2-((2-(Prop-2-yn-1-yloxy)ethyl)disulfaneyl)ethan-1-ol

98%

Reagent Code: #223673
fingerprint
CAS Number 1391914-41-2

science Other reagents with same CAS 1391914-41-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.30 g/mol
Formula C₇H₁₂O₂S₂
badge Registry Numbers
MDL Number MFCD28505558
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a crosslinking agent in polymer chemistry, particularly in the synthesis of functional hydrogels and responsive materials. It contains a disulfide group (reducible to thiols), an alkyne moiety for click chemistry reactions, and a terminal hydroxyl group. These features enable efficient thiol-ene couplings (post-reduction) and azide-alkyne cycloadditions, making it valuable in bioconjugation, surface modification, and controlled network formation. Commonly applied in drug delivery systems and biomaterials. Also utilized in the development of biosensors for anchoring biomolecules onto sensor surfaces through selective coupling.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,200.00
inventory 250mg
10-20 days ฿32,000.00
inventory 1g
10-20 days ฿80,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-((2-(Prop-2-yn-1-yloxy)ethyl)disulfaneyl)ethan-1-ol
No image available

Used as a crosslinking agent in polymer chemistry, particularly in the synthesis of functional hydrogels and responsive materials. It contains a disulfide group (reducible to thiols), an alkyne moiety for click chemistry reactions, and a terminal hydroxyl group. These features enable efficient thiol-ene couplings (post-reduction) and azide-alkyne cycloadditions, making it valuable in bioconjugation, surface modification, and controlled network formation. Commonly applied in drug delivery systems and biom

Used as a crosslinking agent in polymer chemistry, particularly in the synthesis of functional hydrogels and responsive materials. It contains a disulfide group (reducible to thiols), an alkyne moiety for click chemistry reactions, and a terminal hydroxyl group. These features enable efficient thiol-ene couplings (post-reduction) and azide-alkyne cycloadditions, making it valuable in bioconjugation, surface modification, and controlled network formation. Commonly applied in drug delivery systems and biomaterials. Also utilized in the development of biosensors for anchoring biomolecules onto sensor surfaces through selective coupling.

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...