Maleimide(-MAL) PEG

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Catalog No.	Name	M.W.	Purity
In stock BPG-4879	Mal(Br2)-AEEA	401.00	>98%
In stock BPG-4814 CAS: 2739896-54-7	Mal-propionylamido-PEG1-NHS-acetate	367.31	N/A
In stock BPG-4812 CAS: 1373284-24-2	Mal-propionylamido-PEG2-NHS acetate	411.37	N/A
In stock BPG-4811 CAS: 151225-46-6	Mal-propionylamido-PEG5-acetic acid	446.45	N/A
In stock BPG-4810 CAS: 1424363-49-4	Mal-propionylamido-PEG4-acetic acid	402.40	N/A
In stock BPG-4809 CAS: 450368-58-8	Mal-propionylamido-PEG3-acetic acid	358.34	N/A
In stock BPG-4808 CAS: 936616-30-7	Mal-propionylamido-PEG2-acetic acid	314.29	N/A
In stock BPG-4804 CAS: 1127247-28-2	MAL-PEG4-t-boc-hydrazide	530.57	N/A
In stock BPG-4801 CAS: 518044-39-8	Mal-PEG6-CH2COOH	419.42	N/A
In stock BPG-4380	Mal-PEG8-Amine, TFA salt	492.6	≥98%
In stock BPG-4379 CAS: 2170654-73-4	Mal-PEG5-amine TFA salt	360.4	0.98
In stock BPG-4378 CAS: 2221042-92-6	Mal-PEG4-amine TFA salt	316.4	0.98
In stock BPG-4377 CAS: 2101722-60-3	Mal-amido-PEG12-NHS	865.9	0.95
In stock BPG-4376	3,4-Dibromo-Mal-amido-PEG4-azide	557.2	0.95
In stock BPG-4375	N-(t-butyl ester-PEG3)-N-bis(PEG3-Mal)	958.1	N/A
In stock BPG-4374	N-(Mal-PEG8-carbonyl)-N-bis(PEG8-t-butyl ester)	1552.9	0.98
In stock BPG-4373	Tri(Mal-PEG2-amide)-amine	1077.2	0.98
In stock BPG-4372	Diphenylthiol-Mal-PEG8-PEG4-Biotin	1182.5	N/A
In stock BPG-4371	Biotin-PEG4-Amide-PEG8-3,4-Dibromo-Mal	1124	0.98
In stock BPG-4370	Methyltetrazine-PEG4-Amido-PEG8-Mal-3,4-Dibromo	1024.8	0.98

C18-PEG-MAL ³
Small-molecule Maleimide PEG ⁵⁵

Background

What is Maleimide PEG?

Maleimide (-MAL) PEG is a polyethylene glycol (PEG) molecule containing a maleimide functional group. The maleimide functional group in maleimide PEG allows specific conjugation reactions with molecules containing thiol (sulfhydryl) groups, such as cysteine residues in proteins or thiol-modified nucleotides. This conjugation reaction forms a stable covalent bond, making maleimide PEG useful for attaching PEG chains to proteins, peptides, or other molecules for various purposes, such as enhancing solubility, stability, or bioavailability.

Fig. 1. Multiplicity of maleimide functional groups on the PEG chain (Journal of Pharmaceutical and Biomedical Analysis. 2019, 164: 452-459).

Functions of Maleimide PEG

Maleimide PEG has a variety of functions that allow it to be used in a variety of applications. The maleimide group can react with the thiol group to form a stable covalent bond, allowing maleimide PEG to be used for bioconjugation, drug delivery and tissue engineering. The hydrophilic and biocompatible nature of the PEG component allows maleimide PEG to be used as a coating material for pharmaceutical formulations and medical devices. The unique structure and chemistry of maleimide PEG makes it a versatile polymer that can be customized for specific applications.

Applications for Maleimide PEG

Maleimide PEG has a variety of applications in the biomedical field.

Protein and Antibody Labeling - Maleimide-PEG is used for site-specific labeling of proteins and antibodies by concatenating the PEG portion with exposed cysteine residues.
Drug Delivery Systems - Maleimide-PEG can be used to modify drug molecules or nanocarriers to enhance their solubility, stability and targeted delivery.
Bioconjugation Strategies - Maleimide-PEG allows covalent attachment of therapeutic agents, imaging probes or other functional molecules to thiol-containing biomolecules such as peptides and proteins.
Surface Modification - Maleimide-PEG can be used to modify the surface of materials such as nanoparticles and biosensors to enhance stability and biocompatibility.
Diagnostic Assays - Maleimide-PEG can be used in a variety of diagnostic assays, including immunoassays and biosensors, to enable efficient attachment of biomolecules to sensor surfaces.

Benefits of Maleimide PEG

Maleimide-PEG offers several advantages that contribute to its widespread use in bioconjugation and other applications. These advantages include:

High specificity. The maleimide moiety readily reacts with thiol-containing molecules, resulting in site-specific bioconjugation and minimal off-target modifications.
Stable covalent bonding. The maleimide-thiol reaction forms a stable covalent bond, ensuring long-term stability of the bioconjugate.
Controlled splicing. The selective reactivity of maleimide-PEG allows for precise control of the degree of splicing, providing the flexibility to modify the properties of the biomolecule.
Enhanced water solubility. The PEG backbone improves the water solubility of maleimide-PEG, allowing for efficient concatenation in an aqueous environment.
Reduced immunogenicity. The polyethylene glycolization of maleimide-PEG has been shown to reduce immunogenicity, making it suitable for biomedical applications.

BOC Sciences is a leading supplier of high-quality chemicals, including maleimide PEG, which is widely used in a variety of research applications. We offer a wide range of maleimide PEGs with varying molecular weights and functionalities to meet our customers' specific needs. Our maleimide PEG is of high quality and purity and we guarantee the best prices in the market. We also offer custom synthesis of maleimide PEG and other chemicals to meet the specific needs of our customers.

Reference

Wang, J. et al. Multi-arm PEG-maleimide conjugation intermediate characterization and hydrolysis study by a selective HPLC method. Journal of Pharmaceutical and Biomedical Analysis. 2019, 164: 452-459.

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