추천 제품
Quality Level
분석
75%
양식
solid
불순물
20% acenaphthene
bp
280 °C (lit.)
mp
78-82 °C (lit.)
density
0.899 g/mL at 25 °C (lit.)
SMILES string
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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신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - 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)
251.6 °F - closed cup
Flash Point (°C)
122.0 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
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
Ling Zi Sang et al.
Talanta, 78(4-5), 1339-1344 (2009-04-14)
A fluorimetric method for simultaneous determination of dissolved acenaphthylene (Ace) phenanthrene (Ph) and pyrene (Py), mixed in an aqueous mineral salts medium (MSM), was developed. The linear ranges for determination of Ace, Ph and Py dissolved in the mixture were
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
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
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
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