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Merck
CN

48566

Supelco

苊烯

analytical standard

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关于此项目

经验公式(希尔记法):
C12H8
化学文摘社编号:
分子量:
152.19
Beilstein:
774092
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
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等级

analytical standard

质量水平

CofA

current certificate can be downloaded

包装

ampule of 100 mg

技术

HPLC: suitable
gas chromatography (GC): suitable

沸点

280 °C (lit.)

mp

78-82 °C (lit.)

密度

0.899 g/mL at 25 °C (lit.)

应用

environmental

包装形式

neat

储存温度

2-30°C

SMILES字符串

c1cc2C=Cc3cccc(c1)c23

InChI

1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H

InChI key

HXGDTGSAIMULJN-UHFFFAOYSA-N

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应用

Acenaphthylene may be used as an analytical reference standard for the determination of the analyte in water using  gas chromatography-flame ionization detection (GC-FID).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - 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)

251.6 °F - closed cup

闪点(°C)

122.0 °C - closed cup

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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Determination of organic compounds in water using dispersive liquid-liquid microextraction.
Rezaee M, et al.
Journal of Chromatography A, 1116(1-2), 1-9 (2006)
Zhiru Ma et al.
The journal of physical chemistry. A, 111(10), 2020-2027 (2007-03-29)
13C chemical shift tensor data from 2D FIREMAT spectra are reported for 4,7-di-t-butylacenaphthene and 4,7-di-t-butylacenaphthylene. In addition, calculations of the chemical shielding tensors were completed at the B3LYP/6-311G** level of theory. While the experimental tensor data on 4,7-di-t-butylacenaphthylene are in
Onruthai Pinyakong et al.
FEMS microbiology letters, 238(2), 297-305 (2004-09-11)
Sphingomonas sp. strain A4 is capable of utilizing acenaphthene and acenaphthylene as sole carbon and energy sources, but it is unable to grow on other polycyclic aromatic hydrocarbons (PAHs). The genes encoding terminal oxygenase components of ring-hydroxylating dioxygenase (arhA1 and
N D Marsh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(8), 1499-1511 (2000-07-25)
We have examined the UV spectra of six newly-synthesized ethynyl-PAH (1-ethynylnaphthalene, 5-ethynylacenaphthylene, 1-ethynylanthracene, 9-ethynylphenanthrene, 3-ethynylfluoranthene, and 1-ethynylpyrene) and five corresponding CP-PAH (acenaphthylene, aceanthrylene, acephenanthrylene, cyclopenta[cd]fluoranthene, and cyclopenta[cd]pyrene) and have found the following systematic behavior: ethynyl-substitution results in average bathochromic shifts
Xiuhua Zhu et al.
Environmental pollution (Barking, Essex : 1987), 156(2), 461-466 (2008-03-04)
Gaseous emissions of combusted electronic scrap, PVC, carpet and wood were monitored for polycyclic aromatic hydrocarbons (PAHs) by simultaneous use of semipermeable membrane devices (SPMDs) and shoots of spruce needles (Picea abies). It was found that phenanthrene, acenaphthylene and fluorene

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