V3204
4-Vinylpyridine
contains 100 ppm hydroquinone as inhibitor, 95%
Synonym(s):
4-Ethenylpyridine Pyridine
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
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:
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.
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
Rimma S Kalina et al.
Toxins, 12(1) (2020-01-16)
Toxins modulating NaV channels are the most abundant and studied peptide components of sea anemone venom. Three type-II toxins, δ-SHTX-Hcr1f (= RpII), RTX-III, and RTX-VI, were isolated from the sea anemone Heteractis crispa. RTX-VI has been found to be an
M Ploug et al.
Electrophoresis, 13(3), 148-153 (1992-03-01)
For identification of cysteine residues on microsequence analysis it is crucial to derivatize the sulfhydryl groups. This reaction requires a desalting step which often represents a major obstacle, especially if the sample consists of limited amounts of a hydrophobic membrane
Lachlan J Schwarz et al.
Journal of chromatography. A, 1218(16), 2189-2195 (2011-03-18)
(E)-Resveratrol imprinted polymers have been rationally designed with the aid of molecular modelling and NMR spectroscopic titration techniques to determine the optimal ratio of the template to functional monomer for polymer formation. Based on this approach, (E)-resveratrol imprinted polymers were