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| Bz-Tz-NHS Basic information |
Product Name: | Bz-Tz-NHS | Synonyms: | 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;Tz-NHS;5-(4-(1,2,4,5-tetrazin-3-yl)benzylamino)-5-oxopentanoic acid succinimidyl 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 |
density | 1.45±0.1 g/cm3(Predicted) | storage temp. | -20°C | solubility | DMSO : 100 mg/mL (251.02 mM; Need ultrasonic) | pka | 14.57±0.46(Predicted) | form | Solid | color | Pink to red |
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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