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116416

Sigma-Aldrich

1-Benzylimidazole

99%

Synonym(s):

1-(Phenylmethyl)-1H-imidazole, 1-Benzyl-1H-imidazole, N-Benzylimidazole

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About This Item

Empirical Formula (Hill Notation):
C10H10N2
CAS Number:
4238-71-5
Molecular Weight:
158.20
Beilstein:
114571
EC Number:
224-200-4
MDL number:
MFCD00005296
UNSPSC Code:
12352005
eCl@ss:
39161001
PubChem Substance ID:
24847290
NACRES:
NA.22

Assay

99%

bp

310 °C (lit.)

mp

68-70 °C (lit.)

SMILES string

C(c1ccccc1)n2ccnc2

InChI

1S/C10H10N2/c1-2-4-10(5-3-1)8-12-7-6-11-9-12/h1-7,9H,8H2

InChI key

KKKDZZRICRFGSD-UHFFFAOYSA-N

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General description

1-Benzylimidazole has been used to prepare cyclodextrin-ionic liquid polymer (βCD-BIMOTs-TDI).

Biochem/physiol Actions

1-Benzylimidazole is a CYP inhibitor that inhibits the biotransformation of MeO-BDEs (methoxylated-brominated diphenyl ethers) to OH-BDEs (hydroxylated) in fishes.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Guillaume Izzet et al.
Inorganic chemistry, 45(3), 1069-1077 (2006-01-31)
Complexation of copper(II) by calix[6]arene-based ligands bearing either two or three N-benzylimidazole coordinating arms under basic conditions has been studied. Whereas the tris(imidazole) derivative stabilizes dicationic 5-coordinate aqua complexes in a mononuclear state with an intracavity bound guest, in the
Muggundha Raoov et al.
Journal of hazardous materials, 263 Pt 2, 501-516 (2013-11-16)
Cyclodextrin-ionic liquid polymer (βCD-BIMOTs-TDI) was firstly synthesized using functionalized β-Cyclodextrin (CD) with 1-benzylimidazole (BIM) to form monofunctionalized CD (βCD-BIMOTs) and was further polymerized using toluene diisocyanate (TDI) linker to form insoluble βCD-BIMOTs-TDI. SEM characterization result shows that βCD-BIMOTs-TDI exhibits macropore
J Wang et al.
Toxicological sciences : an official journal of the Society of Toxicology, 64(2), 200-207 (2001-11-24)
Fluctuations in several environmental variables, such as salinity, can influence the interactions between organisms and pollutants in aquatic organisms, and, therefore, affect the toxicity of xenobiotics. In this study, after 2 species of fish, rainbow trout (Oncorhynchus mykiss) and hybrid
Fengyan Liu et al.
Aquatic toxicology (Amsterdam, Netherlands), 114-115, 182-188 (2012-03-27)
Polybrominated diphenyl ethers (PBDEs) and their methoxylated- (MeO-) and hydroxylated- (OH-) analogs are ubiquitously distributed in the environment worldwide. The OH-BDEs have greater potency than PBDEs and can be produced from the transformation of MeO-BDEs. The objectives of the current
A Grothusen et al.
Archives of toxicology, 71(1-2), 64-71 (1996-01-01)
Liver microsomes are a frequently used probe to investigate the phase I metabolism of xenobiotics in vitro. Structures containing nucleophilic hetero-atoms are possible substrates for cytochrome P450 enzymes (P450) and flavin-containing monooxygenases (FMO). Both enzymes are located in the endoplasmatic
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