CAS 132-16-1|[29H,31H-Phthalocyaninato(2-)-κ2N29,N31]iron
Introduction：Basic information about CAS 132-16-1|[29H,31H-Phthalocyaninato(2-)-κ2N29,N31]iron, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | [29H,31H-Phthalocyaninato(2-)-κ2N29,N31]iron | ||
|---|---|---|---|
| CAS Number | 132-16-1 | Molecular Weight | 568.368 |
| Density | / | Boiling Point | / |
| Molecular Formula | C32H16FeN8 | Melting Point | / |
| MSDS | ChineseUSA | Flash Point | / |
Names
| Name | Iron phthalocyanine |
|---|---|
| Synonym | More Synonyms |
Chemical & Physical Properties
| Molecular Formula | C32H16FeN8 |
|---|---|
| Molecular Weight | 568.368 |
| Exact Mass | 568.084717 |
| PSA | 84.02000 |
| LogP | 1.46190 |
| InChIKey | MIINHRNQLVVCEW-UHFFFAOYSA-N |
| SMILES | [Fe+2].c1ccc2c(c1)-c1nc-2nc2[n-]c(nc3nc(nc4[n-]c(n1)c1ccccc41)-c1ccccc1-3)c1ccccc21 |
| Water Solubility | It is insoluble in water. It is soluble in conc. sulfuric acid. |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| Safety Phrases | S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
Articles4
More Articles| An efficient mimic of cytochrome P-450 from a zeolite-encaged iron complex in a polymer membrane. Nature 370(6490) , 541-4, (1994) Many attempts have been made to mimic the catalytic oxidative properties of the enzyme cytochrome P-450. For homogeneous systems the mechanisms of oxidation can be readily determined but proper mimicr... | |
| Detection of pesticides using an amperometric biosensor based on ferophthalocyanine chemically modified carbon paste electrode and immobilized bienzymatic system. Biosens. Bioelectron. 18(2-3) , 303-10, (2003) A new highly sensitive amperometric method for the detection of organophosphorus compounds has been developed. The method is based on a ferophthalocyanine chemically modified carbon paste electrode co... | |
| Bonding of nitrosobenzene and phenyl isocyanide to chelated mesoheme, hemoglobin and ferrous phthalocyanine. Biochim. Biophys. Acta 955(2) , 220-30, (1988) Reactions of nitrosobenzene, phenyl isocyanide and their ring-substituted analogues with hemoglobin, ferrous phthalocyanine and a synthetic model compound of hemoglobin were investigated by optical, 1... |
Synonyms
| EINECS 205-047-2 |
| Ferrous phthalocyanine |
| MFCD00015953 |
| Iron(II) Phthalocyanine |
| Fe pythalocyanine |
| Iron, [29H,31H-phthalocyaninato(2-)-κN,κN]- |
| Phthalocyanine Iron(II) |
| [29H,31H-Phthalocyaninato(2-)-κN,N]iron |
| Phthalocyanine iron(II) salt |
| Fe phthalocyanine |
