| Code | Name | Synonym |
| DI-125 | Fmoc-TEPA(Boc3)-Suc | 3‐[(2‐{[(tert‐butoxy)carbonyl](2‐{[(tert‐butoxy)carbonyl](2‐{[(tert‐butoxy)carbonyl][2‐({[(9H‐fluoren‐9‐yl)methoxy]carbonyl}amino)ethyl]amino}ethyl)amino}ethyl)amino}ethyl)carbamoyl]propanoic acid |
| CAS | 2304536-78-3 |  |
| Formula | C42H61N5O11 | |
| MW | 812 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | This reagent is used as a protected polyamine linker or side-chain for various applications. Klein, P. M.; Kern, S.; Lee, D.-J.; Schmaus, J.; Hoehn, M.; Gorges, J.; Kazmaier, U.; Wagner, E. Biomaterials (2018), 178, 630-642, DOI:10.1016/j.biomaterials.2018.03.031. | |
| Code | Name | Synonym |
| DI-124 | TEPA(HBBBH) | 4,7,10-tri-Boc-tetraethylene pentamine // tert‐butyl N,N‐bis({2‐[(2‐aminoethyl)[(tert‐butoxy)carbonyl]amino]ethyl})carbamate // 4,7,10-tris(Boc)tetraethylenepentamine // Tp(boc3) |
| CAS | 556082-09-8 |  |
| Formula | C23H47N5O6 | |
| MW | 489.7 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | TEPA HBBBH is used as a protected polyamine linker or side-chain for various applications. Reineke, T. M. et al, J. Am. Chem. Soc. (2006), 128(25), 8176-8184. DOI:10.1021/ja0585580; Reineke, T. M. et al, Proc. Natl. Acad. Sci. USA (2009), 106(40), 16913-16918, DOI:10.1073/pnas.0904860106; Wagner, E. et al, Org. Lett. (2011), 13(7), 1586-1589, DOI:10.1021/ol200381z; Reineke, T. M. et al, Biomacromolecules (2014), 15(5), 1612-1624, DOI:10.1021/bm401870z. | |
| Code | Name | Synonym |
| DI-120 | Fmoc-TETA(Boc2)-Suc-OH | 3-({2-[(tert-butoxycarbonyl)({2-[(tert- butoxycarbonyl)(2-{[(9H-fluoren-9- ylmethoxy)carbonyl]amino}ethyl)amino]ethyl})amino]ethyl}carbamoyl)propanoic acid |
| CAS | 2389064-35-9 |  |
| Formula | C35H48N4O9 | |
| MW | 668.8 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | ||
| Code | Name | Synonym |
| DI-121 | H-TETA(Boc2)-H | N2,N3-diBoc-triethylene tetramine // 4,7-di-Boc-1,4,7,10-tetraazadecane // tert-butyl N-(2-aminoethyl)-N-{2-[(2- aminoethyl)(tert- butoxycarbonyl)amino]ethyl}carbamate |
| CAS | 206531-21-7 |  |
| Formula | C16H34N4O4 | |
| MW | 346.5 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | H-TETA(Boc2)-H is used as a protected polyamine linker and to produce dendrimer-like structures. J. Am. Chem. Soc. (2006), 128(25), 8176-8184. DOI:10.1021/ja0585580; J. Med. Chem. (2013), 56(23), 9471-9481. DOI:10.1021/jm400794z; PCT Int. Appl. (2018), WO 2018097403 A1. | |
| Code | Name | Synonym |
| DI-104 | 1-(Boc-amino)-4,7,10-trioxa-13-tridecaneazide | tert-butyl N-(3-{2-[2-(3-azidopropoxy)ethoxy]ethoxy}propyl)carbamate // Boc-TOTA-N3 |
| CAS | 1162070-33-8 |  |
| Formula | C15H30N4O5 | |
| MW | 346.4 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Code | Name | Synonym |
| ET-166 | N3-C10H20-COOH | 11-Azidoundecanoic acid // 11-Azido-undecanoic acid |
| CAS | 118162-45-1 |  |
| Formula | C11H21N3O2 | |
| MW | 227.3 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | Used as a hydrophobic bioconjugation linker that can be further modified at the azido-position using Staudinger ligation or Click-chemistry. A substrate of lipoic acid ligase for labeling. Ting, A. Y. et. al. Nature Biotech. 2007, 1483, DOI:10.1038/nbt1355; Leatherbarrow R. J.; Tate E. W. et. al. Org. Biomol. Chem. 2008, 2308, DOI:10.1039/b803258k; Wnuk S. F. et. al. Eur. J. Med. Chem. 2018, 314, DOI:DOI:10.1016/j.ejmech.2018.02.017. | |
| Code | Name | Synonym |
| ET-163 | N3-C10H20-COOSu | 2,5‐dioxopyrrolidin‐1‐yl 11‐azidoundecanoate // 11-azido undecanoic acid NHS ester // 11-azido undecanoic acid N-hydroxysuccinimide ester |
| CAS | 850080-13-6 |  |
| Formula | C15H24N4O4 | |
| MW | 324.4 | |
| Purity | >98% (HPLC) | |
| Storage | -15 ... -25 °C | |
| Note | Used as a hydrophobic bioconjugation linker that can be further modified at the azido-position using Staudinger ligation or Click-chemistry. Bundle, D. R. et al Organic & Biomolecular Chem. (2006), 4(1), 142-154. DOI:10.1039/B513595H; Liu, J.-N. et al Biomacromolecules (2009), 10(4), 877-883. DOI:10.1021/bm8014076; Zundel, M. A. et al PCT Int. Appl. (2005), WO 2005035553. | |
| Code | Name | Synonym |
| ET-175 | 10-Undecynoyl-OSu | 10-Undecynoic acid NHS ester // 10-Undecynoic acid N-hydroxysuccinimide ester // 10-Undecynoic acid NHS ester // 2,5‐dioxopyrrolidin‐1‐yl undec‐10‐ynoate |
| CAS | 1006592-57-9 |  |
| Formula | C15H21NO4 | |
| MW | 279.3 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | Used as a hydrophobic bioconjugation linker that can be further modified at the alkyne using Click-chemistry. WO 2013183656 A1. | |
| Code | Name | Synonym |
| ET-117 | AMCA-OSu | 7-amino-4-methyl-3-coumarinacetic acid N-succinimidyl ester // N-succinimidyl 7-amino-4-methyl-3-coumarinylacetate // AMCA-NHS // succinimidyl-7-amino-4-methylcoumarin-3-acetate |
| CAS | 113721-87-2 |  |
| Formula | C16H14N2O6 | |
| MW | 330.3 | |
| Purity | >95% | |
| Storage | +2 ... +8 °C |
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