3-[2-[2-[(1-Oxo-10-undecyn-1-yl)amino]ethoxy]ethoxy]propanoic Acid 2,5-Dioxo-1-pyrrolidinyl Ester

98%

Reagent Code: #220996
fingerprint
CAS Number 1006592-59-1

science Other reagents with same CAS 1006592-59-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 438.51 g/mol
Formula C₂₂H₃₄N₂O₇
badge Registry Numbers
MDL Number MFCD20229897
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a crosslinking agent in bioconjugation, particularly for coupling peptides or proteins to other molecules via click chemistry. Its activated ester group reacts efficiently with primary amines to form stable amide bonds, while the alkyne group allows for copper-catalyzed azide-alkyne cycloaddition (CuAAC). This dual functionality makes it valuable in drug delivery systems, diagnostic probes, and surface functionalization in biomedical research. Commonly applied in the development of antibody-drug conjugates (ADCs) and labeling biomolecules for imaging.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10mg
10-20 days ฿43,120.00
3-[2-[2-[(1-Oxo-10-undecyn-1-yl)amino]ethoxy]ethoxy]propanoic Acid 2,5-Dioxo-1-pyrrolidinyl Ester
No image available

Used as a crosslinking agent in bioconjugation, particularly for coupling peptides or proteins to other molecules via click chemistry. Its activated ester group reacts efficiently with primary amines to form stable amide bonds, while the alkyne group allows for copper-catalyzed azide-alkyne cycloaddition (CuAAC). This dual functionality makes it valuable in drug delivery systems, diagnostic probes, and surface functionalization in biomedical research. Commonly applied in the development of antibody-drug

Used as a crosslinking agent in bioconjugation, particularly for coupling peptides or proteins to other molecules via click chemistry. Its activated ester group reacts efficiently with primary amines to form stable amide bonds, while the alkyne group allows for copper-catalyzed azide-alkyne cycloaddition (CuAAC). This dual functionality makes it valuable in drug delivery systems, diagnostic probes, and surface functionalization in biomedical research. Commonly applied in the development of antibody-drug conjugates (ADCs) and labeling biomolecules for imaging.

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...