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Merck

422177

Sigma-Aldrich

Ethyl vinyl ether

contains 0.1% KOH as stabilizer, 99%

Szinonimák:

Ethoxyethylene

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

Lineáris képlet:
C2H5OCH=CH2
CAS-szám:
Molekulatömeg:
72.11
Beilstein:
605351
EC-szám:
MDL-szám:
UNSPSC kód:
12162002
eCl@ss:
39021025
PubChem Substance ID:
NACRES:
NA.23

Minőségi szint

Teszt

99%

Forma

liquid

tartalmaz

0.1% KOH as stabilizer
0.1% potassium hydroxide as stabilizer

törésmutató

n20/D 1.376 (lit.)

bp

33 °C (lit.)

mp

−116 °C (lit.)

sűrűség

0.753 g/mL at 25 °C (lit.)

tárolási hőmérséklet

2-8°C

SMILES string

CCOC=C

InChI

1S/C4H8O/c1-3-5-4-2/h3H,1,4H2,2H3

Nemzetközi kémiai azonosító kulcs

FJKIXWOMBXYWOQ-UHFFFAOYSA-N

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Általános leírás

Ethyl vinyl ether, also known as ethoxy ethane is highly reactive due to the presence of the vinyl group and the ether functionality. It can polymerize via different methods like radical polymerization, cationic polymerization, oroxidative polymerization, yielding poly(ethyl vinyl ether) or PVE. It is widely used as a monomer to synthesize copolymers and block polymers with thermal stability and flexibility for various applications such as the synthesis of silicone hydrogel for contact lenses, tissue engineering, 3D bioprinting, drug delivery, and Li-ion batteries.

Alkalmazás

Ethyl vinyl ether can be used as:


  • A monomer to synthesize amphiphilic block copolymers to fabricate protein-repelling polymersomes to produce spherical nanoparticles. These nanoparticles can be used as drug carriers.
  • A precursor to synthesize polymer electrolytes and cathode materials for solid-state lithium-ion batteries via UV photopolymerizations.
  • A monomer to synthesize poly(vinyl ether)s with controlled molecular weight and narrow dispersity via photoinduced free radical-promoted cationic reversible addition–fragmentation chain transfer (RAFT) polymerization. These polymers are used to fabricate 3D objects with different thicknesses by employing stereolithography-based 3D printing.

  • H-bonded Reusable Template Assisted para-Selective Ketonisation: This study discusses the use of ethyl vinyl ether in catalytic processes involving palladium and hexafluoroisopropanol to achieve para-selectivity in ketonisation, relevant for synthesizing complex organic compounds used in pharmaceuticals and materials science (A Maji, A Dahiya, G Lu, T Bhattacharya, 2018).

  • Mechanistic Insight into Photocontrolled Cationic Polymerization: Explores the photocontrolled polymerization of ethyl vinyl ether, providing valuable knowledge for the development of light-responsive materials, which could have applications in drug delivery and smart material systems (Q Michaudel, T Chauviré, V Kottisch, 2017).

Piktogramok

FlameExclamation mark

Figyelmeztetés

Danger

Figyelmeztető mondatok

Óvintézkedésre vonatkozó mondatok

Veszélyességi osztályok

Aquatic Chronic 3 - Flam. Liq. 2 - STOT SE 3

Célzott szervek

Central nervous system

Tárolási osztály kódja

3 - Flammable liquids

WGK

WGK 1

Lobbanási pont (F)

-49.0 °F

Lobbanási pont (C)

-45 °C

Egyéni védőeszköz

Eyeshields, Faceshields, Gloves


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Analitikai tanúsítványok (COA)

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Az ügyfelek ezeket is megtekintették

Polyglycidol-stabilized nanoparticles as a promising alternative to nanoparticle PEGylation: polymer synthesis and protein fouling considerations
Haiqin Du, et al.
Langmuir, 36, 1266-1278 (2020)
A PROXYL-Type Norbornene Polymer for High-Voltage Cathodes in Lithium Batteries
Hatakeyama-Sato, et al.
Macromolecular Rapid Communications, 42, 2100374-2100374 (2021)
Guotao Li et al.
Journal of the American Chemical Society, 130(22), 6944-6945 (2008-05-10)
An efficient Au(I)-catalyzed synthesis of highly strained and functionalized bicyclo[3.2.0]heptanes is developed. Subsequent couplings with various nucleophiles offer additional structural features/complexity. These one-pot, three-component reactions are proposed to proceed via a key 1,3-dipolar cycloaddition between a Au carbenoid-containing carbonyl ylide
Natalia Chernyak et al.
Journal of the American Chemical Society, 134(30), 12466-12469 (2012-07-21)
Anilines and ethyl vinyl ether can be used as precursors for a process that is the synthetic equivalent of the α-arylation of acetaldehyde enolate. The reaction manifests a high level of functional group compatibility, allowing the ready preparation of a
Eden Tesfu et al.
Journal of the American Chemical Society, 128(1), 70-71 (2006-01-05)
A Pd(II) reagent has been generated at preselected sites on an electrochemically addressable chip and used to effect the oxidation of the neighboring alcohols on the polymer coating the chip's surface. The resulting carbonyls were then used to accomplish site-selective

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