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Merck
CN

CRM40071

苯并[a]芘 CRM 溶液

certified reference material, TraceCERT®, 1000 μg/mL in acetone

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关于此项目

经验公式（希尔记法）:
C20H12
化学文摘社编号:
50-32-8
分子量:
252.31
NACRES:
NA.24
PubChem Substance ID:
329798435
UNSPSC Code:
41116107
MDL number:
MFCD00003602

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产品名称

苯并[a]芘 CRM 溶液, certified reference material, TraceCERT®, 1000 μg/mL in acetone

InChI

1S/C20H12/c1-2-7-17-15(4-1)12-16-9-8-13-5-3-6-14-10-11-18(17)20(16)19(13)14/h1-12H

SMILES string

c1ccc2c(c1)cc3ccc4cccc5ccc2c3c45

InChI key

FMMWHPNWAFZXNH-UHFFFAOYSA-N

grade

certified reference material
TraceCERT®

product line

TraceCERT®

CofA

current certificate can be downloaded

feature

standard type calibration

packaging

ampule of 1 mL

concentration

1000 μg/mL in acetone

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Quality Level

300

application(s)

environmental

format

single component solution

storage temp.

2-8°C

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Application

有关合适仪器技术的更多信息，请参考产品分析证书。如需进一步支持，请联系技术服务。

Other Notes

该认证参考物质 (CRM) 按照 ISO 17034 和 ISO/IEC 17025 生产和认证。所有关于此 CRM 的信息均记载在分析证书中。

General description

This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - Muta. 1B - STOT SE 3

target_organs

Respiratory system

supp_hazards

EUH066

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

1.4 °F - closed cup

flash_point_c

-17.0 °C - closed cup

法规信息

易制毒化学品（3类）
危险化学品
此项目有

分析证书(COA)

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A P Wolterbeek et al.
Cancer letters, 89(1), 107-116 (1995-02-10)
Several experimental models have been developed to study respiratory tract carcinogenesis. The most widely applied in vivo model uses Syrian golden hamsters which receive intratracheal instillations of a suspension of benzo[a]pyrene (B[a]P) particles attached to ferric-oxide (Fe2O3) particles in saline;
Gunnar Boysen et al.
Mutation research, 543(1), 17-30 (2003-01-03)
We review studies which investigate the presence, using structure-specific analytical methods, of DNA or protein adducts of the carcinogen benzo[a]pyrene (BaP) in human tissues. The analytical methods include high performance liquid chromatography with fluorescence detection and gas chromatography-mass spectrometry. Although
Kroum Alexandrov et al.
Toxicology letters, 198(1), 63-68 (2010-04-20)
Benzo(a)pyrene (BP) and cadmium are environmental pollutants found in foodstuffs, cigarette smoke, and polluted air. BP is converted in liver and lung to benzo(a)pyrene-7,8-diol-9,10-epoxide (BPDE) by the enzymes of the cytochrome P450 (CYP) superfamily, namely CYP1A1/1A2, and CYP1B1. BPDE reacts
Luchun Duan et al.
Environment international, 70, 192-202 (2014-06-18)
Oral bioavailability of benzo[a]pyrene (B[a]P) was studied in a swine model using eight spiked soil samples after incubation for 50 and/or 90 days. Silica sand was used as a reference material and the relative bioavailability (RB) of B[a]P in soils
K P Miller et al.
Drug metabolism reviews, 33(1), 1-35 (2001-03-29)
Polycyclic aromatic hydrocarbons are ubiquitous contaminants in the environment. Benzo[a]pyrene (BaP), a prototypical member of this class of chemicals, has been extensively studied for its toxic effects in laboratory animals and human populations. BaP toxicity is often mediated by oxidative
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