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69025

Sigma-Aldrich

1-Methylpyrene

suitable for fluorescence, ≥97.0% (GC)

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100 MG
$251.00

$251.00


Estimated to ship onApril 14, 2025


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100 MG
$251.00

About This Item

Empirical Formula (Hill Notation):
C17H12
CAS Number:
Molecular Weight:
216.28
Beilstein/REAXYS Number:
1868500
EC Number:
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.32

$251.00


Estimated to ship onApril 14, 2025


Request a Bulk Order

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[1]

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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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
N. Boens et al.
Chemical Physics Letters, 146, 337-337 (1988)
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
Matthew J Bird et al.
The journal of physical chemistry. A, 124(26), 5487-5495 (2020-05-22)
A novel method to determine redox potentials without electrolyte is presented. The method is based on a new ability to determine the dissociation constant, K°

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