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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

Quality Level

100

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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Related Categories

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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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
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
Daniel Kmiecik et al.
Journal of fluorescence, 20(5), 973-983 (2010-03-31)
We studied effect of 1-aminoanthracene (1-AMA) binding on the structures of dimeric β lactoglobulin, dimeric odorant binding protein (OBP) and monomeric α(1)-acid glycoprotein (lipocalin family proteins) by monitoring fluorescence excitation spectra and measuring fluorescence lifetimes of the tryptophan residues of
Soundarapandian Kannan et al.
Rapid communications in mass spectrometry : RCM, 25(2), 262-270 (2010-12-31)
Vomeronasal type 2 receptor (V2Rx) from Swiss mouse (Mus musculus (L.)) was analyzed by high-resolution ion-exchange chromatography, reversed-phase high-performance liquid chromatography (RP-HPLC), matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS), Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS), Ion Spray tandem
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