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D31206

Sigma-Aldrich

1,2,3,4-二苯并蒽

97%

同義詞:

1,2:3,4-二苯并蒽

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About This Item

經驗公式（希爾表示法）:
C22H14
CAS號碼:
215-58-7
分子量：:
278.35
Beilstein:
1912415
EC號碼:
205-920-8
MDL號碼:
MFCD00003603
分類程式碼代碼:
12352100
PubChem物質ID:
24893724
NACRES:
NA.22
暫時無法取得訂價和供貨情況

化驗

97%

形狀

powder

bp

518 °C (lit.)

mp

205-207 °C (lit.)

SMILES 字串

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 密鑰

RAASUWZPTOJQAY-UHFFFAOYSA-N

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相關類別

象形圖

Skull and crossbonesEnvironment
GHS06,GHS09

訊號詞

Danger

危險分類

Acute Tox. 3 Oral - Aquatic Acute 1

儲存類別代碼

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

水污染物質分類（WGK）

WGK 3

個人防護裝備

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

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分析證明 (COA)

Lot/Batch Number
10525JE
02013AE
1816AH
0923TE

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A P Koley et al.
Biochemistry, 34(6), 1942-1947 (1995-02-14)
The flash photolysis technique was used to examine the kinetics of CO binding to cytochromes P450 in rat liver microsomes. The effect of polycyclic aromatic hydrocarbons (PAHs) and flavones was used to distinguish the kinetic behavior of the PAH-metabolizing P450
The metabolic activation of some polycyclic hydrocarbons: the role of dihydrodiols and diol-epoxides.
P Sims
Advances in experimental medicine and biology, 136 Pt A, 487-500 (1981-01-01)
P Bryla et al.
Cancer letters, 65(1), 35-41 (1992-07-31)
The binding of benzo[a]pyrene, 7,12-dimethylbenz[a]anthracene, 3-methylcholanthrene, benz[a]anthracene, dibenz[a,c]anthracene and phenanthrene to calf thymus DNA in vitro in the absence of enzymatic or chemical activation was investigated using the 32P-postlabeling assay. Reactions were performed in the dark or under white light
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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