Description

Flupropanate (2,2,3,3-Tetrafluoropropionic Acid) is a high-purity fluorinated carboxylic acid with the molecular formula C₃H₂F₄O₂ and CAS number 756-09-2. This specialized chemical is widely utilized in organic synthesis, pharmaceutical intermediates, and agrochemical research due to its strong electron-withdrawing properties and reactivity. Its unique tetrafluorinated structure enhances stability and bioavailability, making it a valuable building block for advanced fluorinated compounds. Available in rigorously controlled batches, our Flupropanate meets stringent purity standards, ensuring consistency for sensitive applications. Suitable for laboratory and industrial use, it is provided with comprehensive analytical documentation, including HPLC, NMR, and MS data.

Properties

• CAS Number: 756-09-2
• Complexity: 121
• IUPAC Name: 2,2,3,3-tetrafluoropropanoic acid
• InChI: InChI=1S/C3H2F4O2/c4-1(5)3(6,7)2(8)9/h1H,(H,8,9)
• InChI Key: PXRROZVNOOEPPZ-UHFFFAOYSA-N
• Exact Mass: 145.99909195
• Molecular Formula: C3H2F4O2
• Molecular Weight: 146.04
• SMILES: C(C(C(=O)O)(F)F)(F)F
• Topological: 37.3
• Monoisotopic Mass: 145.99909195
• Synonyms: Flupropanate, 756-09-2, 2,2,3,3-Tetrafluoropropionic acid, Flupropanate [ISO], 376KS3J2Q6, EINECS 212-049-7, DTXSID7058177, DTXCID3031945, 3H-Tetrafluoropropionic acid, 2,2,3,3-tetrafluoropropanoic acid, MFCD00054686, Propanoic acid, 2,2,3,3-tetrafluoro-, 2,2,3,3-Tetrafluoropropionic acid;3H-Tetrafluoropropionic acid, 3h-tetrafluoropropanoic acid, UNII-376KS3J2Q6, tetrafluoropropionic acid, SCHEMBL128482, SCHEMBL865265, SCHEMBL1155750, CHEBI:82013, PXRROZVNOOEPPZ-UHFFFAOYSA-, ALBB-035770, AC9459, SBB086451, AKOS002662653, BS-42255, SY047513, DB-055971, NS00019239, T1777, EN300-96639, C18854, Q27155689, F0001-1912, InChI=1/C3H2F4O2/c4-1(5)3(6,7)2(8)9/h1H,(H,8,9)

Application

Flupropanate serves as a key intermediate in the synthesis of fluorinated pharmaceuticals, agrochemicals, and specialty materials. Its strong acidity and fluorinated backbone make it ideal for modifying bioactive molecules to enhance metabolic stability and binding affinity. Researchers also employ it in the development of herbicides and plant growth regulators due to its selective herbicidal properties. Additionally, it is used in material science for surface modification and as a precursor for advanced fluoropolymers.

Safety and Hazards

GHS Hazard Statements

• H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]

Precautionary Statements

• P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501

Hazard Classes and Categories

• Skin Corr. 1B (100%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.