69025
1-Methylpyrene
suitable for fluorescence, ≥97.0% (GC)
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About This Item
Empirical Formula (Hill Notation):
C17H12
CAS Number:
Molecular Weight:
216.28
Beilstein:
1868500
EC Number:
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.32
Recommended Products
Quality Level
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
SMILES string
Cc1ccc2ccc3cccc4ccc1c2c34
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
InChI key
KBSPJIWZDWBDGM-UHFFFAOYSA-N
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
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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
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
N. Boens et al.
Chemical Physics Letters, 146, 337-337 (1988)
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
Pavol Jusko et al.
Chemical physics letters, 698, 206-210 (2018-06-09)
The fragment of the 1-methylpyrene cation,
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