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Merck
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Key Documents

502332

Supelco

Benzo[j]fluoranthene solution

certified reference material, 2000 μg/mL in dichloromethane

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About This Item

실험식(Hill 표기법):
C20H12
CAS Number:
Molecular Weight:
252.31
UNSPSC 코드:
12000000

Grade

certified reference material

제품 라인

TraceCERT®

grade

TraceCERT®

CofA

current certificate can be downloaded

포장

ampule of 1 mL

농도

2000 μg/mL in dichloromethane

기술

HPLC: suitable
gas chromatography (GC): suitable

응용 분야

cleaning products
cosmetics
environmental
food and beverages
personal care

형식

single component solution

저장 온도

2-30°C

InChI

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

InChI key

KHNYNFUTFKJLDD-UHFFFAOYSA-N

일반 설명

Benzo[j]fluoranthene is a polycyclic aromatic hydrocarbon, which is carcinogenic in nature and can be generated into the environment via combustion of coal, coal tar and petroleum products.

애플리케이션

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

기타 정보

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

법적 정보

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

픽토그램

Health hazardExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Aquatic Chronic 3 - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Central nervous system

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Report on Carcinogens (12th Ed. ) (2011)
A Comprehensive Guide to the Hazardous Properties of Chemical Substances (2007)
J E Rice et al.
Cancer research, 47(23), 6166-6170 (1987-12-01)
The metabolism of benzo[j]fluoranthene (BjF) in vivo in mouse skin was investigated. trans-4,5-Dihydro-4,5-dihydroxybenzo[j]fluoranthene (BjF-4,5-diol) and trans-9,10-dihydro-9,10-dihydroxybenzo[j]fluoranthene (BjF-9,10-diol) have been identified as major metabolites. In addition, 4- and 10-hydroxybenzo[j]fluoranthene and benzo[j]fluoranthen-4,5-dione have been tentatively identified among the metabolites formed in vivo
E H Weyand et al.
Chemical research in toxicology, 6(1), 117-124 (1993-01-01)
Studies have demonstrated that the metabolic activation of benzo[j]fluoranthene (B[j]F) to a genotoxic agent proceeds through the formation of either the trans-4,5-dihydrodiol (B[j]F-4,5-diol) or the trans-9,10-dihydrodiol (B[j]F-9,10-diol) metabolite of B[j]F. Using 32P-postlabeling analysis, the profiles of DNA adducts formed in
J E Rice et al.
Chemico-biological interactions, 63(3), 227-237 (1987-01-01)
The metabolites of benzo[j]fluoranthene (BjF) as formed in vitro using the 9000 X g supernatant from Aroclor-pretreated rats have been identified. Two dihydrodiols, trans-4,5-dihydro-4,5-dihydroxyBjF and trans-9,10-dihydro-9,10-dihydroxyBjF have been identified as major metabolites by comparison of their spectral and chromatographic properties

프로토콜

GC Analysis of Polynuclear Aromatic Hydrocarbons (PAHs) in Salmon on SPB®-608 (20 m x 0.18 mm I.D., 0.18 µm) after QuEChERS Cleanup using Supel™ QuE Z-Sep, Fast GC Analysis

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