Skip to Content
Merck
All Photos(2)

Documents

A39009

Sigma-Aldrich

1-Aminoanthraquinone

≥96.5% purity, powder, crystals or chunks

Synonym(s):

Azoic Diazo No. 36, Fast Red AL

Sign Into View Organizational & Contract Pricing
All Photos(2)

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

Looking for similar products? Visit Product Comparison Guide

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000185550
SHBP4587
MKCJ8412
MKCH2122
MKBZ7557V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

2-hydroxyanthraquinone AldrichCPR

Sigma-Aldrich

CDS010580

2-hydroxyanthraquinone

Anthraquinone 97%

Sigma-Aldrich

A90004

Anthraquinone

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
Solubility of 1-aminoanthraquinone and 1-nitroanthraquinone in supercritical carbon dioxide
Tamura K, et al.
The Journal of Chemical Thermodynamics, 104, 162-168 (2017)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service