69025
1-Methylpyrene
suitable for fluorescence, ≥97.0% (GC)
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经验公式（希尔记法）:
C17H12
化学文摘社编号:
分子量:
216.28
UNSPSC Code:
12352108
NACRES:
NA.32
PubChem Substance ID:
EC Number:
219-178-8
Beilstein/REAXYS Number:
1868500
MDL number:
产品名称
1-Methylpyrene, suitable for fluorescence, ≥97.0% (GC)
InChI key
KBSPJIWZDWBDGM-UHFFFAOYSA-N
InChI
1S/C17H12/c1-11-5-6-14-8-7-12-3-2-4-13-9-10-15(11)17(14)16(12)13/h2-10H,1H3
SMILES string
Cc1ccc2ccc3cccc4ccc1c2c34
assay
≥97.0% (GC)
form
solid
mp
72-74 °C (lit.)
solubility
DMSO: soluble
acetonitrile: soluble
chloroform: soluble
fluorescence
λex 340 nm; λem 486 nm in chloroform
λex 346 nm; λem 378 nm in DMSO
suitability
suitable for fluorescence
Quality Level
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Analysis Note
In addition to the emission maximum at 378 nm, there are lower maxima at 398, 420 and 445 nm
Other Notes
Fluorescent probe for the determination of micellar aggregation number
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Raouf Bahri et al.
Journal of toxicology and environmental health. Part A, 73(8), 552-564 (2010-04-15)
The cytotoxic effects of two polycyclic aromatic hydrocarbons (PAH) (1-methyplyrene and perylene) were investigated on human skin keratinocytes. Normal human keratinocytes were cultured in the presence of various concentrations of 1-methylpyrene and perylene either alone or in combination. Following incubation
Pavol Jusko et al.
Chemical physics letters, 698, 206-210 (2018-06-09)
The fragment of the 1-methylpyrene cation,
J M Kokontis et al.
Carcinogenesis, 14(4), 645-651 (1993-04-01)
Twenty-eight base complementary oligonucleotides were synthesized with deoxyadenosine residues modified at the N6 position with 1-methylpyrene (MP) specifically positioned 3 bp apart in opposite DNA strands. Doubly modified constructs as well as non-modified and singly modified constructs were ligated into
J M Montejo et al.
Biochemistry, 31(33), 7580-7586 (1992-08-25)
The rotational motions of human fibrinogen in solution at 20 degrees C have been examined, in the 0.2-12-microseconds time range, by measuring the laser-induced dichroism of the triplet state of an erythrosin probe covalently bonded to the protein. The decay
Bernhard H Monien et al.
Chemical research in toxicology, 21(10), 2017-2025 (2008-09-16)
The alkylated polycyclic aromatic hydrocarbon 1-methylpyrene is a carcinogen in rodents and has been detected in various environmental matrices and foodstuffs. It is activated metabolically by benzylic hydroxylation to 1-hydroxymethylpyrene followed by sulfoconjugation to yield electrophilic 1-sulfooxymethylpyrene (1-SMP) that is
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