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)ccc3cc4ccc5ccccc5c4cc23
InChI
1S/C22H14/c1-3-7-19-15(5-1)9-11-17-13-18-12-10-16-6-2-4-8-20(16)22(18)14-21(17)19/h1-14H
InChI key
KLIHYVJAYWCEDM-UHFFFAOYSA-N
Analysis Note
For more information please see:
BCR095
BCR095
Legal Information
BCR is a registered trademark of European Commission
存储类别
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
S V Vulimiri et al.
Chemical research in toxicology, 12(1), 60-67 (1999-01-20)
The formation of DNA adducts in mouse epidermis has been examined following topical application of dibenz[a,j]anthracene (DB[a,j]A) and its metabolites, i.e., DB[a,j]A-3,4-diol, DB[a,j]A-3,4-10, 11-bis-diol, DB[a,j]A-3,4-8,9-bis-diol, 10-OH-DB[a,j]A-3,4-diol, or 11-OH-DB[a,j]A-3,4-diol, using a 32P-postlabeling assay. At initiating doses (400-1600 nmol), DB[a,j]A produced at
Dibenz[a,j]anthracene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 309-313 (1983-12-01)
W Baer-Dubowska et al.
Chemical research in toxicology, 8(2), 292-301 (1995-03-01)
The formation of deoxyribonucleoside adducts in mouse epidermis has been examined following topical application of [3H]dibenz[a,j]anthracene (DB[a,j]A) or by 32P-postlabeling following topical application of unlabeled DB[a,j]A, DB[a,j]A trans-3,4-diol or the anti- or syn-3,4-diol 1,2-epoxides. A single topical application of [3H]DB[a,j]A
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| BCR095-100MG | 04061832656991 |