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258806

Sigma-Aldrich

Mesoporphyrin IX dihydrochloride

synthetic, 95%

Sinonimo/i:

7,12-Diethyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropionic acid dihydrochloride

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About This Item

Formula empirica (notazione di Hill):
C34H38N4O4 · 2HCl
Numero CAS:
68938-72-7
Peso molecolare:
639.61
Numero CE:
273-141-0
Numero MDL:
MFCD00136049
Codice UNSPSC:
12161600
ID PubChem:
24855661
NACRES:
NA.22

Livello qualitativo

100

Saggio

95%

Impiego in reazioni chimiche

core: porphyrin
reagent type: catalyst

λmax

401 nm

Stringa SMILE

Cl.Cl.CCc1c(C)c2cc3[nH]c(cc4nc(cc5[nH]c(cc1n2)c(C)c5CCC(O)=O)c(CCC(O)=O)c4C)c(C)c3CC

InChI

1S/C34H38N4O4.2ClH/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;;/h13-16,35,38H,7-12H2,1-6H3,(H,39,40)(H,41,42);2*1H/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;;
LLAQRSFKJHORNW-HXFTUNQESA-N

Applicazioni

Reactant in constructing efficient dye-sensitized solar cells

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
MKCT8713
MKCR1775
MKCF9445
MKCC8195
MKBV0344V

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Monika S Walczak et al.
The journal of physical chemistry. B, 115(5), 1145-1150 (2010-12-31)
X-ray absorption spectroscopy is used to determine the local atomic structure around the iron atom from a soluble synthetic analogue of malaria pigment (hemozoin), cf. ferrimesoporphyrin IX of mesohematin anhydride, in the absence or presence of chloroquine (CQ) in dimethyl
F A Lara et al.
Biochemical and biophysical research communications, 355(1), 16-22 (2007-02-13)
Epimastigotes multiplies in the insect midgut by taking up nutrients present in the blood meal including heme bound to hemoglobin of red blood cell. During blood meal digestion by vector proteases in the posterior midgut, hemoglobin is clipped off into
J Koster et al.
The journal of physical chemistry. A, 110(39), 11252-11259 (2006-09-29)
The symmetry properties of selected vibrational modes of mesoporphyrin IX dimethyl ester (MP-IX-DME) in solution are investigated under different electronic resonance conditions. The Raman band parameters of the macrocycle modes nu(2), nu(10), nu(11), and nu(19) are determined from a quantitative
Roxanne Kieltyka et al.
Methods in molecular biology (Clifton, N.J.), 608, 223-255 (2009-12-17)
Telomerase inhibition through guanine quadruplex sequestration by small-molecule drugs is of great current interest as an anticancer strategy. G-quadruplexes (GQs) can be formed at the guanine-rich sequences found at the end of the telomere. They possess a large electron-rich pi-surface
Naoki Hosomi et al.
Journal of bioscience and bioengineering, 99(3), 222-229 (2005-10-20)
Monoclonal antibody 2D7 generated against a transition-state analog N-methyl mesoporphyrin catalyzes a reaction for insertion of a cupric ion into mesoporphyrin. To investigate amino acid residues responsible for the catalytic activity, site-directed mutagenesis of the amino acid residues in the
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