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Dihydrorhodamine 123

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Dihydrorhodamine 123 manufacturers

Dihydrorhodamine 123 Basic information
Product Name:Dihydrorhodamine 123
Synonyms:2-(3,6-DIAMINO-9H-XANTHEN-9-YL)-BENZOIC ACID, METHYL ESTER;Dihydrohodamine 123;DIHYDRORHODAMINE 123, FOR FLUOR-ESCENCE;Dihydrorhodamine123(DHR123);Benzoic acid, 2-(3,6-diamino-9H-xanthen-9-yl)-, methyl ester;Methyl 2-(3,6-diamino-9H-xanthen-9-yl)benzoate;D 23806;D 632
CAS:109244-58-8
MF:C21H18N2O3
MW:346.38
EINECS:
Product Categories:Xanthene;AlphabeticalStains and Dyes;DFluorescent Probes, Labels, Particles and Stains;Fluorescent Enzyme Substrates;Fluorescent Enzyme Substrates for Flow Cytometry;Fluorescent Probes, Labels, Particles and Stains;Stains&Dyes, A to
Mol File:109244-58-8.mol
Dihydrorhodamine 123 Structure
Dihydrorhodamine 123 Chemical Properties
Melting point 163–165℃
Boiling point 526.9±50.0 °C(Predicted)
density 1.313±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility DMSO: >5mg/mL
form powder
pka4.70 ± 0.40, most basic, temperature: 25 °C
color Light red or pinkish-white
λmax289 nm
BRN 5989965
Biological ApplicationsGenerating,detecting & measuring reactive oxygen species; generating,detecting & measuring reactive nitrogen species; detecting phosphates,peroxynitrile; measuring respiratory burst; chronic granulomatous disease DHR assay; screening
Major Applicationdiagnostic assay manufacturing
hematology
histology
InChIInChI=1S/C21H18N2O3/c1-25-21(24)15-5-3-2-4-14(15)20-16-8-6-12(22)10-18(16)26-19-11-13(23)7-9-17(19)20/h2-11,20H,22-23H2,1H3
InChIKeyFNEZBBILNYNQGC-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=CC=C1C1C2=C(C=C(N)C=C2)OC2=C1C=CC(N)=C2
Safety Information
Safety Statements 22-24/25
WGK Germany 3
10-23
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
Dihydrorhodamine 123 Usage And Synthesis
DescriptionDHR is a cell-permeable fluorogenic probe that is used as an indicator of intracellular peroxynitrite formation. It is oxidized by peroxynitrite to the highly fluorescent product rhodamine in vitro. Neither nitric oxide, superoxide, nor hydrogen peroxide alone appear to oxidize DHR. Formation of rhodamine can be monitored by fluorescence spectroscopy using excitation and emission wavelengths of 500 and 536 nm, respectively, or by absorbance spectroscopy at 500 nm (ε = 78,800 M−1cm−1). DHR has been used to investigate reactive oxygen intermediates produced by endothelial cells, eosinophils, and reactive microglia.
UsesDihydrorhodamine 123 is the uncharged and nonfluorescent reduction product of the mitochondrion-selective dye rhodamine 123 used for investigation of reacitve oxygen intermediates.
UsesDihydrorhodamine 123 (DHR) has been used for the detection of free intracellular radicals or ROS (reactive oxygen species) in head kidney-derived macrophages. It has also been used in DHR assay in red blood cells and in oxidative burst assay in neutrophils.
General DescriptionCell-permeable fluorogenic probe that is useful for the detection of reactive oxygen species (ROS) such as peroxide and peroxynitrite. Dihydrorhodamine is not fluorescent unless it is converted to rhodamine 123.
Biochem/physiol ActionsCell permeable: yes
References[1] CROW J P. Dichlorodihydrofluorescein and Dihydrorhodamine 123 Are Sensitive Indicators of Peroxynitritein Vitro:Implications for Intracellular Measurement of Reactive Nitrogen and Oxygen Species[J]. Nitric oxide: biology and chemistry, 1997, 1 2: Pages 145-157. DOI: 10.1006/niox.1996.0113
[2] K BRIVIBA. Attenuation of oxidation and nitration reactions of peroxynitrite by selenomethionine, selenocystine and ebselen.[J]. Biochemical Journal, 1996, 319 ( Pt 1): 13-15. DOI: 10.1042/bj3190013
[3] H SIES. Glutathione peroxidase protects against peroxynitrite-mediated oxidations. A new function for selenoproteins as peroxynitrite reductase.[J]. The Journal of Biological Chemistry, 1997, 272 44: 27812-27817. DOI: 10.1074/jbc.272.44.27812
[4] OSAMU HANDA  Gediminas C  Jancy Stephen. Role of endothelial nitric oxide synthase-derived nitric oxide in activation and dysfunction of cerebrovascular endothelial cells during early onsets of sepsis.[J]. American journal of physiology. Heart and circulatory physiology, 2008, 295 4: H1712-9. DOI: 10.1152/ajpheart.00476.2008
[5] PAIGE LACY. Divergence of mechanisms regulating respiratory burst in blood and sputum eosinophils and neutrophils from atopic subjects.[J]. Journal of immunology, 2003, 170 5: 2670-2679. DOI: 10.4049/jimmunol.170.5.2670
[6] JIANRONG LI. Peroxynitrite generated by inducible nitric oxide synthase and NADPH oxidase mediates microglial toxicity to oligodendrocytes.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2005, 102 28: 9936-9941. DOI: 10.1073/pnas.0502552102
Dihydrorhodamine 123 Preparation Products And Raw materials
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