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![苯并 [ b ] 蒽 98%](/deepweb/assets/sigmaaldrich/product/structures/197/885/3a015625-5e09-4f15-8b17-4cc285304fc7/640/3a015625-5e09-4f15-8b17-4cc285304fc7.png)
蒸汽密度
6.15 (vs air)
质量水平
蒸汽压
1 mmHg ( 145 °C)
产品线
ReagentPlus®
方案
99%
表单
powder or flakes
自燃温度
1004 °F
颜色
blue-violet fluorescence
沸点
340 °C (lit.)
mp
210-215 °C (lit.)
溶解性
toluene: soluble 20 mg/mL, clear, colorless to faintly yellow
alcohols: soluble
benzene: soluble
chloroform: soluble
hydronaphthalenes: soluble
supercritical carbon dioxide: soluble
SMILES字符串
c1ccc2cc3ccccc3cc2c1
InChI
1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H
InChI key
MWPLVEDNUUSJAV-UHFFFAOYSA-N
基因信息
human ... CYP1A2(1544)
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一般描述
蒽衍生物可用于制备稳定的蓝光发射有机电致发光器件 。 分枝杆菌 sp 将其氧化为蒽 顺式 -1,2-二氢二醇。菌株 PYR-12 。它通过与[5,6]-富勒烯C60的[4 + 2]-环加成反应形成双加合物。
应用
蒽已被证明可溶于各种环己酮、乙酸乙酯和甲醇的二元和三元混合物中。
蒽用于研究蒽在超临界CO2中的光二聚反应。
法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Warning
危险声明
危险分类
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
249.8 °F - closed cup
闪点(°C)
121.0 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
危险化学品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Anthracene derivatives for stable blue-emitting organic electroluminescence devices.
Jianmin S and Tang CW.
Applied Physics Letters, 80(17), 3201-3203 (2002)
Christopher E. Bunker et al.
The Journal of organic chemistry, 62(21), 7324-7329 (2001-10-24)
The photodimerization reaction of anthracene in supercritical CO(2) was studied systematically at different CO(2) densities. Unlike in normal liquid solvents, the reaction in supercritical CO(2) is significant even at anthracene concentrations as low as a few micromolar. At comparable anthracene
J D Moody et al.
Applied and environmental microbiology, 67(4), 1476-1483 (2001-04-03)
Cultures of Mycobacterium sp. strain PYR-1 were dosed with anthracene or phenanthrene and after 14 days of incubation had degraded 92 and 90% of the added anthracene and phenanthrene, respectively. The metabolites were extracted and identified by UV-visible light absorption
The bis-adducts of the [5, 6]-fullerene C60 and anthracene.
Duarte-Ruiz A, et al.
Tetrahedron, 57(17), 3709-3714 (2001)
Payam Payamyar et al.
Chimia, 67(4), 283-285 (2013-08-24)
We describe the challenges involved with extending the limited lateral size of two-dimensional polymers (2DPs). An amphiphilic monomer with three-fold symmetry is chosen to form an ideally tessellated monolayer at the air/water interface. Anthracene [4+4] photo-dimerization is chosen as the
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