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| Benzotriazole-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate Basic information |
| Benzotriazole-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate Chemical Properties |
| Melting point | 154-156 °C (dec.)(lit.) | | density | 1.438 at 20℃ | | vapor pressure | 0-0Pa at 20-50℃ | | storage temp. | 2-8°C | | solubility | methanol: 25 mg/mL, clear | | form | Fine Crystalline Powder | | color | White to off-white | | Sensitive | Moisture Sensitive | | BRN | 3584612 | | InChIKey | BYCLGHOAELJLOF-UHFFFAOYSA-M | | LogP | -0.3 at 26℃ and pH3.5-3.7 | | CAS DataBase Reference | 128625-52-5(CAS DataBase Reference) |
| Benzotriazole-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate Usage And Synthesis |
| Chemical Properties | Off-White Solid | | Uses | One of the most convenient coupling reagents for peptide synthesis without carcinogenic by-products. It replaces BOP reagent. This is especially suitable for solid-phase peptide synthesis, avoids racemization. | | Uses | 1H-Benzotriazol-1-yloxytri(1-pyrrolidinyl) phosphonium hexafluorophosphate is a peptide coupling reagent utilized in solid phase peptide synthesis. It is also used as a substitute for the (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) reagent. | | Uses | Reagent for: Synthesis of single labeled oligonucleotides that fluoresce upon matched hybridization Generation of endocrine disruptor chemical binders Cycloaddition to template-assembled multivalent peptide conjugates | | General Description | (Benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyBOP) is an activator of carboxyl group commonly used in peptide synthesis. It also participates in the carboxylic acid esterification. It shows characteristics similar to benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and can be utilized as an alternative to BOP in peptide bond formation. |
| Benzotriazole-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate Preparation Products And Raw materials |
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