Benzyl (2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl)carbamate

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Reagent Code: #128247
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CAS Number 206265-31-8

science Other reagents with same CAS 206265-31-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.37 g/mol
Formula C₁₆H₂₅NO₆
badge Registry Numbers
MDL Number MFCD29918235
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

This compound, a Cbz-protected amino-PEG4-ol (tetraethylene glycol with a protected primary amine), serves as a key building block and linker in organic synthesis for peptides, complex molecules, and bioconjugates. The carbamate group protects the amine, allowing selective reactions at the terminal hydroxyl while the polyether chain enhances solubility in polar and aqueous solvents. It is particularly valuable in pharmaceutical applications, such as antibody-drug conjugates (ADCs) and targeted drug delivery systems, where mild deprotection enables precise control and minimizes impact on other functional groups.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,260.00
inventory 1g
10-20 days ฿19,680.00

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Benzyl (2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl)carbamate
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This compound, a Cbz-protected amino-PEG4-ol (tetraethylene glycol with a protected primary amine), serves as a key building block and linker in organic synthesis for peptides, complex molecules, and bioconjugates. The carbamate group protects the amine, allowing selective reactions at the terminal hydroxyl while the polyether chain enhances solubility in polar and aqueous solvents. It is particularly valuable in pharmaceutical applications, such as antibody-drug conjugates (ADCs) and targeted

This compound, a Cbz-protected amino-PEG4-ol (tetraethylene glycol with a protected primary amine), serves as a key building block and linker in organic synthesis for peptides, complex molecules, and bioconjugates. The carbamate group protects the amine, allowing selective reactions at the terminal hydroxyl while the polyether chain enhances solubility in polar and aqueous solvents. It is particularly valuable in pharmaceutical applications, such as antibody-drug conjugates (ADCs) and targeted drug delivery systems, where mild deprotection enables precise control and minimizes impact on other functional groups.

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