Skip to Content
Merck
CN

235466

1-Vinylimidazole

≥99%

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

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

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

OSSNTDFYBPYIEC-UHFFFAOYSA-N

InChI

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

SMILES string

C=Cn1ccnc1

assay

≥99%

form

liquid

Quality Level

100

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.)

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

signalword

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000500263
0000500263
0000500262
0000500262
MKCZ2497

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
Bo Mattiasson et al.
Nature protocols, 2(1), 213-220 (2007-04-03)
Affinity precipitation of proteins uses polymers capable of reversible soluble-insoluble transitions in response to small environmental changes (temperature, pH or solvent composition). Here we describe protocols for (i) the synthesis of responsive polymers with specific affinity to target proteins and
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
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)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service