m-PEG6-Hydrazide

≥95%

Reagent Code: #108828
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CAS Number 1449390-64-0

science Other reagents with same CAS 1449390-64-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.4 g/mol
Formula C₁₄H₃₀N₂O₇
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

m-PEG6-Hydrazide is widely used in bioconjugation and chemical synthesis. It serves as a linker molecule for attaching polyethylene glycol (PEG) chains to various biomolecules, such as proteins, peptides, and antibodies. This modification enhances the solubility, stability, and bioavailability of the conjugated molecules, making it valuable in drug delivery systems. Additionally, it is employed in the development of hydrogels and other biomaterials for tissue engineering and regenerative medicine. Its hydrazide group allows for specific reactions with aldehydes and ketones, enabling precise conjugation in diagnostic assays and targeted therapies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,400.00

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m-PEG6-Hydrazide
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m-PEG6-Hydrazide is widely used in bioconjugation and chemical synthesis. It serves as a linker molecule for attaching polyethylene glycol (PEG) chains to various biomolecules, such as proteins, peptides, and antibodies. This modification enhances the solubility, stability, and bioavailability of the conjugated molecules, making it valuable in drug delivery systems. Additionally, it is employed in the development of hydrogels and other biomaterials for tissue engineering and regenerative medicine. Its hy

m-PEG6-Hydrazide is widely used in bioconjugation and chemical synthesis. It serves as a linker molecule for attaching polyethylene glycol (PEG) chains to various biomolecules, such as proteins, peptides, and antibodies. This modification enhances the solubility, stability, and bioavailability of the conjugated molecules, making it valuable in drug delivery systems. Additionally, it is employed in the development of hydrogels and other biomaterials for tissue engineering and regenerative medicine. Its hydrazide group allows for specific reactions with aldehydes and ketones, enabling precise conjugation in diagnostic assays and targeted therapies.

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