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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
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Quality Level

100

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

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
Ashok Kumar et al.
Biotechnology and bioengineering, 84(4), 494-503 (2003-10-24)
Metal chelate affinity precipitation (MCAP) has been successfully developed as a simple purification process for proteins that have affinity for metal ions. The present lack of widespread applications for this technique as compared to immobilized metal affinity chromatography (IMAC) may
Bilgen Osman et al.
Applied biochemistry and biotechnology, 168(2), 279-294 (2012-06-28)
Designing an immobilised metal ion affinity process on large-scale demands that a thorough understanding be developed regarding the adsorption behaviour of proteins on metal-loaded gels and the characteristic adsorption parameters to be evaluated. In view of this requirement, interaction of
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