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

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Additional ordering information

Telephone	1-800-990-8053
Fax	1-800-609-2943
Email	sales@aatbio.com
Quotation	Request
International	See distributors
Shipping	Standard overnight for United States, inquire for international

Physical properties

Molecular weight	437.21
Solvent	DMSO

Spectral properties

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

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 SDS Protocol

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 mg	0.5 mg	1 mg	5 mg	10 mg
1 mM	228.723 µL	1.144 mL	2.287 mL	11.436 mL	22.872 mL
5 mM	45.745 µL	228.723 µL	457.446 µL	2.287 mL	4.574 mL
10 mM	22.872 µL	114.362 µL	228.723 µL	1.144 mL	2.287 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

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Spectral properties

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

Images

Figure 1. Chemical structure for Bodi Fluor™ R6G NHS Ester [equivalent to Bodipy® R6G, NHS Ester]

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

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