|
HS Code |
382885 |
| Product Name | 2-Trifluoromethyl Thiophenol |
| Cas Number | 13715-44-9 |
| Molecular Formula | C7H5F3S |
| Molecular Weight | 178.18 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 191-193 °C |
| Density | 1.36 g/cm3 at 25 °C |
| Purity | Typically ≥98% |
| Refractive Index | n20/D 1.552 |
| Smiles | C1=CC=C(C(=C1)S)C(F)(F)F |
| Solubility | Insoluble in water; soluble in organic solvents |
| Storage Temperature | Store at 2-8 °C |
| Flash Point | 85 °C |
| Synonyms | 2-(Trifluoromethyl)benzenethiol |
As an accredited 2-Trifluoromethyl Thiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Trifluoromethyl Thiophenol, 25g, is supplied in a sealed amber glass bottle with a secure screw cap for chemical protection. |
| Shipping | 2-Trifluoromethyl Thiophenol must be shipped as a hazardous chemical in accordance with local, national, and international regulations. It should be packed in tightly sealed containers, clearly labeled, and protected from light and moisture. Shipping must adhere to proper documentation and safety protocols, including appropriate hazard labeling and handling instructions. |
| Storage | 2-Trifluoromethyl Thiophenol should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store under inert atmosphere, such as nitrogen or argon, if possible. Use secondary containment to prevent leaks or spills, and clearly label all storage containers with the chemical’s identity and hazard information. |
Competitive 2-Trifluoromethyl Thiophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Anyone who has spent time in a chemical plant knows that some products refuse to be simple formulations. 2-Trifluoromethyl thiophenol (model: TFMT-101) earns its place as one of those tricky, but vital, molecules that keeps showing up on project wishlists. We have produced this compound at commercial scale for over a decade, and learned the gritty details that make a difference for downstream synthesis and process reliability. As a manufacturer, we have discovered that while certain chemicals are often labeled as commodity items, this thiophenol derivative never truly fits that description—its structure and purity demand closer attention.
The molecule itself carries a trifluoromethyl group attached to the benzene ring, and its sulfur functionality makes it a powerful partner in several custom syntheses. Unlike its simpler cousins such as unsubstituted thiophenol or 4-methyl thiophenol, the electron-withdrawing trifluoromethyl group renders this compound less odoriferous and gives it a distinctive reactivity profile. It remains stable through a broader range of reaction conditions compared to many other thiol-based intermediates. Our chemists have watched it outperform other thiol reagents in both yield and selectivity, especially during the manufacture of fine chemicals for pharmaceutical and agricultural applications.
In direct comparison with basic thiophenol, 2-trifluoromethyl thiophenol demonstrates much lower tendency toward air oxidation. We have also seen a marked decrease in the undesired formation of side-products during halogenations and coupling reactions, which translates to cleaner workups and fewer headaches for production teams. The structure, with the CF3 group at the ortho position, helps block some common routes for side reactions, especially those promoted by trace metals. Labs that make substitutions at other positions quickly discover that the ortho placement of the trifluoromethyl group plays a crucial role in ensuring the desired chemistry actually works at larger scale.
Talking about use cases from the perspective of someone with hands-on experience: 2-trifluoromethyl thiophenol serves as a specialty building block for active pharmaceutical ingredient synthesis. Due to its particular substitution pattern, it is regularly called for in the construction of complex sulfur- and fluorine-containing scaffolds, including veterinary drugs and certain crop protection agents. The molecule’s reactivity toward alkylation and acylation agents, especially under phase-transfer or basic conditions, remains a standout feature, and our plant staff knows that a small tweak in reaction temperature can mean the difference between a solid batch and a failed run.
We have developed an instinct for what the downstream chemist needs because we see the production scrap and analytical data ourselves. Batch control reports show that customers using less rigorously manufactured batches (whether from distributors or small-batch importers) often run into higher impurity levels, and sometimes subtle changes in reaction color or by-product odor. Over repeated jobs, these differences rarely go unnoticed by experienced operators on the ground.
Our standard product specification for TFMT-101 guarantees GC purity above 99 percent, verified with reference standards from international suppliers. We learned early that even a single spike of disulfide contaminant over 0.5 percent can ruin column performance for a downstream pharma plant. In answer, we invested in a two-step vacuum distillation protocol, moving away from a single-pot operation common among competitors. Every lot undergoes rigorous Karl Fischer titration for water content, and staff receives training to avoid the pitfalls of moisture creep during packaging.
Where we see the greatest differences with third-party sources is in volatility control and odor profile. Poorly controlled synthesis or shortcuts in purification leave behind organosulfur by-products and higher boiling point residues. In one notable case, a customer switching from our TFMT-101 to a back-channel source saw a fivefold increase in baseline drift on their in-process chromatograms. End users feeding the product into microwave-assisted coupling reactions notice any deviation in sulfur content or volatility, which is another reason we maintain a dedicated analytical lab just for organosulfur QC.
Within our facility, every operator learns early that this compound deserves close handling in inert atmosphere—both for quality and safety. Product leaves our filling lines as a pale yellow to colorless liquid, packed under nitrogen in fluoropolymer-lined containers. When the shipment opens at customer sites, even the most sensitive GC-MS methods show no evidence of atmospheric thiol oxidation, confirming the benefit of exclusion of oxygen during all stages. Bulk users appreciate shipment in seamless drums lined with EPDM, while R&D departments typically request smaller glass-sealed ampoules to minimize risk and enable simple, direct transfer into glove-box systems.
We have watched alternate thiophenols, often supplied as off-white to amber liquids, develop color or crystals during transit—a sign of polymerization or hydrolysis. To prevent these nonconformities, our storage and distribution keep the product below 5°C until arrival, an approach based on years of tracking failure rates from room temperature storage. Direct end-user feedback, along with our own shelf-life trials, points to more predictable reactivity with our process controls than with material handled more casually.
Hands-on manufacturing demonstrates the gulf between guaranteed quality and theoretical specification. We often receive inquiries from companies whose R&D teams, stuck with questionable supply, end up troubleshooting anomalous yields or unexplained residues. Many request analytical support to deconvolute complex impurity profiles, a process which, in our experience, nearly always traces back to off-spec materials or poor control during synthesis and handling.
Unlike generic thiophenols—where cost per kilogram typically rules procurement decisions—2-trifluoromethyl thiophenol commands a premium among users who grasp the true cost of inefficient cleanup or wasted downstream material. We have earned repeat business from customers who initially gambled on cheaper sources, only to find that they paid for product but lost money through hidden inefficiencies.
Not every synthesis route or application suits a generic product line. Our years of custom production taught us to adapt fraction cutpoints, minimize batch-to-batch variability, and consult closely with end users about minor impurities that could undermine specific reaction steps. We have supplied both tightly specified and “standard” grades, always after open discussion with project teams about their sensitivity to halide, moisture, and trace amine contaminants.
Synthetic chemists working at scale rarely possess the bandwidth to resolve issues arising from upstream suppliers. Our practice acknowledges this by emphasizing certificates of analysis that reflect genuine, batch-specific testing, not generic boilerplate. This level of partnership also includes guidance on in-plant storage and transfer, illustrating the practical impact of minor changes in handling, particularly where the material’s volatility or reactivity matter.
Much as regulatory documents emphasize classifications and thresholds, real chemical safety comes from observing patterns over many years. We have seen firsthand how trace decomposition under standard storage conditions can create pressure or off-gassing in sealed drums. Plant walk-throughs during the summer months reveal that relaxed temperature control or allowing containers to “breathe” ambient air quickly translates to staining and odor complaints. Relying on these patterns, we enforce a strict safety data management process in which experienced personnel monitor every batch for off-gassing and color change, instead of depending purely on calendar-based shelf-life estimates.
For users scaling from laboratory to pilot plant, our technical team can overhear concerns about containment, vapor risks, and cross-contamination. We design shipment and delivery routines with those transition points in mind, supplying documentation that comes from tracked observations rather than regulatory checklists. This often means giving direct advice based on how the actual product behaves, a contribution that proves its worth during unplanned process upsets or scale-ups.
In a field where impurity tolerances keep shrinking, we rely on in-house GC-MS and titration labs, not simply paperwork or outdated physical checks, to verify every tank and drum. Over our years in production, we recorded seasonal patterns in minor impurity drift, learning to compensate process settings before they threaten a batch. Each batch pulls composite samples directly from finished drums, not intermediary tanks. We share these profiles with users whenever a refinement in their process might be sensitive to trace impurities.
The experience of troubleshooting at scale teaches the value of investing in maintenance and staff training. Water intrusion from poorly maintained gaskets or rushed drum sealing shows up as product failures just as surely as inconsistency in reaction input weights. Our lab teams stay in regular touch with line operators to catch the small, human-driven causes of off-specification reports before they snowball into lost production time.
By manufacturing 2-trifluoromethyl thiophenol domestically and at high batch volume, we take direct responsibility for our environmental footprint. Waste streams receive on-site treatment for sulfur removal. Our protocols eliminate uncontrolled venting, as we observed early on that inconsiderate handling would result in strong local odors and, over time, material losses significant enough to impact unit economics. Working closely with local authorities, our team maintains emissions well below permitted levels—years of data show it is possible to minimize both cost and risk through integrated design, not just after-the-fact remediation.
We recognize that environmental regulations continue to evolve, and through regular feedback from field staff, continually refine process steps to shrink waste and recover side-products wherever feasible. For end users, this means a supply chain that can respond to environmental auditing processes without scrambling for compliance on short notice.
Users trying to decide between 2-trifluoromethyl thiophenol and related compounds often confront a crowded marketplace filled with substituted thiols and alternative fluorinated aromatics. Direct experience, both from our own synthesis and through conversations with process chemists, suggests that TFMT-101’s unique substitution pattern outperforms typical alternatives—particularly for nucleophilic aromatic substitution, routes to trifluoromethylated heterocycles, and thiol-ene coupling. Compounds with para or meta substitution patterns tend to lag, especially at full plant scale, where small differences in boiling point or volatility rapidly complicate solvent recovery and downstream separation.
Alternate products, such as non-fluorinated thiophenols, have limited value for applications demanding high oxidative resistance or low residual odor. We’ve fielded multiple requests from R&D teams struggling to replace TFMT-101 with less expensive materials, only to watch product performance falter—and sometimes stall—mid-scaleup. These lessons, learned on the shipping dock and laboratory bench alike, reinforce our commitment to the compound’s continued production under strict controls.
It’s easy to take specialty chemicals for granted until a process hiccup exposes the false economy of “close enough.” Our facility routinely fields late-night calls from engineers who trusted a paper specification and ended up with off-color or low-assay batches that threaten expensive downstream steps. Each batch of 2-trifluoromethyl thiophenol we produce strengthens our conviction that engaged, transparent manufacturing delivers value unmatched by lowest-bid trading.
We invest in long-term partnerships, not only through consistent product supply but also by sharing protocols, batch histories, and troubleshooting experience. The reality of modern chemical production is that specifications matter, but first-hand knowledge and adaptive support matter more. The TFMT-101 story continues to evolve, shaped by the everyday details encountered in reactors, warehouses, and at loading docks—far away from paperwork or abstract product descriptions.
Our decades-long commitment to manufacturing 2-trifluoromethyl thiophenol—a compound often overlooked as just one more aromatic thiol—grows from the day-in, day-out realities faced by chemical producers and end users. The molecule rewards careful attention to quality, control, and real-world application, and our experience has taught us there are no shortcuts worth taking when product performance and plant reliability are on the line.