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Merck
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주요 문서

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48574

Supelco

Dibenz[a,h]anthracene

analytical standard

동의어(들):

1,2:5,6-Dibenzanthracene

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About This Item

실험식(Hill 표기법):
C22H14
CAS Number:
53-70-3
Molecular Weight:
278.35
Beilstein:
1912416
EC Number:
200-181-8
MDL number:
MFCD00003708
UNSPSC 코드:
12000000
PubChem Substance ID:
24872126

Grade

analytical standard

CofA

current certificate can be downloaded

포장

vial of 100 mg

기술

HPLC: suitable
gas chromatography (GC): suitable

bp

524 °C (lit.)

mp

262-265 °C (lit.)

응용 분야

cleaning products
cosmetics
environmental
food and beverages
personal care

형식

neat

저장 온도

2-30°C

SMILES string

c1ccc2c(c1)ccc3cc4c(ccc5ccccc45)cc23

InChI

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

InChI key

LHRCREOYAASXPZ-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

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

픽토그램

Health hazardEnvironment
GHS08,GHS09

신호어

Danger

유해 및 위험 성명서

H350,H410

Hazard Classifications

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

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

개인 보호 장비

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

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
LC26902V
LC17792V
LC08119V
LB98826V
LB95471V

적합한 버전을 찾을 수 없으신가요?

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

COA 검색

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 5

1 of 5

Benz[a]anthracene analytical standard

Supelco

48563

Benz[a]anthracene

Dibenzo[a,h]pyrene BCR®, certified reference material

BCR159

Dibenzo[a,h]pyrene

Benzo[k]fluoranthene certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

03323

Benzo[k]fluoranthene

Benzo[e]pyrene 98%

Sigma-Aldrich

B10102

Benzo[e]pyrene

Benzo[a]pyrene ≥96% (HPLC)

Sigma-Aldrich

B1760

Benzo[a]pyrene

P Sartorelli et al.
Toxicology and industrial health, 17(1), 17-21 (2002-05-15)
To understand the dermal uptake of chemicals bound to soil and dust, information on the neat substance is helpful but does not seem sufficient. Because of its content of polycyclic aromatic hydrocarbons (PAHs) coal is suspected to be carcinogenic. However
Heinz Frank et al.
Chemical research in toxicology, 24(12), 2258-2268 (2011-11-18)
The synthesis of the 8 possible stereoisomeric diol epoxides (DEs) at the terminal benzo ring of carcinogenic dibenz[a,h]anthracene (DBA) is reported. trans-3,4-Dihydroxy-3,4-dihydro-DBA (1) afforded the 4 bay region DEs: the enantiomeric pairs of the anti diastereomers (+)-3/(-)-3 and of the
K B Okona-Mensah et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 43(7), 1103-1116 (2005-04-19)
Evidence suggests that people living in urban areas have an increased risk of lung cancer due to higher levels of air pollution in these areas. Benzo[a]pyrene (B[a]P) is currently used as the main indicator of carcinogenic polycyclic aromatic hydrocarbons (PAHs)
S Nesnow et al.
Carcinogenesis, 15(10), 2225-2231 (1994-10-01)
The major routes of metabolic activation of dibenz[a,h]-anthracene (DBA) have been studied in transformable C3H10T1/2CL8 (C3H10T1/2) mouse embryo fibroblasts in culture. The morphological transforming activities of three potential intermediates formed by metabolism of DBA by C3H10T1/2 cells, trans-3,4-dihydroxy-3,4-dihydro-DBA-(DBA-3,4-diol), trans-dihydroxy-3,4-dihydro-DBA-anti-1,2-oxide (DBA-3,4-diol-1,2-oxide)
Zhi-Xin Yuan et al.
Chemical research in toxicology, 16(12), 1581-1588 (2003-12-19)
Benzo[b]phenanthro[2,3-d]thiophene (BPT), a thia analogue of dibenz[a,h]anthracene (DBA), is a carcinogenic environmental pollutant. We have examined the metabolism of BPT by rodent liver microsomes to investigate the mechanism by which BPT produces mutagenic and carcinogenic effects. Both rat and mouse
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