2,2-Dimethyl-4-oxo-3,8,11-trioxa-5,14-diazahexadecan-16-oic acid

95%

Reagent Code: #131701
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CAS Number 356066-44-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.36 g/mol
Formula C₁₃H₂₆N₂O₆
badge Registry Numbers
MDL Number MFCD24465652
thermostat Physical Properties
Boiling Point 460.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.127±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, especially in the development of peptide-based drugs and prodrugs. Its structure allows for selective functionalization, making it valuable in creating biodegradable linkers and spacers that improve drug solubility and bioavailability. Commonly employed in controlled release systems due to its ability to form ester and amide bonds that are cleaved under physiological conditions. Also utilized in the design of polymer-drug conjugates for targeted delivery, particularly in oncology and anti-inflammatory therapies. Its polyether and amino acid-like features support compatibility with biological systems, reducing immunogenicity and enhancing stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,500.00
inventory 250mg
10-20 days ฿29,300.00
2,2-Dimethyl-4-oxo-3,8,11-trioxa-5,14-diazahexadecan-16-oic acid
Used primarily as a key intermediate in the synthesis of pharmaceuticals, especially in the development of peptide-based drugs and prodrugs. Its structure allows for selective functionalization, making it valuable in creating biodegradable linkers and spacers that improve drug solubility and bioavailability. Commonly employed in controlled release systems due to its ability to form ester and amide bonds that are cleaved under physiological conditions. Also utilized in the design of polymer-drug conjugates for targeted delivery, particularly in oncology and anti-inflammatory therapies. Its polyether and amino acid-like features support compatibility with biological systems, reducing immunogenicity and enhancing stability.
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