质量水平
检测方案
99%
bp
310 °C (lit.)
mp
68-70 °C (lit.)
SMILES字符串
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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一般描述
1-苄基咪唑已被用于制备环糊精-离子液体聚合物(βCD-BIMOTs-TDI)。
生化/生理作用
1-苄咪唑是一种 CYP 抑制剂,可抑制鱼类中 MeO-BDEs(甲氧基-溴代二苯醚)生物转化为 OH-BDEs(羟基化)。
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
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
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
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
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
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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