Synonym
JXN10736; JXN 10736; JXN-10736; 5,10-Diphenyl-15,20-di(4-pyridyl)-21H,23H-porphine; 5,20-diphenyl-10,15-di(pyridin-4-yl)porphyrin;
IUPAC/Chemical Name
5,20-diphenyl-10,15-di(pyridin-4-yl)porphyrin
InChi Key
JDYAHFKHYRTJHC-XGGOTWSRSA-N
InChi Code
InChI=1S/C42H28N6/c1-3-7-27(8-4-1)39-31-11-12-32(45-31)40(28-9-5-2-6-10-28)34-14-16-36(47-34)42(30-21-25-44-26-22-30)38-18-17-37(48-38)41(29-19-23-43-24-20-29)35-15-13-33(39)46-35/h1-26,45,48H/b39-31-,39-33-,40-32-,40-34-,41-35-,41-37-,42-36-,42-38-
SMILES Code
C1(/C2=C3N=C(/C(C4=CC=NC=C4)=C(C=C/5)\NC5=C(C6=N/C(C=C6)=C(C7=CC=C2N7)/C8=CC=CC=C8)\C9=CC=NC=C9)C=C/3)=CC=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
616.73
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.) Vidal, et al. A Flexible Synthetic Strategy for the Preparation of Heteroleptic Metallacycles of Porphyrins. Inorg. Chem. 2021, 60, 15, 11503–11513. https://doi.org/10.1021/acs.inorgchem.1c01511
2.) Drain, et al. Self-assembly of square multiporphyrin arrays by metal ion coordination. J. Chem. Soc., Chem. Commun., 1994, 2313-2315. https://doi.org/10.1039/C39940002313
3.) Lengo, et al. A Functionalized Noncovalent Macrocyclic Multiporphyrin Assembly from a Dizinc(II) Bis-Porphyrin Receptor and a Free-Base Dipyridylporphyrin. Chemistry, A European Journal. Volume 9, Issue 23, December 5, 2003, Pages 5879-5887. https://doi.org/10.1002/chem.200304795
4.) Zhang, et al. A Discrete Platinum(II) Amphiphile: Construction, Characterization, and Controllable Self-Assembly in Different Solvents. Inorg. Chem. 2020, 59, 12, 7924–7927. https://doi.org/10.1021/acs.inorgchem.0c01164
5.) Horiguchi, et al. Controllable Direction of Porphyrin Derivatives in Two Cyclodextrin Cavities. EurJOC. Volume 2018, Issue 18, May 15, 2018, Pages 2138-2143. https://doi.org/10.1002/ejoc.201800433
