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Merck

132292

2-Vinylpyridine

97%

Synonyme(s) :

α-Vinylpyridine, 2-Ethenylpyridine, 2-Pyridylethylene

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A propos de cet article

Formule empirique (notation de Hill) :
C7H7N
Numéro CAS:
Poids moléculaire :
105.14
NACRES:
NA.23
PubChem Substance ID:
eCl@ss:
39151715
UNSPSC Code:
12162002
EC Number:
202-879-8
MDL number:
Beilstein/REAXYS Number:
104505
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InChI key

KGIGUEBEKRSTEW-UHFFFAOYSA-N

InChI

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

SMILES string

C=Cc1ccccn1

vapor pressure

10 mmHg ( 44.5 °C)

assay

97%

form

liquid

contains

0.1 wt. % p-tert-butylcatechol as inhibitor

Quality Level

refractive index

n20/D 1.549 (lit.)

bp

79-82 °C/29 mmHg (lit.)

density

0.975 g/mL at 25 °C (lit.)

storage temp.

−20°C

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General description

2-Vinylpyridine (2VP) belongs to the class of monomers known as vinyl monomers. It is used as a monomer in the synthesis of various polymers such as poly(2-vinylpyridine) (P2VP), poly(2-vinylpyridine-co-styrene), poly(2-vinylpyridine-co-butadiene) etc. These polymers find applications in membrane and separation technologies, ion exchange resins, electronic devices, sensors, energy storage systems, and drug delivery systems. Additionally, 2VP polymers are used as binders in adhesives and coatings due to their excellent adhesion properties. They can provide strong bonding to various substrates.

2-Vinylpyridine (2VP) is a water soluble pyridine derivative that can be used in the synthesis of poly(2-vinylpyridine) (P2VP) by anionic polymerization. It can be industrially prepared by treatment of 2-methylpyridine with an aqueous solution of formaldehyde in a temperature range of 150-200°C.

Application

2-Vinylpyridine can be used as a monomer:
  • In the preparation of P2VP oligomers to study their properties and behavior on various surfaces, with a focus on area-selective deposition techniques.
  • To synthesize pH-responsive thin film membranes, which can be used for various applications, such as separation, filtration, and catalysis.
  • To synthesize degradable block copolymer-derived nanoporous membranes, which have potential applications in various fields, including energy-related catalysis and nanoparticle synthesis.
  • To improve the effectiveness of protective polymer coatings on metals.
Additionally, 2VP can be used for a variety of applications such as dye sensitized solar cells (DSSCs) and lithium ion cells.
Vinylation of silacyclobutanes with Ni-catalysis leading to geometrically pure (E)-silylolefins.

Disclaimer

Supply conditions do not apply to the regions and states of Brazil: North, Northeast, Mato Grosso do Sul, Mato Grosso, and Rio Grande do Sul.

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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - Skin Sens. 1

supp_hazards

Classe de stockage

3 - Flammable liquids

wgk

WGK 3

flash_point_f

122.0 °F - closed cup

flash_point_c

50 °C - closed cup

ppe

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


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Consulter la Bibliothèque de documents

Charge recombination in dye-sensitized nanocrystalline TiO2 solar cells
Huang SY, et al.
The Journal of Physical Chemistry B, 101(14), 2576-2582 (1997)
Pyridine and pyridine derivatives
Shimizu S, et al.
Ullmann's Encyclopedia of Industrial Chemistry, 36(13), 4679-4681 (2000)
Igor Pujalté et al.
Particle and fibre toxicology, 8, 10-10 (2011-03-05)
Some manufactured nanoparticles are metal-based and have a wide variety of applications in electronic, engineering and medicine. Until now, many studies have described the potential toxicity of NPs on pulmonary target, while little attention has been paid to kidney which
Ramak Esfandi et al.
Foods (Basel, Switzerland), 8(5) (2019-05-15)
The objective of this work was to find out how the method to extract proteins and subsequent enzymatic hydrolysis affect the ability of hepatic cells to resist oxidative stress. Proteins were isolated from oat brans in the presence of Cellulase
Nickel-catalyzed regio- and stereoselective silylation of terminal alkenes with silacyclobutanes: facile access to vinylsilanes from alkenes.
Koji Hirano et al.
Journal of the American Chemical Society, 129(19), 6094-6095 (2007-04-20)

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