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Merck

160997

Sigma-Aldrich

5,10,15,20-Tetraphenyl-21H,23H-porphine

97%

Sinónimos:

meso-Tetraphenylporphyrin, TPP

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About This Item

Fórmula empírica (notación de Hill):
C44H30N4
Número de CAS:
Peso molecular:
614.74
Beilstein/REAXYS Number:
379542
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

Quality Level

assay

97%

form

powder or crystals

technique(s)

titration: suitable

impurities

1-3% corresponding chlorin

mp

>300 °C (lit.)

solubility

chloroform: 1 mg/mL, clear to opaque

λmax

514 nm

ε (extinction coefficient)

≥3500 at 480-486 nm in toluene
≥4000 at 647-653 nm in toluene
≥5000 at 589-595  nm in toluene
≥8000 at 546-552 nm in toluene

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

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

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-

InChI key

YNHJECZULSZAQK-LWQDQPMZSA-N

Gene Information

human ... TERT(7015)

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General description

5,10,15,20-Tetraphenyl-21H,23H-porphine is a porphyrin compound.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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
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
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
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
Anette Weyergang et al.
Biochimica et biophysica acta, 1830(3), 2659-2670 (2013-05-15)
Tyrosin kinase inhibitors (TKIs) and monoclonal antibodies aimed to target epidermal growth factor receptor (EGFR) have shown limited effect as monotherapies and drug resistance is a major limitation for therapeutic success. Adjuvant therapies to EGFR targeting therapeutics are therefore of

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