Synonym
meso-Tetra (2-carboxyphenyl) porphine;
IUPAC/Chemical Name
2,2',2'',2'''-(porphyrin-5,10,15,20-tetrayl)tetrabenzoic acid
InChi Key
GQUMTQCSESILQU-LWQDQPMZSA-N
InChi Code
InChI=1S/C48H30N4O8/c53-45(54)29-13-5-1-9-25(29)41-33-17-19-35(49-33)42(26-10-2-6-14-30(26)46(55)56)37-21-23-39(51-37)44(28-12-4-8-16-32(28)48(59)60)40-24-22-38(52-40)43(36-20-18-34(41)50-36)27-11-3-7-15-31(27)47(57)58/h1-24,49,52H,(H,53,54)(H,55,56)(H,57,58)(H,59,60)/b41-33-,41-34-,42-35-,42-37-,43-36-,43-38-,44-39-,44-40-
SMILES Code
O=C(O)C1=C(/C2=C3C=C/C(N\3)=C(C4=CC=CC=C4C(O)=O)/C5=N/C(C=C5)=C(C6=CC=CC=C6C(O)=O)\C7=CC=C(N7)/C(C8=CC=CC=C8C(O)=O)=C9N=C2C=C\9)C=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
790.79
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.) Leondiadis, et al. 5,10,15,20-Tetrakis(.alpha.,.alpha.,.alpha.,.alpha.-o-(N-tert-butyl-carbamoyl)phenyl)porphyrin: synthesis and redox properties of zinc(II) and copper(II) complexes. J. Org. Chem. 1989, 54, 26, 6135–6138. https://doi.org/10.1021/jo00287a034
2.) Nishino, et al. Induced circular dichroism of atropisomeric porphyrins by combined amino acid residues. J. Chem. Soc., Chem. Commun., 1992, 692-694. https://doi.org/10.1039/D2CC04230D
3.) Carver, et al. Electrocatalytic Oxygen Reduction by Iron Tetra-arylporphyrins Bearing Pendant Proton Relays. J. Am. Chem. Soc. 2012, 134, 12, 5444–5447. https://doi.org/10.1021/ja211987f
4.) Dai, et al. Ultrathin MOF nanosheet-based resistive sensors for highly sensitive detection of methanol. Chem. Commun., 2022,58, 11543-11546. https://doi.org/10.1039/D2CC04230D
