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BCR159

Dibenzo[a,h]pyrene

BCR®, certified reference material

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100 MG
₩1,233,936

₩1,233,936

예상 입고일2025년 5월 12일세부사항

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모든 사진(1)

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100 MG
₩1,233,936

About This Item

실험식(Hill 표기법):
C24H14
CAS Number:
189-64-0
Molecular Weight:
302.37
Beilstein:
2054067
MDL number:
MFCD00039579
UNSPSC 코드:
41116107
PubChem Substance ID:
329773795
NACRES:
NA.24

₩1,233,936

예상 입고일2025년 5월 12일세부사항

벌크 견적 요청

Grade

certified reference material

Agency

BCR®

제조업체/상표

JRC

기술

HPLC: suitable
gas chromatography (GC): suitable

형식

neat

저장 온도

2-8°C

SMILES string

c1ccc2c(c1)cc3ccc4c5ccccc5cc6ccc2c3c46

InChI

1S/C24H14/c1-3-7-19-15(5-1)13-17-9-12-22-20-8-4-2-6-16(20)14-18-10-11-21(19)23(17)24(18)22/h1-14H

InChI key

RXUSYFJGDZFVND-UHFFFAOYSA-N

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관련 카테고리

분석 메모

For more information please see:
BCR159

법적 정보

BCR is a registered trademark of European Commission

픽토그램

Health hazard
GHS08

신호어

Danger

유해 및 위험 성명서

H341,H350

Hazard Classifications

Carc. 1B - Muta. 2

Storage Class Code

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

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

A W Wood et al.
Cancer research, 41(7), 2589-2597 (1981-07-01)
The mutagenic activities of dibenzo(a,h)(pyrene, dibenzo(a,i)pyrene, and a total of 11 of their benzo-ring derivatives were evaluated in bacterial and mammalian cells in the absence or presence of a mammalian metabolic activation system. trans-1,2-Dihydroxy-1,2-dihydrodibenzo(a,h)pyrene and trans-3,4-dihydroxy-3,4-dihydrodibenzo(a,i)pyrene, the expected dihydrodiol precursors
G A Marsch et al.
Chemical research in toxicology, 5(6), 765-772 (1992-11-01)
The in vivo formation of dibenzo[a,h]pyrene-DNA adducts in mouse skin was assessed by laser-excited fluorescence spectroscopy at 77 and 4.2 K. Two adducts were identified with fluorescence origin bands at approximately 383.5 and 407.2 nm, and these were shown to
Tumorigenicity of bay-region diol-epoxides and other benzo-ring derivatives of dibenzo(a,h)pyrene and dibenzo(a,i)pyrene on mouse skin and in newborn mice.
R L Chang et al.
Cancer research, 42(1), 25-29 (1982-01-01)
Dibenzo[a,h]pyrene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 331-335 (1983-12-01)
B S Hass et al.
Cancer research, 42(5), 1646-1649 (1982-05-01)
The polycyclic aromatic hydrocarbons dibenzo(a,i)pyrene and dibenzo(a,h)pyrene, each of which possesses two bay regions, and their bay-region difluorinated derivatives were tested for mutagenicity for ouabain and 6-thioguanine resistance in Chinese hamster V79 cells. Since V79 cells do not metabolize polycyclic
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Efficient PAH Analysis (EU 15+1) using an Ascentis® Express PAH HPLC Column

This application note describes the fast and efficient separation of the EU’s list of 15 + 1 polynuclear aromatic hydrocarbons (PAHs) using Ascentis® Express PAH HPLC column.

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