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A38606

Sigma-Aldrich

1-Aminoanthracene

technical grade, 90%

Synonym(s):

1-Anthramine

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1 G
73,10 €
5 G
222,00 €

73,10 €

Estimated to ship on12 mai 2025

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1 G
73,10 €
5 G
222,00 €

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

73,10 €

Estimated to ship on12 mai 2025

To order products, please contact your local dealer.

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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Show Differences

1 of 4

This Item
A38800211354932116
1-Aminoanthracene technical grade, 90%

A38606

1-Aminoanthracene

2-Aminoanthracene 96%

A38800

2-Aminoanthracene

(R)-(−)-1-(9-Anthryl)-2,2,2-trifluoroethanol ≥98%

211354

(R)-(−)-1-(9-Anthryl)-2,2,2-trifluoroethanol

9-(Naphthalen-1-yl)-10-(naphthalen-2-yl)anthracene ≥99% (HPLC)

932116

9-(Naphthalen-1-yl)-10-(naphthalen-2-yl)anthracene

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

powder

form

powder

form

-

form

-

mp

114-118 °C (lit.)

mp

238-241 °C (lit.)

mp

132-135 °C (lit.)

mp

-

grade

technical grade

grade

-

grade

-

grade

sublimed grade

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
  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    MKBQ7794V
    STBC7822V
    10401BE
    S29421
    12518CZ

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    Patricia Nagnan-Le Meillour et al.
    Biochimica et biophysica acta, 1794(8), 1142-1150 (2009-05-05)
    Structural and molecular dynamics studies have pointed out the role of aromatic residues in the uptake of ligand by porcine odorant-binding protein (pOBP). The shift of Tyr82 from its position during the opening of the binding cavity has been shown
    Florence Vincent et al.
    European journal of biochemistry, 271(19), 3832-3842 (2004-09-18)
    The structure of bovine odorant-binding protein (bOBP) revealed a striking feature of a dimer formed by domain swapping [Tegoni, M., Ramoni, R., Bignetti, E., Spinelli, S. & Cambillau, C. (1996) Nat. Struct. Biol.3, 863-867; Bianchet, M.A., Bains, G., Pelosi, P.
    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
    S Paolini et al.
    Biochimica et biophysica acta, 1431(1), 179-188 (1999-04-21)
    Infrared spectra show that the binding of the odorants 2-isobuthyl-3-methoxypyrazine (PYR) and 3,7-dimethyl-1-octanol (DMO) stabilises the tertiary structure of porcine OBP-I against thermal denaturation. The fluorescence emission spectrum of the single tryptophan shows a lambdamax at 337 nm, indicating that
    Mariella Parisi et al.
    Biochimica et biophysica acta, 1652(2), 115-125 (2003-12-04)
    Unfolding and refolding studies on porcine odorant binding protein (pOBP) have been performed at pH 7 in the presence of guanidinium hydrochloride (GdnHCl). Unfolding, monitored by following changes of protein fluorescence and circular dichroism (CD), was found to be a
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