2,5-Dioxopyrrolidin-1-yl nonanoate

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Reagent Code: #83216
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CAS Number 104943-23-9

science Other reagents with same CAS 104943-23-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.31 g/mol
Formula C₁₃H₂₁NO₄
badge Registry Numbers
MDL Number MFCD28125395
thermostat Physical Properties
Boiling Point 348.4±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage room temperature, inert atmosphere

description Product Description

This compound is widely used in the field of bioconjugation and protein labeling. It serves as an activated ester, facilitating the attachment of nonanoate groups to amino groups in proteins, peptides, or other biomolecules. This is particularly useful in modifying biomolecules for research, diagnostics, and therapeutic applications. It is also employed in the synthesis of polymers and materials where specific functionalization is required. Additionally, it plays a role in creating drug delivery systems by enabling the conjugation of active pharmaceutical ingredients to carriers or targeting moieties. Its reactivity and stability make it a valuable tool in organic synthesis and biochemical engineering.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,431.00
inventory 1g
10-20 days ฿6,543.00
inventory 250mg
10-20 days ฿2,430.00

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2,5-Dioxopyrrolidin-1-yl nonanoate
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This compound is widely used in the field of bioconjugation and protein labeling. It serves as an activated ester, facilitating the attachment of nonanoate groups to amino groups in proteins, peptides, or other biomolecules. This is particularly useful in modifying biomolecules for research, diagnostics, and therapeutic applications. It is also employed in the synthesis of polymers and materials where specific functionalization is required. Additionally, it plays a role in creating drug delivery systems

This compound is widely used in the field of bioconjugation and protein labeling. It serves as an activated ester, facilitating the attachment of nonanoate groups to amino groups in proteins, peptides, or other biomolecules. This is particularly useful in modifying biomolecules for research, diagnostics, and therapeutic applications. It is also employed in the synthesis of polymers and materials where specific functionalization is required. Additionally, it plays a role in creating drug delivery systems by enabling the conjugation of active pharmaceutical ingredients to carriers or targeting moieties. Its reactivity and stability make it a valuable tool in organic synthesis and biochemical engineering.

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