Synonym
FLN43738; FLN 43738; FLN-43738; meso-Tetra(4-nitrophenyl) porphine; 5,10,15,20-tetrakis(4-nitrophenyl)porphyrin;
IUPAC/Chemical Name
5,10,15,20-tetrakis(4-nitrophenyl)porphyrin
InChi Key
FVHZCBQLLFLQAG-LWQDQPMZSA-N
InChi Code
InChI=1S/C44H26N8O8/c53-49(54)29-9-1-25(2-10-29)41-33-17-19-35(45-33)42(26-3-11-30(12-4-26)50(55)56)37-21-23-39(47-37)44(28-7-15-32(16-8-28)52(59)60)40-24-22-38(48-40)43(36-20-18-34(41)46-36)27-5-13-31(14-6-27)51(57)58/h1-24,45,48H/b41-33-,41-34-,42-35-,42-37-,43-36-,43-38-,44-39-,44-40-
SMILES Code
O=[N+](C(C=C1)=CC=C1/C(C2=N/C(C=C2)=C(C3=CC=C([N+]([O-])=O)C=C3)\C4=CC=C5N4)=C6N/C(C=C/6)=C(C7=CC=C([N+]([O-])=O)C=C7)\C8=N/C(C=C8)=C5/C9=CC=C([N+]([O-])=O)C=C9)[O-]
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
794.74
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.) Li, et al. Porous Azo-Bridged Porphyrin–Phthalocyanine Network with High Iodine Capture Capability. Chemistry – A European Journal, 2016, vol. 22, # 33, p. 11863 – 11868. https://doi.org/10.1002/chem.201602337
2.) Xu, et al. New nitrogen-rich azo-bridged porphyrin-conjugated microporous networks for high performance of gas capture and storage. RSC Advances, 2016, vol. 6, # 36, p. 30048 – 30055. https://doi.org/10.1039/C6RA04077B
3.) Dogan, et al. Gold Recovery from E-Waste by Porous Porphyrin-Phenazine Network Polymers. Chemistry of Materials, 2020, vol. 32, # 12, p. 5343 – 5349. https://doi.org/10.1021/acs.chemmater.0c01734
4.) Feng, et al. Catalytic oxidation of cyclohexane to KA oil by zinc oxide supported manganese 5,10,15,20-tetrakis(4-nitrophenyl)porphyrin. Journal of Molecular Catalysis A: Chemical, 2015, vol. 410, p. 221 – 225. https://doi.org/10.1016/j.molcata.2015.09.027
5.) Zhang, et al. Directing two azo-bridged covalent metalloporphyrinic polymers as highly efficient catalysts for selective oxidation. Applied Catalysis A: General, 2015, vol. 489, # 1, p. 117 – 122. https://doi.org/10.1016/j.apcata.2014.10.023
6.) Huang, et al. Catalysis behavior of boehmite-supported iron tetraphenylporphyrins with nitro and methoxyl substituents for the aerobic oxidation of cyclohexane. Journal of Molecular Catalysis A: Chemical, 2011, vol. 340, # 1-2, p. 60 – 64. https://doi.org/10.1016/j.molcata.2011.03.010
