474223

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecyl methacrylate

contains MEHQ as inhibitor, 97%

• Synonyme(s) : HDFDMA
• Formule linéaire : H₂C=C(CH₃)CO₂CH₂CH₂(CF₂)₇CF₃
• Numéro CAS: 1996-88-9
• Poids moléculaire : 532.19
• Numéro CE : 217-877-2
• Numéro MDL: MFCD00042307
• Code UNSPSC : 12162002
• ID de substance PubChem : 24870971
• Nomenclature NACRES : NA.23

Propriétés

• Pureté: 97%
• Contient: MEHQ as inhibitor
• Indice de réfraction: n20/D 1.343 (lit.)
• Point d'ébullition: 110 °C/4 mmHg (lit.)
• Densité: 1.596 g/mL at 25 °C (lit.)
• Température de stockage: 2-8°C
• Chaîne SMILES: CC(=C)C(=O)OCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
• InChI: 1S/C14H9F17O2/c1-5(2)6(32)33-4-3-7(15,16)8(17,18)9(19,20)10(21,22)11(23,24)12(25,26)13(27,28)14(29,30)31/h1,3-4H2,2H3
• Clé InChI: HBZFBSFGXQBQTB-UHFFFAOYSA-N

Description

Description générale

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecylmethacrylate is a fluorinated acrylate monomer with methacrylate functional group. It imparts excellent water repellency to coatings and materials fabricated using this monomer. It can be used as a surface-modifying agent to alter the properties of different substrates. It can be applied to enhance surface lubricity, reduce friction, improve drug release properties, or modify surface energy. Owing to its hydrophobicity, thermal stability, chemical and oil resistance, it is widely used in the field of coatings, adhesives, and surface treatments.

Application

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecyl methacrylate can be used:

• As a monomer to synthesize poly(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecyl methacrylate) (PFDMA). PFDMA can be used to prepare a super amphiphobic sponge that repels both water and oil via the initiated chemical vapor deposition(iCVD).
• As a surface modification agent to alter the surface energy of steel-use-stainless (SUS) membrane to separate microalgal lipids from wet biomass. This helps to simplify the process of microalgae-derived biodiesel production.
• To fabricate biocompatible polymer coatings for transmucosal delivery of oral drugs. The polymer coating induces hydrophobicity that helps to avoid the release of drugs in unwanted directions.
• As a precursor/monomer to prepare triblock copolymers as electrolytes for Li metal batteries. It enhances mechanical strength, lithium-ion transference number, and cycling stability.

Informations sur la sécurité

• Pictogrammes: GHS08,GHS07
• Mention d'avertissement: Danger
• Mentions de danger: H302 + H332,H351,H360D,H362,H372
• Conseils de prudence: P201 - P202 - P263 - P301 + P312 - P304 + P340 + P312 - P308 + P313
• Classification des risques: Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Lact. - Repr. 1B - STOT RE 1
• Organes cibles: Liver
• Code de la classe de stockage: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): 235.4 °F - closed cup
• Point d'éclair (°C): 113 °C - closed cup
• Équipement de protection individuelle: Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter