116416
1-Benzylimidazole
99%
Synonym(s):
1-(Phenylmethyl)-1H-imidazole, 1-Benzyl-1H-imidazole, N-Benzylimidazole
Sign Into View Organizational & Contract Pricing
All Photos(3)
About This Item
Empirical Formula (Hill Notation):
C10H10N2
CAS Number:
Molecular Weight:
158.20
Beilstein:
114571
EC Number:
MDL number:
UNSPSC Code:
12352005
eCl@ss:
39161001
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
![2,5-Dihydro-3,6-di-2-thienyl-pyrrolo[3,4-c]pyrrole-1,4-dione 97%](/deepweb/assets/sigmaaldrich/product/structures/209/681/63a4048f-a2a7-496b-814d-ccb4b5b76124/640/63a4048f-a2a7-496b-814d-ccb4b5b76124.png)
Quality Level
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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
José María Navas et al.
Environmental toxicology and chemistry, 22(4), 830-836 (2003-04-11)
Xenobiotics can induce cytochrome P4501A (CYP1A) by ligand binding to the aryl hydrocarbon receptor (AhR). Typical AhR ligands are polycyclic aromatic compounds with planar molecular conformation. The present work investigated the ability of the N-imidazole derivative, 1-benzylimidazole (BIM), to induce
P Rothenbach et al.
Journal of applied physiology (Bethesda, Md. : 1985), 83(2), 530-536 (1997-08-01)
This study examines the hypothesis that intestinal ischemia-reperfusion (I/R) injury contributes to renal dysfunction by altered renal eicosanoid release. Anesthetized Sprague-Dawley rats underwent 60 min of sham or superior mesenteric artery (SMA) occlusion with 60 min of reperfusion. The I/R
Jérémie Doiron et al.
European journal of medicinal chemistry, 46(9), 4010-4024 (2011-06-28)
A series of bis- and mono-benzonitrile or phenyl analogues of letrozole 1, bearing (1,2,3 and 1,2,5)-triazole or imidazole, were synthesized and screened for their anti-aromatase activities. The unsubstituted 1,2,3-triazole 10a derivative displayed inhibitory activity comparable with that of the aromatase
K V Dileep et al.
International journal of biological macromolecules, 170, 415-423 (2020-12-30)
Alzheimer's disease (AD), a common chronic neurodegenerative disease, has become a major public health concern. Despite years of research, therapeutics for AD are limited. Overexpression of secretory glutaminyl cyclase (sQC) in AD brain leads to the formation of a highly
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