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Cleavable Linker
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Cleavable Linker

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Catalog Product Name CAS Number
BADC-00673 CL2 Linker 2270986-66-6
CL2 Linker is a cleavable ADC linker designed for controlled drug release and stable antibody conjugation, widely used in antibody-drug conjugate manufacturing for targeted cancer therapeutics. Inquiry
BADC-00676 (2S,2'S)-Bis(2,5-dioxopyrrolidin-1-Yl) 4,4'-disulfanediylbis(2-(((benzyloxy)carbonyl)amino)butanoate) 299402-08-7
(2S,2'S)-Bis(2,5-dioxopyrrolidin-1-Yl) 4,4'-disulfanediylbis(2-(((benzyloxy)carbonyl)amino)butanoate) is a linker for antibody-drug-conjugation (ADC). Inquiry
BADC-00677 Fmoc-PEA 329223-23-6
Fmoc-PEA is a protected amino acid ADC linker intermediate used in peptide synthesis for antibody-drug conjugates. It supports selective conjugation and controlled linker assembly, enhancing ADC stability and payload attachment. Keywords: ADC linker, Fmoc protection, peptide synthesis, linker intermediate, antibody-drug conjugate. Inquiry
BADC-00678 SPP 341498-08-6
SPP is a cleavable peptide ADC linker featuring stable conjugation and enzymatic cleavage properties. Ideal for targeted payload delivery and precision antibody-drug conjugate synthesis. Inquiry
BADC-00679 2,5-dioxopyrrolidin-1-yl 3-(bis(4-methoxyphenyl)(phenyl)methoxy)propanoate 370856-45-4
2,5-dioxopyrrolidin-1-yl 3-(bis(4-methoxyphenyl)(phenyl)methoxy)propanoate is a linker for antibody-drug-conjugation (ADC). Inquiry
BADC-00682 2,5-dioxopyrrolidin-1-yl 3-(4-hydroxyphenoxy)propanoate 616889-42-0
2,5-dioxopyrrolidin-1-yl 3-(4-hydroxyphenoxy)propanoate is an NHS ester ADC linker facilitating efficient antibody conjugation through phenolic hydroxyl groups, enhancing payload stability and targeted delivery in antibody-drug conjugates. Inquiry
BADC-00684 EC089 625827-91-0
EC089 is a proprietary ADC linker designed for stable conjugation and efficient drug release, optimized for enhanced antibody-drug conjugate pharmacodynamics and targeted cancer therapy applications. Inquiry
BADC-00686 2,5-dioxopyrrolidin-1-yl 3-Iodo-4-methoxybenzoate 727659-89-4
2,5-dioxopyrrolidin-1-yl 3-Iodo-4-methoxybenzoate is an NHS ester ADC linker intermediate with iodinated aromatic group for efficient amine-reactive conjugation and enhanced payload stability in antibody-drug conjugates. Keywords: ADC linker, NHS ester, iodinated linker, amine conjugation, payload stability. Inquiry
BADC-00688 2,5-dioxopyrrolidin-1-yl 18-((4-(3,5-dioxohexyl)phenyl)amino)-14,18-dioxo-4,7,10-trioxa-13-azaoctadecan-1-oate 782475-29-0
2,5-dioxopyrrolidin-1-yl 18-((4-(3,5-dioxohexyl)phenyl)amino)-14,18-dioxo-4,7,10-trioxa-13-azaoctadecan-1-oate is a linker for antibody-drug-conjugation (ADC). Inquiry
BADC-00689 (2,5-dioxopyrrolidin-1-yl) 4-methyl-4-(methyldisulfanyl)pentanoate 796073-56-8
(2,5-dioxopyrrolidin-1-yl) 4-methyl-4-(methyldisulfanyl)pentanoate is a cleavable ADC linker intermediate featuring a disulfide bond and NHS ester, designed for efficient thiol-reactive conjugation in antibody-drug conjugates. It enhances controlled payload release and improves linker stability in ADC applications. Keywords: ADC linker, disulfide linker, NHS ester, thiol conjugation, controlled release. Inquiry
BADC-00690 (2,5-dioxopyrrolidin-1-yl) 4-(methyldisulfanyl)pentanoate 796073-59-1
(2,5-dioxopyrrolidin-1-yl) 4-(methyldisulfanyl)pentanoate is an ADC linker intermediate with a disulfide-containing cleavable moiety and NHS ester functionality. It facilitates site-specific thiol conjugation, promoting effective payload delivery and selective drug release in antibody-drug conjugates. Keywords: ADC linker, cleavable disulfide, NHS ester, thiol-reactive, payload delivery. Inquiry
BADC-00691 (2,5-dioxopyrrolidin-1-yl) 3-(2,3-dihydrothieno[3,4-b][1,4]dioxin-3-ylmethoxy)propanoate 853799-72-1
(2,5-dioxopyrrolidin-1-yl) 3-(2,3-dihydrothieno[3,4-b][1,4]dioxin-3-ylmethoxy)propanoate is a linker for antibody-drug-conjugation (ADC). Inquiry
BADC-00695 Fmoc-3VVD-OH 863971-44-2
Fmoc-3VVD-OH is a protected amino acid derivative for peptide-based ADC linker synthesis, enabling controlled conjugation and enhanced stability of antibody-drug conjugates. Inquiry
BADC-00697 Boc-Val-Cit-PABA 870487-09-5
Boc-Val-Cit-PABA is a protected peptide ADC linker featuring valine-citrulline sequence and PABA spacer. It supports enzymatic cleavage and precise payload release in antibody-drug conjugates. Inquiry
BADC-00709 Fmoc-Phe-Lys(Trt)-PAB 1116085-98-3
Fmoc-Phe-Lys(Trt)-PAB is a peptide-based ADC linker intermediate with Fmoc and Trt protections and a para-aminobenzyl (PAB) spacer, designed for enzyme-cleavable payload release in antibody-drug conjugates, improving therapeutic targeting and stability. Keywords: ADC linker, peptide linker, enzyme-cleavable, Fmoc, Trt protection. Inquiry
BADC-00710 Fmoc-Gly3-Val-Cit-PAB 2647914-09-6
Fmoc-Gly3-Val-Cit-PAB is a peptide ADC linker intermediate with tri-glycine spacer, Valine-Citrulline cleavable sequence, and para-aminobenzyl (PAB) group, enabling enzyme-triggered payload release in antibody-drug conjugates for enhanced targeted therapy. Keywords: ADC linker, cleavable peptide, Val-Cit, payload release, targeted delivery. Inquiry
BADC-00711 Fmoc-Gly3-Val-Cit-PAB-PNP 2647914-16-5
Fmoc-Gly3-Val-Cit-PAB-PNP is a peptide-based ADC linker intermediate activated with PNP ester, combining tri-glycine spacer and Valine-Citrulline cleavable linker for controlled drug release and efficient conjugation in antibody-drug conjugates. Keywords: ADC linker, peptide linker, PNP ester, cleavable linker, payload conjugation. Inquiry
BADC-00873 Ald-CH2-PEG3-azide 1002342-83-7
Ald-CH2-PEG3-azide is a bifunctional ADC linker intermediate combining aldehyde and azide groups for versatile conjugation strategies, enhancing targeted payload delivery and stability. Inquiry
BADC-00875 m-PEG6-SS-PEG6-methyl 1007386-15-3
m-PEG6-SS-PEG6-methyl is a cleavable disulfide-containing PEG ADC linker providing enhanced hydrophilicity and controlled intracellular payload release in antibody-drug conjugates. Inquiry
BADC-00876 N-Boc-diethanolamine 103898-11-9
N-Boc-diethanolamine is a versatile intermediate for ADC linker synthesis. Featuring a protected amine and two hydroxyl groups, it is ideal for constructing multi-functional linkers and PEGylated drug carriers. Its flexibility allows further modification for optimized stability and targeting. Inquiry
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