추천 제품
Grade
certified reference material
Agency
BCR®
제조업체/상표
JRC
기술
HPLC: suitable
gas chromatography (GC): suitable
응용 분야
environmental
pharmaceutical (small molecule)
형식
neat
저장 온도
room temp
SMILES string
c1ccc2c(c1)ccc3c2ccc4c5ccccc5ccc34
InChI
1S/C22H14/c1-3-7-17-15(5-1)9-11-21-19(17)13-14-20-18-8-4-2-6-16(18)10-12-22(20)21/h1-14H
InChI key
GBROPGWFBFCKAG-UHFFFAOYSA-N
분석 메모
For more information please see:
BCR168
BCR168
법적 정보
BCR is a registered trademark of European Commission
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Carc. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Alberto Girlando et al.
Physical chemistry chemical physics : PCCP, 14(5), 1694-1699 (2011-12-24)
The paper reports a complete analysis of the phonon structure of crystalline picene, a recently announced organic semiconductor. Both lattice and intramolecular vibrations are investigated. An exhaustive assignment of lattice phonons is obtained through polarized Raman spectra assisted by lattice
K L Platt et al.
Chemico-biological interactions, 66(3-4), 157-175 (1988-01-01)
Picene, a polycyclic aromatic hydrocarbon (PAH) of environmental relevance has recently been predicted to be carcinogenic, based on quantum mechanical calculation, although in several animal studies no carcinogenicity could be detected. In order to find out if the metabolism of
K L Platt et al.
Carcinogenesis, 11(10), 1721-1726 (1990-10-01)
The carcinogenic activity of the two polycyclic aromatic hydrocarbons (PAHs), picene (benzo[a]chrysene) and dibenz[a,h]anthracene (DBA), was determined in NMRI mice by five different experimental protocols in order to find out if picene is a carcinogen as predicted by recent quantum
Andrew P Rutter et al.
Environmental science & technology, 43(20), 7770-7777 (2009-11-20)
Carbonaceous atmospheric particulate matter (PM25) collected in the midwestern United States revealed that soot emissions from incomplete coal combustion were important sources of several organic molecular markers used in source apportionment studies. Despite not constituting a major source of organic
F J Zhang et al.
The Journal of organic chemistry, 65(13), 3952-3960 (2000-06-24)
A new synthetic approach to polycyclic aromatic compounds is described that entails in the key steps double Suzuki coupling of PAH bisboronic acid derivatives with o-bromoaryl aldehydes to furnish aryl dialdehydes that are converted to larger polycyclic aromatic ring systems
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