Boc-10-Adc-OH is a Boc-protected amino acid derivative featuring an amino acid backbone bearing a 10-carbon side chain with a terminal carboxylic acid (Adc), classifying it as a protected, non-free amino acid suitable for peptide-building chemistry. The molecule contains a Boc (tert-butoxycarbonyl) carbamate protecting group on the amino functionality and an unprotected carboxylic acid at the side chain, with the remaining backbone also presenting a carboxyl group that can participate in amide bond formation after activation. In synthesis, it is employed as a stepwise coupling component in peptide synthesis workflows to introduce the side-chain carboxyl functionality while minimizing undesired reactions from the free amine during fragment assembly and subsequent deprotection.
CAT No: CP25467
CAS No:173606-50-3
Synonyms/Alias:Boc-10-Adc-OH;173606-50-3;10-((tert-Butoxycarbonyl)amino)decanoicacid;10-[(TERT-BUTOXYCARBONYL)AMINO]DECANOICACID;AmbotzBAA1321;AC1N8O27;SCHEMBL2702010;10-[(2-methylpropan-2-yl)oxycarbonylamino]decanoicAcid;10-(N-Boc-amino)decanoicAcid;CTK8F0782;BOC-10-AMINODECANOICACID;MolPort-002-345-652;ZINC6186790;6233AH;AKOS007930090;AJ-55938;AK-62617;LP077482;SC-43723;RT-011676;N-T-BUTYLOXYCARBONYL-10-AMINO-DECANOICACID;10-[[(1,1-Dimethylethoxy)carbonyl]amino]decanoicAcid
Chemical Name:N-t-Butyloxycarbonyl-10-amino-decanoic acid
Boc-10-Adc-OH is a Boc-protected amino acid derivative used as a protected building block for constructing amide-containing linkers and ADC-related intermediates. The Boc group provides controlled N-activation during stepwise synthesis, while the "10-Adc" substitution pattern is designed to carry a defined spacer/functional handle appropriate for downstream conjugation chemistry. As a protected, synthetic-grade intermediate, it is typically handled by peptide and linker synthesis teams developing stable, well-defined chemical architectures for bioconjugation workflows.
1. ADC Linker Intermediate
Boc-10-Adc-OH is used by medicinal chemistry and bioconjugation groups to prepare defined linker segments for antibody-drug conjugate (ADC) intermediate assemblies. The Boc-protected amino functionality supports stepwise coupling strategies in which the amine is introduced or transformed under controlled conditions, helping teams maintain structural fidelity of the spacer region that connects a payload to an antibody-reactive motif. In ADC development pipelines, this type of amino acid-derived intermediate is selected to provide a reproducible, chemically characterized junction for subsequent activation and conjugation steps.
2. Peptide-Linker Assembly
Boc-10-Adc-OH is employed in custom peptide-linker synthesis where a Boc-protected amino acid derivative serves as a modular unit for building amide bonds into larger constructs. Research groups developing cleavable or non-cleavable linker architectures often rely on protected amino acid building blocks to manage chemoselectivity across multiple functional groups during assembly. The Boc protection pattern is particularly useful in workflows that require sequential introduction of segments, enabling the preparation of longer, well-defined conjugation-ready intermediates for downstream coupling to biomolecular targets.
3. Pharmaceutical Intermediate Development
Boc-10-Adc-OH is a practical choice for pharmaceutical intermediate development teams who need a stable, isolable precursor bearing a controlled amine protection state for manufacturing-scale synthetic sequences. Intermediate developers value Boc-protected amino acid derivatives because they can be carried through multi-step transformations while limiting unwanted side reactions from the unprotected amine. This product format supports the preparation of standardized batches of linker components used in process development, scale-up studies, and analytical characterization of ADC-related or amide-linked chemical entities.
4. Chemical Biology Conjugation Chemistry
Boc-10-Adc-OH is also used by chemical biology laboratories to generate defined amino acid-based conjugation scaffolds that can be incorporated into bioconjugates for assay development and probe construction. Teams building non-biological reference materials, linker controls, or conjugation standards often prefer protected amino acid intermediates to ensure consistent structure across experimental series. The Boc-protected amine functionality enables downstream derivatization into conjugation-ready forms while preserving the designed spacer characteristics associated with the "10-Adc" motif.
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