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Resorufin, sodium salt *CAS 34994-50-8*

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Physical properties
Molecular weight235.17
SolventWater
Spectral properties
Absorbance (nm)570
Extinction coefficient (cm -1 M -1)650001
Excitation (nm)571
Emission (nm)584
Quantum yield0.751
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

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CAS
34994-50-8
Molecular weight
235.17
Absorbance (nm)
570
Extinction coefficient (cm -1 M -1)
650001
Excitation (nm)
571
Emission (nm)
584
Quantum yield
0.751
Resorufin is used as a calibration standard for resorufin-derived enzyme substrates. It has pH dependent absorption and emission over the range of 5 to 9. It is also the reduction product of resazurin in cells.

Calculators


Common stock solution preparation

Table 1. Volume of Water needed to reconstitute specific mass of Resorufin, sodium salt *CAS 34994-50-8* 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 mM425.224 µL2.126 mL4.252 mL21.261 mL42.522 mL
5 mM85.045 µL425.224 µL850.449 µL4.252 mL8.504 mL
10 mM42.522 µL212.612 µL425.224 µL2.126 mL4.252 mL

Molarity calculator

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Spectrum


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Spectral properties

Absorbance (nm)570
Extinction coefficient (cm -1 M -1)650001
Excitation (nm)571
Emission (nm)584
Quantum yield0.751

Product Family


NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Correction Factor (280 nm)
EDANS sodium salt [5-((2-Aminoethyl)aminonaphthalene-1-sulfonic acid, sodium salt] *CAS 100900-07-0*33645559000.107
Resazurin, sodium salt *CAS 62758-13-8*571584--

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References


View all 31 references: Citation Explorer
Methoxy-resorufin ether as an electrochemically active biological probe for cytochrome P450 O-demethylation
Authors: Jenkins AT, Dash HA, Boundy S, Halliwell CM, ffrench-Constant RH.
Journal: Bioelectrochemistry (2006): 67
Induction of ethoxy-resorufin-O-deethylase activity by halogenated aromatic hydrocarbons and polycyclic aromatic hydrocarbons in primary hepatocytes of the green frog (Rana esculenta)
Authors: Rankouhi TR, Koomen B, S and erson JT, Bosveld AT, Seinen W, van den Berg M.
Journal: Environ Toxicol Chem (2005): 1428
Validation and diagnostic efficacy of a lipase assay using the substrate 1,2-o-dilauryl-rac-glycero glutaric acid-(6' methyl resorufin)-ester for the diagnosis of acute pancreatitis in dogs
Authors: Graca R, Messick J, McCullough S, Barger A, Hoffmann W.
Journal: Vet Clin Pathol (2005): 39
Quantitative structure-activity relationships within a homologous series of 7-alkoxyresorufins exhibiting activity towards CYP1A and CYP2B enzymes: molecular modelling studies on key members of the resorufin series with CYP2C5-derived models of human CYP1A
Authors: Lewis DF, Lake BG, Dickins M.
Journal: Xenobiotica (2004): 501
A resorufin-based fluorescent assay for quantifying NADH
Authors: Batchelor RH, Zhou M.
Journal: Anal Biochem (2002): 118
Functional visualization of the excretory system of adult Schistosoma mansoni by the fluorescent marker resorufin
Authors: Sato H, Kusel JR, Thornhill J.
Journal: Parasitology (2002): 527
The excited-state interaction of resazurin and resorufin with amines in aqueous solutions. Photophysics and photochemical reactions
Authors: Bueno C, Villegas ML, Bertolotti SG, Previtali CM, Neumann MG, Encinas MV.
Journal: Photochem Photobiol (2002): 385
Hydrogen peroxide-induced deacetylation of acetyl resorufin as a novel indicator reaction for fluorometric detection of glucose using only glucose oxidase
Authors: Maeda H, Matsu-ura S, Nishida M, Senba T, Yamauchi Y, Ohmori H.
Journal: Chem Pharm Bull (Tokyo) (2001): 294
Resorufin as an electron acceptor in glucose oxidase-catalyzed oxidation of glucose
Authors: Maeda H, Matsu-ura S, Senba T, Yamasaki S, Takai H, Yamauchi Y, Ohmori H.
Journal: Chem Pharm Bull (Tokyo) (2000): 897
Directed evolution of an esterase from Pseudomonas fluorescens. Random mutagenesis by error-prone PCR or a mutator strain and identification of mutants showing enhanced enantioselectivity by a resorufin-based fluorescence assay
Authors: Henke E, Bornscheuer UT.
Journal: Biol Chem (1999): 1029