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HS Code |
868911 |
| Product Name | 3-(Trifluoromethyl)Benzyl Mercaptan |
| Cas Number | 131747-33-6 |
| Molecular Formula | C8H7F3S |
| Molecular Weight | 192.20 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 220-223°C |
| Density | 1.235 g/mL at 25°C |
| Flash Point | 97°C |
| Refractive Index | 1.529-1.533 |
| Smiles | C1=CC(=CC(=C1)CS)C(F)(F)F |
As an accredited 3-(Trifluoromethyl)Benzyl Mercaptan factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3-(Trifluoromethyl)Benzyl Mercaptan; tamper-evident cap, hazard and safety labels affixed. |
| Shipping | 3-(Trifluoromethyl)Benzyl Mercaptan is shipped in tightly sealed containers under an inert atmosphere, such as nitrogen, to prevent oxidation and degradation. It should be kept away from heat, sparks, and open flame. The chemical is typically classified as hazardous and shipped in compliance with relevant regulations for flammable and toxic substances. |
| Storage | Store 3-(Trifluoromethyl)benzyl mercaptan in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. Protect from direct sunlight and incompatible materials, including strong oxidizers and acids. Proper chemical fume hood storage is recommended. |
Applications of 3-(Trifluoromethyl)Benzyl Mercaptan in Industrial ManufacturingAs a direct manufacturer, we provide 3-(Trifluoromethyl)Benzyl Mercaptan in support of specialized synthesis routes across advanced chemical industries. This intermediate enables distinctive molecular transformations, ensuring precise performance in each downstream sector. We detail major application areas, covering process specifics, compliance, usage ratios, integration points, and finished products. 1. Pharmaceutical API Intermediate Synthesis3-(Trifluoromethyl)Benzyl Mercaptan is essential in constructing sulfur-containing scaffolds for developing specific APIs, such as kinase inhibitors and central nervous system modulators. It serves as a functional group source in selective alkylation or thiolation reactions during late-stage small molecule synthesis, where the trifluoromethyl group contributes to metabolic stability and improved bioavailability. The material must undergo detailed QC, including residual solvent analysis and trace impurity profiling, to ensure it meets the stringent demands of regulated pharma synthesis. Our facility provides this intermediate in cGMP-compliant packaging for pharmaceutical batch manufacturing. Industry compliance standards
Typical usage ratio
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2. Agrochemical Active Ingredient ManufactureThe compound acts as a vital building block in synthesizing trifluoromethylated thiol-substituted agrochemical actives, including herbicides and insecticides. Its use allows for incorporation of both trifluoromethyl and mercapto groups—structures valued for their biological potency and environmental persistence. High-purity mercaptan integration increases yield and ensures compatibility with downstream chlorination, oxidation, or cross-coupling steps. Careful process controls minimize byproduct formation and environmental discharge. Industry compliance standards
Typical usage ratio
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3. Specialty Polymer and Resin ModificationPolymer and resin manufacturers use 3-(Trifluoromethyl)Benzyl Mercaptan to introduce thiol groups that enhance crosslinking and chemical resistance in custom resins, especially those demanding exceptional thermal and chemical tolerance. Incorporating the intermediate as a chain transfer agent or end-capper during polymerization enables precise control of molecular weight and imparts fluorinated surface properties. Formulation chemists select this raw material to achieve functionalized coatings used in electronics and specialty adhesives. Industry compliance standards
Typical usage ratio
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4. Advanced Material Surface ModificationThe trifluoromethyl and mercaptan functionalities make this compound a select agent for post-synthetic surface functionalization of nanoparticles and inorganic substrates. Materials science teams employ it to graft sulfur- and fluorine-bearing groups to silica, gold, or magnetic nanoparticles. This process imparts specific hydrophobicity, anti-fouling properties, or enables bioconjugation for analytical and diagnostic platforms. Materials are tailored for use in next-generation sensor devices and targeted separation membranes, with processing managed in controlled atmosphere reactors to prevent thiol oxidation. Industry compliance standards
Typical usage ratio
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3-(Trifluoromethyl)Benzyl Mercaptan—our trusted team has spent years mastering this particular organosulfur compound, and we put that expertise into every batch. Our plants run with directly observed process controls, and we do our own purification, not farmed out to third-party hands or brokers. That means each order comes to you with the same sharp, consistent profile customers have counted on for years.
Many clients start their inquiry asking why someone would pick 3-(Trifluoromethyl)Benzyl Mercaptan over the dozens of commercial thiols or simple benzyl mercaptans. Direct experience shows you don’t get this particular balance of reactivity, selectivity, and stability from standard products. The trifluoromethyl group at the meta position makes a visible difference. Chemists focused on pharmaceutical intermediates, agrochemical development, or custom specialty resins look for its profile. That means less background reaction, lower risk of by-products in multi-stage syntheses, and an easier path through purification. We’ve seen projects where dialing in this extra reactivity made the difference between batch success or barrels of waste.
Every customer has a spec sheet, but we believe the real test comes during downstream reactions. 3-(Trifluoromethyl)Benzyl Mercaptan leaves our warehouse after fully testing lots using NMR, GC, and titration for free sulfur. You’re purchasing a colorless to pale yellow liquid, purity exceeding 98%, and a thiol group protected from premature oxidation by careful handling with dry nitrogen. We store and ship in acid-washed, moisture-free glass or steel containers to avoid any contamination or off-odors, not just sticking to minimum standards. You won’t spend days scrubbing out side-products from random trace impurities. Our analysis covers more than simple percentages—you get a product that doesn’t introduce unknowns into your process.
Some differences only show up in real-world usage, and we see firsthand what happens when the source chemistry doesn’t line up. An improperly handled thiol will darken, develop offensive odors, or throw off yields due to oxidation. We’ve watched competitors cut corners with open-air transfers and cheap containers. Over the years, we’ve developed closed-cycle handling, cold storage, and a workflow trained on immediate inertization. Our people understand the real hazards—the persistent smell that can hang around a whole facility if leaks go unchecked, or headaches caused by even microgram-level volatiles. Careful, clean work limits these problems before they ever reach you.
Customers tend to notice the difference: less air sensitivity on opening, clear liquid to the last drop, and a much easier time handling the thiol safely in glove boxes or under fume extraction. If your lab is moving up from off-the-shelf benzyl mercaptans, you’ll see a sharp drop in off-notes and undesired sulfurous byproducts. It’s the little details, and every batch we send out reflects the hundreds of times we’ve tweaked the process to get these basics right.
Anyone working with synthesis involving selective alkylations, protective group chemistry, or fine-tuned site-specific coupling reactions will see why this thiol gets repeated demand. The trifluoromethyl group isn’t just a label—it lowers the electron density in a way that reduces unwanted side reactions. We’ve watched clients reduce their purification time when swapping out without worrying about double alkylation or ring reduction steps confusing their process.
In scale-up of pharmaceutical leads, minimizing variation counts for more than just cGMP compliance. We take calls from chemists struggling through route scouting, and they value knowing exactly where their mercaptan comes from. In those moments, reliability can matter more than price or lead time. We field questions on nucleophilicity, discuss solvent systems, and share best-practices for in situ generation or scavenging of excess thiol. It’s not just chemicals—it’s an exchange of real-world lessons built up over years in production and process development.
Labs often reach for plain benzyl mercaptan for generic activation, but our trifluoromethyl variant offers a tighter handle on reaction outcomes. The chemistry gets more predictable—affecting both rate and regioselectivity. You get less random byproduct, fewer headaches during downstream workup, and higher yield of your targeted products. That doesn’t just make lives easier; in regulated settings, it can mean quicker signoff on process validation and fewer failed batches.
Another difference comes down to physical safety and odor control. Standard benzyl mercaptans can be overwhelmingly pungent and tend to persist on surfaces. We built our packing workflow to keep losses to an absolute minimum, using clamped fittings and vapor phase warning systems. Cleaning up an accidental spill of plain mercaptan can mean lingering odors for months, while our product’s strict handling cuts those risks down.
In practical use, our tighter purity specs lead to simpler chromatography, fewer mysterious peaks on an NMR, and shorter troubleshooting sessions. A lot of that comes from knowing exactly which upstream synthetic routes go into the product, and catching deviations upstream before they reach a liter bottle or drum. We’re not just licensing out a production protocol; we’re hands-on during every run, routinely talking with users to hear how the product performs in real reaction settings.
Thiols, especially fluorinated varieties, bring certain headaches. Trifluoromethylated aromatics cost more, and global supply chains for fluoro-building blocks can shift at short notice. Our purchasing team monitors raw material sources months in advance. You can’t just ring up a catalog house and expect a fresh lot every week. That means we maintain buffer inventory, prioritizing incoming orders from established partners, and setting up blanket agreements where possible. In the rare case a supply disruption hits, we notify customers directly and offer alternative lots or forward contracts, sidestepping price spikes or sudden unavailability.
From a production plant view, the biggest risk comes from exposure to moisture and air, which can degrade product or spark safety alarms. We avoid this with real-time detection in tank lines and automated purging. That means you rarely face a rejected lot, and if issues crop up, we’re tracing them back to a specific valve or seal—not guessing from half a world away.
Over time, we’ve grown into a support team as much as a supplier. Labs new to this mercaptan often call in for safe handling tips, as the strong thiol odor can overwhelm ordinary fume hoods. We’ve distributed practical tips—use secondary containment, cold traps, and dry nitrogen—rather than just quoting literature hazards. In multi-step synthesis, isolation and storage tips tend to save more money than reducing the price per kilo, so we share actual case studies drawn from our own work. If you’re blending the thiol into intermediates or planning on large-scale extractions, our chemists walk through the workflow to help minimize exposure and maximize shelf-life.
One useful lesson for small-to-mid scale labs: always check compatibility between your storage vessel and the compound. Ordinary plastics or low-grade steel can discolor or even react with the product over several weeks. Our team routinely audits the performance of our chosen packing solution and records every change, making sure each batch travels in containers that don’t impart flavor or degrade contents. Such details sound small, but any experienced synthetic chemist knows the headaches that stem from avoidable contamination.
Handling mercaptans requires more than just technical documentation; we’ve learned that being above-board with regulatory reporting pays dividends. Fluctuating international shipment limits for organosulfur compounds can affect delivery times, so we keep up with evolving guidelines and routinely update our safety sheets. Our logistics crew is trained in labeling and spill containment that meets or exceeds both local and international rules.
Customers in Europe, the US, and East Asia often have additional documentation requests for import. Our operations team responds directly, providing batch-level analysis, route-of-synthesis letters, or transparency reports on residual substances. By having real chemists on-hand, we avoid the delays and communication breakdowns that sometimes plague large traders. Tight coordination with a handful of trusted freight partners eliminates most issues before orders reach customs inspection.
Disposal also comes up for customers scaling up process runs. We have published guidelines for post-use neutralization and partner with licensed waste handlers to find better downstream disposal or recycling options for spent thiol residues. If you’re managing a pilot campaign, ask us about sustainable options for closed-loop recovery or offsite neutralization rather than guessing from a distance.
We don’t treat 3-(Trifluoromethyl)Benzyl Mercaptan as a fixed product frozen in time. Continuous feedback from research chemists and technical staff sharpens our approach each year. If a new impurity profile turns up on your reaction trace, we’ll dig into our in-house analytics to spot and resolve the cause. We routinely pilot improvements suggested by multiple users, whether that means refining filtration steps, adopting new packing liners, or documenting best practices for handling at ultra-low temperatures.
Being both the manufacturer and primary handler means our chemists see the whole lifecycle, from starting material choice to end-user application. Several times, clients collaborating on new synthetic methods have asked for single-lot, high-purity material, and we’ve adjusted processes in real time. Whether you’re running a small medicinal chem campaign or full-scale agricultural R&D, you’re dealing directly with the source—not getting standard catalog fare.
Demand for 3-(Trifluoromethyl)Benzyl Mercaptan tracks closely with innovation in pharmaceuticals and advanced materials. Every year brings new derivative pipelines—a reflection of the growing appetite for molecules with tailored reactivity. As more companies push into fluorine-containing block synthesis, requests for specialty mercaptans continue to climb. Competition can be fierce for high-quality supplies, especially for research-grade purity.
Because we oversee all stages internally, from raw material procurement to final filling, we can adapt batch schedules rapidly. That reduces lead times when customer projects accelerate or when a large order might otherwise lock out mid-sized buyers. We see this flexibility as a major advantage, preventing disruptions that commonly occur with less agile, multi-stage supply chains. Our long-term clients benefit because they can plan ahead, knowing their supply isn’t subject to sudden rerouting or overseas bottlenecks.
We don’t follow short-term cycles set by traders or brokers. Our years producing mercaptans have rewarded steady planning and strong relationships. As new regulations arrive or raw material sources fluctuate, we keep clients ahead of the curve with stock updates, alternate booking options, and old-fashioned, honest communication about risks in the pipeline.
Beyond simple material provision, we see our core job as partnering with scientists striving for progress. Whether it’s troubleshooting a fouled-up reaction or launching a new material project, hands-on support brings better results than one-sided sales. More than once, a customer’s detailed analytical feedback has sent us back to the drawing board, helping improve purity or rethink minor production steps. These interactions ultimately shape a more robust, reliable thiol—ready for next-generation synthesis.
We continue to invest in both analytical capacity and automation in our production lines, seeking faster turnaround on testing lots or root cause analysis. If you have a challenging request—maybe a super-low sulfur spec, a restricted impurity profile, or unusual packing requirement—bring it to our team. Over the years, these projects have led to permanent improvements in both quality and user safety.
Our commitment to 3-(Trifluoromethyl)Benzyl Mercaptan isn’t abstract. For the people making, testing, and shipping every batch, the focus is always on visible improvements for you, the user. Years standing in the plant, running glassware checks, and recording test results have impressed on us that every shortcut left by a supplier ends up as added work or lost time for a chemist somewhere down the line. We keep to a philosophy rooted in experience—a product that does what you expect, every single lot, and a team that answers questions with the facts, not just scripts.
If you’re new to the compound or familiar with its properties, you’ll notice these differences in your daily work. We’ve learned that strong partnerships outlast trends, produce better outcomes, and build loyalty grounded in trust. Our team encourages all users—whether buying kilos or drums, making gram-scale runs or scaling production—to reach out and become a part of this ongoing conversation.