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HomePolymer PEGActive esterOH-PEG-SC OH-PEG-SC, MW 2K
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OH-PEG-SC, MW 2K

Catalog #: AP15385
Name: OH-PEG-SC, MW 2K
Molecular Weight: 2000
Purity: ≥95%
Availability: In Stock

OH-PEG-SC, MW 2K

$275.00 – $825.00

OH-PEG-SC, MW 2K features a 2 kDa hydrophilic polyethylene glycol chain with terminal hydroxyl and activated succinimidyl carbonate groups. Its heterobifunctional structure supports primary amine conjugation, stable carbamate bond formation, protein and peptide PEGylation, biomaterial surface modification, and further hydroxyl-based functionalization.

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1 g$275
5 g$825

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SKU: AP15385 Category: OH-PEG-SC
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  • Description
  • Synonyms
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Description

OH-PEG-SC, MW 2K provides a heterobifunctional polyethylene glycol derivative for bioconjugation, protein PEGylation, and biomaterials research and specifically combines a 2 kDa hydrophilic PEG chain with a terminal hydroxyl (OH) group and an activated succinimidyl carbonate (SC) group. This structure supports covalent coupling with primary amines while retaining a hydroxyl functionality for subsequent chemical modification.

Key Features and Benefits
  • 2 kDa PEG Chain: Features a hydrophilic polyethylene glycol backbone with a nominal molecular weight of 2,000 Da for bioconjugation and polymer modification.
  • Heterobifunctional Structure: Combines hydroxyl and succinimidyl carbonate groups at opposite PEG termini for especially versatile chemical functionalization.
  • Activated Succinimidyl Carbonate: Provides an amine-reactive carbonate functionality specifically for covalent conjugation with primary amines.
  • Stable Carbamate Bond Formation: Reacts with suitable amino groups to form covalent carbamate linkages between PEG and conjugated molecules.
  • Terminal Hydroxyl Functionality: Retains an OH group for further derivatization, polymer coupling, or surface modification.
  • Hydrophilic PEG Backbone: Supports investigation of aqueous compatibility, molecular hydration, and solubility of PEG-modified compounds.
  • Selective Amine Conjugation: Enables attachment to accessible lysine residues, N-terminal amino groups, and other primary amines under optimized conditions.
  • Short PEG Chain: Provides a 2 kDa PEG spacer specifically for investigating molecular flexibility, steric effects, and surface hydration while introducing less polymer mass than higher-molecular-weight alternatives.
  • Versatile Chemical Modification: Supports preparation of PEGylated proteins, peptides, polymers, and functionalized biomaterials.
Applications
  • Protein PEGylation: Supports covalent attachment of 2 kDa PEG chains to accessible protein amino groups for stability and solubility studies.
  • Peptide Modification: Enables PEGylation of peptides containing suitable primary amines for investigating molecular properties and conjugation efficiency.
  • Bioconjugation Research: Supports succinimidyl carbonate-mediated coupling of PEG to amine-functionalized biomolecules and synthetic compounds.
  • Drug Delivery Research: Enables preparation of PEG-modified molecular constructs for investigating formulation properties and delivery systems.
  • Biomaterial Functionalization: Supports modification of amine-containing hydrogels, polymers, and biomaterial surfaces with hydrophilic PEG chains.
  • Surface Modification: Useful for introducing PEG functionality onto amine-containing surfaces to investigate hydration and nonspecific adsorption.
  • Hydroxyl Functionalization: Enables further chemical modification of the remaining terminal hydroxyl group after amine conjugation.
  • Polymer Conjugate Development: Supports preparation of heterobifunctional PEG conjugates for advanced polymer and materials research.
  • Protein Stability Studies: Enables investigation of PEGylation effects on protein aggregation, molecular interactions, and physicochemical stability.
Storage and Handling
  • Storage: Store at −20°C in a dry, tightly sealed container under an inert atmosphere when possible, unless otherwise specified. Protect from moisture and excessive heat to minimize hydrolysis of the activated carbonate group.
  • Handling: Handle under dry conditions and prepare solutions immediately before use. For amine conjugation, dissolve the reagent in a compatible dry solvent or suitable amine-free reaction buffer. Phosphate-based buffers around pH 7.0–8.5 may be appropriate, depending on the target molecule. Avoid Tris and other primary amine-containing buffers that compete with the conjugation reaction. Minimize prolonged exposure to aqueous solutions to preserve activated carbonate reactivity.

OH-PEG-SC, MW 2K combines an amine-reactive succinimidyl carbonate group with a terminal hydroxyl functionality for versatile PEG conjugation and specifically supports protein and peptide PEGylation, biomaterial functionalization, surface modification, drug delivery research, and development of advanced polymer conjugates.

AxisPharm offers 5000+ PEG Linkers with high purity. Different kinds of PEG Reagents may be available by custom synthesis.

Synonyms
  • SC-PEG-OH, 2000
Shipping & Delivery
Ships within: 24 hours
Storage condition: -20 ° C
Shipping: Ambient Temperature

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