N-Hydroxy-5-norbornene-2,3-dicarboximide perfluoro-1-butanesulfonate

electronic grade, ≥99% trace metals basis

Reagent Code: #220825
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CAS Number 307531-76-6

science Other reagents with same CAS 307531-76-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 461.26 g/mol
Formula C₁₃H₈F₉NO₅S
badge Registry Numbers
MDL Number MFCD02683480
thermostat Physical Properties
Melting Point 55-59 °C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a highly efficient coupling reagent in peptide synthesis, enabling rapid amide bond formation under mild conditions. Its unique structure enhances reactivity and reduces racemization, making it valuable in solid-phase peptide synthesis and the preparation of complex peptides for pharmaceutical research. Also applied in bioconjugation processes, where selective and clean reactions are required, such as labeling biomolecules with fluorescent tags or attaching payloads in antibody-drug conjugates. Shows good solubility in polar aprotic solvents, facilitating its use in automated synthesis platforms.

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inventory 1g
10-20 days ฿19,320.00

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N-Hydroxy-5-norbornene-2,3-dicarboximide perfluoro-1-butanesulfonate
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Used as a highly efficient coupling reagent in peptide synthesis, enabling rapid amide bond formation under mild conditions. Its unique structure enhances reactivity and reduces racemization, making it valuable in solid-phase peptide synthesis and the preparation of complex peptides for pharmaceutical research. Also applied in bioconjugation processes, where selective and clean reactions are required, such as labeling biomolecules with fluorescent tags or attaching payloads in antibody-drug conjugates. S

Used as a highly efficient coupling reagent in peptide synthesis, enabling rapid amide bond formation under mild conditions. Its unique structure enhances reactivity and reduces racemization, making it valuable in solid-phase peptide synthesis and the preparation of complex peptides for pharmaceutical research. Also applied in bioconjugation processes, where selective and clean reactions are required, such as labeling biomolecules with fluorescent tags or attaching payloads in antibody-drug conjugates. Shows good solubility in polar aprotic solvents, facilitating its use in automated synthesis platforms.

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