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Merck
CN

230561

Sulforhodamine G

Dye content 60 %

Synonym(s):

Acid Red 50

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About This Item

Empirical Formula (Hill Notation):
C25H25N2NaO7S2
CAS Number:
5873-16-5
Molecular Weight:
552.60
PubChem Substance ID:
24853820
UNSPSC Code:
12352103
Colour Index Number:
45220
NACRES:
NA.23
EC Number:
227-528-6
MDL number:
MFCD00213704

Key Documents

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Product Name

Sulforhodamine G, Dye content 60 %

InChI key

NWWFZBYHUXCUDI-DJILMAANSA-M

InChI

1S/C25H26N2O7S2.Na/c1-5-26-20-12-22-18(9-14(20)3)25(19-10-15(4)21(27-6-2)13-23(19)34-22)17-8-7-16(35(28,29)30)11-24(17)36(31,32)33;/h7-13,26H,5-6H2,1-4H3,(H,28,29,30)(H,31,32,33);/q;+1/p-1/b27-21-;

SMILES string

[Na+].CCNc1cc2OC3=CC(=N\CC)\C(C)=CC3=C(c2cc1C)c4ccc(cc4S(O)(=O)=O)S([O-])(=O)=O

form

powder

composition

Dye content, 60%

λmax

529 nm

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Application

Sulforhodamine G can be incorporated in composites as a dye for characterizing fluorescent correlation spectroscopy based images. It can also be used in the development of an acceptor molecule that facilitates the emission of white light in a light emitting hybrid.

General description

Sulforhodamine G is an ambipolar fluorescent dye that is used as an acceptor dye for organic electronics. It is a water soluble and hydrophilic dye that shows an absorption peak at a wavelength of 529 nm.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKBT6246V
MKBB4762V
MKBB4762
09525MN
04731MB

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Classifying the photophysical dynamics of single-and multiple-chromophoric molecules by single molecule spectroscopy.
Yip W, et al.
The Journal of Physical Chemistry A, 102(39), 7564-7575 (1998)
Fluorescent dye and media properties affecting sorption and tracer selection
Kasnavia, T., Vu, D., & Sabatini, D. A.
Groundwater, 37(3), 376-381 (1999)
An anisotropic ink based on crystalline nanocellulose: Potential applications in security printing.
Chindawong C and Johannsmann D
Journal of Applied Polymer Science, 131(22) (2014)
Mariana Beija et al.
Chemical Society reviews, 38(8), 2410-2433 (2009-07-23)
Rhodamine dyes are widely used as fluorescent probes owing to their high absorption coefficient and broad fluorescence in the visible region of electromagnetic spectrum, high fluorescence quantum yield and photostability. A great interest in the development of new synthetic procedures
Supramolecular amphiphiles: spontaneous formation of vesicles triggered by formation of a charge-transfer complex in a host.
Jeon YJ, et al.
Angewandte Chemie (International ed. in English), 41(23), 4474-4476 (2002)
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