N,N'-Bis[3-(tert-butoxycarbonylamino)propyl]glycinamide

93%

Reagent Code: #217703
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CAS Number 1822851-77-3

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 388.51 g/mol
Formula C₁₈H₃₆N₄O₅
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in peptide synthesis and bioconjugation processes, this compound functions as a bifunctional linker that enables the coupling of biomolecules or functional groups in a controlled manner. Its protected amine groups allow for selective deprotection and further derivatization, making it valuable in the development of pharmaceuticals, diagnostic agents, and targeted drug delivery systems. It is particularly useful in solid-phase peptide synthesis where precise assembly of amino acid sequences is required. Additionally, its hydrophilic spacer arms can improve solubility and reduce aggregation in complex molecular constructs.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,510.00

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N,N'-Bis[3-(tert-butoxycarbonylamino)propyl]glycinamide
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Used as a key intermediate in peptide synthesis and bioconjugation processes, this compound functions as a bifunctional linker that enables the coupling of biomolecules or functional groups in a controlled manner. Its protected amine groups allow for selective deprotection and further derivatization, making it valuable in the development of pharmaceuticals, diagnostic agents, and targeted drug delivery systems. It is particularly useful in solid-phase peptide synthesis where precise assembly of amino aci

Used as a key intermediate in peptide synthesis and bioconjugation processes, this compound functions as a bifunctional linker that enables the coupling of biomolecules or functional groups in a controlled manner. Its protected amine groups allow for selective deprotection and further derivatization, making it valuable in the development of pharmaceuticals, diagnostic agents, and targeted drug delivery systems. It is particularly useful in solid-phase peptide synthesis where precise assembly of amino acid sequences is required. Additionally, its hydrophilic spacer arms can improve solubility and reduce aggregation in complex molecular constructs.

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