所有图片(2)

文件

A77903

1-氨基芘

Name: 1-氨基芘
Brand: ALDRICH

97%

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所有图片(2)

别名:

1-氨基吡, 3-氨基芘

经验公式（希尔记法）:

C₁₆H₁₁N

CAS号:

1606-67-3

分子量:

217.27

Beilstein:

1875737

EC 号:

216-521-3

MDL编号:

MFCD00004140

PubChem化学物质编号:

24891279

NACRES:

NA.22

质量水平

100

检测方案

97%

形式

powder

mp

115-117 °C (lit.)

SMILES string

Nc1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C16H11N/c17-14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9H,17H2

InChI key

YZVWKHVRBDQPMQ-UHFFFAOYSA-N

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象形图

GHS07

警示用语：

Warning

危险声明

H302

预防措施声明

P264 - P270 - P301 + P312 - P501

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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示例

T1503

货号

25G

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Bismuth Vanadate/Bilirubin Oxidase Photo(bio)electrochemical Cells for Unbiased, Light-Triggered Electrical Power Generation.

Dina Mukha et al.

ChemSusChem, 13(10), 2684-2692 (2020-02-19)

The construction of bias- and donor-free photobioelectrochemical cells for the generation of light-triggered electrical power is presented. The developed oxygen reduction biocathodes are based on bilirubin oxidase (BOD) that originates from Myrothecium verrucaria (MvBOD) and a thermophilic Bacillus pumilus (BpBOD).

Using organic nanoparticle fluorescence to determine nitrite in water.

Lun Wang et al.

Analytical and bioanalytical chemistry, 382(5), 1300-1303 (2005-05-26)

Organic fluorescence nanoparticles (1-aminopyrene nanoparticles) were prepared under ultrasonic radiation and used to determine nitrite. Such nanoparticles have a broad, continuous excitation spectrum, but they are also photochemically stable and water-soluble. Nitrite determination was based upon nitrite quenching the fluorescence

Solution conformation of the N-(deoxyguanosin-8-yl)-1-aminopyrene ([AP]dG) adduct opposite dC in a DNA duplex.

B Mao et al.

Biochemistry, 35(39), 12659-12670 (1996-10-01)

Combined NMR-molecular mechanics computational studies were undertaken on the C8-deoxyguanosine adduct formed by the carcinogen 1-nitropyrene embedded in the d(C5-[AP]G6-C7).d(G16-C17-G18) sequence context in a 11-mer duplex, with dC opposite the modified deoxyguanosine. The exchangeable and nonexchangeable protons of the aminopyrene

Quantitative analysis of the mutagenic potential of 1-aminopyrene-DNA adduct bypass catalyzed by Y-family DNA polymerases.

Shanen M Sherrer et al.

Mutation research, 737(1-2), 25-33 (2012-08-25)

N-(Deoxyguanosin-8-yl)-1-aminopyrene (dG(AP)) is the predominant nitro polyaromatic hydrocarbon product generated from the air pollutant 1-nitropyrene reacting with DNA. Previous studies have shown that dG(AP) induces genetic mutations in bacterial and mammalian cells. One potential source of these mutations is the

Surface immobilized optical probes: pyrene molecules covalently attached to silica and indium-doped tin oxide.

Maciej Mazur et al.

Bioelectrochemistry (Amsterdam, Netherlands), 66(1-2), 89-94 (2005-04-19)

We report on the covalent attachment of pyrene to quartz and indium-doped tin oxide (ITO) surfaces, and its characterization by steady-state and time-resolved emission spectroscopy. We estimate the chromophore surface coverage on the basis of their electrochemical oxidation mechanism in

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