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Merck
모든 사진(1)

문서

416703

Sigma-Aldrich

Acenaphthylene

99%

동의어(들):

Cyclopenta[de]naphthalene

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About This Item

실험식(Hill 표기법):
C12H8
CAS Number:
208-96-8
Molecular Weight:
152.19
Beilstein:
774092
EC Number:
205-917-1
MDL number:
MFCD00003806
UNSPSC 코드:
12352100
PubChem Substance ID:
24865923
NACRES:
NA.22

분석

99%

형태

solid

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

Acenaphthylene has been used to investigate the photodimerization of acenaphthylene in micellar and hydrogel media.

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H302,H315,H319,H335

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

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

Durairajan Madhavan et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2(2), 95-97 (2003-04-01)
The photochemical dimerisation of acenaphthylene in the presence of various cation-exchanged bentonite clays has been studied. While the cis-dimer is the predominant product when smaller cations are present in the clay interlayer, the presence of heavier atoms in the clay
An electron spin resonance study of the carbonization of the aromatic hydrocarbon acenaphthylene.
Singer LS and Lewis IC.
Carbon, 2(2), 115-120 (1964)
Kinetics and products of the gas-phase reactions of acenaphthene with hydroxyl radicals, nitrate radicals and ozone.
Zhou S and Wenger JC.
Atmospheric Environment, 72, 97-104 (2013)
M J Schocken et al.
Applied and environmental microbiology, 48(1), 10-16 (1984-07-01)
A Beijerinckia sp. and a mutant strain, Beijerinckia sp. strain B8/36, were shown to cooxidize the polycyclic aromatic hydrocarbons acenaphthene and acenaphthylene. Both organisms oxidized acenaphthene to the same spectrum of metabolites, which included 1-acenaphthenol, 1-acenaphthenone, 1,2-acenaphthenediol, acenaphthenequinone, and a
Philipp Eyring et al.
Journal of separation science, 44(2), 600-608 (2020-11-14)
Food can contain unwanted compounds and need to be analyzed for compounds like carcinogenic polycyclic aromatic hydrocarbons to ensure consumer safety. The analytes need to be extracted from the sample matrix and cleaned-up to enable detection. However, established methods for
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