199508
吖啶黄 G
Dye content 90 %
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经验公式（希尔记法）:
C15H15N3 · HCl
化学文摘社编号:
分子量:
273.76
PubChem Substance ID:
UNSPSC Code:
12171500
Colour Index Number:
46025
NACRES:
NA.47
EC Number:
205-194-2
MDL number:
InChI key
BGLGAKMTYHWWKW-UHFFFAOYSA-N
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
SMILES string
Cl[H].Cc1cc2cc3cc(C)c(N)cc3nc2cc1N
form
crystalline powder
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
Quality Level
Biochem/physiol Actions
吖啶黄 G（AYG）是一种具有光物理性质的有机染料。它广泛用于光学、医学和光伏电池。AYG 已被用作太阳能光催化剂，可提高生物降解能力并去除废水中的目标污染物阿魏酸。它通过表皮生长因子受体和蛋白激酶 c 激酶的双重抑制来抑制胶质母细胞瘤的生长。
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
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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:
Acridine yellow as solar photocatalyst for enhancing biodegradability and eliminating ferulic acid as model pollutant
Amat AM
Applied Catalysis. B, Environmental, 73, 220-226 (2007)
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
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 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
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