tert-butyl (3,6,9,12-tetraoxapentadec-14-yn-1-yl)carbamate
90%
- Product Code: 241976
CAS:
1219810-90-8
Molecular Weight: | 331.41 g./mol | Molecular Formula: | C₁₆H₂₉NO₆ |
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EC Number: | MDL Number: | ||
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Density: | Storage Condition: | 2-8℃ |
Product Description:
Used as a bifunctional linker in bioconjugation and pharmaceutical synthesis, particularly in the preparation of antibody-drug conjugates (ADCs) and PEGylated compounds. The tert-butyl carbamate (Boc) group provides a protected amine that can be selectively deprotected under mild acidic conditions, allowing for controlled coupling to biomolecules. The terminal alkyne enables efficient conjugation via copper-catalyzed azide-alkyne cycloaddition (CuAAC), commonly known as click chemistry, making it valuable in drug discovery, bioconjugation, and the development of diagnostic probes. Its polyether (PEG-like) spacer enhances solubility and improves pharmacokinetic properties of conjugated molecules.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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50mg | 10-20 days | ฿1,400.00 |
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250mg | 10-20 days | ฿4,140.00 |
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1g | 10-20 days | ฿15,600.00 |
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tert-butyl (3,6,9,12-tetraoxapentadec-14-yn-1-yl)carbamate
Used as a bifunctional linker in bioconjugation and pharmaceutical synthesis, particularly in the preparation of antibody-drug conjugates (ADCs) and PEGylated compounds. The tert-butyl carbamate (Boc) group provides a protected amine that can be selectively deprotected under mild acidic conditions, allowing for controlled coupling to biomolecules. The terminal alkyne enables efficient conjugation via copper-catalyzed azide-alkyne cycloaddition (CuAAC), commonly known as click chemistry, making it valuable in drug discovery, bioconjugation, and the development of diagnostic probes. Its polyether (PEG-like) spacer enhances solubility and improves pharmacokinetic properties of conjugated molecules.
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