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HS Code |
162098 |
| Product Name | 1-Trifluoromethylcyclopropane-1-Carboxylic Acid |
| Cas Number | 119492-30-5 |
| Molecular Formula | C5H5F3O2 |
| Molecular Weight | 170.09 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 60-64°C |
| Density | 1.393 g/cm3 (calculated) |
| Solubility In Water | Slightly soluble |
| Smiles | C1CC1(C(=O)O)C(F)(F)F |
| Inchi | InChI=1S/C5H5F3O2/c6-5(7,8)4(3(9)10)1-2-4/h1-2H2,(H,9,10) |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C |
| Synonyms | 1-(Trifluoromethyl)cyclopropanecarboxylic acid |
As an accredited 1-Trifluoromethylcyclopropane-1-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g amber glass bottle features a secure screw cap, chemical label with hazard symbols, and clear identification: 1-Trifluoromethylcyclopropane-1-Carboxylic Acid. |
| Shipping | 1-Trifluoromethylcyclopropane-1-carboxylic acid is typically shipped in sealed, chemical-resistant containers compliant with UN regulations. It is transported under ambient conditions unless otherwise specified, with clear labeling and documentation. Standard precautions for corrosive and potentially hazardous chemicals apply, ensuring secure packaging to prevent leaks, spills, and exposure during transit. |
| Storage | Store 1-Trifluoromethylcyclopropane-1-carboxylic acid in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases and oxidizing agents. Keep the container tightly closed and protected from light and moisture. Use appropriate corrosion-resistant containers and ensure secondary containment to prevent leaks or spills. Clearly label all storage vessels and follow standard laboratory chemical storage protocols. |
Applications of 1-Trifluoromethylcyclopropane-1-Carboxylic Acid in Industrial ManufacturingAs the direct manufacturer, we supply 1-Trifluoromethylcyclopropane-1-Carboxylic Acid primarily for advanced chemical synthesis across agrochemicals, pharmaceuticals, and high-performance material industries. Its unique trifluoromethylcyclopropane structure delivers crucial building-block functionality for the demanding molecular architectures in regulated downstream fields. 1. Crop Protection Active Ingredient SynthesisManufacturers in the agrochemical sector use this acid as a key intermediate for the synthesis of next-generation pyrethroid insecticides. The cyclopropane ring and trifluoromethyl group introduce both metabolic stability and enhanced bioactivity, supporting the design of highly specific insecticidal actives. Integration occurs during the coupling or esterification step with alcohols or aromatic groups, which sets the bioactive ester profile required by regulatory and market demands. Industry compliance standards
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2. Pharmaceutical API Intermediate – Antiviral and Oncology CompoundsResearch-driven pharmaceutical manufacturers leverage this acid to construct fluorinated cyclopropane motifs for the assembly of complex drug candidates. Its incorporation often occurs through amide bond formation or coupling in late-stage intermediate steps, offering metabolic stability and increased bioavailability. Typical applications include small-molecule antivirals and cancer therapeutics where specific fluorine patterns are required by registration dossiers and patent claims. Industry compliance standards
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3. Fluorinated Specialty Polymers and CoatingsProducers of high-performance polymers utilize this acid as a functional group donor for the development of specialty coatings and engineering plastics. The cyclopropane and trifluoromethyl substituents introduce rigidity and strong hydrophobic properties useful in applications requiring chemical and weather resistance. It is directly copolymerized or grafted in solution polymerization, enabling customized performance for critical end-uses such as electronics and protective films. Industry compliance standards
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4. Agrochemical Safener and Co-Formulant ManufacturingSpecialty agrochemical formulators incorporate this acid to create crop safeners and selective herbicide adjuvants. Its structure enables the synthesis of cyclopropane-based molecules that modulate plant metabolism or enhance pest selectivity. The raw material is introduced at controlled stages of multi-step synthesis, often coupled with amides or heterocyclic fragments that tailor mode of action according to crop-specific registration files. Industry compliance standards
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