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116416

1-Benzylimidazole

Name: 1-Benzylimidazole
Brand: ALDRICH

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

NACRES:

NA.22

PubChem Substance ID:

24847290

eCl@ss:

39161001

UNSPSC Code:

12352005

EC Number:

224-200-4

MDL number:

MFCD00005296

Beilstein/REAXYS Number:

114571

Assay:

99%

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Properties

Quality Level

100

assay

99%

bp

310 °C (lit.)

mp

68-70 °C (lit.)

functional group

phenyl

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

Description

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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Supramolecular assemblies with calix[6]arenes and copper ions: from dinuclear to trinuclear linear arrangements of hydroxo-Cu(II) complexes.

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

Multi-species comparison of the mechanism of biotransformation of MeO-BDEs to OH-BDEs in fish.

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

Removal of 2,4-dichlorophenol using cyclodextrin-ionic liquid polymer as a macroporous material: characterization, adsorption isotherm, kinetic study, thermodynamics.

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

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Global Trade Item Number

SKU	GTIN
116416-5G	04061838704320
116416-25G	04061835521098