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A39009

Sigma-Aldrich

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
Colour Index Number:
37275
Beilstein:
396360
EC Number:
201-423-5
MDL number:
MFCD00001213
UNSPSC Code:
12171500
PubChem Substance ID:
24890825
NACRES:
NA.47

product name

1-Aminoanthraquinone, ≥96.5% (HPLC)

Quality Level

100

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

SMILES string

Nc1cccc2C(=O)c3ccccc3C(=O)c12

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

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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 Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000185550
SHBP4587
MKCJ8412
MKCH2122
MKBZ7557V

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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
Solubility of 1-aminoanthraquinone and 1-nitroanthraquinone in supercritical carbon dioxide
Tamura K, et al.
The Journal of Chemical Thermodynamics, 104, 162-168 (2017)
Sarah J Schmidtke et al.
The journal of physical chemistry. A, 109(32), 7033-7045 (2006-07-13)
The dynamics of a series of 1-acylaminoanthraquinones with varying degrees of excited-state intramolecular proton transfer are studied in acetonitrile and dichloromethane. Events are followed via changes in the third-order intermolecular Raman response as a function of time after resonant excitation
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
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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