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247367

Sigma-Aldrich

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

≥99%

Synonym(s):

meso-Tetraphenylporphyrin, TPP

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About This Item

Empirical Formula (Hill Notation):
C44H30N4
CAS Number:
917-23-7
Molecular Weight:
614.74
Beilstein:
379542
EC Number:
213-025-9
MDL number:
MFCD00011680
UNSPSC Code:
12171500
PubChem Substance ID:
24854864
NACRES:
NA.47

Quality Level

200

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

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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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM4287
MKBX9825V
MKBT1085V
MKBL6051V
MKBH6920V

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G S S Saini et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(13-14), 3070-3076 (2005-09-17)
We present here the infrared absorption spectra of free-base tetraphenylporphine and its dication. Most of the allowed IR bands of porphyrin skeletal are observed in pairs due to two-fold symmetry of the free-base tetraphenylporphine. Observation of some new bands, disappearance
Pradip Chandra Mandal et al.
Journal of hazardous materials, 187(1-3), 600-603 (2011-02-09)
Reactions of nickel-5,10,15,20-tetraphenylporphine (Ni-TPP) were studied in supercritical water in the presence of toluene without the addition of any catalyst, H(2) or H(2)S that is called a green process. The objective of this study was to remove nickel from Ni-TPP
Stefan Müllegger et al.
ACS nano, 5(8), 6480-6486 (2011-07-09)
Supporting functional molecules on crystal facets is an established technique in nanotechnology. To preserve the original activity of ionic metallorganic agents on a supporting template, conservation of the charge and oxidation state of the active center is indispensable. We present
Zerrin Sezgin et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 64(3), 261-268 (2006-08-04)
The objective of this study is to investigate the solubilization of poorly water-soluble anticancer drugs, octaethylporphine (OEP), meso-tetraphenyl porphine (mTPP) and camptothecin (CPT), in Pluronic and polyethylene glycol-distearoylphosphatidylethanolamine (PEG-DSPE) polymeric micelles. Three different Pluronic and PEG-DSPE polymers with various chain
Li Zhang et al.
The journal of physical chemistry. B, 113(42), 14015-14020 (2009-10-16)
The self-assembly and induced supramolecular chirality of a dianionic meso-tetraphenylsulfonato porphyrin (TPPS) on the optically active polylysine has been investigated. Our research has confirmed that in the presence of poly(l-lysine) (PLL) or poly(d-lysine) (PDL), TPPS could form both H and
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