For research use only. Not for therapeutic Use.
Octaethylporphyrin(CAT: I008398) is a synthetic compound that belongs to the family of porphyrins, which are organic molecules that play a critical role in biological processes such as photosynthesis and oxygen transport in the blood. Octaethylporphyrin is often used as a model compound for studying the chemical and physical properties of natural porphyrins due to their structural similarity. It has been investigated for a range of applications including catalysis, photodynamic therapy, and sensing of metal ions. Octaethylporphyrin is typically a dark red solid and is soluble in organic solvents such as chloroform and methanol.
| Catalog Number | I008398 |
| CAS Number | 2683-82-1 |
| Synonyms | Octaethyl-porphyrin; Octaethylporphyrin; Octaethyl porphyrin;2,3,7,8,12,13,17,18-octaethylporphyrin |
| Molecular Formula | C36H46N4 |
| Purity | ≥95% |
| Solubility | Soluble in DMSO, not in water |
| Storage | Store at -20°C |
| IUPAC Name | 2,3,7,8,12,13,17,18-octaethyl-21,22-dihydroporphyrin |
| InChI | InChI=1S/C36H46N4/c1-9-21-22(10-2)30-18-32-25(13-5)26(14-6)34(39-32)20-36-28(16-8)27(15-7)35(40-36)19-33-24(12-4)23(11-3)31(38-33)17-29(21)37-30/h17-20,37-38H,9-16H2,1-8H3 |
| InChIKey | XFIIGRBIXXECHR-UHFFFAOYSA-N |
| SMILES | CCC1=C(C2=CC3=NC(=CC4=NC(=CC5=C(C(=C(N5)C=C1N2)CC)CC)C(=C4CC)CC)C(=C3CC)CC)CC |
| Reference | </br>1:Real-Time Visualization of the Precipitation and Phase Behavior of Octaethylporphyrin in Lipid Microparticles. Parra E, Hervella P, Needham D.J Pharm Sci. 2017 Apr;106(4):1025-1041. doi: 10.1016/j.xphs.2016.11.019. Epub 2016 Dec 9. PMID: 27956095 </br>2:The Unanticipated Dimerization of Ce@C<sub>2v</sub> (9)-C<sub>82</sub> upon Co-crystallization with Ni(octaethylporphyrin) and Comparison with Monomeric M@C<sub>2v</sub> (9)-C<sub>82</sub> (M = La, Sc, and Y). Suzuki M, Yamada M, Maeda Y, Sato S, Takano Y, Uhlík F, Slanina Z, Lian Y, Lu X, Nagase S, Olmstead MM, Balch AL, Akasaka T.Chemistry. 2016 Dec 12;22(50):18115-18122. doi: 10.1002/chem.201602595. Epub 2016 Oct 28. PMID: 27791293 </br>3:Fiber-optic fluorescence-quenching oxygen partial pressure sensor using platinum octaethylporphyrin. Davenport JJ, Hickey M, Phillips JP, Kyriacou PA.Appl Opt. 2016 Jul 20;55(21):5603-9. doi: 10.1364/AO.55.005603. PMID: 27463913 </br>4:Surface directed reversible imidazole ligation to nickel(ii) octaethylporphyrin at the solution/solid interface: a single molecule level study. Nandi G, Chilukuri B, Hipps KW, Mazur U.Phys Chem Chem Phys. 2016 Jul 27;18(30):20819-29. doi: 10.1039/c6cp04454a. PMID: 27416994 </br>5:X-ray Structure and Properties of the Ferrous Octaethylporphyrin Nitroxyl Complex. Kundakarla N, Lindeman S, Rahman MH, Ryan MD.Inorg Chem. 2016 Mar 7;55(5):2070-5. doi: 10.1021/acs.inorgchem.5b02384. Epub 2016 Feb 17. PMID: 26885766 </br>6:Highly sensitive broadband flexible photodetectors based on a blend film with zinc octaethylporphyrin long nanowires embedded in an insulating polymer. Yang JM, Wang FX, Pan GB.Nanoscale. 2016 Feb 7;8(5):2811-8. doi: 10.1039/c5nr08565a. PMID: 26763660 </br>7:Solvatochromic Stokes shift and determination of excited state dipole moments of free base and zinc octaethylporphyrin. Ghosh M, Sinha S.Spectrochim Acta A Mol Biomol Spectrosc. 2015;150:959-65. doi: 10.1016/j.saa.2015.06.057. Epub 2015 Jun 22. PMID: 26123513 </br>8:Effect of dispersion on surface interactions of cobalt(II) octaethylporphyrin monolayer on Au(111) and HOPG(0001) substrates: a comparative first principles study. Chilukuri B, Mazur U, Hipps KW.Phys Chem Chem Phys. 2014 Jul 21;16(27):14096-107. doi: 10.1039/c4cp01762e. Epub 2014 Jun 5. Erratum in: Phys Chem Chem Phys. 2014 Oct 7;16(37):20250. PMID: 24901459 </br>9:Preparation of cocrystal nanofibres of cobalt octaethylporphyrin and tetracyanoquinodimethane with good photoresponse. Wu HD, Xiao Y, Wang FX, Pan GB.J Nanosci Nanotechnol. 2014 Jun;14(6):4097-100. PMID: 24738357 </br>10:Adsorption geometry, conformation, and electronic structure of 2H-octaethylporphyrin on Ag(111) and Fe metalation in ultra high vacuum. Borghetti P, Di Santo G, Castellarin-Cudia C, Fanetti M, Sangaletti L, Magnano E, Bondino F, Goldoni A.J Chem Phys. 2013 Apr 14;138(14):144702. doi: 10.1063/1.4798934. PMID: 24981539 |
