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Merck
CN

V3204

4-Vinylpyridine

contains 100 ppm hydroquinone as inhibitor, 95%

Synonym(s):

4-Ethenylpyridine Pyridine

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About This Item

Empirical Formula (Hill Notation):
C7H7N
CAS Number:
Molecular Weight:
105.14
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
202-852-0
Beilstein/REAXYS Number:
104506
MDL number:
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Quality Level

assay

95%

contains

100 ppm hydroquinone as inhibitor

refractive index

n20/D 1.549 (lit.)

bp

62-65 °C/15 mmHg (lit.)

density

0.975 g/mL at 25 °C (lit.)

storage temp.

−20°C

SMILES string

C=Cc1ccncc1

InChI

1S/C7H7N/c1-2-7-3-5-8-6-4-7/h2-6H,1H2

InChI key

KFDVPJUYSDEJTH-UHFFFAOYSA-N

General description

4-Vinylpyridine is a highly reactive alkene monomer due to the presence of a vinyl group and a heteroaromatic ring. It is widely used as a monomer to produce a variety of polymers and copolymers, which are used in various applications including, contact lenses, nanoelectronics, sensors, optoelectronic devices, smart coatings, drug delivery systems, sensors, gas separation, air filtration, and purification processes.

Application

4-Vinylpyridine can be used as a monomer:
  • In the synthesis or modification of polymers for drug-releasing contact lenses.
  • In the preparation of the zwitterionic polymer, namely poly(4-vinylpyridine propylsulfobetaine). The zwitterionic polymer is utilized for its superior bioinert capability in withstanding clinical sterilization processes, making it suitable for extended medical applications which include the development of biocompatible implants and as a coating material for medical devices.
  • To synthesize the temperature and pH-sensitive copolymer, specifically (N-vinylcaprolactam-co-4-vinylpyridine), which is used in drug delivery systems under certain environmental conditions.
  • The highly charged p(4-vinylpyridine-co-vinylimidazole) particles, which find applications in various fields such as biomedical, catalysis, and environmental applications.
4-Vinylpyridine also plays a role as a functional monomer in the molecular imprinting of the soft contact lens material. Its inclusion, along with other monomers, enhances the affinity of the hydrogel towards brimonidine, resulting in improved binding properties, loading capacity, and controlled release characteristics.


signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - Skin Sens. 1

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

125.0 °F - closed cup

flash_point_c

51.67 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
非剧毒-急性毒性1

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Articles

ATRP is a successful method for precise polymer synthesis with controlled molecular weights and high chain end functionalities.


Turghun Muhammad et al.
Analytica chimica acta, 709, 98-104 (2011-11-30)
Novel water-compatible molecularly imprinted polymers (MIPs) selective for amiodarone (AD) were designed via a new methodology which relies on screening library of non-imprinted polymers (NIPs). The NIP library consisted of eighteen cross-linked co-polymers synthesized from monomers commonly used in molecular
Polymer, 34, 145-145 (1993)
Tzu-Chun Tseng et al.
Molecules (Basel, Switzerland), 23(9) (2018-09-05)
In this work we prepared poly(styrene⁻b⁻vinylphenol) (PS-b-PVPh) by sequential anionic living polymerization and poly(ethylene oxide-b-4-vinylpyridine) (PEO-b-P4VP) by reversible addition fragmentation chain transfer polymerization (RAFT) by using poly(ethylene oxide) 4-cyano-4-(phenylcarbonothioylthio)pentanoate (PEO-SC(S)Ph) as a macroinitiator with two hydrogen bonded acceptor groups. When



Global Trade Item Number

SKUGTIN
V3204-100ML04061837480812
V3204-500ML04061837480829
V3204-5ML04061837480836