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%

Manufacturer: Sigma Aldrich

CAS Number: 1996-88-9

Synonym(S): HDFDMA

Select a Size

Pack Size SKU Availability Price
25 ML 474223-25-ML In Stock ₹ 19,019.53

474223 - 25 ML

₹ 19,019.53

In Stock

Quantity

1

Base Price: ₹ 19,019.53

GST (18%): ₹ 3,423.515

Total Price: ₹ 22,443.045

Quality Level

100

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

Other Options

Image Product Name Manufacturer Price Range
50-147-0522
Matrix Scientific 1H,1H,2H,2H-Heptadecafluorodecyl methacrylate, 1996-88-9, MFCD00042307, 25g
Matrix Scientific ₹ 5,646.96
AB47357
1996-88-9 | 2-(Perfluorooctyl)ethyl methacrylate
A2B Chem ₹ 770.04 - ₹ 7,785.96

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Description

  • 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.[1] [2]
  • 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).[1]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.[2]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.[3]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.[4]

SAFETY INFORMATION

Pictograms

GHS08,GHS07

Signal Word

Danger

Hazard Statements

H302 + H332,H351,H360D,H362,H372

Precautionary Statements

P201 - P202 - P263 - P301 + P312 - P304 + P340 + P312 - P308 + P313

Hazard Classifications

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

Target Organs

Liver

WGK

WGK 3

Flash Point(F)

235.4 °F

Flash Point(C)

113 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Quality Level:
100

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

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