69025
1-Methylpyrene
suitable for fluorescence, ≥97.0% (GC)
质量水平
方案
≥97.0% (GC)
表单
solid
mp
72-74 °C (lit.)
溶解性
DMSO: soluble
acetonitrile: soluble
chloroform: soluble
荧光
λex 340 nm; λem 486 nm in chloroform
λex 346 nm; λem 378 nm in DMSO
适用性
suitable for fluorescence
SMILES字符串
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
分析说明
In addition to the emission maximum at 378 nm, there are lower maxima at 398, 420 and 445 nm
其他说明
Fluorescent probe for the determination of micellar aggregation number
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
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
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°
Pavol Jusko et al.
Chemical physics letters, 698, 206-210 (2018-06-09)
The fragment of the 1-methylpyrene cation,
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 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
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