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关于此项目
经验公式(希尔记法):
C26H18
化学文摘社编号:
分子量:
330.42
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
216-105-1
Beilstein/REAXYS Number:
1914010
MDL number:
InChI key
FCNCGHJSNVOIKE-UHFFFAOYSA-N
InChI
1S/C26H18/c1-3-11-19(12-4-1)25-21-15-7-9-17-23(21)26(20-13-5-2-6-14-20)24-18-10-8-16-22(24)25/h1-18H
SMILES string
c1ccc(cc1)-c2c3ccccc3c(-c4ccccc4)c5ccccc25
assay
97%
form
powder
mp
245-248 °C (lit.)
Quality Level
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Application
- 可进行光子上转换的硅和分子受体之间自旋三重态激子转移的实现:这项研究展示了将三重态激子从硅转移到9,10-二苯基蒽,这是光子上转换技术的关键机制,可能会彻底改变太阳能的收集和光电器件(Xia et al., 2020)。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Anis Arnous et al.
Journal of pharmacological and toxicological methods, 48(3), 171-177 (2004-02-28)
A simple, rapid, sensitive, and enzyme-free analytical method for estimating scavenging of hydrogen peroxide (H2O2) was developed. Peroxyoxalate chemiluminescence (POCL) was measured, using 9,10-diphenylanthracene as fluorophore. The chemiluminescence signal was found to be linear in response to increasing amounts of
M J Steinbeck et al.
The Journal of biological chemistry, 268(21), 15649-15654 (1993-07-25)
The extracellular production of singlet oxygen (O2(1 delta g)) by stimulated macrophages was measured using a modification of our quantitative method initially developed to measure the intracellular production of O2(1 delta g) by neutrophils (Steinbeck, M. J., Khan, A. U.
M J Steinbeck et al.
The Journal of biological chemistry, 267(19), 13425-13433 (1992-07-05)
To determine if singlet oxygen (O2(1 delta g)) is produced by neutrophils (PMNs) during the process of phagocytosis, glass beads were coated with a specific chemical trap for O2(1 delta g), 9,10-diphenylanthracene (DPA). Singlet oxygen, but not other reactive oxygen
Regression analysis of electrochemical data with expanding space grid digital simulation at spherical electrodes.
J V Arena et al.
Analytical chemistry, 58(7), 1481-1488 (1986-06-01)
[Synthesis of novel fluorescent 9,10-bisphenylethynylanthracene-derived pseudonucleoside and its introduction into oligonucleotides].
A D Malakhov et al.
Bioorganicheskaia khimiia, 25(12), 933-937 (2000-03-29)
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