Synonym
meso-Tetra (3-pyridyl) porphine; 5,10,15,20-tetra (pyridin-3-yl)porphyrin; meso-Tetra(3-pyridyl) porphine;
IUPAC/Chemical Name
5,10,15,20-tetra(pyridin-3-yl)porphyrin
InChi Key
GZKPUYJFADMBGO-KHQKEXQOSA-N
InChi Code
InChI=1S/C40H26N8/c1-5-25(21-41-17-1)37-29-9-11-31(45-29)38(26-6-2-18-42-22-26)33-13-15-35(47-33)40(28-8-4-20-44-24-28)36-16-14-34(48-36)39(27-7-3-19-43-23-27)32-12-10-30(37)46-32/h1-24,45,48H/b37-29-,37-30-,38-31-,38-33-,39-32-,39-34-,40-35-,40-36-
SMILES Code
C1(/C(C2=CC=C(N2)/C(C3=CC=CN=C3)=C4N=C5C=C\4)=C6N=C(/C(C7=CN=CC=C7)=C(N/8)/C=CC8=C5/C9=CN=CC=C9)C=C/6)=CN=CC=C1
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
Preparing Stock Solutions
The following data is based on the
product
molecular weight
618.70
Batch specific molecular weights may vary
from batch to batch
due to the degree of hydration, which will
affect the solvent
volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass |
1 mg |
5 mg |
10 mg |
| 1 mM |
1.15 mL |
5.76 mL |
11.51 mL |
| 5 mM |
0.23 mL |
1.15 mL |
2.3 mL |
| 10 mM |
0.12 mL |
0.58 mL |
1.15 mL |
| 50 mM |
0.02 mL |
0.12 mL |
0.23 mL |
1.) Lipstman, et al. Versatile Molecular Recognition Features of Tetra(3-pyridyl)porphyrin in Crystal Engineering. Cryst. Growth Des. 2010, 10, 10, 4596–4606. https://doi.org/10.1021/cg1008973
2.) Zakavi, et al. Effects of Core and/or Peripheral Protonation of meso-Tetra(2-, 3-, and 4-pyridyl)Porphyrin and meso-Tetra(3-methylpyridyl)Porphyrin on Their UV-vis Spectra. Journal of Spectroscopy. Volume 2013, Article ID 713745 https://doi.org/10.1155/2013/713745
3.) Martyanov, T.P., Tovstun, S.A., Vasil’ev, S.G. et al. Adsorption of meso-tetra(3-pyridyl)porphyrin on InP/ZnS colloidal quantum dots. J Nanopart Res 24, 129 (2022). https://doi.org/10.1007/s11051-022-05513-4
4.) Choi, et al. An Interdigitated Metalloporphyrin Framework: Two-Dimensional Tessellation, Framework Flexibility, and Selective Guest Accommodation. Cryst. Growth Des. 2010, 10, 1, 171–176. https://doi.org/10.1021/cg900816h
5.) Le, et al. Bcl-2 Promoter Sequence G-Quadruplex Interactions with Three Planar and Non-Planar Cationic Porphyrins: TMPyP4, TMPyP3, and TMPyP2. PLOS ONE. Published: August 20, 2013. https://doi.org/10.1371/journal.pone.0072462
6.) Dutikova, Y.V., Borisova, O.F., Shchyolkina, A.K. et al. 5,10,15,20-Tetra-(N-methyl-3-pyridyl)porphyrin destabilizes the antiparallel telomeric quadruplex d(TTAGGG)4 . Mol Biol 44, 823–831 (2010). https://doi.org/10.1134/S0026893310050201
7.) Dutton, et al. The Influence of Redox-Active Linkers on the Stability and Physical Properties of a Highly Electroactive Porphyrin Nanoprism. Inorg. Chem. 2020, 59, 17, 12616–12624. https://doi.org/10.1021/acs.inorgchem.0c01719
