Dibenzyl 2,2'-((3,3'-disulfanediylbis(2-benzylpropanoyl))bis(azanediyl))diacetate

98%

Reagent Code: #179240
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CAS Number 141437-88-9

science Other reagents with same CAS 141437-88-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 684.86 g/mol
Formula C₃₈H₄₀N₂O₆S₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a multifunctional crosslinking agent in polymer chemistry, particularly in the development of sulfur-containing polyamide networks. Its structure allows for the formation of disulfide bridges, enabling self-healing properties and enhanced mechanical resilience in specialty coatings and elastomers. Commonly applied in advanced material science for stimuli-responsive films and controlled drug delivery matrices due to its redox-sensitive cleavage characteristics. Also utilized in synthesizing dendritic macromolecules where precise branching and stability under physiological conditions are required.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿9,680.00
inventory 10mg
10-20 days ฿14,500.00
inventory 25mg
10-20 days ฿30,230.00

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Dibenzyl 2,2'-((3,3'-disulfanediylbis(2-benzylpropanoyl))bis(azanediyl))diacetate
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Used as a multifunctional crosslinking agent in polymer chemistry, particularly in the development of sulfur-containing polyamide networks. Its structure allows for the formation of disulfide bridges, enabling self-healing properties and enhanced mechanical resilience in specialty coatings and elastomers. Commonly applied in advanced material science for stimuli-responsive films and controlled drug delivery matrices due to its redox-sensitive cleavage characteristics. Also utilized in synthesizing dendri

Used as a multifunctional crosslinking agent in polymer chemistry, particularly in the development of sulfur-containing polyamide networks. Its structure allows for the formation of disulfide bridges, enabling self-healing properties and enhanced mechanical resilience in specialty coatings and elastomers. Commonly applied in advanced material science for stimuli-responsive films and controlled drug delivery matrices due to its redox-sensitive cleavage characteristics. Also utilized in synthesizing dendritic macromolecules where precise branching and stability under physiological conditions are required.

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