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45235

Sigma-Aldrich

Eosin Y disodium salt

suitable for electrophoresis

Synonym(s):

2′,4′,5′,7′-Tetrabromofluorescein disodium salt, Acid Red 87, Bromo acid J. TS, XL, or XX, Bromofluorescein, Bronze Bromo ES, D&C;Red No. 22, Eosin yellowish

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About This Item

Empirical Formula (Hill Notation):
C20H6Br4Na2O5
CAS Number:
17372-87-1
Molecular Weight:
691.85
Colour Index Number:
45380
Beilstein:
3586809
EC Number:
241-409-6
MDL number:
MFCD00005040
UNSPSC Code:
12171500
PubChem Substance ID:
57650265

technique(s)

electrophoresis: suitable

solubility

H2O: 0.1 g/mL, dark red

fluorescence

λex 520 nm; λem 540 nm in H2O

suitability

in accordance for electrophoresis test

SMILES string

[Na+].[Na+].[O-]C(=O)c1ccccc1C2=C3C=C(Br)C(=O)C(Br)=C3Oc4c(Br)c([O-])c(Br)cc24

InChI

1S/C20H8Br4O5.2Na/c21-11-5-9-13(7-3-1-2-4-8(7)20(27)28)10-6-12(22)17(26)15(24)19(10)29-18(9)14(23)16(11)25;;/h1-6,25H,(H,27,28);;/q;2*+1/p-2

InChI key

SEACYXSIPDVVMV-UHFFFAOYSA-L

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Other Notes

Reversible staining of peptides and proteins after PAGE, followed by recovery of proteins

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H317 - H319

Hazard Classifications

Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

376.9 °F - Pensky-Martens closed cup

Flash Point(C)

191.6 °C - Pensky-Martens closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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M E Selsted et al.
Analytical biochemistry, 155(2), 270-274 (1986-06-01)
A method for the rapid staining of polypeptides in low-pH, urea-containing polyacrylamide gels is described. After 30 s of immersion in an alkaline solution of eosin Y, a variety of proteins stained with intensities similar to those seen with Coomassie
Han Shih et al.
ACS applied materials & interfaces, 5(5), 1673-1680 (2013-02-07)
Interfacial visible light-mediated thiol-ene photoclick reactions were developed for preparing step-growth hydrogels with multilayer structures. The effect of a noncleavage type photoinitiator eosin-Y on visible-light-mediated thiol-ene photopolymerization was first characterized using in situ photorheometry, gel fraction, and equilibrium swelling ratio.
Han Shih et al.
Macromolecular rapid communications, 34(3), 269-273 (2013-02-07)
The utility of visible-light-mediated polymerization in tissue engineering has been limited due to the necessary use of potentially cytotoxic coinitiator and comonomer. Here, we report a visible-light-mediated thiol-ene hydrogelation scheme using eosin-Y as the only photoinitiator. Under visible light exposure
Patricia S Nielsen et al.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 26(3), 404-413 (2012-11-24)
Cellular proliferation is correlated with the progression of melanoma. Accordingly, the proliferation index of H&E-stained thin melanomas was recently included in the staging system of the American Joint Committee on Cancer. Yet, the immunohistochemical markers of proliferation phosphohistone H3 and
Toshihisa Yashiro et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(48), 17212-17217 (2014-11-19)
Males and females are in conflict over genetic transmission in the evolution of parthenogenesis, because it enhances female reproductive output but deprives the males' genetic contribution. For males, any trait that coerces females into sexual reproduction should increase their fitness.
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