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A39009

1-Aminoanthrachinon

Name: 1-Aminoanthrachinon
Brand: SIAL

≥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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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)

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Analysenzertifikate (COA)

Lot/Batch Number

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Ultrafast investigation of photoinduced charge transfer in aminoanthraquinone pharmaceutical product.

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

Reversed-phase stepwise gradient thin-layer chromatography of test dye mixtures with controlled developing solvent velocity.

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)

Dissolved natural organic matter (NOM) impacts photosynthetic oxygen production and electron transport in coontail Ceratophyllum demersum.

S Pflugmacher et al.

The Science of the total environment, 357(1-3), 169-175 (2005-05-12)

Dissolved natural organic matter (NOM) is dead organic matter exceeding, in freshwater systems, the concentration of organic carbon in all living organisms by far. 80-90% (w/w) of the NOM is made up of humic substances (HS). Although NOM possesses several

Solvent Front Position Extraction procedure with thin-layer chromatography as a mode of multicomponent sample preparation for quantitative analysis by instrumental technique.

A Klimek-Turek et al.

Journal of chromatography. A, 1530, 204-210 (2017-11-25)

A concept of using thin-layer chromatography to multicomponent sample preparation for quantitative determination of solutes followed by instrumental technique is presented. Thin-layer chromatography (TLC) is used to separate chosen substances and their internal standard from other components (matrix) and to

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