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Merck

199508

Sigma-Aldrich

Acridine Yellow G

Dye content 90 %

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About This Item

Fórmula empírica (notación de Hill):
C15H15N3 · HCl
Número de CAS:
Peso molecular:
273.76
Colour Index Number:
46025
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

form

crystalline powder

Quality Level

composition

Dye content, 90%

solubility

water: 1 mg/mL, clear, yellow to orange

λmax

442 nm

ε (extinction coefficient)

44000 at 262-268 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

Cl[H].Cc1cc2cc3cc(C)c(N)cc3nc2cc1N

InChI

1S/C15H15N3.ClH/c1-8-3-10-5-11-4-9(2)13(17)7-15(11)18-14(10)6-12(8)16;/h3-7H,16-17H2,1-2H3;1H

Biochem/physiol Actions

Acridine Yellow G (AYG) is an organic dye with photophysical properties. It is widely used in optics, medicine and photovoltaic cells.[1] AYG has been used as a solar photocatalyst to increase biodegradability and remove ferulic acid, a target pollutant from wastewater.[1] It retards the growth of glioblastoma via dual inhibition of epidermal growth factor receptor and protein kinase c kinases.[2]

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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N Houba-Herin et al.
Stain technology, 58(3), 161-170 (1983-05-01)
Commercial samples of acridine yellow, all labeled C.I. 46025, have been analyzed by thin layer chromatography, UV and visible light spectroscopy, mass spectrometry, and photodynamic efficiency in the inactivation of bacteriophage phi X174. Three types of sample were clearly delineated:
J P Martin et al.
Photochemistry and photobiology, 46(1), 45-53 (1987-07-01)
Acridine dyes, fluorescein and lucifer yellow CH are fluorescent photosensitizers used experimentally to selectively stain and photodynamically destroy eukaryotic cells and subcellular structures. We have determined that the mechanism of light- and oxygen-dependent inactivation of E. coli by these dyes
Shao Pu Liu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 64(4), 817-822 (2006-02-07)
In near neutral to weak basic media, sodium carboxymethyl cellulose (NaCMC) will dissociate to become a macro polymeric anion, which can react with acridine yellow (AY) or acridine orange (AO) to form an ion-association complex resulting in fluorescence quenching of
J M Coddington et al.
Chemico-biological interactions, 50(1), 97-110 (1984-06-01)
Variable temperature 1H-nuclear magnetic resonance (NMR) has been used to study the interaction of the RNA trimer, GpCpA, with the intercalators ethidium bromide and the acridine derivatives; proflavin, 9-amino-acridine, acridine orange, acridine yellow and acriflavin. The complexes formed were studied
Rapid preparation of covalently closed circular DNA by acridine yellow affinity chromatography.
W S Vincent et al.
Analytical biochemistry, 110(1), 123-127 (1981-01-01)

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