17-Azido-3,6,9,12,15-pentaoxaheptadecan-1-amine

98%

Reagent Code: #76968
fingerprint
CAS Number 516493-93-9

science Other reagents with same CAS 516493-93-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.36 g/mol
Formula C₁₂H₂₆N₄O₅
badge Registry Numbers
MDL Number MFCD16619318
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is widely used in bioconjugation and click chemistry applications due to its azide functional group. It serves as a linker or spacer molecule, enabling the attachment of biomolecules, such as proteins, peptides, or nucleic acids, to other functional groups or surfaces. Its polyether chain provides hydrophilicity and flexibility, making it suitable for use in aqueous environments and reducing steric hindrance during reactions. It is particularly valuable in the development of drug delivery systems, diagnostic probes, and biomaterial modifications. Additionally, its azide group allows for efficient and selective reactions with alkynes via copper-catalyzed azide-alkyne cycloaddition (CuAAC), a cornerstone of bioorthogonal chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to light yellow liquid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,980.00
inventory 1g
10-20 days ฿11,220.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
17-Azido-3,6,9,12,15-pentaoxaheptadecan-1-amine
No image available
This compound is widely used in bioconjugation and click chemistry applications due to its azide functional group. It serves as a linker or spacer molecule, enabling the attachment of biomolecules, such as proteins, peptides, or nucleic acids, to other functional groups or surfaces. Its polyether chain provides hydrophilicity and flexibility, making it suitable for use in aqueous environments and reducing steric hindrance during reactions. It is particularly valuable in the development of drug delivery systems, diagnostic probes, and biomaterial modifications. Additionally, its azide group allows for efficient and selective reactions with alkynes via copper-catalyzed azide-alkyne cycloaddition (CuAAC), a cornerstone of bioorthogonal chemistry.
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...