Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

More Documents

252883

Sigma-Aldrich

5,10,15,20-Tetrakis(4-methoxyphenyl)-21H,23H-porphine

Dye content 95 %

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C48H38N4O4
CAS Number:
22112-78-3
Molecular Weight:
734.84
MDL number:
MFCD00012072
UNSPSC Code:
12171500
PubChem Substance ID:
24855247
NACRES:
NA.47

form

powder or crystals

Quality Level

100

composition

Dye content, 95%

λmax

424 nm
653 nm (2nd)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

COc1ccc(cc1)-c2c3ccc(n3)c(-c4ccc(OC)cc4)c5ccc([nH]5)c(-c6ccc(OC)cc6)c7ccc(n7)c(-c8ccc(OC)cc8)c9ccc2[nH]9

InChI

1S/C48H38N4O4/c1-53-33-13-5-29(6-14-33)45-37-21-23-39(49-37)46(30-7-15-34(54-2)16-8-30)41-25-27-43(51-41)48(32-11-19-36(56-4)20-12-32)44-28-26-42(52-44)47(40-24-22-38(45)50-40)31-9-17-35(55-3)18-10-31/h5-28,49,52H,1-4H3/b45-37-,45-38-,46-39-,46-41-,47-40-,47-42-,48-43-,48-44-

InChI key

PJOJZHHAECOAFH-PJEPRTEXSA-N

General description

5,10,15,20-Tetrakis(4-methoxyphenyl)-21H,23H-porphine is an achiral porphyrin derivative. It forms chiral supramolecular assemblies via spontaneous symmetry breaking at the air or water interface.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKBC2545
91197LJ
35996CJ
10296MH
00327HH

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

M Belén Ballatore et al.
European journal of medicinal chemistry, 83, 685-694 (2014-07-11)
A covalently linked porphyrin-fullerene C60 dyad 5 was synthesized by 1,3-dipolar cycloaddition using 5-(4-formylphenyl)-10,15,20-tris[3-(N-ethylcarbazoyl)]porphyrin, N-methylglycine and fullerene C60. Methylation of 5 was used to obtain a cationic dyad 6. Spectroscopic properties were compared in toluene, N,N-dimethylformamide (DMF) and toluene/sodium bis(2-ethylhexyl)sulfosuccinate
Chirality amplification of porphyrin assemblies exclusively constructed from achiral porphyrin derivatives.
Chen P, et al.
ChemPhysChem, 7(11), 2419-2423 (2006)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service