357774

1-Phenylimidazole

97%

• Empirical Formula (Hill Notation): C₉H₈N₂
• CAS Number: 7164-98-9
• Molecular Weight: 144.17
• MDL number: MFCD00041204
• UNSPSC Code: 12352005
• PubChem Substance ID: 24861941
• NACRES: NA.22

Properties

• Quality Level: 100
• assay: 97%
• form: liquid
• bp: 142 °C/15 mmHg (lit.)
• mp: 13 °C (lit.)
• density: 1.14 g/mL at 25 °C (lit.)
• SMILES string: c1ccc(cc1)-n2ccnc2
• InChI: 1S/C9H8N2/c1-2-4-9(5-3-1)11-7-6-10-8-11/h1-8H
• InChI key: SEULWJSKCVACTH-UHFFFAOYSA-N

Description

General description

1-Phenylimidazole is an imidazole derivative. It induces 7-ethoxyresorufin-O-deethylase (EROD) activity in rainbow trout (Oncorhynchus mykiss) hepatocytes. The S(1)→S(0) transition of 1-phenylimidazole has been investigated in a supersonic jet expansion by resonant two-photon ionization. 1-Phenylimidazole is reported to be inhibitor of calmodulin-dependent nitric-oxide synthase from bovine brain and GHs pituitary cells.

Application

1-Phenylimidazole is a suitable reagent used to investigate its effect on the citrulline formation by bovine brain nitric-oxide synthase.

Safety Information

• pictograms: GHS07
• signalword: Warning
• hcodes: H302 + H312 + H332,H315,H319,H335
• pcodes: P261 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338
• Hazard Classifications: Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 3
• flash_point_f: 235.4 °F - closed cup
• flash_point_c: 113 °C - closed cup
• ppe: Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter