2-(2,2-Dimethoxyethoxy)ethanamine

97%

Reagent Code: #176401
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CAS Number 1228258-40-9

science Other reagents with same CAS 1228258-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.18 g/mol
Formula C₆H₁₅NO₃
badge Registry Numbers
MDL Number MFCD19215935
inventory_2 Storage & Handling
Storage -20°C, inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized polymers. Its amine and ether groups allow for versatile reactivity, enabling conjugation in drug delivery systems and the development of specialty chemicals. Commonly employed in the synthesis of polymeric ligands and as a building block in creating biologically active molecules. Also finds use in modifying surfaces for biomedical applications due to its bifunctional nature.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,410.00
1g
10-20 days ฿1,870.00
25g
10-20 days ฿21,240.00
5g
10-20 days ฿6,790.00
2-(2,2-Dimethoxyethoxy)ethanamine
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized polymers. Its amine and ether groups allow for versatile reactivity, enabling conjugation in drug delivery systems and the development of specialty chemicals. Commonly employed in the synthesis of polymeric ligands and as a building block in creating biologically active molecules. Also finds use in modifying surfaces for biomedical applications due to its bifunctional nature.

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized polymers. Its amine and ether groups allow for versatile reactivity, enabling conjugation in drug delivery systems and the development of specialty chemicals. Commonly employed in the synthesis of polymeric ligands and as a building block in creating biologically active molecules. Also finds use in modifying surfaces for biomedical applications due to its bifunctional nature.

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