D146706
9,10-ジメチルアントラセン
99%
別名:
9,10-Dimethylanthracene
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この商品について
実験式（ヒル表記法）:
C16H14
CAS番号:
分子量:
206.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-308-4
Beilstein/REAXYS Number:
1909028
MDL number:
Assay:
99%
Form:
crystals
SMILES string
Cc1c2ccccc2c(C)c3ccccc13
InChI key
JTGMTYWYUZDRBK-UHFFFAOYSA-N
InChI
1S/C16H14/c1-11-13-7-3-5-9-15(13)12(2)16-10-6-4-8-14(11)16/h3-10H,1-2H3
assay
99%
form
crystals
mp
182-184 °C (lit.)
Quality Level
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関連するカテゴリー
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Resp. Sens. 1 - Skin Sens. 1
保管分類
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
D146706-1G: + D146706-BULK: + D146706-VAR:
jan
Alan Sholto et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 7(3), 344-351 (2008-04-05)
Six amphiphilic silicon phthalocyanines (SiPc's) axially linked to a dimethylated amino alkyl group of varying length have been examined for their potential suitability as photosensitizers for photodynamic therapy (PDT). This group of molecules was chosen because the length of the
David Bailey et al.
Chemical communications (Cambridge, England), (20)(20), 2569-2571 (2005-05-19)
Irradiating 2,3,6,7-tetraphenylanthracene in the presence of 9,10-dimethylanthracene leads to exclusive formation of the cross-dimer. No photochemical reaction is observed when either of these chromophores is irradiated in the absence of the other.
E Gross et al.
Photochemistry and photobiology, 57(5), 808-813 (1993-05-01)
Two new sensitizers are introduced for a potential use in photodynamic therapy: Zn(2+)- and MG(2+)-tetrabenzoporphyrin (ZnTBP and MgTBP). A comparative study of the quantum yields of singlet oxygen generation (phi delta) of hematoporphyrin derivative (HpD), Photofrin II (PF-II), Zn(2+)-phthalocyanine tetrahydroxyl
E W Vogel et al.
Mutation research, 250(1-2), 291-298 (1991-09-01)
A set of six Drosophila strains was developed, by inducing by chemical treatment with N-ethyl-N-nitrosourea (ENU) new white and, in some strains, yellow mutations in 3 wild-type (WT) and 3 insecticide-resistant (IR) populations. These strains were previously shown to vary
M Elisa Milanesio et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2(9), 926-933 (2003-10-17)
A novel 5-[4-(trimethylammonium)phenyl]-10,15,20-tris(2,4,6-trimethoxyphenyl)porphyrin iodide (2) has been synthesized. A positive charge was incorporated at a peripheral position to increase the amphiphilic character of the structure. The photodynamic effect of the cationic porphyrin 2 was compared with that of non-charged 5-(4-aminophenyl)-10,15,20-tris(2,4,6-trimethoxyphenyl)porphyrin
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