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HS Code |
282179 |
| Chemicalname | 4-(Trifluoromethyl)Cyclohexanecarboxylic Acid |
| Casnumber | 139173-41-2 |
| Molecularformula | C8H11F3O2 |
| Molecularweight | 196.17 |
| Appearance | White to off-white solid |
| Meltingpoint | 64-68°C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Density | 1.3 g/cm³ (approximate) |
| Smiles | C1CC(CC(C1)C(=O)O)C(F)(F)F |
| Inchi | InChI=1S/C8H11F3O2/c9-8(10,11)6-3-1-2-5(4-6)7(12)13/h5-6H,1-4H2,(H,12,13) |
| Synonyms | 4-(Trifluoromethyl)cyclohexane-1-carboxylic acid |
| Storagetemperature | Store at 2-8°C |
| Hazardclass | Irritant |
As an accredited 4-(Trifluoromethyl)Cyclohexanecarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a secure cap, featuring a white label displaying product name, chemical formula, and safety information. |
| Shipping | 4-(Trifluoromethyl)Cyclohexanecarboxylic Acid is shipped in tightly sealed, chemical-resistant containers to ensure safety and prevent contamination. It is handled as a non-hazardous material under normal conditions, but should be kept away from incompatible substances. Shipment complies with relevant regulations, including labelling and documentation, to maintain safe transport and storage. |
| Storage | Store **4-(Trifluoromethyl)cyclohexanecarboxylic acid** in a tightly closed container, in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and bases. Protect from moisture, heat, and direct sunlight. Use chemical-resistant containers and clearly label all storage vessels. Ensure proper grounding and spill containment measures are in place for safe handling and storage. |
Applications of 4-(Trifluoromethyl)Cyclohexanecarboxylic Acid in Industrial ManufacturingAs the direct manufacturer of 4-(Trifluoromethyl)Cyclohexanecarboxylic Acid, we supply this advanced building block to established sectors where its unique structure is required for high-value, application-critical products. Below, we detail real market application scenarios based on concrete industry practices, formulation needs, and compliant downstream usage. 1. Pharmaceutical API Synthesis: Cardiovascular Drug IntermediatesSeveral leading pharmaceutical producers incorporate this raw material as a key amido acid intermediate in the synthesis of regulatory-approved antihypertensive actives. The compound’s cycloalkyl trifluoromethyl group imparts improved metabolic stability and selective biological activity in new chemical entities. Manufacturers qualify each batch via multi-stage purification, and downstream transformations often involve amide coupling and selective reduction. Industry compliance standards
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2. Agrochemical Intermediate for Selective HerbicidesIn the agrochemical sector, formulators use this acid as a precursor for constructing highly selective cyclohexyl-containing herbicide actives. Its trifluoromethyl-cyclohexane structure improves field stability and foliar uptake. Downstream processes involve esterification and subsequent halogenation before formulation with adjuvants compliant to regulatory standards. Industry compliance standards
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3. Fluorinated Polymer Additive ManufacturingSpecialty polymer producers employ this compound as a chain-modifying acid for high-performance fluoropolymer blends. The unique trifluoromethylated cyclohexane moiety enhances chemical resistance and surface properties in polymer resins intended for demanding industrial applications. Compound integration requires careful ratio control during the copolymerization step, often in continuous or semi-batch reactors. Industry compliance standards
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4. Synthesis of Specialty Fragrance IntermediatesFragrance manufacturers synthesize complex cycloaliphatic ketones and lactones using this acid as a building block to introduce unique odor profiles and effective volatility modulation. The downstream processes include catalytic reduction and selective cyclization under process conditions where stringent impurity control is required to meet IFRA safety guidelines. Industry compliance standards
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Working with specialty fluorinated compounds means respecting tight controls, technical challenges, and years of steady improvement. At our manufacturing site, the synthesis of 4-(Trifluoromethyl)cyclohexanecarboxylic acid (CAS 872774-23-7) stands out as a milestone in both scale-up reliability and batch consistency. The trifluoromethyl group attached to the cyclohexane ring gives this molecule its unique character—balancing both chemical stability and reactivity. Unlike straightforward aromatic fluorinated acids, this cycloaliphatic structure reacts a little differently in both pharmaceutical and agrochemical synthesis.
Comparison talks in the industry usually focus on access to raw trifluoroacetic derivatives or even common perfluorinated acids, but here a simple side-group modification on the cyclohexane makes a real difference. The dense trifluoromethyl group interacts with reagents in justified ways, influencing both solubility and steric profile through every stage of the process.
Chemists on the floor know the importance of every reaction parameter though it goes far beyond simply hitting a purity threshold. We always emphasize getting genuine reproducibility at practical scale ranges—all without introducing costly purification or unplanned impurities. We developed proprietary approaches to manage the introduction of the trifluoromethyl group (–CF3), using careful temperature gradients and solvent swaps to suppress unwanted side products. Compared to routes for simpler mono- or difluorinated carboxylic acids, managing this extra fluorine content demands stricter containment techniques and monitoring protocols.
Every month's production logs show a similar pattern: high yields more typical of smaller pilot runs, continuously validated by NMR, GC-MS, and chiral HPLC. Standard practice for us never means cutting corners. Quality comes from well-trained staff and a strong commitment to tracking every stage, from starting materials to finished product containers.
Isomeric purity and residual solvent levels matter greatly when this acid enters regulated or research-focused projects. Our 4-(Trifluoromethyl)cyclohexanecarboxylic acid averages ≥99% chemical purity, with low moisture content and well-documented spectral data ready for every client’s audit. LC-MS and 19F-NMR confirm the right structure and exclude common process residuals. This focus on chemical clarity supports both synthetic uses and detailed downstream analysis.
We have seen over time that careful control of enantiopurity benefits specific research programs in both pharmaceuticals and asymmetric catalysis sectors. While our standard bulk offering is racemic, project-based resolutions support specialized chiral applications. We prioritise stability and storage over arbitrary supply chain efficiency, keeping crystalline solid available throughout seasonal demand fluctuations.
This acid draws specialists who want the well-defined steric profile offered by the six-membered cyclohexane ring and the electron-withdrawing trifluoromethyl group. Synthetic chemists frequently rely on it as a key building block in complex molecule construction—especially those tuning metabolic stability or looking to modulate bioavailability in preclinical drug candidates. The –CF3 moiety brings metabolic resistance in drug discovery and extends molecule half-life—a quality that more conventional non-fluorinated carboxylic acids simply cannot deliver.
Agrochemical developers, too, explore this intermediate for crop protection product research, taking advantage of the increased lipophilicity and environmental persistence that comes with fluorination. As a cycloaliphatic acid, it resists rapid oxidation and microbial breakdown, making it a component of interest when project chemists want a clear point of difference from benzoic or acetic acid alternatives.
Creating new fluorinated intermediates often leads to surprises—solubility shifts, unexpected side reactions, even minor issues like adherence to glassware or filter media due to the compound’s surface characteristics. Early builds with 4-(Trifluoromethyl)cyclohexanecarboxylic acid taught us to scrutinize every stage: is buffer pH correct, is filtration slow, are stirrer speeds adequate for phase separations? Practical answers stem from hard-won lab experience and ongoing investment in new purification setups.
Inconsistent product flow is disruptive to every customer’s timeline—so we doubled down on material handling steps. Packing, storage temp, and routine visual inspection after synthesis all get attention. The tiny tricks—using specific liners in drums, scheduling rapid post-filtration cooling cycles—save days downstream and move projects from bulk delivery to use in pilot labs without backward steps. Customers have told us that off-the-shelf options from traders aren’t enough: maintaining tight particle size, color, and bulk density makes a difference. Experienced labs notice quickly if material drags in solution steps, and those conversations always feed back into our process controls.
Commercial orders usually fall between 5 and 500 kg, though we retain flexibility both above and below that range. Material leaves our site as a crystalline white solid, sometimes faintly off-white depending on batch scale and container type. We keep free acid form as the primary product, rather than switching to sodium or potassium salt forms, unless project requirements dictate otherwise.
Not every competitor wants to deal with the practical headaches of a fluorinated cycloaliphatic acid. Logistics, regulatory requirements, and the basic chemistry all stack up. Our material must withstand both short-term storage in climate-controlled warehouses and long-haul overseas transport. We monitor each shipment for both moisture uptake and hydrolysis during transit, learning a lot from years of customer feedback. Material stored in stainless steel with vapor barriers retains clarity and performance even after months at rest.
Any chemist with bench or production experience will notice that switching from a trifluoromethylbenzene carboxylic acid to a cyclohexane-based one is never a drop-in substitution. The aromatic system brings rigidity and distinct electron-withdrawing effects, while the cyclohexane platform adds three-dimensional shape, flexibility, and different partitioning. In medicinal chemistry projects, teams often report less tendency for ring stacking and more room for functionalization or linker replacement.
Compared to its aromatic cousins, 4-(Trifluoromethyl)cyclohexanecarboxylic acid interacts differently in multistep syntheses, resisting Friedel-Crafts acylation and offering more reliable outcomes in hydrogenation or Grignard additions. This distinction lets project chemists solve problems that often stall with common aromatic acid derivatives. The strength of the carboxyl group remains intact, but with fewer surprises in reduction-sensitive pathways.
Long-term handling experience shows that dust control and ventilation count for more than the hazard pictograms let on. Although this acid doesn’t carry the acute toxicity of strong mineral acids or high-reactivity perfluoroalkyls, the –CF3 group can present mild volatility challenges at elevated temps. We never substitute containment procedures for shortcut shipping or unpacking. Workers stay attentive during scale-up, keeping material in sealed drums or lined containers, observing standard PPE guidelines and engineered ventilation.
Spill scenarios—rare in our shop—reinforce lessons about choosing the right absorbents and maintaining good air flow to prevent pressure buildup in sealed waste drums. Safety stories circulate among the most experienced staff and land in quarterly training sessions. Workers recognize the unique “sharp” odor of trace trifluoromethyl compounds, using regular monitoring in and around blending stations as a quality backstop. Continuous improvement isn't a slogan, it’s a weekly commitment.
Global attention to fluorine chemistry keeps evolving. Some perfluorinated acids draw attention for persistence, but this trifluoromethyl-cyclohexane acid doesn’t share their extreme environmental stability. We comply with both local and international frameworks for waste reduction and effluent management, investing in up-to-date solvent recovery and secondary containment. In-plant recycling means most water streams don’t leave our site until treated and checked by a licensed third-party lab for residual organofluorines.
Regular reporting goes beyond regulatory minimums—annual summaries demonstrate our low-waste approaches and confirm there’s no measurable discharge of persistent organic pollutants. Our customers asked for upstream diligence; we opened environmental audits and shared best practices. In practice, this looks like continuous reagent efficiency programs, frequent process tweaks to improve yield, and long-term relationships with certified waste partners. The result is a track record with few surprises and no regulatory setbacks.
Research programs a decade ago often ordered 4-(Trifluoromethyl)cyclohexanecarboxylic acid by the single gram while evaluating new structure-activity relationships. Now, this compound sits on the manifests of mid-sized plants and pilot kilo-labs, feeding directly into larger trial batches for both regulated APIs and advanced lead optimization. As a manufacturer, we value the feedback loop—that push-and-pull between what labs want to try and what we can deliver repeatedly.
Teams tell us that purity drift or out-of-spec density makes their next experiments unreliable. So, for every improvement suggestion, we trace results back to both raw sourcing and shift notes. Several years back, a partner screening new agrochemical candidates reported a faint but persistent off-odor. We traced it, batch by batch, to a minor change in starting material supplier. Those conversations change how we select and qualify every new feedstock, especially when it affects profile or trace byproduct content.
Today, chemists work to create platforms rather than isolated endpoints. Flexible functionalized acids support "late-stage functionalization," where the carboxyl group acts both as a handle for derivatization and as a strategically placed anchor for bioconjugation. The non-aromatic, non-linear nature of the cyclohexane ring serves better in macrocycle construction and for fitting into enzyme binding sites where flat molecules just don’t suffice.
Several of our service partners request custom packaging—measured aliquots for rapid handling or pre-mixed with co-solvents for immediate downstream use. Having both pre-packaged and made-to-order forms available answers teams racing to beat schedule. We take pride in adapting, moving away from commodity assumptions and working with hands-on scientists to solve both new and old challenges.
Most global markets still see low overall tonnage for trifluoromethyl-functionalized cycloalkanes compared to simple monochloro chemistries or benzoic acid derivatives. That said, demand from R&D-driven organizations keeps growing as more projects chase metabolic stability and new IP claims. Early investments in not only synthesis but also quality assurance bear fruit. Repeat orders and project expansions reward flexibility and deep technical understanding of both the molecule and the greater market.
Working as a manufacturer means answering more than just customer specifications—we jump into troubleshooting calls, host in-plant visits, and open up batch history when shipping documents leave any room for ambiguity. Regulatory registrations in multiple jurisdictions, as well as internal reviews, keep the feedback honest. Our experience tells us: understated differences in structure translate to measurable advantages in process yield, environmental profile, and end-product consistency.
Producing 4-(Trifluoromethyl)cyclohexanecarboxylic acid at commercial scale demands more than the usual attention to reaction purity, yield, or logistics. Through years of close work with downstream customers and in-house technical specialists, we’ve learned to shape process controls to real-world conditions rather than some theoretical ideal. The cycloaliphatic structure offers solution paths that aromatic acids can’t match; the trifluoromethyl function delivers both chemical resilience and differentiation in design. Every lesson learned, from production floor to regulatory audit, feeds our commitment to providing a molecule ready for the next challenge—from discovery to manufacture—delivered with the perspective only hands-on production brings.