Octaethylporphyrin

Octaethylporphyrin
Names
	Other names 2,3,7,8,12,13,17,18-Octaethyl-21H,23H-porphine
Identifiers
CAS Number	2683-82-1;
3D model (JSmol)	Interactive image;
Beilstein Reference	379798
ChEBI	CHEBI:52183;
ChemSpider	10445887;
EC Number	220-243-8;
PubChem CID	102311;
CompTox Dashboard (EPA)	DTXSID2062589;
	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/h17-20,37,40H,9-16H2,1-8H3/b29-17-,30-18-,31-17-,32-18-,33-19-,34-20-,35-19-,36-20- Key: HCIIFBHDBOCSAF-MUZKIALCSA-N;
	SMILES CCC1=C(C2=CC3=NC(=CC4=C(C(=C(N4)C=C5C(=C(C(=N5)C=C1N2)CC)CC)CC)CC)C(=C3CC)CC)CC;
Properties
Chemical formula	C36H46N4
Molar mass	534.792 g·mol−1
Appearance	purple solid
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Octaethylporphyrin (H₂OEP) is an organic compound that is a relative of naturally occurring heme pigments. The compound is used in the preparation of models for the prosthetic group in heme proteins. It is a dark purple solid that is soluble in organic solvents. When treated with ferric chloride in hot acetic acid solution, it forms the square pyramidal complex Fe(OEP)Cl.[1] It also forms the square planar complexes Ni(OEP) and Cu(OEP).

Saturated solution of H₂OEP in dichloromethane.

Unlike naturally occurring porphyrins, the conjugate base of H₂OEP has four-fold symmetry, which simplifies spectroscopic analysis. In contrast to tetraphenylporphyrin and related analogues, H2OEP features unprotected meso positions. In this way, it is a more accurate model for naturally occurring porphyrins.

H₂OEP is prepared by condensation of 3,4-diethylpyrrole with formaldehyde.[2]

References

Chang, C. K.; DiNello, R. K.; Dolphin, D. (1980). "Iron Porphines". Inorg. Synth. 20: 147. doi:10.1002/9780470132517.ch35.
Sessler, Jonathan L.; Mozaffari, Azadeh; Johnson, Martin R. (1992). "3,4-Diethylpyrrole and 2,3,7,8,12,13,17,18-Octaethylporphyrin". Org. Synth. 70: 68. doi:10.15227/orgsyn.070.0068.

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[1] Chang, C. K.; DiNello, R. K.; Dolphin, D. (1980). "Iron Porphines". Inorg. Synth. 20: 147. doi:10.1002/9780470132517.ch35.

[2] Sessler, Jonathan L.; Mozaffari, Azadeh; Johnson, Martin R. (1992). "3,4-Diethylpyrrole and 2,3,7,8,12,13,17,18-Octaethylporphyrin". Org. Synth. 70: 68. doi:10.15227/orgsyn.070.0068.