Tert-butyl (2-acrylamidoethyl)carbamate

95%

Reagent Code: #242617
fingerprint
CAS Number 165196-44-1

science Other reagents with same CAS 165196-44-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.26 g/mol
Formula C₁₀H₁₈N₂O₃
badge Registry Numbers
MDL Number MFCD24468676
inventory_2 Storage & Handling
Storage -20°C, dry, sealed

description Product Description

Used as a reactive monomer in the synthesis of functional polymers, particularly in controlled radical polymerization techniques like RAFT or ATRP. Its acrylamide group enables polymerization, while the tert-butoxycarbonyl (Boc)-protected amine allows for post-polymerization modification after deprotection. Commonly employed in creating stimuli-responsive hydrogels, drug delivery carriers, and bioconjugates due to its biocompatibility and ability to introduce cationic amine groups upon Boc removal. Also utilized in surface grafting applications to modify material properties such as wettability, adhesion, or biointerfacial behavior.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,030.00
inventory 1g
10-20 days ฿12,000.00
inventory 100mg
10-20 days ฿4,050.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Tert-butyl (2-acrylamidoethyl)carbamate
No image available

Used as a reactive monomer in the synthesis of functional polymers, particularly in controlled radical polymerization techniques like RAFT or ATRP. Its acrylamide group enables polymerization, while the tert-butoxycarbonyl (Boc)-protected amine allows for post-polymerization modification after deprotection. Commonly employed in creating stimuli-responsive hydrogels, drug delivery carriers, and bioconjugates due to its biocompatibility and ability to introduce cationic amine groups upon Boc removal. Also

Used as a reactive monomer in the synthesis of functional polymers, particularly in controlled radical polymerization techniques like RAFT or ATRP. Its acrylamide group enables polymerization, while the tert-butoxycarbonyl (Boc)-protected amine allows for post-polymerization modification after deprotection. Commonly employed in creating stimuli-responsive hydrogels, drug delivery carriers, and bioconjugates due to its biocompatibility and ability to introduce cationic amine groups upon Boc removal. Also utilized in surface grafting applications to modify material properties such as wettability, adhesion, or biointerfacial behavior.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...