tert-Butyl 1-iodo-3,6,9,12-tetraoxapentadecan-15-oate

95%

Reagent Code: #132018
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CAS Number 1291090-31-7

science Other reagents with same CAS 1291090-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 432.29 g/mol
Formula C₁₅H₂₉IO₆
badge Registry Numbers
MDL Number MFCD31656967
thermostat Physical Properties
Boiling Point 431.2±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.334±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of functionalized polymers and PEGylated compounds. Its iodo terminus allows for further coupling reactions, such as in click chemistry or nucleophilic substitutions, while the PEG-like chain provides water solubility and biocompatibility. Commonly employed in bioconjugation to attach payloads like drugs, probes, or nanoparticles to targeting molecules. Also utilized in surface modification of nanoparticles and biosensors due to its ability to anchor via the iodine group and present a reactive ester for subsequent functionalization.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,310.00
inventory 1g
10-20 days ฿8,740.00
inventory 5g
10-20 days ฿33,010.00

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tert-Butyl 1-iodo-3,6,9,12-tetraoxapentadecan-15-oate
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Used as a key intermediate in the synthesis of functionalized polymers and PEGylated compounds. Its iodo terminus allows for further coupling reactions, such as in click chemistry or nucleophilic substitutions, while the PEG-like chain provides water solubility and biocompatibility. Commonly employed in bioconjugation to attach payloads like drugs, probes, or nanoparticles to targeting molecules. Also utilized in surface modification of nanoparticles and biosensors due to its ability to anchor via the io

Used as a key intermediate in the synthesis of functionalized polymers and PEGylated compounds. Its iodo terminus allows for further coupling reactions, such as in click chemistry or nucleophilic substitutions, while the PEG-like chain provides water solubility and biocompatibility. Commonly employed in bioconjugation to attach payloads like drugs, probes, or nanoparticles to targeting molecules. Also utilized in surface modification of nanoparticles and biosensors due to its ability to anchor via the iodine group and present a reactive ester for subsequent functionalization.

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