Azide-PEG3-azide
Cat. # | Quantity | Price | Lead time | Buy this product |
---|---|---|---|---|
207-1g | 1 g | $95 | in stock | |
207-5g | 5 g | $390 | in stock | |
207-25g | 25 g | please inquire | in stock |
PEG3 (triethylene glycol) diazide (1,8-diazido-3,6-dioxaoctane) is a symmetrical bifunctional crosslinker bearing two azide groups.
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Alkyne hydrazide
Bifunctional reagent containing alkyne group and hydrazide function. It reacts with aldehydes and ketones. Alkyne group can then be coupled with various azides via CuAAC reaction.Azide-PEG3-amine
A bifunctional linker with azide and amine groups flanking PEG3 (triethylene glycol)Hexynoic acid NHS ester
Hexynoic acid NHS ester for the labeling of biomolecules with alkyne group for copper-catalyzed click chemistry.General properties
Appearance: | colorless/yellowish liquid |
Molecular weight: | 200.2 |
CAS number: | 59559-06-7 |
Molecular formula: | C6H12N6O2 |
IUPAC name: | 1,8-diazido-3,6-dioxaoctane, 1,2-bis(2-azidoethoxy)ethane |
Solubility: | good in water and most organic solvents |
Quality control: | NMR 1H, GC-MS (95%) |
Storage conditions: | Storage: 24 months after receival at -20°C. Transportation: at room temperature for up to 3 weeks. Desiccate. |
MSDS: | Download |
Product specifications |
Product citations
- Rapp, T.L.; DeForest, C.A. Tricolor visible wavelength-selective photodegradable hydrogel biomaterials. Nature Communications, 2023, 14, 5250. doi: 10.1038/s41467-023-40805-w
- Santiana, J.J. ; Sawant, S.S.; Gomez, N.; Rouge, J. L. Multi-Layered Stimuli Responsive DNA Micelles for the Stepwise Controlled Release of Small Molecules. Journal of Materials Chemistry B, 2022, 10(37), 7518–7526. doi: 10.1039/D1TB02722K
- Hull, S.M.; Lindsay, C.D.; Brunel, L.G.; Shiwarski, D.J.; Tashman, J.W.; Roth, J.G.; Myung, D.; Feinberg, A.W.; Heilshorn, S.C. 3D Bioprinting using UNIversal Orthogonal Network (UNION) Bioinks. Advanced Functional Materials, 2021, 31(7), 2007983. doi: 10.1002/adfm.202007983
- Tolentino, M.Q.; Hartmann, A.K.; Loe, D.T.; Rouge, J.L. Controlled release of small molecules and proteins from DNA-surfactant stabilized metal organic frameworks. Journal of Materials Chemistry B, 2020, 8(26), 5627–5635. doi: 10.1039/d0tb00767f
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