Propargyl-peg1-t-butyl ester

95%

Reagent Code: #109388
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CAS Number 488150-84-1

science Other reagents with same CAS 488150-84-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.23 g/mol
Formula C₁₀H₁₆O₃
badge Registry Numbers
MDL Number MFCD26793744
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various compounds, particularly in the creation of prodrugs and targeted drug delivery systems. Its structure allows for efficient conjugation with other molecules, making it valuable in the design of PEGylated compounds, which enhance solubility, stability, and bioavailability of therapeutic agents. Additionally, it is employed in click chemistry reactions due to its propargyl group, enabling the formation of stable triazole linkages. This property is particularly useful in bioconjugation and the development of novel biomaterials.

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Test Parameter Specification
Appearance Colorless Liquid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿77,049.00

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Propargyl-peg1-t-butyl ester
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This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various compounds, particularly in the creation of prodrugs and targeted drug delivery systems. Its structure allows for efficient conjugation with other molecules, making it valuable in the design of PEGylated compounds, which enhance solubility, stability, and bioavailability of therapeutic agents. Additionally, it is employed in click chemistry reactions due to it

This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various compounds, particularly in the creation of prodrugs and targeted drug delivery systems. Its structure allows for efficient conjugation with other molecules, making it valuable in the design of PEGylated compounds, which enhance solubility, stability, and bioavailability of therapeutic agents. Additionally, it is employed in click chemistry reactions due to its propargyl group, enabling the formation of stable triazole linkages. This property is particularly useful in bioconjugation and the development of novel biomaterials.

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