Synonym
MYK07216; MYK-07216; MYK 07216; Fe(III) Deuteroporphyrin IX chloride;
InChi Key
MITFTGOXJCCKJD-YEGLKJMZSA-K
InChi Code
InChI=1S/C30H30N4O4.ClH.Fe/c1-15-9-20-12-25-17(3)21(5-7-29(35)36)27(33-25)14-28-22(6-8-30(37)38)18(4)26(34-28)13-24-16(2)10-19(32-24)11-23(15)31-20;;/h9-14H,5-8H2,1-4H3,(H4,31,32,33,34,35,36,37,38);1H;/q;;+3/p-3/b19-11-,20-12-,23-11-,24-13-,25-12-,26-13-,27-14-,28-14-;;
SMILES Code
CC1=C/C2=C/C3=C(C)C=C(N34)/C=C(C(C)=C5CCC(O)=O)\N=C5/C=C(C(CCC(O)=O)=C/6C)\N([Fe]4Cl)C6=C/C1=N2
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
599.87
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.) Wyllie, et al. NO Orientation and Tilting in (Nitrosyl)iron(II) Deuteroporphyrin IX. Inorg. Chem. 2003, 42, 14, 4259–4261. https://doi.org/10.1021/ic034364e
2.) Kelly, et al. Chlorite ion oxidation of the iron(III) complex of deuteroporphyrin IX. Inorg. Chem. 1981, 20, 4, 1086–1090. https://doi.org/10.1021/ic50218a026
3.) Teng, et al. Singlet Oxygen Generation in Ferriporphyrin-Polymer Dots Catalyzed Chemiluminescence System for Cancer Therapy. ACS Appl. Bio Mater. 2020, 3, 8, 5020–5029. https://doi.org/10.1021/acsabm.0c00522
4.) Kuter, et al. Hydrating the Bispropionate Notch in Malaria Pigment: A New Structural Motif in the Iron(III)(deuteroporphyrin) Dimer. Chemistry, a European Journal. Volume 25, Issue 17, March 21, 2019, Pages 4373-4378. https://doi.org/10.1002/chem.201805116
5.) Zhou, et al. Metallo-deuteroporphyrin as a novel catalyst for p-xylene oxidation using molecular oxygen. Inorganica Chimica Acta. Volume 382, 15 March 2012, Pages 167-170.
6.) Brault, et al. Reactions of iron(III) porphyrins with peroxyl radicals derived from halothane and halomethanes. J. Phys. Chem. 1984, 88, 13, 2857–2862. https://doi.org/10.1021/j150657a038
