Merck
CN
所有图片(1)

文件

D31206

Sigma-Aldrich

1,2,3,4-二苯并蒽

97%

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别名:
1,2:3,4-二苯并蒽
经验公式（希尔记法）:
C22H14
CAS号:
215-58-7
分子量:
278.35
Beilstein:
1912415
EC 号:
205-920-8
MDL编号:
MFCD00003603
PubChem化学物质编号:
24893724
NACRES:
NA.22

质量水平

100

检测方案

97%

形式

powder

bp

518 °C (lit.)

mp

205-207 °C (lit.)

SMILES string

c1ccc2cc3c4ccccc4c5ccccc5c3cc2c1

InChI

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

InChI key

RAASUWZPTOJQAY-UHFFFAOYSA-N

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相关类别

象形图

Skull and crossbonesEnvironment
GHS06,GHS09

警示用语：

Danger

危险分类

Acute Tox. 3 Oral - Aquatic Acute 1

储存分类代码

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

WGK

WGK 3

个人防护装备

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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S Kumar et al.
Mutation research, 242(4), 337-343 (1990-12-01)
The mutagenic activities of dibenz[a,c]anthracene (DB[a,c]A), and its 11 derivatives, including 3 diols, 6 phenols and 2 oxepines, were studied in the TA100 strain of Salmonella typhimurium at doses varying from 0 to 20 micrograms/plate in the presence of a
A Hewer et al.
Carcinogenesis, 2(12), 1345-1352 (1981-01-01)
In rat liver microsomal preparations, the 10,11-dihydrodiol of dibenz[a,c]anthracene (DBA) is metabolized to r-10,t-11-dihydroxy-t-12,13-oxy-10,11,12,13-tetrahydrodibenz[a,c]anthracene (anti-DBA 10,11-diol 12,13-oxide), the anti isomer of a non-bay-region diol-epoxide of DBA. When 3H-labelled DBA or trans-10,11-dihydro-10,11-dihydroxydibenz[a,c]anthracene were metabolized in this system in the presence of
Dibenz[a,c]anthracene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 289-297 (1983-12-01)
I Chouroulinkov et al.
Cancer letters, 19(1), 21-26 (1983-05-01)
The tumor-initiating activities of dibenz[a,c]anthracene (DBA) and of the related trans-1,2-, 3,4- and 10,11-dihydrodiols have been examined on mouse skin subsequently promoted with 12-O-tetradecanoyl-phorbol-13-acetate (TPA). The 1,2- and 10,11-dihydrodiols were active and were more active than equivalent doses of either
M Hall et al.
Carcinogenesis, 9(5), 865-868 (1988-05-01)
Incubation of r-1,t-2-dihydroxy-t-3,4-oxy-1,2,3,4-tetrahydrochrysene (anti-chrysene-1,2-diol 3,4-oxide), the bay-region diol-epoxide of chrysene, with rat liver microsomes in the presence of NADP+ and DNA, followed by 32P-postlabelling analysis of the DNA, revealed the presence of at least two adducts not detected when anti-chrysene-1,2-diol
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