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474223

Sigma-Aldrich

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

contains MEHQ as inhibitor, 97%

Synonym(s):

HDFDMA

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About This Item

Linear Formula:
H2C=C(CH3)CO2CH2CH2(CF2)7CF3
CAS Number:
Molecular Weight:
532.19
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

Quality Level

Assay

97%

contains

MEHQ as inhibitor

refractive index

n20/D 1.343 (lit.)

bp

110 °C/4 mmHg (lit.)

density

1.596 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

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

InChI key

HBZFBSFGXQBQTB-UHFFFAOYSA-N

General description

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.

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Lact. - Repr. 1B - STOT RE 1

Target Organs

Liver

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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