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Bodi Fluor™ 488 SE [equivalent to Bodipy® FL, SE] *CAS 146616-66-2*
Ordering information
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Additional ordering information
| Telephone | 1-800-990-8053 |
| Fax | 1-800-609-2943 |
| sales@aatbio.com | |
| International | See distributors |
| Bulk request | Inquire |
| Custom size | Inquire |
| Shipping | Standard overnight for United States, inquire for international |
Physical properties
| Molecular weight | 389.16 |
| Solvent | DMSO |
Spectral properties
| Correction Factor (260 nm) | 0.015 |
| Correction Factor (280 nm) | 0.018 |
| Extinction coefficient (cm -1 M -1) | 81000 |
| Excitation (nm) | 504 |
| Emission (nm) | 510 |
Storage, safety and handling
| H-phrase | H303, H313, H333 |
| Hazard symbol | XN |
| Intended use | Research Use Only (RUO) |
| R-phrase | R20, R21, R22 |
| Storage | Freeze (< -15 °C); Minimize light exposure |
| UNSPSC | 12171501 |
| Overview |  SDSProtocol |
CAS 146616-66-2 | Molecular weight 389.16 | Correction Factor (260 nm) 0.015 | Correction Factor (280 nm) 0.018 | Extinction coefficient (cm -1 M -1) 81000 | Excitation (nm) 504 | Emission (nm) 510 |
Bodi Fluor™ 488, SE is the same molecule to Bodipy® FL, SE (Bodipy® is the trademark of Invitrogen). Bodi Fluor™ 488 has the excitation and emission spectra similar to those of fluorescein. Compared to fluorescein, Bodi Fluor™ 488 is a neutral molecule, and its fluorescence is not pH-dependent. Bodi Fluor™ 488 gives bright green fluorescence with a sharp emission peak. Bodi Fluor™ 488 has been used for developing fluorescent intracellular tracers. Its conjugates are cell-permeable as long as its carriers are cell-permeable.
Calculators
Common stock solution preparation
Table 1. Volume of DMSO needed to reconstitute specific mass of Bodi Fluor™ 488 SE [equivalent to Bodipy® FL, SE] *CAS 146616-66-2* to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.
| 0.1 mg | 0.5 mg | 1 mg | 5 mg | 10 mg | |
| 1 mM | 256.964 µL | 1.285 mL | 2.57 mL | 12.848 mL | 25.696 mL |
| 5 mM | 51.393 µL | 256.964 µL | 513.927 µL | 2.57 mL | 5.139 mL |
| 10 mM | 25.696 µL | 128.482 µL | 256.964 µL | 1.285 mL | 2.57 mL |
Molarity calculator
Enter any two values (mass, volume, concentration) to calculate the third.
| Mass (Calculate) | Molecular weight | Volume (Calculate) | Concentration (Calculate) | Moles | ||||
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Spectrum
Open in Advanced Spectrum Viewer
Spectral properties
| Correction Factor (260 nm) | 0.015 |
| Correction Factor (280 nm) | 0.018 |
| Extinction coefficient (cm -1 M -1) | 81000 |
| Excitation (nm) | 504 |
| Emission (nm) | 510 |
Product Family
| Name | Excitation (nm) | Emission (nm) | Extinction coefficient (cm -1 M -1) | Correction Factor (260 nm) | Correction Factor (280 nm) |
| Bodi Fluor™ 488 acid [equivalent to Bodipy® FL] *CAS 165599-63-3* | 504 | 510 | 81000 | 0.015 | 0.018 |
Images
Figure 1. Chemical structure for Bodi Fluor™ 488 SE [equivalent to Bodipy® FL, SE] *CAS 146616-66-2*
Citations
View all 1 citations: Citation Explorer
A synthetic strategy for conjugation of paromomycin to cell-penetrating Tat (48-60) for delivery and visualization into Leishmania parasites
Authors: Defaus, Sira and Gallo, Maria and Abengózar, María A and Rivas, Luis and Andreu, David
Authors: Defaus, Sira and Gallo, Maria and Abengózar, María A and Rivas, Luis and Andreu, David
References
View all 153 references: Citation Explorer
Fluorescent BODIPY-based Zn(II) complex as a molecular probe for selective detection of neurofibrillary tangles in the brains of Alzheimer's disease patients
Authors: Ojida A, Sakamoto T, Inoue MA, Fujishima SH, Lippens G, Hamachi I.
Journal: J Am Chem Soc (2009): 6543
Authors: Ojida A, Sakamoto T, Inoue MA, Fujishima SH, Lippens G, Hamachi I.
Journal: J Am Chem Soc (2009): 6543
Non-covalent functionalized SWNTs as delivery agents for novel Bodipy-based potential PDT sensitizers
Authors: Erbas S, Gorgulu A, Kocakusakogullari M, Akkaya EU.
Journal: Chem Commun (Camb) (2009): 4956
Authors: Erbas S, Gorgulu A, Kocakusakogullari M, Akkaya EU.
Journal: Chem Commun (Camb) (2009): 4956
Switching the photo-induced energy and electron-transfer processes in BODIPY-phthalocyanine conjugates
Authors: Liu JY, Ermilov EA, Roder B, Ng DK.
Journal: Chem Commun (Camb) (2009): 1517
Authors: Liu JY, Ermilov EA, Roder B, Ng DK.
Journal: Chem Commun (Camb) (2009): 1517
Improved push-pull-push E-Bodipy fluorophores for two-photon cell-imaging
Authors: Didier P, Ulrich G, Mely Y, Ziessel R.
Journal: Org Biomol Chem (2009): 3639
Authors: Didier P, Ulrich G, Mely Y, Ziessel R.
Journal: Org Biomol Chem (2009): 3639
A selective fluoroionophore based on BODIPY-functionalized magnetic silica nanoparticles: removal of Pb2+ from human blood
Authors: Lee HY, Bae DR, Park JC, Song H, Han WS, Jung JH.
Journal: Angew Chem Int Ed Engl (2009): 1239
Authors: Lee HY, Bae DR, Park JC, Song H, Han WS, Jung JH.
Journal: Angew Chem Int Ed Engl (2009): 1239
Synthesis and characterization of a BODIPY-labeled derivative of Soraphen A that binds to acetyl-CoA carboxylase
Authors: Raymer B, Kavana M, Price A, Wang B, Corcoran L, Kulathila R, Groarke J, Mann T.
Journal: Bioorg Med Chem Lett (2009): 2804
Authors: Raymer B, Kavana M, Price A, Wang B, Corcoran L, Kulathila R, Groarke J, Mann T.
Journal: Bioorg Med Chem Lett (2009): 2804
Solid-state emissive BODIPY dyes with bulky substituents as spacers
Authors: Ozdemir T, Atilgan S, Kutuk I, Yildirim LT, Tulek A, Bayindir M, Akkaya EU.
Journal: Org Lett (2009): 2105
Authors: Ozdemir T, Atilgan S, Kutuk I, Yildirim LT, Tulek A, Bayindir M, Akkaya EU.
Journal: Org Lett (2009): 2105
Synthesis of the core compound of the BODIPY dye class: 4,4'-Difluoro-4-bora-(3a,4a)-diaza-s-indacene
Authors: Schmitt A, Hinkeldey B, Wild M, Jung G.
Journal: J Fluoresc (2009): 755
Authors: Schmitt A, Hinkeldey B, Wild M, Jung G.
Journal: J Fluoresc (2009): 755
A versatile, modular synthesis of monofunctionalized BODIPY dyes
Authors: Leen V, Braeken E, Luckermans K, Jackers C, Van der Auweraer M, Boens N, Dehaen W.
Journal: Chem Commun (Camb) (2009): 4515
Authors: Leen V, Braeken E, Luckermans K, Jackers C, Van der Auweraer M, Boens N, Dehaen W.
Journal: Chem Commun (Camb) (2009): 4515
Star-shaped multichromophoric arrays from Bodipy dyes grafted on truxene core
Authors: Diring S, Puntoriero F, Nastasi F, Campagna S, Ziessel R.
Journal: J Am Chem Soc (2009): 6108
Authors: Diring S, Puntoriero F, Nastasi F, Campagna S, Ziessel R.
Journal: J Am Chem Soc (2009): 6108