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Bodi Fluor™ R6G NHS Ester [equivalent to Bodipy® R6G, NHS Ester]

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Physical properties
Molecular weight437.21
SolventDMSO
Spectral properties
Extinction coefficient (cm -1 M -1)116000
Excitation (nm)528
Emission (nm)547
Storage, safety and handling
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
UNSPSC12171501

OverviewpdfSDSpdfProtocol


Molecular weight
437.21
Extinction coefficient (cm -1 M -1)
116000
Excitation (nm)
528
Emission (nm)
547
Bodi Fluor™R6G, NHS ester is the same molecule to Bodipy® R6G, NHS ester (Bodipy® is the trademark of Invitrogen). Bodi Fluor™R6G has the excitation and emission spectra similar to rhodamine 6G. Compared to rhodamine 6G, Bodi Fluor™R6G is a neutral molecule, and its fluorescence is not pH-dependent. Bodi Fluor™R6G gives bright green fluorescence with a sharp emission peak. Bodi Fluor™R6G 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™ R6G NHS Ester [equivalent to Bodipy® R6G, NHS Ester] to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM228.723 µL1.144 mL2.287 mL11.436 mL22.872 mL
5 mM45.745 µL228.723 µL457.446 µL2.287 mL4.574 mL
10 mM22.872 µL114.362 µL228.723 µL1.144 mL2.287 mL

Molarity calculator

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Spectrum


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spectrum

Spectral properties

Extinction coefficient (cm -1 M -1)116000
Excitation (nm)528
Emission (nm)547

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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 Abeng&oacute;zar, Mar&iacute;a 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
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
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
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
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
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
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
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
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
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