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A77903

Sigma-Aldrich

1-Aminopyrene

97%

Synonym(s):

1-Pyrenamine, 3-Aminopyrene

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About This Item

Empirical Formula (Hill Notation):
C16H11N
CAS Number:
Molecular Weight:
217.27
Beilstein:
1875737
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

powder

mp

115-117 °C (lit.)

SMILES string

Nc1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C16H11N/c17-14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9H,17H2

InChI key

YZVWKHVRBDQPMQ-UHFFFAOYSA-N

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Application

  • Synthesis and evaluation of aromatic stationary phases based on linear solvation energy relationship model for expanded application in supercritical fluid chromatography.: Explores the use of 1-Aminopyrene in the development of advanced stationary phases for chromatography, enhancing the efficiency and application range in pharmaceutical and environmental analysis (Ge et al., 2024).
  • Two-Dimensional Porphyrinic Metal-Organic Framework Composites as a Photocatalytic Platform for Chemoselective Hydrogenation.: Highlights the integration of 1-Aminopyrene into metal-organic frameworks, providing a new avenue for creating highly efficient photocatalytic systems for organic synthesis, relevant to both academic research and industrial chemical manufacturing (Dong et al., 2023).
  • Exploiting and Engineering Neuroglobin for Catalyzing Carbene N-H Insertions and the Formation of Quinoxalinones.: Discusses the role of 1-Aminopyrene in enhancing enzymatic reactions within engineered proteins, paving the way for novel synthetic pathways in pharmaceutical research (Sun et al., 2023).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

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

Certificates of Analysis (COA)

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Dina Mukha et al.
ChemSusChem, 13(10), 2684-2692 (2020-02-19)
The construction of bias- and donor-free photobioelectrochemical cells for the generation of light-triggered electrical power is presented. The developed oxygen reduction biocathodes are based on bilirubin oxidase (BOD) that originates from Myrothecium verrucaria (MvBOD) and a thermophilic Bacillus pumilus (BpBOD).
R Shapiro et al.
Chemical research in toxicology, 11(4), 335-341 (1998-05-05)
While the one-ring amine aniline (AN) has only slight genetic activity, the polycyclic aromatic amines 2-aminofluorene (AF) and 1-aminopyrene (AP) are significant mutagens and carcinogens. Moreover, the bulkier AP is more mutagenic per adduct than AF in the tetracycline-resistance gene
O Wongwattanasathien et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48(4), 1045-1051 (2010-01-27)
The mutagenicity of dichloromethane, methanol and water extracts of Antigonon leptopus Hook. & Arn., Curcuma sessilis Gage, Hibiscus rosa-sinensis Linn., Ixora coccinea Linn., Millingtonia hortensis Linn., Nelumbo nucifera Gaertn., Plumeria obtusa Linn., Punica granatum Linn., Rhinacanthus nasutus ((Linn.) Kurz.) and
A Ferancová et al.
Bioelectrochemistry (Amsterdam, Netherlands), 67(2), 191-197 (2005-08-27)
The aim of this work was voltammetric determination of 1-aminopyrene and 1-hydroxypyrene using carbon paste electrodes modified with cyclodextrin derivatives and double stranded deoxyribonucleic acid (dsDNA). The detection schemes based on a preconcentration and differential pulse voltammetric (DPV) determination at
Tianzhu Zhou et al.
Nature communications, 11(1), 2077-2077 (2020-05-01)
Flexible reduced graphene oxide (rGO) sheets are being considered for applications in portable electrical devices and flexible energy storage systems. However, the poor mechanical properties and electrical conductivities of rGO sheets are limiting factors for the development of such devices.

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