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HS Code |
272411 |
| Productname | 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea |
| Casnumber | 2388-13-4 |
| Molecularformula | C8H7F3N2S |
| Molecularweight | 220.21 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 139-143°C |
| Solubility | Slightly soluble in water; soluble in organic solvents like DMSO and ethanol |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=CC=C1NC(=S)N)C(F)(F)F |
| Inchikey | UGZFKMGLZIAGHS-UHFFFAOYSA-N |
| Storageconditions | Store in a cool, dry place; keep container tightly closed |
| Synonyms | N-(4-Trifluoromethylphenyl)thiourea |
As an accredited 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle labeled **"1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea, 25g"**, with hazard symbols, lot number, and manufacturer details. |
| Shipping | **Shipping Description:** 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea is shipped in tightly sealed containers, protected from moisture and light. It is classified as non-hazardous, but standard chemical handling procedures apply. Packaging complies with regulatory requirements and includes labeling for chemical identity and safety. Store and transport at ambient temperature, avoiding extreme heat or direct sunlight. |
| Storage | 1-[4-(Trifluoromethyl)Phenyl]-2-thiourea should be stored in a tightly sealed container, away from incompatible substances such as strong oxidizers and acids. Keep it in a cool, dry, and well-ventilated area, protected from moisture and direct sunlight. Use appropriate personal protective equipment during handling, and store in a designated chemical storage cabinet following institutional safety guidelines. |
Applications of 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea in Industrial ManufacturingAs a specialized producer, we deliver 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea to manufacturers operating at the core of several critical chemical transformation sectors. Clients rely on its performance characteristics in select, controlled downstream applications where purity, consistent composition, and regulatory compliance are paramount. The following application scenarios reflect established markets and existing industrial practices, highlighting formulation specifics, quality expectations, and integration points within customer production flows. 1. Rubber Vulcanization AcceleratorsTire and industrial rubber compounders frequently use this thiourea derivative as a secondary accelerator in sulfur vulcanization. Its electron-withdrawing group enables rapid cross-linking with reduced scorch risk, particularly in high-performance rubber grades for automotive and engineered mechanical goods. The additive’s chemical structure supports uniform cure rates in both continuous and batch press processes, assisting manufacturers in maintaining quality standards for dynamic and static sealing applications. Industry compliance standards
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2. Specialty Agrochemical Synthesis (Herbicide Intermediates)Agrochemical manufacturers incorporate this compound as a critical intermediate in the creation of substituted thiourea herbicides for selectivity enhancement. The trifluoromethyl group increases metabolic stability in active molecules. Downstream customers synthesize target actives through nucleophilic substitution or heterocyclic ring closure, ensuring consistent product profiles required for regional pesticide registrations and product stewardship programs. Industry compliance standards
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3. Photographic and Imaging Chemical ManufacturingThis compound acts as a silver halide crystal growth regulator and antifogging agent in the formulation of high-sensitivity photographic emulsions and specialty imaging layers. Its unique electron affinity modulates nucleation rates in silver/halide deposition, providing finer grain structures required for advanced medical X-ray films and precision laser image recorders. Stringent raw material validation supports GMP-level trace metal control and batch-to-batch reproducibility. Industry compliance standards
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4. Corrosion Inhibitor Formulations for Acid PicklingSteel processing and surface finishing operations employ this thiourea derivative as an active ingredient in acid pickling inhibitor blends. Its molecular structure forms persistent monolayer films on steel surfaces, slowing corrosion by blocking aggressive ion attack during hydrochloric and sulfuric acid treatments. Specialty chemical blenders precisely dose the additive to manage hydrogen evolution and pitting without inhibiting scale removal. Industry compliance standards
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5. Organic Electronics Synthesis (OLED Intermediates)Display technology manufacturers utilize this compound as a crucial synthon for the construction of heterocyclic ligands and electron injection layers in organic light-emitting diode (OLED) devices. Its trifluoromethyl group facilitates enhanced electron mobility and thermal stability in finished small-molecule compounds. Precision-controlled synthesis environments manage trace impurities for optimal electronic properties, aligning with device fabrication standards for reliability and emission consistency. Industry compliance standards
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Working day in and day out with fine chemicals like 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea changes the way one thinks about the building blocks of pharmaceuticals, agrochemicals, and specialty substances. There’s a certain satisfaction that comes from watching a raw material transform. This satisfaction grows when the compound has the performance and edge that we see in this thiourea derivative. Speaking directly from the tanks and reactors rather than behind a polished sales desk, I’ll share why this molecule earns its place in our production schedule and how our experience has shaped its appeal.
Inside our plant, the moniker 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea isn’t just a catalog entry. The compound carries a unique identity—a trifluoromethyl group sitting on a phenyl ring, linking with a thiourea core. This structure grants the molecule properties neither seen in plain thiourea nor non-fluorinated derivatives. Over years, we have observed that the CF3 substituent, more than just a decorative addition, alters reactivity, boosts metabolic stability, and often introduces lipophilicity sought by medicinal chemists.
Many think of models and specs as vague numbers on a datasheet. We view them as a reflection of real-life process control and consistency. When we craft this compound, every batch aligns with precise melting range and purity thresholds. The melting point is no accident—it’s honed through careful temperature ramps and purity checks. Reagents are controlled so residual levels stay well within accepted ranges. Recrystallization techniques, agitation speeds, and filter selections come from hands-on experience to strip out colored by-products or unwanted isomers. Each time, we run HPLC and NMR to confirm the identity and percentage purity, not just out of regulation, but from habit born of responsibility for downstream users.
Long before our compound sees any paperwork or certificate, teams in pharmaceutical and crop protection labs put it to work. They value that thioureas often serve as nucleophilic partners or intermediates in heterocycle synthesis. The trifluoromethylated version brings that extra push in bioactivity, something plain derivatives simply don’t match. We’ve seen our compound serve as a vital precursor in the preparation of benzothiazoles and related frameworks. Some clients leverage its unique electronic effects to drive selectivity in multistep organic reactions, a tactic that pays off only with tightly controlled material.
When formulation scientists order this compound, they aren’t just filling a shelf. They’ve picked it for its solubility profile, electronic effects, and, in several cases, its application in developing antithyroid drugs or specialty fungicides. They call back with feedback—telling us which solvents delivered the best results, or how trace impurities showed up in their analytics, guiding us on further tightening our controls.
On the surface, this compound can look like just another member of the thiourea family. In practice, there’s a world of difference. Substituting a trifluoromethyl group at the para position does more than change a spectral fingerprint. It adds resistance to metabolic breakdown—making downstream active ingredients more robust in biological systems. Unlike plain phenylthiourea, this variant shows greater stability under oxidative conditions. Laboratories tell us it often provides a better yield and selectivity in cyclization reactions, factors that matter during both R&D and scale-up for production.
We’ve run head-to-head trials, setting 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea against its non-fluorinated cousins in the lab. Data confirm what the synthetic chemists report: the trifluoromethyl group can dramatically switch up a molecule’s polarity, leading to altered partition coefficients and easier separation from reaction mixtures. From a synthetic point of view, this difference can mean an extra crystallization step gets skipped, or a single-pass column is enough rather than running several rounds—saving both time and material.
Few people think much about what’s involved in producing 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea at scale. Inside our facility, it starts with the selection of the right starting materials. 4-Trifluoromethyl aniline, itself not the easiest compound to manage, requires careful handling to avoid inhalation exposure and water ingress that might foul a reaction batch. A controlled addition of isothiocyanate reagents—under nitrogen atmosphere, with precise temperature management—avoids side products and ensures the thiourea bond forms cleanly.
This isn’t the sort of synthesis you can set and forget. Every batch sees close monitoring through real-time infrared spectroscopy, helping us judge endpoint conversion before moving to cooling and filtration. The fine, pale powder that emerges still carries traces of impurities, most often subtle oligomers—not dangerous, but enough to affect certain high-sensitivity uses. Repeated washing with chilled solvent and slow filtration on sintered glass give a finer product. These details don’t just check a regulatory box, they anchor reliability for our clients.
From our end, trust means knowing a medicinal chemist or process engineer across the globe isn’t left puzzling over strange peaks in their quality control sheet. We maintain batch records and hold samples indefinitely, not because it’s required, but because the odd troubleshooting call years down the line sometimes traces straight back to an early lot. Every bottle leaving our plant carries a QC history and authentic, original analysis data.
Whenever we update our purification approach, every change passes through a pilot trial and client feedback loop. Sometimes, shaving off a few ppm of a side reagent might not make a visible difference in preliminary screens, but can mean the world further along in a scale-up project. Our facility technicians don’t just note these tweaks—they bring them into the next production cycle, keeping real use cases in mind.
Consistent product performance really comes down to two-way communication. Over the years, process engineers and lead chemists have reached out to us, reporting how a subtle difference in granule size impacts their feed rates into reaction vessels, or how shifts in crystallinity make for easier or harder dissolutions. We adapt. If a certain particle size proves ideal for automated sampling, we retain that granulation approach. Should a batch test higher in residual solvents (within safe ranges), we tweak drying steps—even if it stretches a cycle by a few hours.
A few years back, a pharmaceutical developer working on kinase inhibitors mentioned that a very slight color tint altered downstream purification, possibly introducing new chromatographic challenges. Tracking back, we caught minute, otherwise harmless, decomposition during a hot drying stage. Now, drying temperatures are checked not just at startup and shutdown, but every hour. This kind of feedback shapes every shift.
No matter how familiar we become with a substance, vigilance remains non-negotiable. 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea does not present the acutely hazardous profile of some high-toxicity lab reagents, but it deserves respect. Exposure to dust can irritate mucous membranes, and improper handling during weighing or mixing may trigger skin sensitivity for some individuals on our line.
Regular training and robust PPE discipline keep our teams safe. We enforce immediate clean-up routines, operate under effective local ventilation near charging points, and replace gloves and sleeves at the first sign of wear. Each exposure event, no matter how minor, is logged and tracked—a policy learned from years of seeing that even trace contamination can affect not just product quality but worker well-being.
Manufacturing stability requires a steady flow of raw materials. Global disruptions in the chemical trade—sometimes a blockage at a port, other times regulatory changes in key countries—put pressure on sourcing 4-trifluoromethyl aniline or specialty isothiocyanate reagents. Our supply teams develop relationships not with the cheapest source, but with ones willing to share analytical data, delivery records, and batch performance.
During the Covid-19 pandemic shock, we nearly ran short on a key precursor. Instead of improvising with unvetted alternatives, production lines paused until approved stocks arrived; clients were updated about the delay. This decision came at a cost, but protected users from the risk of uncharacterized side products. A reputation for reliability is built one decision at a time.
Synthetically, chemists could get away with less specialized compounds. Plenty of standard thioureas furnish the nucleophilicity or ability to build heterocycles in standard reactions. Still, repeating customers tell us that the para-trifluoromethyl version consistently enhances their results—yield bumps by as much as twenty percent, or the emergence of fewer by-products during scale-up. Often, the structure improves the shelf-life of their intermediates, giving them more latitude in planning downstream chemistry.
Analytically, trifluoromethylated thioureas present more defined NMR and IR signatures than unsubstituted analogs, reducing headaches for quality teams who must track impurities down to minuscule levels.
These recurring improvements run deeper than the baseline properties found on a technical bulletin. Bench scientists speak in practical outcomes—less gumming in isolation solid, reduced column fouling, cleaner spectra before stepwise derivatization. Production records back these testimonials, batch after batch.
Increasingly, labs ask for adjusted specifications: reduced particle sizes, alternate solvent residues, or fine-tuned moisture content. These tweaks require skill at the reactor controls and an open line with end users, not just to hit numbers on a page, but to bring tangible improvements to their day-to-day processes.
Sometimes, a new application springs up—from a group developing next-generation herbicides, for example. In these cases, our team is called to adjust synthesis, purification, or packaging to protect the molecule’s activity through months of storage or exposure to light and humidity. These requests rarely come with a manual. Solutions spring from years of collective plant experience—the operator who knows just how much agitation prevents caking, or the chemist who’s seen how tiny solvent tweaks improve crystal habit.
Modern industry raises the bar for sustainable chemistry. Manufacturing 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea on scale means examining every process stream—recycling mother liquors, reducing water consumption, and carefully managing by-product disposal. Regulatory standards guide these activities, but internal targets—driven by pride in our work—push further. Most solvent recovery now routes through continuous distillation until purity meets reuse requirements.
Spent filtrates undergo chemical treatment to limit organic release. Over time, tracking solvent balances and energy use led us to redesign operation schedules for minimal utility peaks, smoothing out electrical demand and reducing emissions. Not every step draws outside praise, but knowing our output leaves a smaller mark on the world gives the team renewed sense of responsibility.
Every chemist or process engineer who picks up 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea does so in the hope that it supports their discovery or production goals. For us, supplying this compound isn’t about chasing the next trend, but about acting as real partners to laboratories worldwide. We listen to changing requirements, improve by embracing feedback—both praise and criticism—and push quality control as far as possible.
From melting point checks to the way we clean equipment between runs, all steps build trust that the material in the drum will do what clients expect—no surprises, no sudden changes. This attention ensures direct continuity from our reactors to their research benches.
As pharmaceutical and crop science demand grows, and as innovations in heterocyclic chemistry reveal new uses for this unique thiourea, our commitment holds steady. Every batch tells the story of those who made it and all the scientists who depend on its consistency. To us, it’s a shared effort—one that stretches from the first loading of a reactor through every line of analytical data, until a new discovery arrives. Experience on the manufacturing floor isn’t just about following protocol; it’s the foundation of reliability, integrity, and long-term partnership. So the next time 1-[4-(Trifluoromethyl)Phenyl]-2-Thiourea makes a breakthrough in a novel synthesis, rest assured that a focused, experienced team stood behind each step that brought it to your door.