromatic thiols often struggle here due to volatility and cross-contamination risk. By contrast, the four methyl groups of our thiol of choice grant just the right level of reactivity, minimized odor impact, and a reliability seldom matched in less-engineered alternatives.
Being the manufacturer means owning every challenge and every solution for the life of the product. Direct lines between production teams, application scientists, and final users create a transparency and problem-solving ecosystem impossible to replicate with one-off purchases from a trading house. Every repeat order isn’t just a transaction; it’s a mark of earned trust, reinforced through accountability and a willingness to listen and adjust, not just claim expertise.
In specialty chemicals, real benefits stem from an ongoing conversation. Whether facing unexpected changes in global shipping, new regulatory requirements, or technical surprises at the plant, our team stands ready. We bring not just molecules, but hard-earned experience, collaborative troubleshooting, and a responsive mindset to every customer relationship. 1,1,3,3-Tetramethyl-1-Butanethiol’s value grows from this foundation—a product shaped not just by synthetic pathways or quality numbers, but by a daily commitment to those who rely on it.