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BCR140

苯并[c]屈

Name: 苯并[c]屈
Brand: SIAL

BCR^®, certified reference material

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About This Item

经验公式（希尔记法）:

C₂₂H₁₄

CAS号:

194-69-4

分子量:

278.35

Beilstein:

1876196

MDL號碼:

MFCD00667762

分類程式碼代碼:

41116107

PubChem物質ID:

329774229

NACRES:

NA.24

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四氯化碳

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Sigma-Aldrich

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四氯化碳

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等級

certified reference material

agency

BCR^®

製造商／商標名

JRC

技術

HPLC: suitable
gas chromatography (GC): suitable

格式

neat

儲存溫度

2-8°C

SMILES 字串

c1ccc2c(c1)ccc3c2ccc4ccc5ccccc5c34

InChI

1S/C22H14/c1-3-7-18-15(5-1)11-14-21-20(18)13-12-17-10-9-16-6-2-4-8-19(16)22(17)21/h1-14H

InChI 密鑰

YZWGEMSQAMDWEM-UHFFFAOYSA-N

分析報告

For more information please see:
BCR140

法律資訊

BCR is a registered trademark of European Commission

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

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Location of the epoxide function determines specificity of the allelic variants of human glutathione transferase Pi toward benzo[c]chrysene diol epoxide isomers.

A Pal et al.

FEBS letters, 486(2), 163-166 (2000-12-13)

Carcinogenic activity of many polycyclic aromatic hydrocarbons (PAHs) is mainly attributed to their respective diol epoxides, which can be classified as either bay or fjord region depending upon the location of the epoxide function. The Pi class human glutathione (GSH)

Synthesis of fjord region tetraols and their use in hepatic biotransformation studies of dihydrodiols of benzo[c]chrysene, benzo[g]chrysene and dibenzo[a,l]pyrene.

A Luch et al.

Carcinogenesis, 19(4), 639-648 (1998-05-26)

Metabolic activation of the racemic benzo[c]chrysene-trans-9,10-, benzo[g]chrysene-trans-11,12- and dibenzo[a,l]pyrene-trans-11,12-dihydrodiols to fjord region syn- and anti-dihydrodiol epoxides by microsomes of Aroclor 1254-treated Sprague-Dawley rats has been examined. Since the fjord region dihydrodiol epoxides were hydrolytically unstable under the experimental conditions, their

Covalent DNA adducts formed by benzo[c]chrysene in mouse epidermis and by benzo[c]chrysene fjord-region diol epoxides reacted with DNA and polynucleotides.

A S Giles et al.

Chemical research in toxicology, 10(11), 1275-1284 (1997-12-24)

The metabolic activation in mouse skin of benzo[c]chrysene (B[c]C), a weakly carcinogenic polycyclic aromatic hydrocarbon (PAH) present in coal tar and crude oil, was investigated. Male Parkes mice were treated topically with 0.5 mumol of B[c]C, and DNA was isolated

Gas chromatographic retention behavior of polycyclic aromatic hydrocarbons (PAHs) and alkyl-substituted PAHs on two stationary phases of different selectivity.

Federica Nalin et al.

Analytical and bioanalytical chemistry, 410(3), 1123-1137 (2017-11-10)

Retention indices (I) for 45 polycyclic aromatic hydrocarbons (PAHs) and 63 methyl-substituted PAHs were determined by gas chromatography - mass spectrometry (GC-MS) using two different stationary phases: a Rxi-PAH phase (a "higher phenyl-content stationary phase") and a 50% (mole fraction)

Metabolism of benzo[c]chrysene and comparative mammary gland tumorigenesis of benzo[c]chrysene bay and fjord region diol epoxides in female CD rats.

Shantu Amin et al.

Chemical research in toxicology, 16(2), 227-231 (2003-02-18)

Benzo[c]chrysene (BcC), an environmental pollutant, is a unique polycyclic aromatic hydrocarbon that possesses both a bay region and a fjord region in the same molecule. We previously demonstrated that both bay region and fjord region terminal rings are involved in

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苯并[c]屈