Bioactivity | 10-(4-(Bis(2-hydroxyethyl)amino)phenyl)-5,5-difluoro-1,3,7,9-tetramethyl-5H-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium-5-uide, a BODIPY derivative, is a fluorescent indicator for detecting Pb2+ (Ex=504 nM, Em=510 nM)[1][2]. |
Target | Pb2+ |
Invitro | Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs)[2].1. Prepare the stock solutions (1 mM) of the perchlorate salts of various metal ions separately.2. stock solution of host (0.1 mM) in acetonitrile. 3. Prepare the test solutions by placing 4-40 μL of the probe stock solution into a test tube.4. Add an appropriate aliquot of each metal stock, and dilute the solution to 4 mL with acetonitrile.5. Excited at 504 nm. |
Name | 10-(4-(Bis(2-hydroxyethyl)amino)phenyl)-5,5-difluoro-1,3,7,9-tetramethyl-5H-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium-5-uide |
CAS | 886212-86-8 |
Formula | C23H28BF2N3O2 |
Molar Mass | 427.30 |
Transport | Room temperature in continental US; may vary elsewhere. |
Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Reference | [1]. Hye Young Lee, et al. A selective fluoroionophore based on BODIPY-functionalized magnetic silica nanoparticles: removal of Pb2+ from human blood. Angew Chem Int Ed Engl. 2009;48(7):1239-43. [2]. Xin Qi, et al. New BODIPY Derivatives as OFF−ON Fluorescent Chemosensor and Fluorescent Chemodosimeter for Cu2+: Cooperative Selectivity Enhancement toward Cu2+. J Org Chem. 2006 Mar 31;71(7):2881-4. |