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A38606

Sigma-Aldrich

1-Aminoanthracene

technical grade, 90%

Synonym(s):

1-Anthramine

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About This Item

Empirical Formula (Hill Notation):
C14H11N
CAS Number:
610-49-1
Molecular Weight:
193.24
Beilstein:
2209406
EC Number:
210-225-8
MDL number:
MFCD00003579
UNSPSC Code:
12352100
PubChem Substance ID:
24890819
NACRES:
NA.22

grade

technical grade

Assay

90%

form

powder

mp

114-118 °C (lit.)

SMILES string

Nc1cccc2cc3ccccc3cc12

InChI

1S/C14H11N/c15-14-7-3-6-12-8-10-4-1-2-5-11(10)9-13(12)14/h1-9H,15H2

InChI key

YUENFNPLGJCNRB-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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
0000373846
0000373846
0000323012
0000235766
0000285939

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B Siddlingeshwar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(3), 490-495 (2008-12-06)
The ground state (micro(g)) and the excited state (micro(e)) dipole moments of three substituted anthraquinones, namely 1-aminoanthracene-9,10-dione (AAQ), 1-(methylamino)anthracence-9,10-dione (MAQ) and 1,5-diaminoanthracene-9,10-dione (DAQ) were estimated in various solvents. The dipole moments (micro(g) and micro(e)) were estimated from Lippert, Bakhshiev, Kawski-Chamma-Viallet
Jixun Zhan et al.
Bioorganic & medicinal chemistry, 16(9), 5085-5089 (2008-04-02)
The carcinogen and mutagen, 1-aminoanthracene, was efficiently metabolized by the fungal strain Beauveria bassiana ATCC 7159 to yield three new metabolites identified as 1-acetamido-5-[(4'-O-methyl-beta-d-glucopyranosyl)oxy]anthracene, 1-acetamido-8-[(4'-O-methyl-beta-d-glucopyranosyl)oxy]anthraquinone, and 1-acetamido-6-[(4'-O-methyl-beta-d-glucopyranosyl)oxy]anthraquinone, together with 1-acetamidoanthracene and 1-acetamidoanthraquinone. Formation of these metabolites suggests that the metabolic
Christopher A Butts et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(16), 6501-6506 (2009-04-07)
We identified a fluorophore, 1-aminoanthracene (1-AMA), that is anesthetic, potentiates GABAergic transmission, and gives an appropriate dissociation constant, K(d) approximately 0.1 mM, for binding to the general anesthetic site in horse spleen apoferritin (HSAF). 1-AMA fluorescence is enhanced when bound
A Longo et al.
Journal of chromatography. B, Biomedical applications, 686(2), 129-139 (1996-11-15)
A new sensitive high-performance liquid chromatographic procedure for the determination of L-carnitine (LC), acetyl-L-carnitine (ALC) and propionyl-L-carnitine (PLC) in human plasma has been developed. Precolumn derivatization with 1-aminoanthracene (1AA), performed in phosphate buffer in the presence of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC)
T Kato et al.
Mutation research, 249(1), 243-254 (1991-07-01)
Arylamines including aniline (I), 1-naphthylamine (II), 2-naphthylamine (III), 2-aminofluorene (IV), 1-aminoanthracene (V) and 1-aminopyrene (VI) were treated with 4 equivalent amounts of nitrite at pH3 and 37 degrees C for 4 h. The reaction mixtures of I, IV, V and
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