|
HS Code |
845549 |
| chemical_name | 3-Methyl-1-Butanethiol |
| cas_number | 2084-18-6 |
| molecular_formula | C5H12S |
| molar_mass | 104.22 g/mol |
| appearance | Colorless to pale yellow liquid |
| odor | Unpleasant, skunky odor |
| boiling_point | 104-106°C |
| density | 0.847 g/cm³ at 25°C |
| flash_point | 20°C (closed cup) |
| solubility_in_water | Insoluble |
| refractive_index | 1.458 (20°C) |
| pubchem_cid | 11537 |
As an accredited 3-Methyl-1-Butanethiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 mL of 3-Methyl-1-Butanethiol, sealed with a secure cap and labeled with hazard warnings. |
| Shipping | 3-Methyl-1-Butanethiol is shipped in tightly sealed containers, typically glass or corrosion-resistant metal, to prevent leaks due to its strong odor and volatility. The container is clearly labeled as flammable and toxic, requiring cool, well-ventilated storage. Complies with relevant transport regulations for hazardous chemicals to ensure safe delivery. |
| Storage | 3-Methyl-1-butanethiol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Keep it away from oxidizing agents, acids, and strong bases. Store in a dedicated flammable liquids cabinet, and ensure proper labeling and containment to prevent leaks, as it has a strong, unpleasant odor and is highly flammable. |
Applications of 3-Methyl-1-Butanethiol in Industrial Manufacturing3-Methyl-1-Butanethiol finds targeted use in several well-established downstream industrial sectors, valued for its high impact olfactory properties and chemical reactivity. As the direct manufacturer, we supply industrial-grade material suitable for regulated processes requiring consistent performance, traceability, and integration with quality-focused production systems. The following scenarios detail precise application cases, each reflecting the real-world role of 3-Methyl-1-Butanethiol across four critical points: compliance, formulation ratio, process incorporation, and the resulting market-ready products. 1. Food Flavor Formulation for Savory SeasoningsGlobal flavor houses and seasoning manufacturers utilize 3-Methyl-1-Butanethiol as a key sulfur-containing note to formulate authentic cheese, onion, and meat profiles. The compound’s ability to mimic natural enzymatic hydrolysis products supports clean-label trends and enhances product realism in snack coatings and ready meals. Food safety and traceability demands dictate strict alignment to food additive regulations and adherence to validated flavor frameworks for responsible use. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Aroma Ingredient in Fragrance ManufacturingFine fragrance and personal care formulators employ 3-Methyl-1-Butanethiol to replicate complex natural odor nuances in premium and industrial perfumes. Its potent character is carefully dosed to create authentic truffle, tropical fruit, or mature cheese facets, particularly in masculine and gourmand fragrance compositions. Due to high olfactive potency, strict IFRA guidelines and batch certification processes govern material handling. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Gas Odorization for Leak DetectionUtility companies, gas cylinder filler plants, and detector manufacturers rely on 3-Methyl-1-Butanethiol to create unmistakable warning odors in otherwise scentless natural gas and LPG products. The compound’s low odor threshold is exploited for safety-critical dosing; robust QA systems confirm every batch meets regulatory requirements for olfactory impact in field conditions across distribution networks and end-user installations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Chemical Intermediate in Pharmaceutical SynthesisActive pharmaceutical ingredient (API) manufacturers and custom synthesis providers utilize 3-Methyl-1-Butanethiol as a key alkylthiol building block in synthesizing specific organosulfur compounds, especially within anti-infective and CNS drug development projects. The material’s defined impurity profile and traceable supply chain support regulatory filings and validated process qualification across scale-up to commercial production. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Methyl-1-Butanethiol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
After years in the lab and plant, I have found 3-Methyl-1-Butanethiol stands out in the toolkit for anyone formulating flavors, fragrances, or specialized intermediates. The moment it leaves our reactor, there’s no mistaking its potent, roasted, almost tropical sulfur aroma. From a production standpoint, this substance always demands the kind of caution reserved for the most pungent thiols. The chemical world knows the molecule as 3-methylbutane-1-thiol, but the common term usually gets shortened to 3-methyl-1-butanethiol. We run strict odor containment: a single drop spreads its aroma through the vents. There are many thiols out there, but this one leaves an impression both olfactory and industrial.
In the plant, we rely on the CAS number 2084-18-6 to avoid mistakes. We check for colorless to slightly yellow liquid as typical of good product. Our specifications measure up as we guarantee a minimum purity of 98%, based on GC. This sets our material apart from many batches circulating with lower threshold impurities, which compromise downstream use. Every drum, every flask, we record batch identity along with detailed characteristic notes, so users can track every shipment right back to the reactor it came from.
Moisture retention is tightly controlled. Our methods prevent trace water content from drifting above 0.5%. Nobody wants a hydrolyzed thiol, and in our quality lab, analysts run Karl Fischer and GC-FID on each batch before transfer. By the time our product reaches your line, it fits required specifications for food, flavor, and fragrance precursors as well as industrial intermediates.
Years of customer feedback and in-house experiments show this thiol’s impact profile in both gourmet and specialty chemical sectors. Various food and beverage labs depend on 3-methyl-1-butanethiol for natural, roasted onion or tropical, savory enhancement. In low ppm quantities, it becomes the heart of meaty, cheesy, or durian flavor notes. Fragrance applications lean on its ability to shade compositions with realistic savory, green, or leathery accords, especially when perfumers chase authenticity in gourmand or naturalistic scent profiles. Working at low dosages prevents overpowering, and our customers often dilute it to suit formulation preferences.
Beyond flavor and fragrance, the chemical research sector investigates this compound as a reference material in odorant studies or as a marker molecule in trace detection protocols. Specialists in analytical chemistry have sought our high-purity batches for GC calibration work, due to the reproducible chromatographic profile and minimal impurity footprint present in carefully managed synthesis conditions.
Producing 3-methyl-1-butanethiol isn’t like synthesizing a standard ester or amine. The odor threshold sits impossibly low, sometimes below a single part per billion. That means the first challenge is containment. Our staff work in custom-ventilated synthesis suites, using closed-loop transfer between vessels. Glass-lined reactors help minimize loss through atmospheric leakage, and secondary scrubbers manage any fugitive emissions that escape the containment. Years ago, more basic facilities struggled to keep odors from escaping, but we have updated our handling to world-class suppression.
We synthesize using alkylation of sodium hydrosulfide with 3-methyl-1-bromobutane under controlled conditions, using nitrogen blanketing to avoid oxidation and minimization of side products. After the aqueous workup, the crude is redistilled under vacuum to drive off low-boiling impurities. Our fractional distillation columns work overtime, tuned specifically for the boiling point of 3-methyl-1-butanethiol, typically 105-108 °C at atmospheric pressure. Only careful fraction collection yields the high purity recognized by flavorists and chromatographers as genuine. Our final containers consist of HDPE drums with Teflon gaskets—anything else suffers from permeation or attack by the aggressive sulfur atom.
People sometimes confuse this thiol with its cousins: 2-methyl-1-propanethiol, n-butanethiol, or tert-butylthiol. It pays to clarify the difference. 3-Methyl-1-butanethiol shows a meatier, heavier aroma than the lighter, more ethereal character from compounds like ethanethiol or propanethiol. Fragrance developers who need richness turn to this molecule, because lighter thiols can feel too sharp or volatile, especially in food simulants or savory flavor notes. The methyl branching on our product’s backbone enhances both persistence and roundness, a trait missing from unbranched sn-1 thiols.
From an industrial angle, our thiol resists oxidation slightly better due to steric hindrance around the sulfur. It reduces the tendency toward unpleasantly acrid degradation products during storage, so both shelf life and delivery windows stay tighter. Chemists running large synthesis or flavor formulators building shelf-stable products appreciate this stability, because small differences in molecular structure can mean big headaches in stability tests.
Handling high-impact sulfur compounds demands more than a simple spec sheet. Our quality control program spans from on-line monitoring during the reaction step to final GC-MS scans prior to bottling. Besides confirming purity, we also assess trace nitrate and halide levels—both of which can sabotage downstream synthesis or analytic work. Each tank and container receives not just gas chromatography analysis, but also a separate panel odor assessment by experienced analysts trained in thiol detection well below detection thresholds. This detailed approach springs from experience: batches that don’t pass both instrumental and sensory tests never reach the packaging line.
Over the years, we’ve partnered directly with flavor chemists to understand which impurities disrupt their recipes. Even isomeric impurities, below half a percent, can lead to off-notes in cheese or tropical fruit flavors. By recirculating feedback from the field back into in-process quality checks, we tailor our reaction times and distillation procedures to drive those trace compounds as close to zero as practical. It’s become clear across projects that thiol-sensitive applications need more than just percentage purity—they need a sensory experience unspoiled by unpleasant edge notes. We tailor our operational controls based on this reality.
From firsthand shipping notes, I can say thiols like this won’t forgive careless packaging. Material transfer in open air leads to both product loss and odor complaints. We use pressure-tested HDPE drums with fluoropolymer inner liners and anti-tamper seals to help ensure that every kilogram that leaves the plant reaches the customer in the same state. Tracking temperature during transit matters too, since elevated heat encourages oxidation. Our warehouse runs on a cool, shaded cycle and we only load-out early in the morning. Customers often appreciate being spared unwanted surprises, as improper storage leads to the appearance of side products, which both affect aroma and reduce value.
Mishandling can also impact workplace safety. We build training into every outbound shipment—both on paper and direct communication—to guide users through each step of handling, so that the potent aroma stays where it belongs, inside closed processing. This keeps both workers and facility neighbors comfortable, and local regulation satisfied.
Chefs and flavorists pushing the limits of savory effect say this thiol is indispensable. They teach us that creative work demands materials not just pure on paper, but reliable batch to batch. There’s little frustration worse than reformulating successful blends after an unexpected impurity creeps in. We accept returned samples for analysis, even gaining insights from customer complaints. Often, application teams share blending strategies to mask or shape the aroma—feedback which finds its way into both our analytical methods and practical advice for new end users.
Sometimes, innovation in one sector spills into another. Researchers in biosensor calibration, for example, started requesting this compound for instrument validation, owing to the predictably detectible odor signature. Their requirements for reproducibility outstrip even the strictest food additive norms. We adapt by tuning fineness of separation and adjusting storage duration, making sure batch-to-batch consistency satisfies analytical-grade specifications, not just food code minimums.
Regulatory environments grow more demanding every year. Surveillance for potential allergens, trace metallics, or banned precursors now shapes both how we synthesize and how we label every container. We no longer view compliance as box-ticking. Instead, every change in international law—such as shifts in allowable flavoring agents in Asia or labeling standards in North America—prompts a review of our upstream supply chain and process management. We maintain a transparent chain of documentation for each batch, tracking it through every step and holding back material if any compliance uncertainty arises.
Users in the fragrance and flavor sector confirm that documented transparency speeds up their own product registrations. Our experience proves that early, clear traceability saves time later, and builds lasting partnerships. Batch records, odor notes, and synthesis logs hang together as a single file, available to clients on request.
People seldom mention the struggle of managing fugitive thiol vapor until they’ve run a plant themselves. Controlling these gases involves not just scrubbers and carbon filters, but procedural discipline. Our teams rotate jobs to prevent olfactory fatigue, and we invest in continuous improvement of local ventilation and exhaust design. Safety isn’t just PPE: it’s day-to-day reality when working with high-impact aroma chemicals. Every single complaint from a neighbor or worker means a review and improvement round, so our staff know their daily routines actively shape plant policy.
Waste handling also forms a core focus. Byproducts and rinsate never exit untreated: we’ve committed to on-site neutralization and incineration systems that capture the vast majority of sulfur compounds before any waste leaves the gate. Sometimes, plant neighbors comment on our almost odor-free site, a direct result of continuous engineering improvement rather than off-the-shelf solutions. Decisions about environmental controls grow from every shift report, as nothing compares to learning from on-the-floor experience.
Our customers often bring us new ways to solve problems. Robust partnerships build on open communication, whether the concern is batch release timing, impurity thresholds, or blending recommendations. More often than not, a small change in how we run a purification step, or tank transfer, was inspired by feedback from a downstream user needing a more stable or less volatile product. A relationship with those who use our material means we do not simply set specifications in-house and hope they suit; we widen our window to include the practicalities of formulation, blending, and handling beyond our walls.
Internal plant meetings focus on future-proofing, based on both evolving compliance requirements and the shifting standards expected by global end-users. Improvements in odor management, batch tracking, and even documentation systems rarely happen in isolation; they follow from an ongoing dialogue within and outside the facility. Only a company deeply engaged with the hands-on details can maintain both high-quality output and transparent customer trust. In many ways, the story of 3-methyl-1-butanethiol is the story of how we build practices that suit not only production, but every user handling the compound on the other end.
As demands grow for unique, convincing flavors and true-to-nature sensory experiences, the role of specialty thiols like 3-methyl-1-butanethiol only increases. This compound carves out a niche no artificial alternative has fully captured. Its rich, meaty, subtly fruity character brings complexity and depth that basic compounds struggle to match. That reputation is won product by product, batch by batch. For those of us at the synthesis and bottling line, the story of this molecule comes down to learning from every process step—from reaction design to odor control and end-user satisfaction.
More so than many aroma chemicals, 3-methyl-1-butanethiol refuses to play by the rules. Its handling teaches next-generation chemists to respect both power and precision. Formulators, in turn, find both challenge and reward in crafting blends where this sulfur note rounds out, rather than dominates, finished goods. Few molecules demand as much attention across the trade: from the minute care in plant workflows, all the way through to the creative touches on a chef's worktable or a perfumer's bench.
Ongoing improvements in how 3-methyl-1-butanethiol is manufactured, purified, and shipped come from shared purpose between our team and those in the field. No matter how much technology advances, the best results spring from minds and hands working together, from feedback cycles and deep operational experience. Old mistakes like releasing low-purity, unstable material have taught us where not to cut corners. Embracing collaboration—in handling, formulation, compliance, and problem-solving—has pushed our standards higher over time.
With each batch, we return to what experience has shown us: the details matter, from reaction timing to container selection. Every day in production reinforces how this particular thiol challenges our assumptions and processes. Chemical manufacturing often depends on process for process’s sake, but producing high-quality 3-methyl-1-butanethiol requires flexibility, careful upgrades, and a willingness to try new approaches. The results speak for themselves in the form of stable, predictable, batch-tested product, trusted by chemists, analysts, flavorists, and perfumers alike.