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A39009

Sigma-Aldrich

1-Aminoanthrachinon

≥96.5% purity, powder, crystals or chunks

Synonym(e):

Azoic Diazo No. 36, Fast Red AL

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About This Item

Empirische Formel (Hill-System):
C14H9NO2
CAS-Nummer:
82-45-1
Molekulargewicht:
223.23
Farbindexnummer:
37275
Beilstein:
396360
EG-Nummer:
201-423-5
MDL-Nummer:
MFCD00001213
UNSPSC-Code:
12171500
PubChem Substanz-ID:
24890825
NACRES:
NA.47

product name

1-Aminoanthrachinon, ≥96.5% (HPLC)

Qualitätsniveau

100

Assay

≥96.5% (HPLC)

Form

powder, crystals or chunks

Farbe

dark brown

mp (Schmelzpunkt)

253-255 °C (lit.)

Anwendung(en)

diagnostic assay manufacturing
hematology
histology

Lagertemp.

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

InChIKey

KHUFHLFHOQVFGB-UHFFFAOYSA-N

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Verwandte Kategorien

Biochem./physiol. Wirkung

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
0000185550
SHBP4587
MKCJ8412
MKCH2122
MKBZ7557V

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Sigma-Aldrich

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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
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
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