235474
Acridine Orange base
Dye content 75 %
동의어(들):
3,6-Bis(dimethylamino)acridine, Solvent Orange 15
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제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C17H19N3
CAS 번호:
Molecular Weight:
265.35
Colour Index Number:
46005
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47
MDL number:
form
powder
Quality Level
composition
Dye content, 75%
technique(s)
microbe id | staining: suitable
mp
165 °C (dec.) (lit.)
solubility
1 M HCl: 1 mg/mL, clear
λmax
488 nm
ε (extinction coefficient)
≥14000 at 227-233 nm, ≥20000 at 289-295 nm, ≥35000 at 486-492 nm, ≥40000 at 266-272 nm
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
room temp
SMILES string
CN(C)c1ccc2cc3ccc(cc3nc2c1)N(C)C
InChI
1S/C17H19N3/c1-19(2)14-7-5-12-9-13-6-8-15(20(3)4)11-17(13)18-16(12)10-14/h5-11H,1-4H3
InChI key
DPKHZNPWBDQZCN-UHFFFAOYSA-N
General description
Acridine Orange base (3,6-Bis(dimethylamino)acridine) is a cell-permeable fluorescent dye that binds to nucleic acids. It emits green fluorescence when bound to dsDNA and red fluorescence when bound to ssDNA or RNA. It is also known to be a positive solvatochromic dye.
Application
Acridine orange has also been used as a lysosomal dye. It is widely used to detect the presence of homeopathic potencies.
저장 등급
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Demethylation of Acridine Orange by Arthrobacter globiformis
Itoh K
Bulletin of Environmental Contamination and Toxicology, 60, 781-785 (1998)
Ravichandran Rekha et al.
Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS), 51, 191-203 (2018-11-24)
Herein, we reported a method to synthesize selenium nanowires (Cr-SeNWs) relying to purified cysteine-rich antimicrobial peptide crustin in presence of ascorbic acid. Cr-SeNWs were characterized by UV-vis, XRD, FTIR and Raman spectroscopy, as well as SEM, HR-TEM and EDAX. The
Basudev Maity et al.
European journal of medicinal chemistry, 57, 250-258 (2012-10-16)
Polypyridyl platinum(II) complexes (1-5), viz., [Pt(pyphen)Cl]Cl (1), [Pt(pyphen)(C≡CFc)]Cl (2), [Pt(pydppz)Cl]Cl (3), [Pt(pydppz)(C≡CPh)]Cl (4) and [Pt(pydppz)(C≡CFc)]Cl (5), where pyphen is 6-(2-pyridyl)-1,10-phenanthroline, pydppz is 6-(2-pyridyl)-dipyrido-[3,2-a:2',3'-c]-phenazine, FcC≡CH is ferrocenyl acetylene and PhC≡CH is phenyl acetylene, were synthesized, characterized and their DNA binding and