O-(2-Aminoethyl)-O'-[2-(Boc-amino)ethyl]tetraethylene Glycol

95%

Reagent Code: #221460
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CAS Number 189209-27-6

science Other reagents with same CAS 189209-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 380.48 g/mol
Formula C₁₇H₃₆N₂O₇
inventory_2 Storage & Handling
Storage 2~8°C, inert gas atmosphere

description Product Description

Used as a hydrophilic linker in bioconjugation and pharmaceutical development, particularly in the synthesis of antibody-drug conjugates (ADCs) and peptide-based therapeutics. Its tetraethylene glycol backbone provides water solubility and flexibility, reducing aggregation and improving bioavailability. The Boc-protected amine and terminal aminoethyl groups allow for sequential, controlled coupling reactions—enabling stepwise assembly of complex molecules. Commonly employed in solid-phase peptide synthesis and PEGylation strategies where moderate chain length and biocompatibility are required. Also utilized in creating spacers for surface immobilization of biomolecules in diagnostic assays and biosensors.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,120.00
250mg
10-20 days ฿2,400.00
5g
10-20 days ฿29,600.00
10g
10-20 days ฿57,600.00
1g
10-20 days ฿7,680.00
25g
10-20 days ฿128,000.00
O-(2-Aminoethyl)-O'-[2-(Boc-amino)ethyl]tetraethylene Glycol
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Used as a hydrophilic linker in bioconjugation and pharmaceutical development, particularly in the synthesis of antibody-drug conjugates (ADCs) and peptide-based therapeutics. Its tetraethylene glycol backbone provides water solubility and flexibility, reducing aggregation and improving bioavailability. The Boc-protected amine and terminal aminoethyl groups allow for sequential, controlled coupling reactions—enabling stepwise assembly of complex molecules. Commonly employed in solid-phase peptide synthes

Used as a hydrophilic linker in bioconjugation and pharmaceutical development, particularly in the synthesis of antibody-drug conjugates (ADCs) and peptide-based therapeutics. Its tetraethylene glycol backbone provides water solubility and flexibility, reducing aggregation and improving bioavailability. The Boc-protected amine and terminal aminoethyl groups allow for sequential, controlled coupling reactions—enabling stepwise assembly of complex molecules. Commonly employed in solid-phase peptide synthesis and PEGylation strategies where moderate chain length and biocompatibility are required. Also utilized in creating spacers for surface immobilization of biomolecules in diagnostic assays and biosensors.

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