Alfa Chemistry Materials 5 - Products
Alfa Chemistry Materials is specialized in material chemistry and offers an extensive catalog of materials in a wide range of applications, including Metals and Materials, 3D Printing Materials, Biomaterials.
| Product | Description | |
|---|---|---|
| 5-Propyl-1,3-dithiolo[4,5-d][1,3]dithiole-2-thione, ≥93% | 5-Propyl-1,3-dithiolo[4,5-d][1,3]dithiole-2-thione, ≥93%. Group: Electronic chemicals. CAS No. 202126-48-5. Product ID: 2-propyl-[1,3]dithiolo[4,5-d][1,3]dithiole-5-thione. Molecular formula: 252.5g/mol. Mole weight: C7H8S5. CCCC1SC2=C(S1)SC(=S)S2. InChI=1S/C7H8S5/c1-2-3-4-9-5-6 (10-4)12-7 (8)11-5/h4H, 2-3H2, 1H3. QVGTUNLOIXSBRJ-UHFFFAOYSA-N. |  |
| 5-(p-Tolyl)-1H-tetrazole | 5-(p-Tolyl)-1H-tetrazole. Group: Ligands for functional metal complexes. CAS No. 24994-04-5. Product ID: 5-(4-methylphenyl)-2H-tetrazole. Molecular formula: 160.18g/mol. Mole weight: C8H8N4. CC1=CC=C(C=C1)C2=NNN=N2. InChI=1S/C8H8N4/c1-6-2-4-7 (5-3-6)8-9-11-12-10-8/h2-5H, 1H3, (H, 9, 10, 11, 12). BCCJIAZPYBJASR-UHFFFAOYSA-N. | |
| 6, 13-Bis (triisopropylsilylethynyl)pentacene (This product is unavailable in the U.S.) | 6, 13-Bis (triisopropylsilylethynyl)pentacene (This product is unavailable in the U.S.). Group: Electronic materials. CAS No. 373596-08-8. Product ID: tri(propan-2-yl)-[2-[13-[2-tri(propan-2-yl)silylethynyl]pentacen-6-yl]ethynyl]silane. Molecular formula: 639.1g/mol. Mole weight: C44H54Si2. CC (C)[Si] (C#CC1=C2C=C3C=CC=CC3=CC2=C (C4=CC5=CC=CC=C5C=C41)C#C[Si] (C (C)C) (C (C)C)C (C)C) (C (C)C)C (C)C. InChI=1S/C44H54Si2/c1-29 (2) 45 (30 (3) 4, 31 (5) 6) 23-21-39-41-25-35-17-13-15-19-37 (35) 27-43 (41) 40 (22-24-46 (32 (7) 8, 33 (9) 10) 34 (11) 12) 44-28-38-20-16-14-18-36 (38) 26-42 (39) 44/h13-20, 25-34H, 1-12H3. FMZQNTNMBORAJM-UHFFFAOYSA-N. | |
| 6,6'-Bis(chloromethyl)-2,2'-bipyridyl | 6,6'-Bis(chloromethyl)-2,2'-bipyridyl. Group: Ligands for functional metal complexes. Alternative Names: 2-(Chloromethyl)-6-[6-(chloromethyl)pyridin-2-yl]pyridine. CAS No. 74065-64-8. Product ID: 2-(chloromethyl)-6-[6-(chloromethyl)pyridin-2-yl]pyridine. Molecular formula: 253.12. Mole weight: C12H10Cl2N2. C1=CC(=NC(=C1)CCl)C2=NC(=CC=C2)CCl. InChI=1S / C12H10Cl2N2 / c13-7-9-3-1-5-11 (15-9) 12-6-2-4-10 (8-14) 16-12 / h1-6H, 7-8H2. CUWSIBMCPYEBPL-UHFFFAOYSA-N. 98%+. | |
| (6,6)Carbon Nanobelt Bis(tetrahydrofuran) Adduct | (6,6)Carbon Nanobelt Bis(tetrahydrofuran) Adduct. Group: Carbon nano materials. CAS No. 2245104-25-8. | |
| 6,6'-Diamino-2,2'-bipyridyl | 6,6'-Diamino-2,2'-bipyridyl. Group: Ligands for functional metal complexes. Alternative Names: AKOS015854225; CTK3I6165; 6,6'-Diamino-2,2'-bipyridyl; TR-029181; VP12389; D2913; 6-(6-aminopyridin-2-yl)pyridin-2-amine; FCH1122679; 93127-75-4; ANW-39986. CAS No. 93127-75-4. Product ID: 6-(6-aminopyridin-2-yl)pyridin-2-amine. Molecular formula: 186.218g/mol. Mole weight: C10H10N4. C1=CC(=NC(=C1)N)C2=NC(=CC=C2)N. InChI=1S/C10H10N4/c11-9-5-1-3-7 (13-9)8-4-2-6-10 (12)14-8/h1-6H, (H2, 11, 13) (H2, 12, 14). YKSWVQYWQSZDPR-UHFFFAOYSA-N. | |
| 6,6''-Dibromo-2,2':6',2''-terpyridine | 6,6''-Dibromo-2,2':6',2''-terpyridine. Group: Ligands for functional metal complexes. Alternative Names: 2,6-Bis(6-Bromopyridin-2-Yl)Pyridine; 2,2':6',2''-Terpyridine, 6,6''-Dibromo-. CAS No. 100366-66-3. Product ID: 2,6-bis(6-bromopyridin-2-yl)pyridine. Molecular formula: 391.06. Mole weight: C15H9Br2N3. C1=CC (=NC (=C1)C2=NC (=CC=C2)Br)C3=NC (=CC=C3)Br. InChI=1S/C15H9Br2N3/c16-14-8-2-6-12 (19-14)10-4-1-5-11 (18-10)13-7-3-9-15 (17)20-13/h1-9H. PYMBATDYUCQLBC-UHFFFAOYSA-N. 94%+. | |
| 6,6'-Dibromo-2,2'-bipyridyl | 6,6'-Dibromo-2,2'-bipyridyl. Group: Ligands for functional metal complexes. Alternative Names: 2-Bromo-6-(6-Bromopyridin-2-Yl)Pyridine. CAS No. 49669-22-9. Product ID: 2-bromo-6-(6-bromopyridin-2-yl)pyridine. Molecular formula: 313.97. Mole weight: C10H6Br2N2. C1=CC(=NC(=C1)Br)C2=NC(=CC=C2)Br. InChI=1S/C10H6Br2N2/c11-9-5-1-3-7 (13-9)8-4-2-6-10 (12)14-8/h1-6H. WZVWSOXTTOJQQQ-UHFFFAOYSA-N. 95%+. | |
| 6,6'-Dibromo-9,9'-diphenyl-3,3'-bicarbazole | 6,6'-Dibromo-9,9'-diphenyl-3,3'-bicarbazole. Group: Small molecule semiconductor building blocks. CAS No. 354135-75-4. Product ID: 3-bromo-6-(6-bromo-9-phenylcarbazol-3-yl)-9-phenylcarbazole. Molecular formula: 642.4g/mol. Mole weight: C36H22Br2N2. C1=CC=C (C=C1)N2C3=C (C=C (C=C3)C4=CC5=C (C=C4)N (C6=C5C=C (C=C6)Br)C7=CC=CC=C7)C8=C2C=CC (=C8)Br. InChI=1S / C36H22Br2N2 / c37-25-13-17-35-31 (21-25) 29-19-23 (11-15-33 (29) 39 (35) 27-7-3-1-4-8-27) 24-12-16-34-30 (20-24) 32-22-26 (38) 14-18-36 (32) 40 (34) 28-9-5-2-6-10-28 / h1-22H. VTIPHPNQFUCDAW-UHFFFAOYSA-N. | |
| 6,6'-Dibromoisoindigo | 6,6'-Dibromoisoindigo. Uses: Electron accepting building block for the preparation of electroactive materials for organic electronics. Group: Small molecule semiconductor building blockssynthetic tools and reagents polymers. Alternative Names: 6, 6'-Dibromo-[3, 3'-biindolinylidene]-2, 2'-dione. CAS No. 1147124-21-7. Pack Sizes: 1 g in glass bottle. Product ID: 6-bromo-3-(6-bromo-2-hydroxy-1H-indol-3-yl)indol-2-one. Molecular formula: 420.06. Mole weight: C16H8Br2N2O2. O=C1NC2=C (C=CC (Br)=C2)/C1=C3C (NC4=C\3C=CC (Br)=C4)=O. InChI=1S/C16H8Br2N2O2/c17-7-1-3-9-11 (5-7)19-15 (21)13 (9)14-10-4-2-8 (18)6-12 (10)20-16 (14)22/h1-6, 19, 21H. FMIGDKYPJSFPDF-UHFFFAOYSA-N. >96.0%(HPLC)(N). | |
| [6,6]-Pentadeuterophenyl C61 butyric acid methyl ester | [6,6]-Pentadeuterophenyl C61 butyric acid methyl ester (PC60BM) is a deuterated fullerene that can be used as an acceptor molecule. It has a fullerene as the core and deuterium and benzyl as the attachment. The deuterium atoms facilitate an increase in the quantum efficiency of the electrochemical devices. Uses: Pc60bm is a conjugating polymer that can be used as an alternative to the conventionally used pcbm for the organic electronic based applications, which include polymeric solar cells and organic light emitting diodes (oleds). Group: Carbon nano materials organic solar cell (opv) materials. Alternative Names: 1-[3-(Methoxycarbonyl)propyl]-1-pentadeuterophenyl-[6.6] C61,d5-PCBM. CAS No. 749898-80-4. Pack Sizes: 100 mg in glass insert. Molecular formula: 915.91. [2H]c1c ([2H]) c ([2H]) c (c ([2H]) c1[2H]) C2 (CCCC (=O) OC) [C]3=4c5c6c7c8c9c% 10c (c% 11c% 12c3c% 13c5c% 14c% 15c6c% 16c7c% 17c9c% 18c% 19c% 10c% 20c% 11c% 21c% 12c% 22c% 13c% 23c% 14c% 24c% 15c% 25c% 16c% 26c% 17c% 18c% 27c% 28c% 19c% 20c% 29c% 21c% 30c% 22c% 23c% 31c% 24c% 32c% 25c% 26c% 27c% 33c% 28c% 29c% 30c% 31c% 32% 33) [C]2=48. | |
| [6,6]-Phenyl-C61 butyric acid butyl ester | [6,6]-Phenyl-C61 butyric acid butyl ester ([60]PCB-C4) is a fullerene derivative that is used as an acceptor molecule with good field effect mobility in organic electronics. It has a structural similarity to PCBM based fullerene and its aliphatic groups facilitate an increase in its solubility. Uses: [60]pcb-c4 is a conducting polymer, which can be used in a variety of applications such as organic photovoltaic cells (opvs) and bulk heterojunction (bhj) solar cells. Group: Carbon nano materials organic field effect transistor (ofet) materials organic solar cell (opv) materials. Alternative Names: 1-(3-Butoxycarbonylpropyl)-1-phenyl-[6.6]C61,PCBB,PCB-C4. CAS No. 571177-66-7. Pack Sizes: 1 g in glass bottle. Product ID: butyl 4-[(28S, 30R)-29-phenyl-29-heptadecacyclo[10.8.8.813, 17.55, 28.04, 22.08, 32.09, 30.016, 40.020, 35.021, 36.023, 33.024, 37.025, 31.026, 38.027, 41.028, 30.034, 39]hentetraconta-1(20), 2, 4, 6, 8, 10, 12, 14, 16, 18, 21, 23, 25(31), 26, 32, 34, 36, 38, 40-nonadecaenyl]butanoate. Molecular formula: 952.96. Mole weight: C55H30O2. CCCCOC (=O) CCCC2 (c1ccccc1) C34c5c6c7c8c9c% 10c (c% 11c% 12c3c% 13c5c% 14c% 15c6c% 16c7c% 17c9c% 18c% 19c% 10c% 20c% 11c% 21c% 12c% 22c% 13c% 23c% 14c% 24c% 15c% 25c% 16c% 26c% 17c% 18c% 27c% 28c% 19c% 20c% 29c% 21c% 30c% 22c% 23c% 31c% 24c% 32c% 25c% 26c% 27c% 33c% 28c% 29c% 30c% 31c% 32% 33) C248. InChI= 1S / C55H30O2 / c1-2-3-22-57-34 (56) 10-7-21-5 | |
| [6,6]-Phenyl-C61-butyric Acid Butyl Ester | [6,6]-Phenyl-C61-butyric Acid Butyl Ester. Group: Semiconducting materials carbon nano materials dye-sensitized solar cell (dssc) materials electronic materials organic solar cell (opv) materials. CAS No. 571177-66-7. Product ID: butyl 4-[(28S, 30R)-29-phenyl-29-heptadecacyclo[10.8.8.813, 17.55, 28.04, 22.08, 32.09, 30.016, 40.020, 35.021, 36.023, 33.024, 37.025, 31.026, 38.027, 41.028, 30.034, 39]hentetraconta-1(20), 2, 4, 6, 8, 10, 12, 14, 16, 18, 21, 23, 25(31), 26, 32, 34, 36, 38, 40-nonadecaenyl]butanoate. Molecular formula: 722.8g/mol. Mole weight: C55H30O2. CCCCOC (=O) CCCC1 (C23C14C5=C6C=CC7=C8C=CC9=C1C=CC% 10=C% 11C=CC (=C2C=C5) C2=C% 11C5=C% 11C% 12=C (C1=C% 105) C9=C8C1=C% 12C (=C4C6=C71) C% 11=C32) C1=CC=CC=C1. InChI= 1S / C55H30O2 / c1-2-3-22-57-34 (56) 10-7-21-53 (23-8-5-4-6-9-23) 54-32-19-20-33-31-18-16-29-27-14-12-2 5-24-11-13-26-28-15-17-30 (32) 41-39 (28) 44-37 (26) 35 (24) 43-36 (25) 38 (27) 45-40 (29) 42 (31) 52 (55 (33, 53) 54) 50-48 (45) 46 (43) 47 (44) 49 (50) 51 ( 41) 54 / h4-6, 8-9, 11-20H, 2-3, 7, 10, 21-22H2, 1H3 / t53? , 54-, 55 +. FZYQHMHIALEGMG-MVOHYUIRSA-N. | |
| [6,6]-Phenyl-C61-butyric Acid Dodecyl Ester | [6,6]-Phenyl-C61-butyric Acid Dodecyl Ester. Group: Semiconducting materials carbon nano materials dye-sensitized solar cell (dssc) materials electronic materials organic solar cell (opv) materials. Alternative Names: [60]PCB-C12. CAS No. 571177-69-0. Molecular formula: 1065.20. Mole weight: C83H36O2. >98.0%HPLC. | |
| [6,6]-Phenyl-C61-butyric Acid Methyl Ester | [6,6]-Phenyl-C61-butyric Acid Methyl Ester. Group: Carbon nano materials dye-sensitized solar cell (dssc) materials organic field effect transistor (ofet) materials organic solar cell (opv) materials perovskite solar cell (psc) materials. Alternative Names: Methyl [6,6]-Phenyl-C61-butyrate [60]PCBM PCBM. CAS No. 160848-22-6. Molecular formula: 910.90. Mole weight: C72H14O2. COC (=O) CCCC1 (C23C14C5=C6C7=C8C5=C9C1=C5C% 10=C% 11C% 12=C% 13C% 10=C% 10C1=C8C1=C% 10C8=C% 10C% 14=C% 15C% 16=C% 17C (=C% 12C% 12=C% 17C% 17=C% 18C% 16=C% 16C% 15=C% 15C% 10=C1C7=C% 15C1=C% 16C (=C% 18C7=C2C2=C% 10C (=C5C9=C42) C% 11=C% 12C% 10=C% 177) C3=C16) C% 14=C% 138) C1=CC=CC=C1. InChI=1S/C72H14O2/c1-74-11 (73) 8-5-9-70 (10-6-3-2-4-7-10) 71-66-59-52-40-32-23-14-12-13-15-18 (14) 27-34 (32) 42-43-35 (27) 33-24 (15) 26-22-17 (13) 20-19-16 (12) 21-25 (23) 38 (40) 46-44-30 (21) 28 (19) 36-37-29 (20) 31 (22) 45-47-39 (26) 41 (33) 53-55 (43) 64 (63 (66) 54 (42) 52) 67-60 (53) 58 (47) 62-51 (45) 49 (37) 56-48 (36) 50 (44) 61 (57 (46) 59) 68 (71) 65 (56) 69 (62) 72 (67, 70) 71/h2-4, 6-7H, 5, 8-9H2, 1H3. MCEWYIDBDVPMES-UHFFFAOYSA-N. >99.5%(HPLC). | |
| [6,6]-Phenyl-C61-butyric Acid Methyl Ester [for organic electronics] | [6,6]-Phenyl-C61-butyric Acid Methyl Ester [for organic electronics]. Group: Small molecule semiconductor building blockscarbon nano materials dye-sensitized solar cell (dssc) materials organic field effect transistor (ofet) materials organic semiconductorsorganic solar cell (opv) materials perovskite solar cell (psc) materials. CAS No. 160848-22-6. Molecular formula: 910.9g/mol. Mole weight: C72H14O2. COC (=O) CCCC1 (C23C14C5=C6C7=C8C5=C9C1=C5C% 10=C% 11C% 12=C% 13C% 10=C% 10C1=C8C1=C% 10C8=C% 10C% 14=C% 15C% 16=C% 17C (=C% 12C% 12=C% 17C% 17=C% 18C% 16=C% 16C% 15=C% 15C% 10=C1C7=C% 15C1=C% 16C (=C% 18C7=C2C2=C% 10C (=C5C9=C42) C% 11=C% 12C% 10=C% 177) C3=C16) C% 14=C% 138) C1=CC=CC=C1. InChI=1S/C72H14O2/c1-74-11 (73) 8-5-9-70 (10-6-3-2-4-7-10) 71-66-59-52-40-32-23-14-12-13-15-18 (14) 27-34 (32) 42-43-35 (27) 33-24 (15) 26-22-17 (13) 20-19-16 (12) 21-25 (23) 38 (40) 46-44-30 (21) 28 (19) 36-37-29 (20) 31 (22) 45-47-39 (26) 41 (33) 53-55 (43) 64 (63 (66) 54 (42) 52) 67-60 (53) 58 (47) 62-51 (45) 49 (37) 56-48 (36) 50 (44) 61 (57 (46) 59) 68 (71) 65 (56) 69 (62) 72 (67, 70) 71/h2-4, 6-7H, 5, 8-9H2, 1H3. MCEWYIDBDVPMES-UHFFFAOYSA-N. | |
| [6,6]-Phenyl-C61-butyric Acid n-Octyl Ester | [6,6]-Phenyl-C61-butyric Acid n-Octyl Ester. Group: Semiconducting materials carbon nano materials dye-sensitized solar cell (dssc) materials electronic materials organic solar cell (opv) materials. CAS No. 571177-68-9. | |
| [6,6]-Phenyl-C61 butyric acid octyl ester | functionalized fullerene. Uses: Soluble n-channel organic semiconductor. Group: Carbon nano materials organic field effect transistor (ofet) materials organic solar cell (opv) materials. Alternative Names: 1-(3-Octoxycarbonylpropyl)-1-phenyl-[6.6]C61,PCBO. CAS No. 571177-68-9. Pack Sizes: 100 mg in glass insert. Molecular formula: 1009.07. CCCCCCCCOC (=O) CCCC2 (c1ccccc1) [C]3=4c5c6c7c8c9c% 10c (c% 11c% 12c3c% 13c5c% 14c% 15c6c% 16c7c% 17c9c% 18c% 19c% 10c% 20c% 11c% 21c% 12c% 22c% 13c% 23c% 14c% 24c% 15c% 25c% 16c% 26c% 17c% 18c% 27c% 28c% 19c% 20c% 29c% 21c% 30c% 22c% 23c% 31c% 24c% 32c% 25c% 26c% 27c% 33c% 28c% 29c% 30c% 31c% 32% 33) [C]2=48. | |
| [6,6]-Phenyl-C71-butyric Acid Methyl Ester (mixture of isomers) | [6,6]-Phenyl-C71-butyric Acid Methyl Ester (mixture of isomers). Group: Carbon nano materials dye-sensitized solar cell (dssc) materials organic field effect transistor (ofet) materials organic solar cell (opv) materials perovskite solar cell (psc) materials. Alternative Names: [70]PCBM (mixture of isomers) Methyl [6,6]-Phenyl-C71-butyrate (mixture of isomers). CAS No. 609771-63-3. Molecular formula: 1031.01. Mole weight: C82H14O2. COC (=O) CCCC1 (C23C14C5=C6C7=C8C9=C1C% 10=C% 11C9=C9C% 12=C% 13C% 14=C% 15C% 16=C% 17C% 18=C% 19C% 20=C% 21C% 22=C% 23C% 24=C% 25C% 26=C% 27C% 28=C (C% 14=C% 14C% 12=C% 11C% 11=C% 14C% 28=C% 26C% 12=C% 11C% 10=C% 10C% 12=C% 25C% 23=C% 11C% 10=C1C7=C% 11C% 22=C6C4=C% 21C% 19=C2C% 17=C1C% 15=C% 13C2=C9C8=C5C2=C31) C% 16=C% 18C% 27=C% 24% 20) C1=CC=CC=C1. InChI=1S / C82H14O2 / c1-84-11 (83) 8-5-9-80 (10-6-3-2-4-7-10) 81-76-68-60-50-40-33-24-18-12-13-15-1 7-16-14 (12) 20-27-22 (16) 31-32-23 (17) 28-21 (15) 30-26 (19 (13) 24) 35-41 (33) 51 (50) 61-55-45 (35) 37 (30) 47-39 (28) 49-43 (32) 53-52-42 (31) 48-38 (27) 46-36-29 (20) 25 (18) 34 (40) 44 (36) 54 ( 60) 64-58 (46) 66-56 (48) 62 (52) 70-71-63 (53) 57 (49) 67-59 (47) 65 (55) 73 (77 (81) 69 (61) 68) 75 (67) 79 (71) 82 (80, 81) 78 ( 70) 74 (66) 72 (64) 76 / h2-4, 6-7H, 5, 8-9H2, 1H3. AZSFNTBGCTUQFX-UHFFFAOYSA-N. >99.0%(HPLC). | |
| [6,6]-Phenyl-C71-butyric Acid Methyl Ester (mixture of isomers) [for organic electronics] | [6,6]-Phenyl-C71-butyric Acid Methyl Ester (mixture of isomers) [for organic electronics]. Group: Small molecule semiconductor building blockscarbon nano materials dye-sensitized solar cell (dssc) materials organic field effect transistor (ofet) materials organic semiconductorsorganic solar cell (opv) materials perovskite solar cell (psc) materials. CAS No. 609771-63-3. Molecular formula: 1031g/mol. Mole weight: C82H14O2. COC (=O) CCCC1 (C23C14C5=C6C7=C8C9=C1C% 10=C% 11C9=C9C% 12=C% 13C% 14=C% 15C% 16=C% 17C% 18=C% 19C% 20=C% 21C% 22=C% 23C% 24=C% 25C% 26=C% 27C% 28=C (C% 14=C% 14C% 12=C% 11C% 11=C% 14C% 28=C% 26C% 12=C% 11C% 10=C% 10C% 12=C% 25C% 23=C% 11C% 10=C1C7=C% 11C% 22=C6C4=C% 21C% 19=C2C% 17=C1C% 15=C% 13C2=C9C8=C5C2=C31) C% 16=C% 18C% 27=C% 24% 20) C1=CC=CC=C1. InChI= 1S / C82H14O2 / c1-84-11 (83) 8-5-9-80 (10-6-3-2-4-7-10) 81-76-68-60-50-40-33-24-18-12-13-15-1 7-16-14 (12) 20-27-22 (16) 31-32-23 (17) 28-21 (15) 30-26 (19 (13) 24) 35-41 (33) 51 (50) 61-55-45 (35) 37 (30) 47-39 (28) 49-43 (32) 53-52-42 (31) 48-38 (27) 46-36-29 (20) 25 (18) 34 (40) 44 (36) 54 ( 60) 64-58 (46) 66-56 (48) 62 (52) 70-71-63 (53) 57 (49) 67-59 (47) 65 (55) 73 (77 (81) 69 (61) 68) 75 (67) 79 (71) 82 (80, 81) 78 ( 70) 74 (66) 72 (64) 76 / h2-4, 6-7H, 5, 8-9H2, 1H3. AZSFNTBGCTUQFX-UHFFFAOYSA-N. | |
| [6,6]-Thienyl C61 butyric acid methyl ester | [6,6]-Thienyl C61 butyric acid methyl ester. Uses: [6,6]-thienyl c61 butyric acid methyl ester is a class of thienyl based pcbm that can be used for the fabrication of optoelectronic devices such as organic solar cells (oscs). Group: Carbon nano materials organic field effect transistor (ofet) materials organic solar cell (opv) materials. Alternative Names: [60]ThPCBM. Pack Sizes: 100 mg in glass insert. Molecular formula: 916.91. COC (=O) CCCC2 (c1cccs1) [C]3=4c5c6c7c8c9c% 10c (c% 11c% 12c3c% 13c5c% 14c% 15c6c% 16c7c% 17c9c% 18c% 19c% 10c% 20c% 11c% 21c% 12c% 22c% 13c% 23c% 14c% 24c% 15c% 25c% 16c% 26c% 17c% 18c% 27c% 28c% 19c% 20c% 29c% 21c% 30c% 22c% 23c% 31c% 24c% 32c% 25c% 26c% 27c% 33c% 28c% 29c% 30c% 31c% 32% 33) [C]2=48. | |
| 6-Aminohexylphosphonic acid hydrochloride salt | 6-Aminohexylphosphonic acid hydrochloride salt. Group: Self-assembly materials. CAS No. 1433996-75-8. Product ID: 6-aminohexylphosphonic acid; hydrochloride. Molecular formula: 217.63g/mol. Mole weight: C6H17ClNO3P. C(CCCP(=O)(O)O)CCN.Cl. InChI=1S/C6H16NO3P. ClH/c7-5-3-1-2-4-6-11(8, 9)10; /h1-7H2, (H2, 8, 9, 10); 1H. WQDFKCNDHMSGQQ-UHFFFAOYSA-N. | |
| 6arm-PEG17K | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 6arm-PEG. Molecular formula: average Mn 17000. | |
| 6-Bromo-2,2'-bipyridyl | 6-Bromo-2,2'-bipyridyl. Group: Ligands for functional metal complexes. Alternative Names: 6-Bromo-2,2-bipyridine; CTK4A3518; DB-027142; J-400771; AM84321; AJ-68924; 6-bromo-2-(2-pyridyl)pyridine; CB-2545; NCRIDSGPLISUEU-UHFFFAOYSA-N; MFCD01318953. CAS No. 10495-73-5. Product ID: 2-bromo-6-pyridin-2-ylpyridine. Molecular formula: 235.084g/mol. Mole weight: C10H7BrN2. C1=CC=NC(=C1)C2=NC(=CC=C2)Br. InChI=1S/C10H7BrN2/c11-10-6-3-5-9 (13-10)8-4-1-2-7-12-8/h1-7H. NCRIDSGPLISUEU-UHFFFAOYSA-N. | |
| 6-Bromo-4,4'-dimethyl-2,2'-bipyridyl | 6-Bromo-4,4'-dimethyl-2,2'-bipyridyl. Group: Ligands for functional metal complexes. Alternative Names: 6-Bromo-4,4'-Dimethyl-2,2'-Bipyridyl; 2-Bromo-4-Methyl-6-(4-Methylpyridin-2-Yl)Pyridine. CAS No. 850413-36-4. Product ID: 2-bromo-4-methyl-6-(4-methylpyridin-2-yl)pyridine. Molecular formula: 263.13. Mole weight: C12H11BrN2. CC1=CC(=NC=C1)C2=NC(=CC(=C2)C)Br. InChI=1S/C12H11BrN2/c1-8-3-4-14-10 (5-8)11-6-9 (2)7-12 (13)15-11/h3-7H, 1-2H3. UEJJXCRFGURPDR-UHFFFAOYSA-N. 97%. | |
| [6]Cycloparaphenylene | [6]Cycloparaphenylene. Group: Supramolecular host materials carbon nano materials. CAS No. 156980-13-1. Product ID: heptacyclo[20.2.2.22, 5.26, 9.210, 13.214, 17.218, 21]hexatriaconta-1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35-octadecaene. Molecular formula: 456.6g/mol. Mole weight: C36H24. C1=CC2=C3C=CC (=C4C=CC (=C5C=CC (=C6C=CC (=C7C=CC (=C1C=C2)C=C7)C=C6)C=C5)C=C4)C=C3. InChI=1S/C36H24/c1-2-26-4-3-25 (1)27-5-7-29 (8-6-27)31-13-15-33 (16-14-31)35-21-23-36 (24-22-35)34-19-17-32 (18-20-34)30-11-9-28 (26)10-12-30/h1-24H. HNGGBZMJWQRDDA-UHFFFAOYSA-N. | |
| [6]Cycloparaphenylene, 98% | [6]Cycloparaphenylene, 98%. Group: Carbon nano materials. CAS No. 156980-13-1. Product ID: heptacyclo[20.2.2.22, 5.26, 9.210, 13.214, 17.218, 21]hexatriaconta-1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35-octadecaene. Molecular formula: 456.6g/mol. Mole weight: C36H24. C1=CC2=C3C=CC (=C4C=CC (=C5C=CC (=C6C=CC (=C7C=CC (=C1C=C2)C=C7)C=C6)C=C5)C=C4)C=C3. InChI=1S/C36H24/c1-2-26-4-3-25 (1)27-5-7-29 (8-6-27)31-13-15-33 (16-14-31)35-21-23-36 (24-22-35)34-19-17-32 (18-20-34)30-11-9-28 (26)10-12-30/h1-24H. HNGGBZMJWQRDDA-UHFFFAOYSA-N. | |
| 6'-(Diethylamino)-1',2'-benzofluoran | Alfa Chemistry offers high-purity 6'-(Diethylamino)-1',2'-benzofluoran 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: This technique has been applied to print on commuter passes or prepaid cards. by combining acid-generating methods with the coloring mechanism, new applications can be expected for these materials. Group: Pressure & heat sensitive recording materials heat & pressure sensitive dyes other materials. CAS No. 26628-47-7. Product ID: 9'-(diethylamino)spiro[2-benzofuran-3,12'-benzo[a]xanthene]-1-one. Molecular formula: 421.5. Mole weight: C28H23NO3. CCN (CC)C1=CC2=C (C=C1)C3 (C4=CC=CC=C4C (=O)O3)C5=C (O2)C=CC6=CC=CC=C65. InChI=1S/C28H23NO3/c1-3-29 (4-2)19-14-15-23-25 (17-19)31-24-16-13-18-9-5-6-10-20 (18)26 (24)28 (23)22-12-8-7-11-21 (22)27 (30)32-28/h5-17H, 3-4H2, 1-2H3. HMNGPLGXLQFPFN-UHFFFAOYSA-N. >98.0%(GC)(T). | |
| 6H-Indolo[2,3-b]quinoxaline | 6H-Indolo[2,3-b]quinoxaline. Group: Small molecule semiconductor building blocks. CAS No. 243-59-4. Product ID: 6H-indolo[3,2-b]quinoxaline. Molecular formula: 219.25. Mole weight: C14H9N3. C1=CC=C2C(=C1)C3=NC4=CC=CC=C4N=C3N2. InChI=1S/C14H9N3/c1-2-6-10-9 (5-1)13-14 (16-10)17-12-8-4-3-7-11 (12)15-13/h1-8H, (H, 16, 17). LCKIWLDOHFUYDV-UHFFFAOYSA-N. >98.0%(GC)(T). | |
| 6-O-Alpha-maltosyl-beta-cyclodextrin hydrate | 6-O-Alpha-maltosyl-beta-cyclodextrin hydrate. Group: Macrocycles. Alternative Names: 6-O-ALPHA-D-MALTOSYL-BETA-CYCLODEXTRIN; 6-O-ALPHA-MALTOSYL-BETA-CYCLODEXTRIN; 6-O-ALPHA-MALTOSYL-BETA-CYCLODEXTRIN HYDRATE; 6-O-alpha-D-Maltosyl-?cyclodextrin; 6-O-A-maltosyl-B-cyclodextrin hydrate; MALTOSYL CYCLODEXTRIN; 6-O-ALPHA-D-MALTOSYL-BETA-CYCLODEXTRIN 98+%; 6-o-α -maltosyl-β -cyclodextrin hydrate. CAS No. 104723-60-6. Product ID: 6-O-α -MALTOSYL-β -CYCLODEXTRIN HYDRATE. Molecular formula: 1459.27. Mole weight: C54< / sub>H90< / sub>O45< / sub>. C (C1C (C (C (C (O1) OC2C (OC (C (C2O) O) OCC3C4C (C (C (O3) OC5C (OC (C (C5O) O) OC6C (OC (C (C6O) O) OC7C (OC (C (C7O) O) OC8C (OC (C (C8O) O) OC9C (OC (C (C9O) O) OC1C (OC (O4) C (C1O) O) CO) CO) CO) CO) CO) CO) O) O) CO) O) O) O) O. QFSFPJHBIGWPMD-PBVGKYIBSA-N. 95%. | |
| 6-Phenylpyridine-3-carboxylic acid | 6-Phenylpyridine-3-carboxylic acid. Group: Small molecule semiconductor building blocks. Alternative Names: 3-Pyridinecarboxylic Acid. CAS No. 29051-44-3. Product ID: 6-phenylpyridine-3-carboxylic acid. Molecular formula: 199.21. Mole weight: C12H9NO2. C1=CC=C(C=C1)C2=NC=C(C=C2)C(=O)O. DLFLQXUYRFIFOK-UHFFFAOYSA-N. InChI=1S/C12H9NO2/c14-12 (15)10-6-7-11 (13-8-10)9-4-2-1-3-5-9/h1-8H, (H, 14, 15). 98%+. | |
| (6-Phosphonohexyl)phosphonic acid | (6-Phosphonohexyl)phosphonic acid. Group: Self-assembly materials. CAS No. 4721-22-6. Product ID: 6-phosphonohexylphosphonic acid. Molecular formula: 246.14g/mol. Mole weight: C6H16O6P2. C(CCCP(=O)(O)O)CCP(=O)(O)O. InChI=1S/C6H16O6P2/c7-13(8, 9)5-3-1-2-4-6-14(10, 11)12/h1-6H2, (H2, 7, 8, 9)(H2, 10, 11, 12). WDYVUKGVKRZQNM-UHFFFAOYSA-N. | |
| 6-[(tert-Butoxycarbonyl)amino]hexanoic Acid N-Succinimidyl Ester, ≥98% | 6-[(tert-Butoxycarbonyl)amino]hexanoic Acid N-Succinimidyl Ester, ≥98%. Group: Crosslinkers. CAS No. 51513-80-5. Product ID: (2,5-dioxopyrrolidin-1-yl) 6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoate. Molecular formula: 328.36g/mol. Mole weight: C15H24N2O6. CC (C) (C)OC (=O)NCCCCCC (=O)ON1C (=O)CCC1=O. InChI=1S/C15H24N2O6/c1-15 (2, 3)22-14 (21)16-10-6-4-5-7-13 (20)23-17-11 (18)8-9-12 (17)19/h4-10H2, 1-3H3, (H, 16, 21). TYJPSIQEEXOQLC-UHFFFAOYSA-N. | |
| 7,7-Dimethyl-7H-benzo[c]fluorene | 7,7-Dimethyl-7H-benzo[c]fluorene. Group: Small molecule semiconductor building blocks. CAS No. 112486-09-6. Product ID: 7,7-dimethylbenzo[c]fluorene. Molecular formula: 244.3g/mol. Mole weight: C19H16. CC1 (C2=C (C3=CC=CC=C3C=C2)C4=CC=CC=C41)C. InChI=1S/C19H16/c1-19 (2)16-10-6-5-9-15 (16)18-14-8-4-3-7-13 (14)11-12-17 (18)19/h3-12H, 1-2H3. SJVOYVUTRSZMKW-UHFFFAOYSA-N. | |
| 7-Amino-3-[(5-methyl-1,3,4-thiadiazol-2-ylthio)methyl]-3-cephem-4-carboxylic Acid, 99% | 7-Amino-3-[(5-methyl-1,3,4-thiadiazol-2-ylthio)methyl]-3-cephem-4-carboxylic Acid, 99%. Group: other glass and ceramic materials. CAS No. 30246-33-4. Product ID: (7R)-7-amino-3-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. Molecular formula: 344.4g/mol. Mole weight: C11H12N4O3S3. CC1=NN=C (S1)SCC2=C (N3C (C (C3=O)N)SC2)C (=O)O. InChI=1S/C11H12N4O3S3/c1-4-13-14-11 (21-4)20-3-5-2-19-9-6 (12)8 (16)15 (9)7 (5)10 (17)18/h6, 9H, 2-3, 12H2, 1H3, (H, 17, 18)/t6-, 9?/m1/s1. HJSGHKMSDOLGJJ-VJSCVCEBSA-N. | |
| 7-Bromo-2,1,3-benzothiadiazole-4-carbonitrile | 7-Bromo-2,1,3-benzothiadiazole-4-carbonitrile. Group: Small molecule semiconductor building blocks. Alternative Names: 7-Bromo-4-cyano-2,1,3-benzothiadiazole. CAS No. 1331742-86-9. Product ID: 4-bromo-2,1,3-benzothiadiazole-7-carbonitrile. Molecular formula: 240.08. Mole weight: C7H2BrN3S. C1=C(C2=NSN=C2C(=C1)Br)C#N. InChI=1S/C7H2BrN3S/c8-5-2-1-4 (3-9)6-7 (5)11-12-10-6/h1-2H. ORLZWSSVSNUQAZ-UHFFFAOYSA-N. >96.0%(GC). | |
| 7-Bromo-2,1,3-benzothiadiazole-4-carboxaldehyde | 7-Bromo-2,1,3-benzothiadiazole-4-carboxaldehyde. Group: Small molecule semiconductor building blocks. Alternative Names: 7-Bromo-4-formyl-2,1,3-benzothiadiazole. CAS No. 1071224-34-4. Product ID: 4-bromo-2,1,3-benzothiadiazole-7-carbaldehyde. Molecular formula: 243.08. Mole weight: C7H3BrN2OS. C1=C(C2=NSN=C2C(=C1)Br)C=O. InChI=1S/C7H3BrN2OS/c8-5-2-1-4 (3-11)6-7 (5)10-12-9-6/h1-3H. VPDPNJVAWKCZEH-UHFFFAOYSA-N. >98.0%(GC). | |
| 7-Bromo-2,3-dihydrothieno[3,4-b][1,4]dioxine-5-carboxaldehyde | 7-Bromo-2,3-dihydrothieno[3,4-b][1,4]dioxine-5-carboxaldehyde. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 852054-42-3. Product ID: 5-bromo-2,3-dihydrothieno[3,4-b][1,4]dioxine-7-carbaldehyde. Molecular formula: 249.08g/mol. Mole weight: C7H5BrO3S. C1COC2=C(SC(=C2O1)C=O)Br. InChI=1S/C7H5BrO3S/c8-7-6-5 (4 (3-9)12-7)10-1-2-11-6/h3H, 1-2H2. YEKBJVHBVICUOZ-UHFFFAOYSA-N. | |
| 7-Bromo-2-naphthol | 7-Bromo-2-naphthol. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 116230-30-9. Product ID: 7-bromonaphthalen-2-ol. Molecular formula: 223.07g/mol. Mole weight: C10H7BrO. C1=CC(=CC2=C1C=CC(=C2)Br)O. InChI=1S/C10H7BrO/c11-9-3-1-7-2-4-10 (12)6-8 (7)5-9/h1-6, 12H. VWSBGGRCEQOTNU-UHFFFAOYSA-N. | |
| (7-Bromo-9,9-dimethyl-9H-fluoren-2-yl)boronic Acid (contains varying amounts of Anhydride) | (7-Bromo-9,9-dimethyl-9H-fluoren-2-yl)boronic Acid (contains varying amounts of Anhydride). Group: Small molecule semiconductor building blocks. CAS No. 1213768-48-9. Product ID: (7-bromo-9,9-dimethylfluoren-2-yl)boronic acid. Molecular formula: 316.99g/mol. Mole weight: C15H14BBrO2. B (C1=CC2=C (C=C1)C3=C (C2 (C)C)C=C (C=C3)Br) (O)O. InChI=1S/C15H14BBrO2/c1-15 (2)13-7-9 (16 (18)19)3-5-11 (13)12-6-4-10 (17)8-14 (12)15/h3-8, 18-19H, 1-2H3. CYZUULREWZKGJP-UHFFFAOYSA-N. | |
| 7-(Bromomethyl)pentadecane | 7-(Bromomethyl)pentadecane. Group: Solubility enhancing reagents solubilizer. CAS No. 52997-43-0. Product ID: 7-(bromomethyl)pentadecane. Molecular formula: 305.34g/mol. Mole weight: C16H33Br. CCCCCCCCC(CCCCCC)CBr. InChI=1S / C16H33Br / c1-3-5-7-9-10-12-14-16 (15-17) 13-11-8-6-4-2 / h16H, 3-15H2, 1-2H3. RWEKWRQKAHQYNE-UHFFFAOYSA-N. | |
| [7]Cycloparaphenylene | [7]Cycloparaphenylene. Group: Supramolecular host materials carbon nano materials. CAS No. 1222105-42-1. Product ID: octacyclo[24.2.2.22, 5.26, 9.210, 13.214, 17.218, 21.222, 25]dotetraconta-1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37, 39, 41-henicosaene. Molecular formula: 532.7g/mol. Mole weight: C42H28. C1=CC2=C3C=CC (=C4C=CC (=C5C=CC (=C6C=CC (=C7C=CC (=C8C=CC (=C1C=C2) C=C8) C=C7) C=C6) C=C5) C=C4) C=C3. InChI=1S/C42H28/c1-2-30-4-3-29 (1)31-5-7-33 (8-6-31)35-13-15-37 (16-14-35)39-21-23-41 (24-22-39)42-27-25-40 (26-28-42)38-19-17-36 (18-20-38)34-11-9-32 (30)10-12-34/h1-28H. WGYDELDXZJCAJB-UHFFFAOYSA-N. | |
| 7-Diethylamino-4-methylcoumarin (purified by sublimation) | 7-diethylamino-4-methylcoumarin is a light tan grains. Gives bright blue-white fluorescence in very dilute solutions. (NTP, 1992);DryPowder. Group: other material building blocks. CAS No. 91-44-1. Product ID: 7-(diethylamino)-4-methylchromen-2-one. Molecular formula: 231.29g/mol. Mole weight: C14H17NO2. CCN(CC)C1=CC2=C(C=C1)C(=CC(=O)O2)C. InChI=1S/C14H17NO2/c1-4-15 (5-2)11-6-7-12-10 (3)8-14 (16)17-13 (12)9-11/h6-9H, 4-5H2, 1-3H3. AFYCEAFSNDLKSX-UHFFFAOYSA-N. | |
| 7-(Dimethylamino)-4-methylcoumarin (purified by sublimation) | 7-(Dimethylamino)-4-methylcoumarin (purified by sublimation). Group: other material building blocks. CAS No. 87-01-4. Product ID: 7-(dimethylamino)-4-methylchromen-2-one. Molecular formula: 203.24g/mol. Mole weight: C12H13NO2. CC1=CC(=O)OC2=C1C=CC(=C2)N(C)C. InChI=1S/C12H13NO2/c1-8-6-12 (14)15-11-7-9 (13 (2)3)4-5-10 (8)11/h4-7H, 1-3H3. GZEYLLPOQRZUDF-UHFFFAOYSA-N. | |
| 7H-benzo[c]carbazole | 7H-benzo[c]carbazole. Group: Small molecule semiconductor building blocks. Alternative Names: 3,4-Benzocarbazole. CAS No. 205-25-4. Product ID: 7H-benzo[c]carbazole. Molecular formula: 217.27. Mole weight: C16H11N. C1=CC=C2C(=C1)C=CC3=C2C4=CC=CC=C4N3. InChI=1S/C16H11N/c1-2-6-12-11 (5-1)9-10-15-16 (12)13-7-3-4-8-14 (13)17-15/h1-10, 17H. UGFOTZLGPPWNPY-UHFFFAOYSA-N. 99.5%+. | |
| 8-[2-(2-Pyridyl)phenyl]-5H-pyrido[3,2-b]indole | 8-[2-(2-Pyridyl)phenyl]-5H-pyrido[3,2-b]indole. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 1251503-35-1. Product ID: 8-(2-pyridin-2-ylphenyl)-5H-pyrido[3,2-b]indole. Molecular formula: 321.38. Mole weight: C22H15N3. C1=CC=C (C (=C1)C2=CC3=C (C=C2)NC4=C3N=CC=C4)C5=CC=CC=N5. InChI=1S/C22H15N3/c1-2-7-17 (19-8-3-4-12-23-19)16 (6-1)15-10-11-20-18 (14-15)22-21 (25-20)9-5-13-24-22/h1-14, 25H. ROQWGQBJRGUPAG-UHFFFAOYSA-N. >98.0%(GC). | |
| 8-Amino-1-octanethiol hydrochloride | 8-Amino-1-octanethiol hydrochloride. Group: Self-assembly materials. CAS No. 937706-44-0. | |
| 8arm-PEG10K 7arm-OH, 1arm-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 10000. | |
| 8arm-PEG10K 7arm-OH, 1arm-COOH, tripentaerythritol core | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG 7arm-OH, 1arm-COOH, tripentaerythritol core, 8arm PEG, 7arm-Hydroxyl, 1arm-Carboxyl. Molecular formula: average Mn 10000. | |
| 8arm-PEG10K-Acrylate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 10000. | |
| 8arm-PEG10K-COOH, hexaglycerol core | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-COOH, hexaglycerol core, 8arm-PEG-COOH. Molecular formula: average Mn 10000. | |
| 8arm-PEG10K-COOH, tripentaerythritol core | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-COOH, tripentaerythritol core, 8arm-PEG-COOH. Molecular formula: average Mn 10000. | |
| 8arm-PEG10K-Maleimide | 8arm-PEG10K-Maleimide. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 8-arm PEG10K-Methacrylate (hexaglycerol core) | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 10000. | |
| 8-arm PEG10K-Methacrylate (tripentaerythritol core) | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 10000. | |
| 8arm-PEG10K-NH2, hexaglycerol core | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-NH2, hexaglycerol core, 8arm-PEG-NH2. Molecular formula: average Mn 10000. | |
| 8arm-PEG10K-NH2, tripentaerythritol core | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-NH2, 8arm-PEG-NH2, tripentaerythritol core. Molecular formula: average Mn 10000. | |
| 8-arm PEG10K-PCL2K-Acrylate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 8-arm PEG10K-PLA2K-Acrylate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 8arm-PEG10K-SH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-SH. Molecular formula: average Mn 10000. | |
| 8arm-PEG10K-SH, tripentaerythritol core | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-SH, tripentaerythritol core, 8arm-PEG-SH. Molecular formula: average Mn 10000. | |
| 8arm-PEG10K-Succinimidyl Glutarate | 8arm-PEG10K-Succinimidyl Glutarate. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 8arm-PEG10K-Succinimidyl Succinate | 8arm-PEG10K-Succinimidyl Succinate. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 8arm-PEG10K-Vinylsulfone, tripentaerythritol core | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-VS, 8arm-PEG-Vinylsulfone, tripentaerythritol core. Molecular formula: average Mn 10000. | |
| 8arm-PEG15K-Succinimidyl Glutarate | 8arm-PEG15K-Succinimidyl Glutarate. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 8arm-PEG15K-Succinimidyl Succinate | 8arm-PEG15K-Succinimidyl Succinate. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 8arm-PEG20K 7arm-OH, 1arm-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 20000. | |
| 8arm-PEG20K 7arm-OH, 1arm-COOH, tripentaerythritol core | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG 7arm-OH, 1arm-COOH, tripentaerythritol core, 8arm PEG, 7arm-Hydroxyl, 1arm-Carboxyl. Molecular formula: average Mn 20000. | |
| 8arm-PEG20K-Acrylate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-Acrylate, hexaglycerol core. Molecular formula: average Mn 20000. | |
| 8arm-PEG20K-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 8arm-PEG-COOH. Molecular formula: average Mn 20000. | |
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