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A77903

Sigma-Aldrich

1-Aminopyrene

97%

Synonyme(s) :

1-Pyrenamine, 3-Aminopyrene

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About This Item

Formule empirique (notation de Hill):
C16H11N
Numéro CAS:
Poids moléculaire :
217.27
Numéro Beilstein :
1875737
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Pureté

97%

Forme

powder

Pf

115-117 °C (lit.)

Chaîne SMILES 

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

Clé InChI

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).

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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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).
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
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
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.
Man Jae Park et al.
Chemical communications (Cambridge, England), 48(89), 11008-11010 (2012-10-06)
Excess electron transfer dynamics in DNA hairpins was investigated by femtosecond laser flash photolysis of a donor-DNA-acceptor system using N,N-dimethylaminopyrene and diphenylacetylene as an electron donor and acceptor, respectively. It was revealed that the excess electron hopping rate between T's

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