Description

5,5,5-Trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-yl methacrylate (CAS No. 630414-85-6) is a highly specialized fluorinated methacrylate monomer with the molecular formula C₁₀H₁₂F₆O₃. This compound features a unique trifluoromethyl and hydroxyl functional group arrangement, making it an ideal candidate for advanced polymer synthesis and surface modification applications. Its IUPAC name, [5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-yl] 2-methylprop-2-enoate, reflects its precise chemical structure. The presence of multiple fluorine atoms enhances its thermal stability, chemical resistance, and hydrophobicity, which are critical for high-performance materials. This monomer is particularly valuable in the development of fluorinated acrylic polymers, coatings, and adhesives where low surface energy and durability are required. It is supplied with high purity and strict quality control to ensure consistency in research and industrial applications.

Properties

• CAS Number: 630414-85-6
• Complexity: 343
• IUPAC Name: [4,4,4-trifluoro-3-hydroxy-1-methyl-3-(trifluoromethyl)butyl] 2-methylprop-2-enoate
• InChI: InChI=1S/C10H12F6O3/c1-5(2)7(17)19-6(3)4-8(18,9(11,12)13)10(14,15)16/h6,18H,1,4H2,2-3H3
• InChI Key: CZDKPGBADTUZLK-UHFFFAOYSA-N
• Exact Mass: 294.06906321
• Molecular Formula: C10H12F6O3
• Molecular Weight: 294.19
• SMILES: CC(CC(C(F)(F)F)(C(F)(F)F)O)OC(=O)C(=C)C
• Topological: 46.5
• Monoisotopic Mass: 294.06906321
• Synonyms: 630414-85-6, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-yl methacrylate, 1,1,1-trifluoro-2-trifluoromethyl-2-hydroxy-4-pentyl Methacrylate, 5,5,5-TRIFLUORO-4-HYDROXY-4-(TRIFLUOROMETHYL)PENTAN-2-YL 2-METHYLPROP-2-ENOATE, SCHEMBL75248, FD2105, MFCD28137626, [5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-yl] 2-methylprop-2-enoate, DA-30483, 1,1,1 -trifluoro-2-trifluoromethyl-2-hydroxy-4-pentyl methacrylate, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-ylmethacrylate

Application

This fluorinated methacrylate monomer is widely used in the synthesis of advanced polymeric materials, particularly for applications requiring enhanced chemical resistance and low surface energy. It is employed in the development of hydrophobic coatings for electronic components, optical devices, and medical implants. Researchers also utilize it to create high-performance adhesives and sealants with superior durability in harsh environments. Its unique structure allows for tailored polymer properties, making it a valuable tool in material science and engineering.

Safety and Hazards

GHS Hazard Statements

• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Skin Irrit. 2 (100%)
• Eye Irrit. 2 (100%)
• STOT SE 3 (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.