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Merck

235466

1-Vinylimidazole

≥99%

Synonym(s):

1-Ethenyl-1H-imidazole, 1-Ethenylimidazole, 1-Vinyl-1H-imidazole, N-Vinylimidazole

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About This Item

Empirical Formula (Hill Notation):
C5H6N2
CAS Number:
1072-63-5
Molecular Weight:
94.11
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
24854105
EC Number:
214-012-0
Beilstein/REAXYS Number:
105321
MDL number:
MFCD00005297
Assay:
≥99%
Form:
liquid

Key Documents

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assay

≥99%

form

liquid

refractive index

n20/D 1.533 (lit.)

bp

192-194 °C (lit.), 78-79 °C/13 mmHg (lit.)

density

1.039 g/mL at 25 °C (lit.)

SMILES string

C=Cn1ccnc1

InChI

1S/C5H6N2/c1-2-7-4-3-6-5-7/h2-5H,1H2

InChI key

OSSNTDFYBPYIEC-UHFFFAOYSA-N

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Application

1-Vinylimidazole has been employed:
  • as functional monomer in the synthesis of molecularly imprinted polymers
  • as monomer in the preparation of magnetic-poly(divinylbenzene-1-vinylimidazole) [m-poly(DVB-VIM)] microbeads
  • in the synthesis of novel ion imprinted polyvinylimidazole-silica hybrid copolymer (IIHC)
  • in removal of the vinyl protecting group via isoprene-catalyzed lithiation process

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

183.2 °F - Pensky-Martens closed cup

flash_point_c

84 °C - Pensky-Martens closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
0000500263
0000500263
0000500262
0000500262
MKCZ2497

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Chartchalerm Isarankura-Na-Ayudhya et al.
Molecules (Basel, Switzerland), 13(12), 3077-3091 (2008-12-17)
Molecular imprinting is one of the most efficient methods for preparing synthetic receptors that possess user defined recognition properties. Despite general success of non-covalent imprinting for a large variety of templates, some groups of compounds remain difficult to tackle due
César Ricardo Teixeira Tarley et al.
Analytica chimica acta, 703(2), 145-151 (2011-09-06)
A novel ion imprinted polyvinylimidazole-silica hybrid copolymer (IIHC) was synthesized and used as a selective solid sorbent for Pb(2+) ions preconcentration using an on-line solid phase extraction (SPE) system coupled to TS-FF-AAS. The ionic hybrid sorbent was prepared using 1-vinylimidazole
Li-Na Yi et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 38(13), 2136-2139 (2013-10-02)
Picroside II, separated from Chinese herbal medicine, is an active compound with neroprotective activity. Molecularly imprinted polymers (MIPs) have high affinity toward template molecules synthesized by molecularly imprinted technology for its specific combined sites, which can overcome the shortcomings of
Hong Wang et al.
Nature communications, 8, 13592-13592 (2017-01-05)
Nanoporous graphitic carbon membranes with defined chemical composition and pore architecture are novel nanomaterials that are actively pursued. Compared with easy-to-make porous carbon powders that dominate the porous carbon research and applications in energy generation/conversion and environmental remediation, porous carbon
N Pietruszka et al.
Biotechnology progress, 16(3), 408-415 (2000-06-03)
A new type of polymer, starch-modified by acrylamide, has been developed for application in aqueous two-phase systems (ATPS) for protein separation. Partial hydrolysis and acrylamide modification of starch to different degrees make it suitable for forming ATPS with poly(ethylene glycol)
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