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BCR156R

Dibenz[c,h]acridine

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C21H13N
CAS Number:
224-53-3
Molecular Weight:
279.33
Beilstein:
209259
MDL number:
MFCD00215937
UNSPSC Code:
41116107
PubChem Substance ID:
329773792
NACRES:
NA.24

grade

certified reference material

Agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

neat

storage temp.

2-8°C

SMILES string

c1ccc2c(c1)ccc3cc4ccc5ccccc5c4nc23

InChI

1S/C21H13N/c1-3-7-18-14(5-1)9-11-16-13-17-12-10-15-6-2-4-8-19(15)21(17)22-20(16)18/h1-13H

InChI key

BTVBCAKHMZHLFR-UHFFFAOYSA-N

Related Categories

Analysis Note

For more information please see:
BCR156R

Legal Information

BCR is a registered trademark of European Commission

Pictograms

Health hazard
GHS08

Signal Word

Warning

Hazard Statements

H351

Precautionary Statements

P201 - P308 + P313

Hazard Classifications

Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

BCR156R-10MG:

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Certificates of Analysis (COA)

Lot/Batch Number

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Myriam Coulet et al.
Toxicology in vitro : an international journal published in association with BIBRA, 59, 281-291 (2019-05-06)
Nitrogen-containing polycyclic aromatic hydrocarbons (PANHs or azaarenes) are compounds structurally similar to PAHs (carbon substituted by a nitrogen) reported to occur at low levels in food. Although limited, literature may suggest possible higher toxicity than for PAHs. Using a battery
A H Conney et al.
Advances in experimental medicine and biology, 500, 697-707 (2002-01-05)
Chinese hamster V79 cells were exposed to a high or low concentration of the highly carcinogenic (R,S,S,R) or the less active (S,R,R,S) bay- or fjord-region diol epoxides of benzo[a]pyrene, benzo[c]phenanthrene or dibenz[c,h]acridine. Independent 8-azaguanine-resistant clones were isolated, and base substitutions

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