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Merck
CN

247367

5,10,15,20-四苯基-21 H ,23 H -卟吩

≥99%

别名:

内消旋 -四苯基卟啉, 四苯基卟啉

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关于此项目

经验公式(希尔记法):
C44H30N4
化学文摘社编号:
分子量:
614.74
UNSPSC Code:
12171500
NACRES:
NA.47
PubChem Substance ID:
EC Number:
213-025-9
Beilstein/REAXYS Number:
379542
MDL number:
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InChI key

YNHJECZULSZAQK-LWQDQPMZSA-N

InChI

1S/C44H30N4/c1-5-13-29(14-6-1)41-33-21-23-35(45-33)42(30-15-7-2-8-16-30)37-25-27-39(47-37)44(32-19-11-4-12-20-32)40-28-26-38(48-40)43(31-17-9-3-10-18-31)36-24-22-34(41)46-36/h1-28,45,48H/b41-33-,41-34-,42-35-,42-37-,43-36-,43-38-,44-39-,44-40-

SMILES string

c1ccc(cc1)-c2c3ccc(n3)c(-c4ccccc4)c5ccc([nH]5)c(-c6ccccc6)c7ccc(n7)c(-c8ccccc8)c9ccc2[nH]9

assay

≥99%

form

crystalline powder

technique(s)

titration: suitable

impurities

<0.1% corresponding chlorin

mp

>300 °C (lit.)

solubility

toluene: 0.03 g/L, clear

λmax

415 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

Gene Information

human ... TERT(7015)

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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)


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Maria Bassiouk et al.
Journal of nanoscience and nanotechnology, 11(6), 5457-5468 (2011-07-21)
The self-assembly of porphyrins into highly organized functional arrays supported on appropriate solid substrates is an area of research with multiple potential applications in the "bottom-up" approach to manufacturing. In order to analyze the self-assembly of meso-tetraphenylporphine (H2TPP) on the
Satoshi Tsukahara et al.
Analytical and bioanalytical chemistry, 395(4), 1047-1053 (2009-07-09)
Rhombic-ordered microdomains of diprotonated 5,10,15,20-tetraphenylporphine aggregate, whose sizes were 10-200 microm, were formed at dodecane/aqueous H(2)SO(4) interfaces. The light excitation of their two absorption bands (410 and 473 nm for H- and J-bands, respectively) led to one fluorescence band at
A V Udal'tsov et al.
Biophysical chemistry, 83(2), 141-152 (2000-02-15)
Properties of protonated dimeric forms of meso-tetraphenylporphine (TPP) and meso-tetra(p-aminophenyl)porphine (TAPP) bound with copolymer and also complexes produced by associated TAPP bound with copolymer, Mn2+, and Fe3+ are investigated by absorption, luminescence, and Raman spectroscopy. According to absorption spectra of
Zachary J Tonzetich et al.
Inorganic chemistry, 50(4), 1570-1579 (2011-01-20)
Several nitrosyl complexes of Fe and Co have been prepared using the sterically hindered Ar-nacnac ligand (Ar-nacnac = anion of [(2,6-diisopropylphenyl)NC(Me)](2)CH). The dinitrosyliron complexes [Fe(NO)(2)(Ar-nacnac)] (1) and (Bu(4)N)[Fe(NO)(2)(Ar-nacnac)] (2) react with [Fe(III)(TPP)Cl] (TPP = tetraphenylporphine dianion) to generate [Fe(II)(NO)(TPP)] and
Zerrin Sezgin et al.
International journal of pharmaceutics, 332(1-2), 161-167 (2006-10-24)
Meso-tetraphenyl porphine (mTPP) is a highly lipophilic, fluorescent porphyrin derivate and it is used as photosensitizer on the treatment of malign neoplasms. The aim of this study was to prepare mTPP loaded pluronic F127 and polyethylene glycol-distearoyl phosphatidylethanolamine (PEG(2000)-DSPE) micelles

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