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B10102

Sigma-Aldrich

Benzo[e]pyren

98%

Synonym(e):

1,2-Benzpyren, 4,5-Benzpyren

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About This Item

Empirische Formel (Hill-System):
C20H12
CAS-Nummer:
192-97-2
Molekulargewicht:
252.31
Beilstein:
1911334
EG-Nummer:
205-892-7
MDL-Nummer:
MFCD00003605
UNSPSC-Code:
12352103
PubChem Substanz-ID:
24891539
NACRES:
NA.23

Assay

98%

Form

crystals

mp (Schmelzpunkt)

177-180 °C (lit.)

SMILES String

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

InChIKey

TXVHTIQJNYSSKO-UHFFFAOYSA-N

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Allgemeine Beschreibung

This polycyclic aromatic hydrocarbon is soluble in acetone. It is a non-carcinogenic benzopyrene isomer. Studies report its lack of immunosuppressive activity following in vivo and in vitro exposure.In nature, it is metabolized by strains of C. elegans to 3-benzo[e]Pyrene sulphate, 1-hydroxy-3-benzi[e]pyrenyl sulfate and bezo[e]Pyrene 3-O-ß-glucopyranoside.

Anwendung

Used for studies of immune suppressive activity of bezo[e]Pyrene on antibody response to DNP-Ficoll and sheep erythrocytes and "dispersive liquid -liquid micro extraction” technique by extracting organic compounds from water samples.

Piktogramme

Health hazardEnvironment
GHS08,GHS09

Signalwort

Danger

H-Sätze

H350,H410

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Coronen 97%

Sigma-Aldrich

C84801

Coronen

1-Methylpyren suitable for fluorescence, ≥97.0% (GC)

Sigma-Aldrich

69025

1-Methylpyren

Perylen sublimed grade, ≥99.5%

Sigma-Aldrich

394475

Perylen

Coronen BCR®, certified reference material

BCR272

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EPA TCL PAH-Mischung certified reference material, in acetonitrile: methanol (9:1) (varied)

Supelco

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EPA TCL PAH-Mischung

Benzo[a]pyren-d12 98 atom % D

Sigma-Aldrich

451797

Benzo[a]pyren-d12

K L White et al.
Cancer research, 44(8), 3388-3393 (1984-08-01)
The role of metabolic activation of benzo(a)pyrene B(a)P in mediating its suppression of humoral immune responsiveness of the female C57BL/6 X C3H F1 (hereafter called B6C3F1) mouse was addressed in these studies. The model was the in vitro antibody response
Mohammad Rezaee et al.
Journal of chromatography. A, 1116(1-2), 1-9 (2006-04-01)
A new microextraction technique termed dispersive liquid-liquid microextraction (DLLME) was developed. DLLME is a very simple and rapid method for extraction and preconcentration of organic compounds from water samples. In this method, the appropriate mixture of extraction solvent (8.0 microL
D W Rosenberg et al.
Archives of biochemistry and biophysics, 300(1), 186-192 (1993-01-01)
The consequences of altered cytochrome P450-dependent monooxygenase activities in colonic tissue are unknown. As an initial step toward elucidating underlying mechanisms that regulate cytochrome P450 levels in colonic epithelium, we have characterized CYP1A1(3) induction in cultured human colonic cells (Caco-2).
S Faiderbe et al.
Cancer research, 52(10), 2862-2865 (1992-05-15)
High levels of anti-phosphatidylinositol (PtdIns) autoantibodies (autoAb) have been previously described in sera of cancer patients and in plasma of dimethylbenzanthracene-treated female Sprague-Dawley rats. The presence of anti-PtdIns autoAb was tested in a model of highly malignant sarcomas induced by
K Sterling et al.
Toxicology and applied pharmacology, 128(1), 18-24 (1994-09-01)
Hepa 1c1c7 (WT), TAOc1BPrc1 (CI), and BPrc1 (CII) mouse hepatoma cells were exposed to benzo[e]pyrene (B[e]P) or benzo[a]pyrene (B[a]P). B[e]P induced activity of a rat CYP1A1 reporter gene construct (-3015 to +2545 bp) by 1.8- to 2-fold and 5-fold in
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