추천 제품
Quality Level
분석
≥97.0% (GC)
양식
solid
mp
72-74 °C (lit.)
solubility
DMSO: soluble
acetonitrile: soluble
chloroform: soluble
형광
λex 340 nm; λem 486 nm in chloroform
λex 346 nm; λem 378 nm in DMSO
적합성
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
분석 메모
In addition to the emission maximum at 378 nm, there are lower maxima at 398, 420 and 445 nm
기타 정보
Fluorescent probe for the determination of micellar aggregation number
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
Chemical physics letters, 698, 206-210 (2018-06-09)
The fragment of the 1-methylpyrene cation,
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
Chemical Physics Letters, 146, 337-337 (1988)
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
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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