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Safety Information

A39009

Sigma-Aldrich

1-Aminoanthraquinone

≥96.5%

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

Quality Level

100

Assay

≥96.5%

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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Related Categories

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Class II Designated Chemical Substances

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

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Certificates of Analysis (COA)

Lot/Batch Number
MKCJ8412
MKCH2122
MKBZ7557V
MKBS8947V
MKBN6432V

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Anthraquinone 97%

Sigma-Aldrich

A90004

Anthraquinone

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
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)
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
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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