Chloro protoporphyrinato iron 3 hemin

Manufactured by Merck Group

Chloro(protoporphyrinato)iron(III), commonly known as Hemin, is a chemical compound that consists of an iron(III) center coordinated to a protoporphyrin IX ligand. It is a reddish-brown crystalline solid that is widely used in various research and laboratory applications.

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Lab products found in correlation

Sodium hydroxide (naoh), by Merck Group (1 mentions) Milli q water 18 mω cm, by Merck Group (1 mentions) Phenol, by Merck Group (1 mentions) Benzaldehyde, by Merck Group (1 mentions) Benzyl alcohol, by Merck Group (1 mentions) Ferrocenecarboxylic acid, by ABCR (1 mentions) N n diisopropylethylamine diea, by Merck Group (1 mentions)

Close spelling variants of this product

Hemin (689 citations) Iron III (2 citations)

2 protocols using chloro protoporphyrinato iron 3 hemin

Hemin Preparation in Aqueous NaOH

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Chloro(protoporphyrinato)iron(III) (Hemin) and NaOH were purchased from Sigma Aldrich (St. Louis, MO). Milli-Q water (18 MΩ-cm, Millipore Corp., Burlington MA) was used to prepare 10 mM hemin solution in 0.1M aqueous NaOH. Blood-collection bags (4R1582) were purchased from Fenwal Inc. (Lake Zurich, IL).

Gautam R., Oh J.Y., Patel R.P, & Dluhy R.A. (2018). Non-Invasive Analysis of Stored Red Blood Cells Using Diffuse Resonance Raman Spectroscopy. The Analyst, 143(24), 5950-5958.

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Synthesis of Iron(III) Porphyrin Complexes

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All reagents and chemicals were purchased from commercial sources and used without further purification. Ferrocenecarboxylic acid was purchased from Abcr. Chloro(protoporphyrinato)iron(III) (hemin), benzyl alcohol, benzaldehyde, phenol and N,N-diisopropylethylamine (DIEA) were purchased from Sigma-Aldrich.

Śmiłowicz D., Kogelheide F., Schöne A.L., Stapelmann K., Awakowicz P, & Metzler-Nolte N. (2020). Catalytic oxidation of small organic molecules by cold plasma in solution in the presence of molecular iron complexes†. Scientific Reports, 10, 21652.

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