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Propargyl-PEG8-acid is a polyethylene glycol (PEG) based linker bearing a terminal propargyl (alkyne) group and a carboxylic acid, used for conjugation in PROTAC and antibody-drug conjugate (ADC) synthesis.
Contains a terminal propargyl alkyne for click chemistry.
Provides a carboxylic acid handle for amide coupling.
Approximate molecular weight 436.49 g/mol.
High purity (98.0%) suitable for research applications.
Available in multiple pack sizes, including 1 G for lab-scale use.
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Propargyl-PEG3-acid is a PEG-based bifunctional linker bearing a terminal propargyl (alkyne) group and a carboxylic acid handle, used for click chemistry and conjugation in small-molecule and bioconjugate synthesis.
Terminal alkyne functional group for copper-catalyzed azide-alkyne cycloaddition
Carboxylic acid end group for amide coupling and further derivatization
Three-unit PEG spacer imparts solubility and flexibility
High reported purity suitable for synthetic applications
Available in 1 g pack for small-scale synthesis
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Bis-PEG1-C-PEG1-CH2COOH is a PEG-based bifunctional linker bearing a terminal carboxylic acid; it serves as a building block for the synthesis of PROTACs and other conjugates. The material is supplied as an off-white to yellow oil, and is typically offered at research-grade purity for small-scale synthetic work.
PEG-based bifunctional linker for PROTAC and conjugate synthesis.
Terminal carboxylic acid enables standard amide or ester coupling reactions.
Low molecular weight building block (MW 350.4) for modular design.
Supplied as an off-white to yellow oil suitable for solution-phase synthesis.
High purity appropriate for research applications (95.0%).
Available in small pack sizes for screening and library synthesis.
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Propargyl-PEG5-acid is a polyethylene glycol-based linker with a terminal propargyl (alkyne) group and a terminal carboxylic acid. It is used as a non-cleavable PEG spacer in bioconjugation, including antibody-drug conjugate and PROTAC synthesis, and as a reagent for copper-catalyzed azide-alkyne cycloaddition (CuAAC).
Propargyl-PEG3-acid is a PEG-based bifunctional linker bearing a terminal propargyl (alkyne) group and a carboxylic acid. It is used in bioconjugation and medicinal chemistry applications such as click chemistry and PROTAC or ADC linker construction.
Contains a terminal alkyne for copper-catalyzed azide-alkyne cycloaddition
Three-unit PEG spacer improves solubility and flexibility
Carboxylic acid functionality enables standard coupling chemistries
High purity (99.14%) and liquid form, colorless to light yellow
Available in multiple sizes, including a 5 g package; recommended storage: -20°C for long-term stability
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Propargyl-PEG2-acid (CAS 1859379-85-3) is a polyethylene glycol (PEG)-based small molecule featuring a terminal propargyl (alkyne) group and a carboxylic acid moiety The alkyne functionality facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions commonly referred to as click chemistry This enables site-specific conjugation to azide-containing molecules for the synthesis of bioconjugates such as antibody-drug conjugates (ADCs) labeling probes or other functionalized biomolecules Its PEG2 spacer increases solubility and flexibility supporting its application in biomedical research requiring stable and efficient heterobifunctional linkers
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Propargyl-PEG7-acid is a PEG7-based linker bearing a terminal propargyl (alkyne) group used for assembling PROTACs, synthesizing antibody-drug conjugates, and performing copper-catalyzed azide-alkyne click reactions.
Terminal alkyne for CuAAC click chemistry
PEG7 spacer improves solubility and linker flexibility
Suitable for PROTAC and ADC linker synthesis
Available in multiple pack sizes for scalable use
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Propargyl-PEG3-acid is a PEG-based bifunctional linker featuring a terminal propargyl (alkyne) group and a carboxylic acid; it is used as a non-cleavable three-unit PEG linker for antibody-drug conjugates and as a PEG linker for PROTACs, enabling copper-catalyzed azide-alkyne cycloaddition (CuAAC) click chemistry.
Non-cleavable three-unit PEG linker suitable for ADC and PROTAC synthesis.
Terminal alkyne enables copper-catalyzed azide-alkyne cycloaddition for conjugation to azide-containing molecules.
High purity appropriate for research-scale bioconjugation workflows.
Available in multiple pack sizes to support small-scale and larger preparative work.
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Propargyl-PEG7-acid is a polyethylene glycol (PEG)-based linker with a terminal propargyl (alkyne) group and a carboxylic acid. It is used as a click-chemistry compatible linker for assembling PROTACs and antibody-drug conjugates, enabling copper-catalyzed azide-alkyne cycloaddition (CuAAC) to attach payloads or targeting moieties.
Cleavable PEG linker suitable for PROTAC and ADC synthesis.
Contains a terminal alkyne for CuAAC (click chemistry) conjugation.
High purity supports reliable coupling reactions.
Stable as a dry powder when stored under inert atmosphere at low temperature.
Available in small research packs for medicinal chemistry use.
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Propargyl-PEG6-acid is a PEG6-based linker and click-chemistry reagent containing a terminal propargyl (alkyne) group and a carboxylic acid. It is used to introduce a PEG6 spacer in the synthesis of PROTACs and antibody-drug conjugates (ADCs) and undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAC) for bioconjugation.
Propargyl-PEG7-acid is a PEG-based linker and click chemistry reagent containing a terminal alkyne that enables copper-catalyzed azide-alkyne cycloaddition. It is used as a PROTAC linker and as a cleavable linker in antibody-drug conjugate synthesis.
Contains terminal alkyne suitable for CuAAc
PEG7 spacer provides solubility and conformational flexibility
Applicable as a cleavable linker for ADC synthesis
High purity: ≥98.0% (NMR)
Available in small-scale pack sizes for research use
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Propargyl-PEG5-acid is a PEG-based linker bearing a terminal propargyl (alkyne) group and a free carboxylic acid. It is used as a click-chemistry reagent and as a non-cleavable five-unit PEG spacer for bioconjugation workflows such as PEGylation and antibody-drug conjugate linker synthesis. The material is supplied as a colorless to light-yellow liquid with ≥98.0% purity and is intended for research use; store protected from light at -20°C, or in solution at -80°C for longer-term storage.
Contains terminal propargyl alkyne for copper-catalyzed azide-alkyne cycloaddition.
Five-unit PEG spacer improves solubility and reduces aggregation.
Free carboxylic acid enables conjugation through standard activation chemistries.
High purity (≥98.0%) for reproducible research results.
Colorless to light-yellow liquid; stable when stored protected from light at -20°C.
Intended for research use only; not validated for clinical applications.
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Propargyl-PEG7-acid is a PEG-based linker bearing a terminal propargyl (alkyne) group used for click chemistry, PROTAC assembly, and antibody-drug conjugate (ADC) synthesis. It is supplied as a light yellow liquid of high purity suitable for research bioconjugation workflows.
Contains a terminal alkyne for copper-catalyzed azide-alkyne cycloaddition (CuAAC).
Suitable for PROTAC and ADC linker synthesis.
High purity (≥98.0%), compatible with analytical workflows.
Light yellow liquid form, convenient for solution-phase conjugation.
Available in small-scale and bulk pack sizes for synthesis needs.
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Propargyl-PEG6-acid is a PEG-based linker bearing a terminal propargyl (alkyne) group, used as a click-chemistry reagent and as a linker in the synthesis of PROTACs and antibody-drug conjugates. The PEG6 spacer increases hydrophilicity and enables conjugation via copper-catalyzed azide-alkyne cycloaddition (CuAAC).
Contains a terminal propargyl (alkyne) functional group.
Suitable for copper-catalyzed azide-alkyne cycloaddition (CuAAC).
Used in synthesis of PROTACs and antibody-drug conjugates.
PEG6 spacer provides hydrophilicity and improved solubility.
Storage recommendations: pure form refrigerated or frozen for long-term stability; store solutions frozen.
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Propargyl-PEG6-acid is a PEG-based linker and click chemistry reagent containing a terminal alkyne. It is used as a linker in PROTAC and ADC synthesis and for copper-catalyzed azide-alkyne cycloaddition (CuAAc) bioconjugation reactions.
cleavable PEG6 linker suitable for PROTAC and ADC synthesis
contains a terminal propargyl (alkyne) group for click chemistry
high purity (≥97.0% by NMR) suitable for research applications
molecular weight 348.39 g/mol, molecular formula C16H28O8
storage: pure form -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month)
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