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379549

Sigma-Aldrich

Iron(II) phthalocyanine

Dye content ~90 %

Synonym(s):

Phthalocyanine iron(II) salt

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About This Item

Empirical Formula (Hill Notation):
C32H16FeN8
CAS Number:
132-16-1
Molecular Weight:
568.37
EC Number:
205-047-2
MDL number:
MFCD00015953
UNSPSC Code:
12352103
PubChem Substance ID:
24863668
NACRES:
NA.23

form

powder

composition

Dye content, ~90%

λmax

657 nm

SMILES string

[Fe]1n2c3nc4nc(nc5n1c(nc6nc(nc2c7ccccc37)c8ccccc68)c9ccccc59)c%10ccccc4%10

InChI

1S/C32H16N8.Fe/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25;/h1-16H;/q-2;+2

InChI key

MIINHRNQLVVCEW-UHFFFAOYSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Anton A Ciucu et al.
Biosensors & bioelectronics, 18(2-3), 303-310 (2002-12-18)
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 coupled with acetylcholinesterase and choline oxidase co-immobilized onto the surface of a dialysis
J Fukui et al.
Journal of the American Geriatrics Society, 38(8), 889-892 (1990-08-01)
The authors designed a new pad for urinary incontinence. It is composed of a cloth of acrylonitrile copper sulfide and another cloth of iron-phthalocyanine. In vitro experiments showed that acrylonitrile copper sulfide cloth inhibited the growth of most bacteria causing
H Ozaki et al.
Biochimica et biophysica acta, 955(2), 220-230 (1988-07-20)
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, 1H-NMR and infrared spectroscopy. Complexes of chelated ferromesoheme, the model compound, with 2-methyl-, 2-ethyl, 2-isopropyl- or
R F Parton et al.
Nature, 370(6490), 541-544 (1994-08-18)
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 mimicry of the protein environment is difficult to achieve. Heterogeneous mimics

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