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69025

Sigma-Aldrich

1-Methylpyrene

suitable for fluorescence, ≥97.0% (GC)

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About This Item

Fórmula empírica (Notação de Hill):
C17H12
Número CAS:
2381-21-7
Peso molecular:
216.28
Beilstein:
1868500
Número CE:
219-178-8
Número MDL:
MFCD00014329
Código UNSPSC:
12352108
ID de substância PubChem:
57652170
NACRES:
NA.32

Ensaio

≥97.0% (GC)

forma

solid

pf

72-74 °C (lit.)

solubilidade

DMSO: soluble
acetonitrile: soluble
chloroform: soluble

fluorescência

λex 340 nm; λem 486 nm in chloroform
λex 346 nm; λem 378 nm in DMSO

adequação

suitable for fluorescence

cadeia de caracteres SMILES

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

chave InChI

KBSPJIWZDWBDGM-UHFFFAOYSA-N

Nota de análise

In addition to the emission maximum at 378 nm, there are lower maxima at 398, 420 and 445 nm

Outras notas

Fluorescent probe for the determination of micellar aggregation number

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Pavol Jusko et al.
Chemical physics letters, 698, 206-210 (2018-06-09)
The fragment of the 1-methylpyrene cation,
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
N. Boens et al.
Chemical Physics Letters, 146, 337-337 (1988)
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
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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