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Merck
CN

69025

Sigma-Aldrich

1-Methylpyrene

suitable for fluorescence, ≥97.0% (GC)

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关于此项目

经验公式(希尔记法):
C17H12
化学文摘社编号:
分子量:
216.28
Beilstein:
1868500
EC 号:
MDL编号:
UNSPSC代码:
12352108
PubChem化学物质编号:
NACRES:
NA.32
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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

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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

象形图

Exclamation mark

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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
J Horn et al.
Biochemical and biophysical research communications, 228(1), 105-109 (1996-11-01)
1-Hydroxymethylpyrene and 1-sulfooxymethylpyrene were tested for complete carcinogenic activity by repeated s.c. injection in groups of 12 female Sprague-Dawley rats, respectively. A dose of 0.2 mumol of either 1-sulfooxymethylpyrene or 1-hydroxymethylpyrene was administered every other weekday for 20 doses (i.e.

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