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HS Code |
378560 |
| Product Name | 1-[4-(Trifluoromethyl)Phenyl]-1H-Pyrrole-2-Carbaldehyde |
| Molecular Formula | C12H8F3NO |
| Molecular Weight | 239.19 g/mol |
| Cas Number | 110590-18-8 |
| Appearance | off-white to pale yellow solid |
| Purity | typically ≥ 97% |
| Melting Point | 82-86°C |
| Solubility | soluble in organic solvents (e.g., DMSO, methanol, chloroform) |
| Smiles | C1=CN(C=C1C=O)C2=CC=C(C=C2)C(F)(F)F |
| Inchi | InChI=1S/C12H8F3NO/c13-12(14,15)10-4-2-9(3-5-10)16-7-1-8(6-17)11-16/h1-7H |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Hazard Statements | Irritant; Harmful if swallowed or inhaled |
| Synonyms | 4-(Trifluoromethyl)phenyl-1H-pyrrole-2-carbaldehyde |
As an accredited 1-[4-(Trifluoromethyl)Phenyl]-1H-Pyrrole-2-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5-gram amber glass bottle, sealed with a screw cap, labeled with the chemical name, structure, lot number, and safety warnings. |
| Shipping | **Shipping Description:** 1-[4-(Trifluoromethyl)Phenyl]-1H-Pyrrole-2-Carbaldehyde is shipped in tightly sealed, inert containers to prevent moisture and light exposure. It is handled as a laboratory chemical, complying with all relevant safety, transport, and labeling regulations. Shipping typically occurs under ambient or cooled conditions, with appropriate documentation and hazard communication as required. |
| Storage | Store 1-[4-(Trifluoromethyl)phenyl]-1H-pyrrole-2-carbaldehyde in a tightly sealed container, protected from light and moisture. Keep at room temperature in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers or acids. Ensure appropriate chemical labeling and restrict access to trained personnel only. |
Applications of 1-[4-(Trifluoromethyl)Phenyl]-1H-Pyrrole-2-Carbaldehyde in Industrial Manufacturing1-[4-(Trifluoromethyl)Phenyl]-1H-Pyrrole-2-Carbaldehyde serves as a specialized intermediate for advanced chemical synthesis in regulated industries. We support direct integration of this compound into downstream processes, targeting sectors where unique electronic, pharmacological, or catalytic properties are required. Below we summarize major application scenarios based on real industrial consumption, technical requirements, and standards adherence. 1. Active Pharmaceutical Ingredient (API) SynthesisThis molecule is widely used in the preparation of heterocyclic frameworks needed for new-generation pharmaceuticals, particularly where a trifluoromethyl substitution enhances metabolic stability or receptor specificity. Medicinal chemistry teams introduce this intermediate during early-stage condensation or coupling, focusing on selective transformation and high-yield processes. It requires consistent purity and traceability under pharmaceutical GMP systems, with usage strictly based on validated synthetic routes for final API registration. Manufacturers choose this compound for late-stage functionalization, maximizing control over fluorine group introduction as required by modern regulatory filings. Industry compliance standards
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2. Advanced Agrochemical SynthesisIn agrochemical manufacturing, this building block enables the introduction of fluorine-containing heterocycles, improving pest resistance and metabolic stability for next-generation crop protection products. Its structure supports high conversion in key steps, such as pyrrole-based herbicide or fungicide starter units. Compliance with agro standards is critical to ensure safe environmental release and to facilitate downstream registration under global regulatory regimes. Agro formulators employ robust analytical monitoring, determining exact incorporation rate during structure–activity studies and pilot-scale runs. Industry compliance standards
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3. OLED and Functional Material SynthesisElectronic materials manufacturers utilize this compound for the synthesis of functional pyrrole derivatives critical to organic light-emitting diode (OLED) layers and semiconductors. Control over trifluoromethyl orientation in the molecule directly influences charge mobility and layer stability. Downstream users require rigorous batch-testing and materials traceability, matched to electronic-grade quality standards. Adoption occurs during monomer or pre-polymer scale-up, where accurate feed ratios guarantee consistent electronic and optical performance in end-device fabrication. Industry compliance standards
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4. Specialty Dye and Pigment PrecursorManufacturers in pigment and dye sectors select this molecule as a key precursor for fluorinated heterocyclic pigments, targeting high-performance coatings, inks, and fiber colorants. Its unique electronic profile permits stable colorfastness and UV resistance in specialty applications. Integration occurs at the dye coupling stage, where it undergoes further ring fusion or electrophilic substitution. End users rely on precise composition control and batch-to-batch reproducibility to meet textile and coatings regulatory approvals. Industry compliance standards
Typical usage ratio
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In manufacturing laboratories, the pursuit of reliability and performance continues to guide our daily routines. Chemicals like 1-[4-(Trifluoromethyl)Phenyl]-1H-pyrrole-2-carbaldehyde show this best. This compound stands out for its unique structure—a pyrrole ring linked to a trifluoromethyl-substituted phenyl group, with the distinct aldehyde function setting it apart from standard aromatic intermediates. We have watched this molecule gain ground among our synthetic partners, especially with the constant need for building blocks that can handle tough downstream processing and tight project timelines.
In the world of fine chemicals, impurities always seem to rear their head at the worst possible moment. Our team dedicates itself to minimizing these headaches, both through process control and raw material management. Early on, we realized that inconsistent starting materials can set back an entire chain of downstream chemistry. Our production method—crafted through years of adjustments—prioritizes the purity of 1-[4-(Trifluoromethyl)Phenyl]-1H-pyrrole-2-carbaldehyde at each stage. This pays off in both chemical yield and reliability, especially for researchers scaling projects from grams to kilograms.
Impurities can affect the electrophilic reactivity of the aldehyde group or even lead to color changes that disrupt product isolation. Keeping batches as colorless and clear as possible signals to our customers—and our own QC team—that we've done our job right. Rigorous analytical checks, particularly using NMR and HPLC, ensure conformity to expected results. Each month, we spot-check random samples and track any drift in spectral characteristics to prevent surprises.
Our clients come from diverse sectors, but the ones who return most frequently work in pharmaceutical research, semiconductor coating projects, and advanced materials exploration. The distinctive substitution pattern of 1-[4-(Trifluoromethyl)Phenyl]-1H-pyrrole-2-carbaldehyde makes it more than just another pyrrole derivative. The trifluoromethyl group boosts electron-withdrawing effects, which in turn adjusts the reactivity of both pyrrole and aldehyde sites. In practice, this opens doors for clean, directed transformations.
Medicinal chemists appreciate this, because electron-rich and electron-poor environments play off each other during drug candidate synthesis. In our own pilot facility, we've tested this compound in Suzuki and Heck-type couplings. Some who order from us use this intermediate to prepare heterocyclic scaffolds, finding its reactivity considerably different compared to non-fluorinated analogues. For teams building combinatorial libraries, subtle differences in reactivity speed up the discovery process.
Materials scientists also value this compound's properties. Incorporating trifluoromethyl groups changes the solubility and polarity of final products. For instance, creating high-performance polymers and pigments often demands starting points that deliver specialized solubility or stability under extreme conditions. This pyrrole carbaldehyde brings that advantage to the table—sometimes as a unique monomer, sometimes as part of a more complex molecular architecture.
Our standard lot offers material at ≥98% GC purity, achieved through repetitive recrystallization and careful vacuum drying. If a customer runs into solubility problems during scale-up, we help with tailored advice, since solvent choices for this molecule matter—polar aprotic solvents like DMF or DMSO often deliver the best results for reactions. From our perspective as a manufacturer, matching material quality to intended usage prevents most troubleshooting headaches before they occur. Past clients seldom return material; most post-purchase inquiries revolve around crystallization details or ideal storage and transport conditions, rather than unresolved impurities.
Unlike generic aldehydes or unsubstituted pyrroles, this compound calls for storage in cool, dry conditions to prevent slow hydrolysis or polymerization, especially over several months. We believe in honest timelines and open storage guidelines. From year to year, we may tweak packaging based on season or shipping distance, choosing amber glass with PTFE liners to thwart air and light degradation. Fielding feedback directly from users—sometimes after international transit—helps us improve both the packaging design and batch scheduling for distant clients.
Customers often ask how this building block compares to more standard aldehydes or pyrrole-based intermediates. Unlike common benzaldehydes, the combination of the trifluoromethyl group at the para position and the fused pyrrole structure confers both unique reactivity and physical behavior. Trifluoromethyl groups, notorious for their strong electron-withdrawing effect, tune the overall behavior of connected aromatic systems. In lab-scale tests, we notice higher chemical resistance and greater selectivity in transition-metal catalyzed cross-coupling. These features prove handy for synthetic teams aiming for purity and difficult bond formation.
Unsubstituted or lightly substituted pyrrole carbaldehydes tend to suffer from rapid oxidation or even unwanted condensation, which leads to yield loss. By contrast, 1-[4-(Trifluoromethyl)Phenyl]-1H-pyrrole-2-carbaldehyde demonstrates a certain robustness that allows it to stand up to rougher reaction conditions. Most first-time buyers quickly realize the benefit: greater confidence during upscaling or directed functionalization steps.
From where we stand in the supply chain, feedback counts as much as quality control. Working directly with process chemists and scale-up teams in pharmaceutical and electronics manufacturing gives us a clear view of what works and where things go wrong in the field. One significant pain point among users centers on reaction scalability. Not all intermediates scale smoothly—this is where our ongoing monitoring and regular process reviews sharpen our edge.
Years ago, we encountered batch-to-batch drift during a hot summer, when minor solvent contamination caused an uptick in side products. Rather than distribute subpar material, we suspended shipments and isolated the problem—an upstream solvent tank had picked up trace water. Since then, we included additional checks for residual moisture content and maintain backup solvent lines. Our consistency translates to fewer project delays for our partners—a lesson learned the hard way.
Another common theme involves crystal habit and particle size. Many synthetic chemists run into filtration clogs if particle size distributions shift unexpectedly. By tuning our recrystallization conditions and taking time to grind to a consistent particle size, we help researchers avoid lost afternoons hunched over vacuum filtrations. It’s these technical details that reinforce trust. Some customers report seeing clean NMR spectra right out of the package, with no baseline noise or trace impurities—feedback we use to drive internal improvements across all products, not just this intermediate.
New mechanisms and catalytic pathways continually reshape the way this compound finds use. Over the years, we've seen a steady uptick in orders around late Q1 and Q3—times when grant-funded discovery programs and semester-long academic studies ramp up. Exposure to different research sectors sharpens our awareness of shifting end-use needs.
Several collaborations with university groups have deepened our appreciation for the chemical’s performance envelope. In transition-metal-mediated cross-couplings, such as with palladium or nickel catalysts, the unique electronics of the trifluoromethyl group can sharpen reaction selectivity and suppress undesired side reactions. This allows researchers to push yields and scalability farther than with classic benzaldehyde derivatives.
On the materials side, researchers have flagged the benefit of integrating fluorinated aromatics for the tailored tuning of polymer backbones. Such design enables better hydrophobicity, enhanced resistance to oxidative breakdown, or optimized electronic properties for devices. We remain responsive to these trends, occasionally modifying batch size, delivery schedule, or impurity profiles to support special projects without disrupting our core process.
Our experience runs deeper than point-of-sale logistics. Manufacturers hold unique product insights, built from years troubleshooting the quirks that appear only at scale. Throughout the years, we have received requests to tweak not only purity, but also to generate documentation—analytical traces, stability data, storage notes—that downstream handlers and regulatory gates keep asking for.
A major advantage remains our direct oversight of every process step. We select starting materials based on long-standing supplier relationships, and we periodically qualify alternatives to keep costs and timelines viable. By controlling key reaction conditions—temperature, stirring rates, solvent selection—we tighten batch reproducibility. For customers, this means less time spent running in-house QC, chasing batch variance, or negotiating headaches with customs and storage during transit. When problems arise, our technical staff responds directly, removing third-party delays.
Over the years, we’ve watched trading companies repackage bulk lots, sometimes introducing risk or confusion with handling methods, relabeling, or aggregation from multiple sources. From a chemist’s perspective, direct relationships with the manufacturer translate to better traceability and accountability. Several institutional clients, especially in regulated settings, prefer this—full visibility from synthesis to bench application.
Every year, expectations rise. Downstream partners ask for higher purity, better documentation, and increasingly niche application support. Industry trends continue to push for greener synthesis and lower residual solvent content, prompting us to upgrade selective process stages when possible. Solvent recovery and more efficient purification columns, along with increased automation in in-process controls, keep us competitive while reducing both cost and environmental impact.
Supply chain disruptions taught us the value of backup suppliers for key precursors. Periodic stress tests on our inventory management now run twice yearly rather than just after major events. Every improvement builds from lessons learned during less predictable years, such as border shutdowns that force rapid adaptation in logistics planning. We keep revisiting our documentation package, ensuring that new regulatory requests can be covered without delay or overpromised lead times.
Industry certifications—ISO and internal GMP adherence—prompt us to document not just best practices but also areas for continuous improvement. Fielding client requests for specification tweaks, or newly needed analytical traces, stimulates both our R&D and production crews to innovate. Over time, technical knowledge and direct field experience have proven themselves as the keys to reliability, not bulk scale or superficial cost savings alone.
Most queries that come our way still revolve around finding the best reaction conditions and handling advice for this pyrrole derivative. We recommend storing material in a cool, desiccated space, away from direct light to keep the aldehyde function fully reactive over time. If customers need larger batches, we offer pre-packed kilogram lots in moisture-resistant drums or bottles for extended stability. Our team often follows up with tailored research support—clarifying experimental recipes, providing safety documentation, or simply sharing best practices gleaned from hundreds of client interactions.
Analytical consistency surfaces as a major concern, particularly among those scaling up reactions or validating production for regulated environments. Offering reliable spectral data—alongside rapid requalification support—remains one of our core strengths, built on direct investment in analytical infrastructure. Whether a client runs into crystallization difficulties, post-reaction discoloration, or simply wants to fine-tune method development, we draw on both hands-on lab experience and a growing database of real-world client examples.
For projects requiring the most stringent trace impurity levels, we accommodate custom production schedules and more intensive purification stages upon request. Over time, these capabilities have grown from a handful of one-off requests to a pillar of our regular service portfolio—at heart, a result of staying engaged with chemistry’s advancing edge.
1-[4-(Trifluoromethyl)Phenyl]-1H-pyrrole-2-carbaldehyde shows that the details of manufacture matter as much as molecular structure itself. Working on the production floor means seeing not just what lab protocols say should happen, but what real-world conditions require. Each lot reflects the combined effort of careful process optimization, attention to customer needs, and hard experience recovering from the occasional setback. Through direct engagement with users—whether in pharma, electronics, or advanced materials design—we move the product forward, keeping pace with the evolving standards and practical demands of chemistry.
Our faith in this intermediate comes from repeated technical success, informed adjustments, and steady dialogue across the supply chain. From high-performance drug building blocks to emerging electronic materials, 1-[4-(Trifluoromethyl)Phenyl]-1H-pyrrole-2-carbaldehyde represents more than a chemical name—it’s an outcome of continuous problem-solving, rigorous control, and persistent attention to the needs of the people and projects that depend on it.