Dihydrofluorescein diacetate [Fluorescin diacetate] *CAS 35340-49-9*
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Physical properties
Molecular weight | 418.4 |
Solvent | DMSO |
Spectral properties
Absorbance (nm) | 487 |
Correction Factor (260 nm) | 0.32 |
Correction Factor (280 nm) | 0.35 |
Extinction coefficient (cm -1 M -1) | 800001 |
Excitation (nm) | 498 |
Emission (nm) | 517 |
Quantum yield | 0.79001, 0.952 |
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 | 12352200 |
Overview | SDSProtocol |
See also: Fluoresceins, Reactive Oxygen Species (ROS)
CAS 35340-49-9 | Molecular weight 418.4 | Absorbance (nm) 487 | Correction Factor (260 nm) 0.32 | Correction Factor (280 nm) 0.35 | Extinction coefficient (cm -1 M -1) 800001 | Excitation (nm) 498 | Emission (nm) 517 | Quantum yield 0.79001, 0.952 |
Dihydrofluorescein diacetate (also called fluorescin diacetate) is hydrolyzed by cellular esterases to dihydrofluorescein (also called fluorescin) and is then oxidized to fluorescein primarily by H2O2. Dihydrofluorescein diacetate might be reactive toward a broad range of oxidizing reactions that may be increased during intracellular oxidant stress. Cell-loading studies indicate that dihydrofluorescein achieves higher intracellular concentrations than the other redox sensors such as 2',7'-dichlorodihydrofluorescein and Dihydrorhodamine 123.
Calculators
Common stock solution preparation
Table 1. Volume of DMSO needed to reconstitute specific mass of Dihydrofluorescein diacetate [Fluorescin diacetate] *CAS 35340-49-9* 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 | 239.006 µL | 1.195 mL | 2.39 mL | 11.95 mL | 23.901 mL |
5 mM | 47.801 µL | 239.006 µL | 478.011 µL | 2.39 mL | 4.78 mL |
10 mM | 23.901 µL | 119.503 µL | 239.006 µL | 1.195 mL | 2.39 mL |
Molarity calculator
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Spectrum
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Spectral properties
Absorbance (nm) | 487 |
Correction Factor (260 nm) | 0.32 |
Correction Factor (280 nm) | 0.35 |
Extinction coefficient (cm -1 M -1) | 800001 |
Excitation (nm) | 498 |
Emission (nm) | 517 |
Quantum yield | 0.79001, 0.952 |
Images
References
View all 11 references: Citation Explorer
Mitochondrial localization of reactive oxygen species by dihydrofluorescein probes
Authors: Diaz G, Liu S, Isola R, Diana A, Falchi AM.
Journal: Histochem Cell Biol (2003): 319
Authors: Diaz G, Liu S, Isola R, Diana A, Falchi AM.
Journal: Histochem Cell Biol (2003): 319
Kinetic analysis of fluorescein and dihydrofluorescein effluxes in tumour cells expressing the multidrug resistance protein, MRP1
Authors: Saengkhae C, Loetchutinat C, Garnier-Suillerot A.
Journal: Biochem Pharmacol (2003): 969
Authors: Saengkhae C, Loetchutinat C, Garnier-Suillerot A.
Journal: Biochem Pharmacol (2003): 969
Dihydrofluorescein diacetate is superior for detecting intracellular oxidants: comparison with 2',7'-dichlorodihydrofluorescein diacetate, 5(and 6)-carboxy-2',7'-dichlorodihydrofluorescein diacetate, and dihydrorhodamine 123
Authors: Hempel SL, Buettner GR, O'Malley YQ, Wessels DA, Flaherty DM.
Journal: Free Radic Biol Med (1999): 146
Authors: Hempel SL, Buettner GR, O'Malley YQ, Wessels DA, Flaherty DM.
Journal: Free Radic Biol Med (1999): 146
A rapid diagnostic test for the viability of early cattle and rabbit embryos using diacetyl-fluorescin
Authors: Schilling E, Dopke HH.
Journal: Naturwissenschaften (1978): 658
Authors: Schilling E, Dopke HH.
Journal: Naturwissenschaften (1978): 658
Determination of fluorescin sodium in ophthalmic solutions
Authors: Robertson EJ, Patel JA.
Journal: Am J Hosp Pharm (1968): 598
Authors: Robertson EJ, Patel JA.
Journal: Am J Hosp Pharm (1968): 598
Experimental research on insulin antibodies. III. Immunohistology of the endocrine pancreas with guinea pig anti-bovine insulin serum, conjugated with fluorescin isothiocyanate.
Authors: Costanzi G, Mancini UM, Zampa GA.
Journal: Boll Soc Ital Biol Sper (1961): 1233
Authors: Costanzi G, Mancini UM, Zampa GA.
Journal: Boll Soc Ital Biol Sper (1961): 1233
Experimental research on insulin antibodies. II. Immunochemical characterization of guinea pig anti-ox insulin serum conjugated with fluorescin isothiocyanate.
Authors: Mancini AM, Zampa GA, Costanzi G.
Journal: Boll Soc Ital Biol Sper (1961): 1230
Authors: Mancini AM, Zampa GA, Costanzi G.
Journal: Boll Soc Ital Biol Sper (1961): 1230
Two simple media for the demonstration of pyocyanin and fluorescin
Authors: King EO, Ward MK, Raney DE.
Journal: J Lab Clin Med (1954): 301
Authors: King EO, Ward MK, Raney DE.
Journal: J Lab Clin Med (1954): 301
Influence of the concentration of iron on the production of fluorescin by Pseudomonas aeruginosa
Authors: Totter JR, Moseley FT.
Journal: J Bacteriol (1953): 45
Authors: Totter JR, Moseley FT.
Journal: J Bacteriol (1953): 45
Determination of circulation time with fluorescin in normal children and in congenital or acquired cardiopathy.
Authors: Bulgarelli R, Garioni F.
Journal: Minerva Pediatr (1952): 576
Authors: Bulgarelli R, Garioni F.
Journal: Minerva Pediatr (1952): 576
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Fluorescent Oligonucleotide Labeling Reagents