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グレード
certified reference material
認証
BCR®
メーカー／製品名
JRC
テクニック
HPLC: suitable
gas chromatography (GC): suitable
mp
177-180 °C (lit.)
フォーマット
neat
保管温度
2-8°C
SMILES記法
c1ccc2c(c1)c3cccc4ccc5cccc2c5c34
InChI
1S/C20H12/c1-2-8-16-15(7-1)17-9-3-5-13-11-12-14-6-4-10-18(16)20(14)19(13)17/h1-12H
InChI Key
TXVHTIQJNYSSKO-UHFFFAOYSA-N
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アナリシスノート
For more information please see:
BCR050
BCR050
法的情報
BCR is a registered trademark of European Commission
シグナルワード
Danger
危険有害性情報
危険有害性の分類
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B
保管分類コード
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
BCR050-100MG:
最新バージョンのいずれかを選択してください：
Saffar Mansoor et al.
Investigative ophthalmology & visual science, 51(5), 2601-2607 (2009-12-05)
To study the inhibitory effects of some agents or drugs (inhibitors) on benzo(e)pyrene (B(e)P)-induced cell death and apoptosis on human retinal pigment epithelial (ARPE-19) cells in vitro. ARPE-19 cells were pretreated with varying concentrations of different classes of inhibitors (calpain
W H Houser et al.
Molecular carcinogenesis, 5(3), 232-237 (1992-01-01)
In the rat, expression of the CYP1A1 gene is closely associated with arylhydrocarbon hydroxylase (AHH) enzyme activity. AHH is an inducile enzyme activity known to play an important role in the bioactivation of polycyclic aromatic hydrocarbons (PAHs) to mutagenic and
Silvina Fioressi et al.
Environmental science & technology, 39(10), 3646-3655 (2005-06-16)
The photodegradation of benzo[e]pyrene (BeP), a ubiquitous polycyclic aromatic hydrocarbon (PAH) contaminant, was investigated in solution and adsorbed on surfaces modeling the atmospheric particulate matter to provide fundamental information that could help to clarify its fate in the atmosphere. Diones
Gabriela L Borosky et al.
Organic & biomolecular chemistry, 5(14), 2234-2242 (2007-07-05)
A DFT study aimed at understanding structure-reactivity relationships and fluorine substitution effects on carbocation stability in benzo[a]pyrene (BaP), benzo[e]pyrene (BeP), and aza-benzo[a]pyrene (aza-BaP) derivatives are reported. The relative energies of the resulting carbocations are examined and compared, taking into account
Joris J H Haftka et al.
Environmental toxicology and chemistry, 27(7), 1526-1532 (2008-02-12)
The uptake kinetics of fluorene, phenanthrene, fluoranthene, pyrene, and benzo[e]pyrene by solid-phase microextraction fibers was studied in the presence of dissolved organic matter (DOM) obtained from sediment pore water and resulted in increased fiber absorption and desorption rate coefficients. Compared
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