Other grades of this product :
| Bz-Tz-NHS Basic information |
| Product Name: | Bz-Tz-NHS | | Synonyms: | 2,5-dioxopyrrolidin-1-yl 5-((4-(1,2,4,5-tetrazin-3-yl)benzyl)amino)-5-oxopentanoate;5-Oxo-5-[[[4-(1,2,4,5-tetrazin-3-yl)phenyl]methyl]amino]pentanoic acid 2,5-dioxo-1-pyrrolidinyl ester;Benzylamino tetrazine N-hydroxysuccinimidyl ester;Benzylaminotetrazine-NHS;Bz-Tz-NHS;2,5-Dioxo-1-pyrrolidinyl 5-[4-(1,2,4,5-tetrazin-3-yl)benzylamino]-5-oxopentanoate;Tetrazine-Ph-NHCO-C3-NHS ester;2,5-Dioxo-1-pyrrolidinyl 5-[4-(1,2,4,5-tetrazin-3-yl)benzylamino]-5-oxopentanoate >=90% | | CAS: | 1244040-64-9 | | MF: | C18H18N6O5 | | MW: | 398.37272 | | EINECS: | | Product Categories: | | Mol File: | 1244040-64-9.mol |
| Bz-Tz-NHS Chemical Properties |
| Hazard Codes | Xn | | Risk Statements | 22 | | WGK Germany | 3 |
| Bz-Tz-NHS Usage And Synthesis |
| Uses | Succinimidyl ester functionalized tetrazine for inverse electron demand Diels-Alder cycloaddition reactions. Succinimidyl ester will react with amines for small molecule, biomolecule or surface modification. Tetrazine will react with strained alkenes such as transcyclooctene, norbornene and cyclopropene to yield a stable covalent linkage. Tetrazines have proven useful in bioorthogonal reactions for many biological imaging and bioconjugation applications. |
| Bz-Tz-NHS Preparation Products And Raw materials |
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