A77903
1-Aminopyrene
97%
Synonym(s):
1-Pyrenamine, 3-Aminopyrene
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All Photos(2)
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
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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).
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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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
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
P D Josephy et al.
Mutation research, 429(2), 199-208 (1999-10-20)
The mutagenic actions of many chemicals depend on the activities of bacterial "mutagenesis proteins", which allow replicative bypass of DNA lesions. Genes encoding these proteins occur on bacterial chromosomes and plasmids, often in the form of an operon (such as
Lun Wang et al.
Analytical and bioanalytical chemistry, 382(5), 1300-1303 (2005-05-26)
Organic fluorescence nanoparticles (1-aminopyrene nanoparticles) were prepared under ultrasonic radiation and used to determine nitrite. Such nanoparticles have a broad, continuous excitation spectrum, but they are also photochemically stable and water-soluble. Nitrite determination was based upon nitrite quenching the fluorescence
B Mao et al.
Biochemistry, 35(39), 12659-12670 (1996-10-01)
Combined NMR-molecular mechanics computational studies were undertaken on the C8-deoxyguanosine adduct formed by the carcinogen 1-nitropyrene embedded in the d(C5-[AP]G6-C7).d(G16-C17-G18) sequence context in a 11-mer duplex, with dC opposite the modified deoxyguanosine. The exchangeable and nonexchangeable protons of the aminopyrene
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