tert-butyl 2-(bis(2-hydroxyethyl)amino)acetate

≥95%

Reagent Code: #244325
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CAS Number 660440-94-8

science Other reagents with same CAS 660440-94-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.28 g/mol
Formula C₁₀H₂₁NO₄
badge Registry Numbers
MDL Number MFCD16152336
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of betaine derivatives and amino acid-based compounds. Its hydroxyl and ester functionalities allow for further chemical modifications, making it valuable in creating biologically active molecules. Commonly employed in the preparation of zwitterionic compounds for use in cosmetic formulations, where it contributes to moisturizing and skin-conditioning properties. Also utilized in the design of prodrugs due to its biodegradable ester group and water-soluble character when deprotected.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,760.00
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tert-butyl 2-(bis(2-hydroxyethyl)amino)acetate
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Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of betaine derivatives and amino acid-based compounds. Its hydroxyl and ester functionalities allow for further chemical modifications, making it valuable in creating biologically active molecules. Commonly employed in the preparation of zwitterionic compounds for use in cosmetic formulations, where it contributes to moisturizing and skin-conditioning properties. Also utilized in the design of

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of betaine derivatives and amino acid-based compounds. Its hydroxyl and ester functionalities allow for further chemical modifications, making it valuable in creating biologically active molecules. Commonly employed in the preparation of zwitterionic compounds for use in cosmetic formulations, where it contributes to moisturizing and skin-conditioning properties. Also utilized in the design of prodrugs due to its biodegradable ester group and water-soluble character when deprotected.

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