N-(2-Amino-2-oxoethyl)acrylamide

98%

Reagent Code: #218407
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CAS Number 2479-62-1

science Other reagents with same CAS 2479-62-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.13 g/mol
Formula C₅H₈N₂O₂
badge Registry Numbers
MDL Number MFCD12091068
thermostat Physical Properties
Melting Point 129 °C
Boiling Point 430.6±37.0 °C at 760 mmHg (Predicted)
inventory_2 Storage & Handling
Density 1.134±0.06 g/cm3 (Predicted)
Storage 2-8°C, stored in inert gas, avoiding light

description Product Description

Used in the synthesis of biologically active compounds and pharmaceutical intermediates. Its structure allows for incorporation into peptide-like chains, making it useful in drug development where amide and amino functionalities are needed. Commonly employed in modifying biomolecules due to its ability to form stable amide bonds and participate in further conjugation reactions. Also applied in polymer chemistry to introduce functional groups into hydrogels and other functional materials, especially those designed for biomedical applications such as drug delivery systems and tissue engineering scaffolds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿650.00
inventory 5g
10-20 days ฿3,050.00
inventory 25g
10-20 days ฿11,400.00
inventory 100g
10-20 days ฿32,940.00

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N-(2-Amino-2-oxoethyl)acrylamide
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Used in the synthesis of biologically active compounds and pharmaceutical intermediates. Its structure allows for incorporation into peptide-like chains, making it useful in drug development where amide and amino functionalities are needed. Commonly employed in modifying biomolecules due to its ability to form stable amide bonds and participate in further conjugation reactions. Also applied in polymer chemistry to introduce functional groups into hydrogels and other functional materials, especially those

Used in the synthesis of biologically active compounds and pharmaceutical intermediates. Its structure allows for incorporation into peptide-like chains, making it useful in drug development where amide and amino functionalities are needed. Commonly employed in modifying biomolecules due to its ability to form stable amide bonds and participate in further conjugation reactions. Also applied in polymer chemistry to introduce functional groups into hydrogels and other functional materials, especially those designed for biomedical applications such as drug delivery systems and tissue engineering scaffolds.

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