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| Product | Description | |
|---|---|---|
| 5,10,15,20-Tetra(4-pyridyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetra(4-pyridyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetra(4-pyridyl)-21H,23H-porphine. CAS No. 16834-13-2. Pack Sizes: 1G-Glass Bottle with Plastic Insert. Product ID: 5,10,15,20-tetrapyridin-4-yl-21,23-dihydroporphyrin. Molecular formula: 618.7. Mole weight: C40H26N8. C1=CC2=C (C3=NC (=C (C4=CC=C (N4) C (=C5C=CC (=N5) C (=C1N2) C6=CC=NC=C6) C7=CC=NC=C7) C8=CC=NC=C8) C=C3) C9=CC=NC=C9. DNZSHSJERXNJGX-UHFFFAOYSA-N. InChI=1S/C40H26N8/c1-2-30-38 (26-11-19-42-20-12-26)32-5-6-34 (47-32)40 (28-15-23-44-24-16-28)36-8-7-35 (48-36)39 (27-13-21-43-22-14-27)33-4-3-31 (46-33)37 (29 (1)45-30)25-9-17-41-18-10-25/h1-24, 45, 48H. >93.0%(HPLC). |  |
| 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphine. CAS No. 37083-37-7. Pack Sizes: 100MG-Glass Bottle with Plastic Insert. Product ID: 5,10,15,20-tetrakis(2,6-dichlorophenyl)-21,23-dihydroporphyrin. Molecular formula: 890.29. Mole weight: C44H22Cl8N4. C1=CC (=C (C (=C1)Cl)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=C (C=CC=C7Cl)Cl)C8=C (C=CC=C8Cl)Cl)C=C4)C9=C (C=CC=C9Cl)Cl)N3)Cl. InChI=1S/C44H22Cl8N4/c45-21-5-1-6-22 (46)37 (21)41-29-13-15-31 (53-29)42 (38-23 (47)7-2-8-24 (38)48)33-17-19-35 (55-33)44 (40-27 (51)11-4-12-28 (40)52)36-20-18-34 (56-36)43 (32-16-14-30 (41)54-32)39-25 (49)9-3-10-26 (39)50/h1-20, 53, 56H. UQASJTNIEXIESH-UHFFFAOYSA-N. >95.0%(HPLC). | |
| 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)-21H,23H-porphine. CAS No. 145764-54-1. Product ID: 5-[10,15,20-tris(3,5-dihydroxyphenyl)-21,24-dihydroporphyrin-5-yl]benzene-1,3-diol. Molecular formula: 742.74. Mole weight: C44H30N4O8. C1=CC2=C (C3=NC (=C (C4=CC=C (N4)C (=C5C=CC (=N5)C (=C1N2)C6=CC (=CC (=C6)O)O)C7=CC (=CC (=C7)O)O)C8=CC (=CC (=C8)O)O)C=C3)C9=CC (=CC (=C9)O)O. InChI=1S/C44H30N4O8/c49-25-9-21 (10-26 (50)17-25)41-33-1-2-34 (45-33)42 (22-11-27 (51)18-28 (52)12-22)36-5-6-38 (47-36)44 (24-15-31 (55)20-32 (56)16-24)40-8-7-39 (48-40)43 (37-4-3-35 (41)46-37)23-13-29 (53)19-30 (54)14-23/h1-20, 45, 48-56H. XDVQXKKXBXLGCO-UHFFFAOYSA-N. >90.0%(HPLC). | |
| 5,10,15,20-Tetrakis(3,5-dimethoxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(3,5-dimethoxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(3,5-dimethoxyphenyl)-21H,23H-porphine. CAS No. 74684-34-7. Product ID: 5,10,15,20-tetrakis(3,5-dimethoxyphenyl)-21,23-dihydroporphyrin. Molecular formula: 854.96. Mole weight: C52H46N4O8. COC1=CC (=CC (=C1)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC (=CC (=C7)OC)OC)C8=CC (=CC (=C8)OC)OC)C=C4)C9=CC (=CC (=C9)OC)OC)N3)OC. InChI=1S/C52H46N4O8/c1-57-33-17-29 (18-34 (25-33)58-2)49-41-9-11-43 (53-41)50 (30-19-35 (59-3)26-36 (20-30)60-4)45-13-15-47 (55-45)52 (32-23-39 (63-7)28-40 (24-32)64-8)48-16-14-46 (56-48)51 (44-12-10-42 (49)54-44)31-21-37 (61-5)27-38 (22-31)62-6/h9-28, 53, 56H, 1-8H3. YNXRFPUCCCJMPX-UHFFFAOYSA-N. >95.0%(HPLC). | |
| 5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(4-hydroxyphenyl)-21H,23H-porphine. CAS No. 51094-17-8. Product ID: 4-[10,15,20-tris(4-hydroxyphenyl)-21,23-dihydroporphyrin-5-yl]phenol. Molecular formula: 678.75. Mole weight: C44H30N4O4. C1=CC (=CC=C1C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC=C (C=C7)O)C8=CC=C (C=C8)O)C=C4)C9=CC=C (C=C9)O)N3)O. InChI=1S/C44H30N4O4/c49-29-9-1-25 (2-10-29)41-33-17-19-35 (45-33)42 (26-3-11-30 (50)12-4-26)37-21-23-39 (47-37)44 (28-7-15-32 (52)16-8-28)40-24-22-38 (48-40)43 (36-20-18-34 (41)46-36)27-5-13-31 (51)14-6-27/h1-24, 45, 48-52H. VFHDWGAEEDVVPD-UHFFFAOYSA-N. >95.0%(HPLC). | |
| 5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexes other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(4-methoxyphenyl)-21H,23H-porphine. CAS No. 22112-78-3. Product ID: 5,10,15,20-tetrakis(4-methoxyphenyl)-21,23-dihydroporphyrin. Molecular formula: 734.86. Mole weight: C48H38N4O4. COC1=CC=C (C=C1)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC=C (C=C7)OC)C8=CC=C (C=C8)OC)C=C4)C9=CC=C (C=C9)OC)N3. InChI=1S/C48H38N4O4/c1-53-33-13-5-29 (6-14-33)45-37-21-23-39 (49-37)46 (30-7-15-34 (54-2)16-8-30)41-25-27-43 (51-41)48 (32-11-19-36 (56-4)20-12-32)44-28-26-42 (52-44)47 (40-24-22-38 (45)50-40)31-9-17-35 (55-3)18-10-31/h5-28, 49, 52H, 1-4H3. PJOJZHHAECOAFH-UHFFFAOYSA-N. >97.0%(T)(HPLC). | |
| [5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrinato]cobalt(II) | Alfa Chemistry offers [5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrinato]cobalt(II) products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Magnetic metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: [5,10,15,20-Tetrakis(4-methoxyphenyl)-21H,23H-porphinato]cobalt(II). CAS No. 28903-71-1. Product ID: cobalt(2+); 5,10,15,20-tetrakis(4-methoxyphenyl)porphyrin-22,23-diide. Molecular formula: 791.77. Mole weight: C48H36CoN4O4. COC1=CC=C (C=C1)C2=C3C=CC (=C (C4=CC=C ([N-]4)C (=C5C=CC (=N5)C (=C6C=CC2=N6)C7=CC=C (C=C7)OC)C8=CC=C (C=C8)OC)C9=CC=C (C=C9)OC)[N-]3. [Co+2]. QBCIMRXPMLWVML-UHFFFAOYSA-N. >96.0%(T). | |
| 5,10,15,20-Tetrakis[4-(per-O-methyl-α-cyclodextrin-6-yloxy)phenyl]porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis[4-(per-O-methyl-α-cyclodextrin-6-yloxy)phenyl]porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Supramolecular host materials. Alternative Names: 5,10,15,20-Tetrakis[4-(per-O-methyl-α-cyclodextrin-6-yloxy)phenyl]-21H,23H-porphine. Molecular formula: 5451.91. Mole weight: C256H398N4O120. | |
| 5,10,15,20-Tetrakis(pentafluorophenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(pentafluorophenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexes other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(perfluorophenyl)porphyrin 5,10,15,20-Tetrakis(pentafluorophenyl)-21H,23H-porphine. CAS No. 25440-14-6. Pack Sizes: 100MG-Glass Bottle with Plastic Insert. Product ID: 5,10,15,20-tetrakis(2,3,4,5,6-pentafluorophenyl)-21,23-dihydroporphyrin. Molecular formula: 974.56. Mole weight: C44H10F20N4. C1=CC2=C (C3=NC (=C (C4=CC=C (N4)C (=C5C=CC (=N5)C (=C1N2)C6=C (C (=C (C (=C6F)F)F)F)F)C7=C (C (=C (C (=C7F)F)F)F)F)C8=C (C (=C (C (=C8F)F)F)F)F)C=C3)C9=C (C (=C (C (=C9F)F)F)F)F. InChI=1S/C44H10F20N4/c45-25-21 (26 (46)34 (54)41 (61)33 (25)53)17-9-1-2-10 (65-9)18 (22-27 (47)35 (55)42 (62)36 (56)28 (22)48)12-5-6-14 (67-12)20 (24-31 (51)39 (59)44 (64)40 (60)32 (24)52)16-8-7-15 (68-16)19 | |
| [5, 15-Bis (phenylethynyl) -10, 20-bis[ (triisopropylsilyl) ethynyl]porphyrinato]magnesium (II) | Alfa Chemistry offers [5, 15-Bis (phenylethynyl) -10, 20-bis[ (triisopropylsilyl) ethynyl]porphyrinato]magnesium (II) products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Dye-sensitized solar cell (dssc) materials electronic materials organic solar cell (opv) materials phthalocyanine dyes, porphyrin dyes. CAS No. 1397288-30-0. Molecular formula: 893.62. Mole weight: C58H60MgN4Si2. >95.0%(HPLC). | |
| 5,15-Diphenylporphyrin | Alfa Chemistry offers 5,15-Diphenylporphyrin Chloride products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,15-Diphenyl-21H,23H-porphine. CAS No. 22112-89-6. Product ID: 10,20-diphenyl-21,22-dihydroporphyrin. Molecular formula: 462.56. Mole weight: C32H22N4. C1=CC=C (C=C1)C2=C3C=CC (=CC4=CC=C (N4)C (=C5C=CC (=N5)C=C6C=CC2=N6)C7=CC=CC=C7)N3. InChI=1S/C32H22N4/c1-3-7-21 (8-4-1)31-27-15-11-23 (33-27)19-25-13-17-29 (35-25)32 (22-9-5-2-6-10-22)30-18-14-26 (36-30)20-24-12-16-28 (31)34-24/h1-20, 33, 35H. QIBKIAFNCVIIMG-UHFFFAOYSA-N. >90.0%(HPLC). | |
| 5-(4-CArboxyphenyl)-10,15,20-triphenylporphyrin | Alfa Chemistry offers 5-(4-Carboxyphenyl)-10,15,20-triphenylporphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexes other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: 5-(4-Carboxyphenyl)-10,15,20-triphenyl-21H,23H-porphine. CAS No. 95051-10-8. Product ID: 4-(10,15,20-triphenyl-21,23-dihydroporphyrin-5-yl)benzoic acid. Molecular formula: 658.76. Mole weight: C45H30N4O2. C1=CC=C (C=C1)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC=CC=C7)C8=CC=C (C=C8)C (=O)O)C=C4)C9=CC=CC=C9)N3. GZTMFXHPFNRUNU-UHFFFAOYSA-N. InChI=1S/C45H30N4O2/c50-45 (51)32-18-16-31 (17-19-32)44-39-26-24-37 (48-39)42 (29-12-6-2-7-13-29)35-22-20-33 (46-35)41 (28-10-4-1-5-11-28)34-21-23-36 (47-34)43 (30-14-8-3-9-15-30)38-25-27-40 (44)49-38/h1-27, 46, 49H, (H, 50, 51). >98.0%(HPLC). | |
| 5-(4-Methoxycarbonylphenyl)-10,15,20-triphenylporphyrin | Alfa Chemistry offers 5-(4-Methoxycarbonylphenyl)-10,15,20-triphenylporphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexes other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: 5-(4-Carbomethoxyphenyl)-10,15,20-triphenylporphyrin 5-(4-Methoxycarbonylphenyl)-10,15,20-triphenyl-21H,23H-porphine. CAS No. 119730-06-2. Product ID: methyl 4-(10,15,20-triphenyl-21,23-dihydroporphyrin-5-yl)benzoate. Molecular formula: 672.79. Mole weight: C46H32N4O2. COC (=O) C1=CC=C (C=C1) C2=C3C=CC (=N3) C (=C4C=CC (=C (C5=NC (=C (C6=CC=C2N6) C7=CC=CC=C7) C=C5) C8=CC=CC=C8) N4) C9=CC=CC=C9. AUUXSDUVWMAVMR-UHFFFAOYSA-N. InChI=1S/C46H32N4O2/c1-52-46 (51)33-19-17-32 (18-20-33)45-40-27-25-38 (49-40)43 (30-13-7-3-8-14-30)36-23-21-34 (47-36)42 (29-11-5-2-6-12-29)35-22-24-37 (48-35)44 (31-15-9-4-10-16-31)39-26-28-41 (45)50-39/h2-28, 47, 50H, 1H3. >90.0%(HPLC). | |
| Bilirubin oxidase | Bilirubin oxidase (BOD) is a multi-copper oxidase that catalyzes the oxidation of bilirubin to biliverdin and reduces molecular oxygen to water. Bilirubin oxidase can participate in the metabolism of porphyrin and chlorophyll, and is widely used in biochemical research as a catalyst for oxygen reduction [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BOD. CAS No. 80619-01-8. Pack Sizes: 250 U; 500 U; 1000 U. Product ID: HY-P2888. |  |
| Cobalt(II) Tetraphenylporphyrin | Alfa Chemistry offers Cobalt(II) Tetraphenylporphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Magnetic metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetraphenyl-21H,23H-porphine Cobalt(II) Cobalt(II) TPP CoTPP (meso-Tetraphenylporphinato)Cobalt(II) Cobalt(II) meso-Tetraphenylporphine. CAS No. 14172-90-8. Product ID: cobalt(2+); 5,10,15,20-tetraphenylporphyrin-22,24-diide. Molecular formula: 671.67. Mole weight: C44H28CoN4. C1=CC=C (C=C1) C2=C3C=CC (=C (C4=NC (=C (C5=CC=C ([N-]5) C (=C6C=CC2=N6) C7=CC=CC=C7) C8=CC=CC=C8) C=C4) C9=CC=CC=C9) [N-]3. [Co+2]. InChI=1S/C44H28N4. Co/c1-5-13-29 (14-6-1)41-33-21-23-35 (45-33)42 (30-15-7-2-8-16-30)37-25-27-39 (47-37)44 (32-19-11-4-12-20-32)40-28-26-38 (48-40)43 (31-17-9-3-10-18-31)36-24-22-34 (41)46-36; /h1-28H; /q-2; +2. LSZLYWSRWXFMOI-UHFFFAOYSA-N. >80.0%(HPLC). | |
| Cobalt(II) TPP | 5,10,15,20-Tetraphenyl-21H,23H-porphine cobalt(II), commonly known as CoTPP or cobalt porphyrin, is a coordination compound. 5,10,15,20-Tetraphenyl-21H,23H-porphine cobalt(II) is widely used in various fields such as catalysis, sensing, and organic electronics because of its unique electronic and optical properties. An efficient catalyst for reactions including oxidation, reduction, and CH bond activation, moreover, it has been used as a fluorescent probe for detecting oxygen content in biological systems and as an active material in organic solar cells. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 14172-90-8. Pack Sizes: 100 mg; 500 mg; 1 g. Product ID: HY-W073013. | |
| Fetpps | FeTPPS, a 5,10,15,20-tetrakis (4-sulfonatophenyl) porphyrin iron III chloride peroxynitrite decomposition catalyst, possesses evident neuroprotective effects in a experimental model of spinal cord damage. FeTPPS acts as a peroxynitrite scavenger and anti-nitrating agent in vivo. FeTPPS reduces nitric oxide (NO) production and apoptosis process. Uses: Designed for use in research and industrial production. Additional or Alternative Names: FeTPPS;Fe(III) meso-tetra(4-sulfonatophenyl)porphine chloride (acid form). Product Category: Inhibitors. Appearance: Solid. CAS No. 90384-82-0. Molecular formula: C44H28ClFeN4O12S4. Mole weight: 1024.27. Canonical SMILES: O=S([O-])(C1=CC=C(C(C(C=C2)=[N]3C2=C(C4=CC=C5C(C6=CC=C(S(=O)([O-])=O)C=C6)=C7C=C8)C9=CC=C(S(=O)([O-])=O)C=C9)=C%10C=CC%11=C(C%12=CC=C(S(=O)([O-])=O)C=C%12)C8=[N]7[Fe+3]3([Cl-])([N-]45)[N-]%10%11)C=C1)=O.[4H+]. Product ID: ACM90384820. Alfa Chemistry ISO 9001:2015 Certified. Categories: Fe(TPP)Cl. |  |
| FeTPPS | A peroxynitrite decomposition catalyst. An iron porphyrin complex that catalytically isomerizes peroxynitrite to nitrate both in vivo and in vitro thus serving as a decomposition catalyst and a selective peroxynitrite scavenger. Does not complex with nitric oxide and exhibits little SOD mimetic activity. Group: Biochemicals. Alternative Names: 5, 10, 15, 20-Tetrakis (4-sulfonatophenyl) porphyrinato Iron (III), Chloride. Grades: Highly Purified. CAS No. 90384-82-0. Pack Sizes: 25mg, 100mg. US Biological Life Sciences. |  Worldwide |
| FeTPPS | FeTPPS, a 5,10,15,20-tetrakis (4-sulfonatophenyl) porphyrin iron III chloride peroxynitrite decomposition catalyst, possesses evident neuroprotective effects in a experimental model of spinal cord damage [1]. FeTPPS acts as a peroxynitrite scavenger and anti-nitrating agent in vivo. FeTPPS reduces nitric oxide ( NO ) production and apoptosis process [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 90384-82-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-131697. | |
| Manganese Tetrakis (2, 6-dichlorophenyl) porphyrin Chloride | Manganese Tetrakis (2, 6-dichlorophenyl) porphyrin Chloride is a catalyst used for oxidation of hydrocarbons. Group: Biochemicals. Grades: Highly Purified. CAS No. 91463-17-1. Pack Sizes: 5mg, 50mg. Molecular Formula: C44H20Cl9MnN4, Molecular Weight: 978.67. US Biological Life Sciences. | Worldwide |
| YD2 | Alfa Chemistry offers YD2 products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Dye-sensitized solar cell (dssc) materials phthalocyanine dyes, porphyrin dyes. Alternative Names: [5-[Bis(4-hexylphenyl)amino]-15-[2-(4-carboxyphenyl)ethynyl]-10,20-bis(3,5-di-tert-butylphenyl)porphyrinato]zinc(II). CAS No. 1201915-91-4. Product ID: zinc; 4-[2-[10,20-bis(3,5-ditert-butylphenyl)-15-(4-hexyl-N-(4-hexylphenyl)anilino)porphyrin-22,24-diid-5-yl]ethynyl]benzoic acid. Molecular formula: 1230.02. Mole weight: C81H89N5O2Zn. CCCCCCC1=CC=C (C=C1)N (C2=CC=C (C=C2)CCCCCC)C3=C4C=CC (=N4)C (=C5C=CC (=C (C6=NC (=C (C7=CC=C3[N-]7)C8=CC (=CC (=C8)C (C) (C)C)C (C) (C)C)C=C6)C#CC9=CC=C (C=C9)C (=O)O)[N-]5)C1=CC (=CC (=C1)C (C) (C)C)C (C) (C)C. [Zn+2]. InChI=1S/C81H90N5O2. Zn/c1-15-17-19-21-23-53-27-34-63 (35-28-53) 86 (64-36-29-54 (30-37-64) 24-22-20-18-16-2) 76-72-45-43-70 (84-72) 74 (57-47-59 (78 (3, 4) 5) 51-60 (48-57) 79 (6, 7) 8) 68-41-39-66 (82-68) 65 (38-31-55-25-32-56 (33-26-55) 7 | |
| Zinc(II) Tetraphenylporphyrin | Alfa Chemistry offers Zinc(II) Tetraphenylporphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetraphenyl-21H,23H-porphine Zinc(II) Zinc(II) TPP ZnTPP (meso-Tetraphenylporphinato)Zinc(II) Zinc(II) meso-Tetraphenylporphine. CAS No. 14074-80-7. Pack Sizes: 1G-Glass Bottle with Plastic Insert. Product ID: zinc; 5,10,15,20-tetraphenylporphyrin-22,24-diide. Molecular formula: 678.12. Mole weight: C44H28N4Zn. C1=CC=C (C=C1) C2=C3C=CC (=C (C4=NC (=C (C5=CC=C ([N-]5) C (=C6C=CC2=N6) C7=CC=CC=C7) C8=CC=CC=C8) C=C4) C9=CC=CC=C9) [N-]3. [Zn+2]. InChI=1S/C44H28N4. Zn/c1-5-13-29 (14-6-1)41-33-21-23-35 (45-33)42 (30-15-7-2-8-16-30)37-25-27-39 (47-37)44 (32-19-11-4-12-20-32)40-28-26-38 (48-40)43 (31-17-9-3-10-18-31)36-24-22-34 (41)46-36; /h1-28H; /q-2; +2. XPVVGUHKLPZAEN-UHFFFAOYSA-N. >97.0%(HPLC). | |
| Zinc phthalocyanine | Zinc (II) phthalocyanine (ZnPc) complexes show photosensitizing properties. Phthalocyanines show significant Π-Π interactions and easy formation of H aggregates. Uses: Zinc phthalocyanine finds general applications in industry (catalysts, photoconductors etc) and biomedical (photodynamic therapy, pdt). znpc may be used to photooxidise cyclohexane. a study reports functionalization of polymer membrane with znpc. Group: Phthalonitriles & naphthalonitrilesdye-sensitized solar cell (dssc) materials electronic materials molecular conductorsorganic field effect transistor (ofet) materials organic solar cell (opv) materials perovskite solar cell (psc) materials other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: [29H, 31H-Phthalocyaninato(2-)-N29, N30, N31, N32]zinc. CAS No. 14320-04-8. Pack Sizes: 5, 25 g in glass bottle. Product ID: Zinc; 2, 11, 20, 29, 37, 39-hexaza-38, 40-diazanidanonacyclo[28.6.1.13, 10.112, 19.121, 28.04, 9.013, 18.022, 27.031, 36]tetraconta-1, 3, 5, 7, 9, 11, 13, 15, 17, 19(39), 20, 22, 24, 26, 28, 30(37), 31, 33, 35-nonadecaene. Molecular formula: 577.9. Mole weight: C32H16N8Zn. C1=CC=C2C (=C1)C3=NC4=NC (=NC5=C6C=CC=CC6=C ([N-]5)N=C7C8=CC=CC=C8C (=N7)N=C2[N-]3)C9=CC=CC=C94. [Zn+2]. InChI=1S/C32H16N8. Zn/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. PODBBOVV | |
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