V900634
1-Acetylimidazole
Vetec™, reagent grade, 98%
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About This Item
Empirical Formula (Hill Notation):
C5H6N2O
CAS Number:
Molecular Weight:
110.11
Beilstein:
108425
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
grade
reagent grade
product line
Vetec™
Assay
98%
mp
99-105 °C (lit.)
storage temp.
2-8°C
SMILES string
CC(=O)n1ccnc1
InChI
1S/C5H6N2O/c1-5(8)7-3-2-6-4-7/h2-4H,1H3
InChI key
VIHYIVKEECZGOU-UHFFFAOYSA-N
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Feng Zhang et al.
Biochemistry, 44(2), 719-725 (2005-01-12)
To study its contribution to the assembly of the green plant manganese stabilizing protein (MSP) into photosystem II (PSII), tyrosine residues were specifically acetylated using N-acetylimidazole (NAI). In soluble MSP, three groups of Tyr residues could be differentiated by NAI
Y F Keng et al.
Archives of biochemistry and biophysics, 335(1), 73-81 (1996-11-01)
Aspartokinase III (AK III) has been purified from a plasmid-containing strain of Escherichia coli. The enzyme shows broad specificity for the phosphoryl acceptor substrate. Structural analogs of aspartic acid with a derivatized alpha-carboxyl group are accepted as alternative substrates by
B G Vertessy et al.
Biochimica et biophysica acta, 1205(1), 146-150 (1994-03-16)
dUTP nucleotidohydrolase (dUTPase, EC 3.6.1.23) from E. coli contains a total of six tyrosine residues per trimer. About half of them were found to be susceptible to acetylation with N-acetylimidazole or to nitration with tetranitromethane with concomitant loss of activity.
Yuan Liu et al.
Biochemical and biophysical research communications, 325(2), 600-604 (2004-11-09)
Carotenoids in the peripheral light-harvesting complexes (LH2) of the green mutant (GM309) of Rhodobacter sphaeroides were identified as containing neurosporenes, which lack the polar CH(3)O group, compared to spheroidenes in native-LH2 of R. sphaeroides 601. After LH2 complexes were treated
G D Cymes et al.
International journal of peptide and protein research, 42(1), 33-38 (1993-07-01)
Reaction of ovine prolactin (oPRL) with a 150-fold molar excess of N-acetylimidazole over protein content resulted in the modification of 2.5 tyrosine residues and 1.2 lysine residues. Acetylation greatly decreased the in vitro binding capacity to lactogenic sites. This binding
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