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Merck
CN

A39009

1-Aminoanthraquinone

≥96.5% purity, powder, crystals or chunks

Synonym(s):

Azoic Diazo No. 36, Fast Red AL

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About This Item

Empirical Formula (Hill Notation):
C14H9NO2
CAS Number:
82-45-1
Molecular Weight:
223.23
NACRES:
NA.47
PubChem Substance ID:
24890825
UNSPSC Code:
12171500
Colour Index Number:
37275
EC Number:
201-423-5
MDL number:
MFCD00001213
Beilstein/REAXYS Number:
396360

Key Documents

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Product Name

1-Aminoanthraquinone, ≥96.5% (HPLC)

InChI

1S/C14H9NO2/c15-11-7-3-6-10-12(11)14(17)9-5-2-1-4-8(9)13(10)16/h1-7H,15H2

InChI key

KHUFHLFHOQVFGB-UHFFFAOYSA-N

SMILES string

Nc1cccc2C(=O)c3ccccc3C(=O)c12

assay

≥96.5% (HPLC)

form

powder, crystals or chunks

color

dark brown

mp

253-255 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

100

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Biochem/physiol Actions

1-Aminoanthraquinone has the ability to increase the solubility of derivatives of anthraquinone in supercritical carbon dioxide.

Storage Class

11 - Combustible Solids

wgk

WGK 1

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
SHBS7854
0000185550
0000185550
SHBP4587
MKCJ8412

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Solubility of 1-aminoanthraquinone and 1-nitroanthraquinone in supercritical carbon dioxide
Tamura K, et al.
The Journal of Chemical Thermodynamics, 104, 162-168 (2017)
Aneta Hałka-Grysińska et al.
Journal of chromatography. A, 1610, 460516-460516 (2019-09-19)
The new approach to the development of planar chromatogram with controlled developing solvent velocity was implemented for gradient reversed-phase chromatography of a test mixture of dyes. The developing solvent components were directly delivered onto the surface of the C18 type
Song Zhang et al.
Scientific reports, 7, 43419-43419 (2017-02-25)
We investigated the mechanism of intramolecular charge transfer and the following radiationless dynamics of the excited states of 1-aminoanthraquinone using steady state and time-resolved absorption spectroscopy combined with quantum chemical calculations. Following photoexcitation with 460 nm, conformational relaxation via twisting of
Vsevolod Katritch et al.
Journal of medicinal chemistry, 53(4), 1799-1809 (2010-01-26)
The recent progress in crystallography of G-protein coupled receptors opens an unprecedented venue for structure-based GPCR drug discovery. To test efficiency of the structure-based approach, we performed molecular docking and virtual ligand screening (VLS) of more than 4 million commercially
Jin-Shui Liu et al.
Guang pu xue yu guang pu fen xi = Guang pu, 25(1), 76-78 (2005-04-28)
Anthracene, perylene and 1-aminoanthraquinone colloids have been prepared by reprecipitation method. In comparison with the fluorescence emission spectra of colloids and molecules (in acetone solution), it was indicated that collids fluorescence spectra are red-shifted and easy emission. Base on the
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