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Merck
모든 사진(1)

문서

258806

Sigma-Aldrich

Mesoporphyrin IX dihydrochloride

synthetic, 95%

동의어(들):

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

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About This Item

실험식(Hill 표기법):
C34H38N4O4 · 2HCl
CAS Number:
Molecular Weight:
639.61
EC Number:
MDL number:
UNSPSC 코드:
12161600
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

95%

반응 적합성

core: porphyrin
reagent type: catalyst

λmax

401 nm

SMILES string

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-;;

InChI key

LLAQRSFKJHORNW-HXFTUNQESA-N

애플리케이션

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)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


시험 성적서(COA)

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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)
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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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