N-BOC-2-MaleMidoethylaMine

97%

Reagent Code: #218406
fingerprint
CAS Number 134272-63-2

science Other reagents with same CAS 134272-63-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.26 g/mol
Formula C₁₁H₁₆N₂O₄
badge Registry Numbers
MDL Number MFCD03425523
thermostat Physical Properties
Melting Point 110-115 °C
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Widely used in pharmaceutical and peptide synthesis, this compound serves as a protected amine building block that enables selective reactions in multi-step organic syntheses. Its maleimide group allows for efficient conjugation with thiol-containing molecules via Michael addition, making it valuable in the development of bioconjugates, drug delivery systems, and antibody-drug conjugates (ADCs). The BOC (tert-butoxycarbonyl) group provides reversible protection of the amine, ensuring stability during reactions and easy removal under mild acidic conditions when needed. It is particularly useful in creating linker systems in targeted therapies and in the preparation of functionalized polymers or surfaces in bioengineering applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,290.00
inventory 1g
10-20 days ฿5,120.00
N-BOC-2-MaleMidoethylaMine
No image available

Widely used in pharmaceutical and peptide synthesis, this compound serves as a protected amine building block that enables selective reactions in multi-step organic syntheses. Its maleimide group allows for efficient conjugation with thiol-containing molecules via Michael addition, making it valuable in the development of bioconjugates, drug delivery systems, and antibody-drug conjugates (ADCs). The BOC (tert-butoxycarbonyl) group provides reversible protection of the amine, ensuring stability during rea

Widely used in pharmaceutical and peptide synthesis, this compound serves as a protected amine building block that enables selective reactions in multi-step organic syntheses. Its maleimide group allows for efficient conjugation with thiol-containing molecules via Michael addition, making it valuable in the development of bioconjugates, drug delivery systems, and antibody-drug conjugates (ADCs). The BOC (tert-butoxycarbonyl) group provides reversible protection of the amine, ensuring stability during reactions and easy removal under mild acidic conditions when needed. It is particularly useful in creating linker systems in targeted therapies and in the preparation of functionalized polymers or surfaces in bioengineering applications.

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...