N-Succinimidyl Acetate

98%

Reagent Code: #217130
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CAS Number 14464-29-0

science Other reagents with same CAS 14464-29-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.13 g/mol
Formula C₆H₇NO₄
badge Registry Numbers
MDL Number MFCD00037916
thermostat Physical Properties
Melting Point 132.0 to 136.0 deg-C
inventory_2 Storage & Handling
Storage 2~8°C, sealed

description Product Description

N-Succinimidyl acetate is an active ester used as a selective acetylating agent in organic synthesis. It is particularly valuable for introducing acetyl groups to primary amine functionalities, such as lysine residues or N-terminal amines in peptides, proteins, and other biomolecules, under mild aqueous conditions. This modification helps block reactive amines, enhance protein stability, reduce immunogenicity, or prepare acetylated derivatives for biochemical and pharmaceutical research. It is also employed in the synthesis of modified antibodies, therapeutic proteins, and in applications related to drug delivery and diagnostic development.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿300.00
25g
10-20 days ฿1,010.00
100g
10-20 days ฿4,010.00
500g
10-20 days ฿12,020.00
N-Succinimidyl Acetate
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N-Succinimidyl acetate is an active ester used as a selective acetylating agent in organic synthesis. It is particularly valuable for introducing acetyl groups to primary amine functionalities, such as lysine residues or N-terminal amines in peptides, proteins, and other biomolecules, under mild aqueous conditions. This modification helps block reactive amines, enhance protein stability, reduce immunogenicity, or prepare acetylated derivatives for biochemical and pharmaceutical research. It is also emplo

N-Succinimidyl acetate is an active ester used as a selective acetylating agent in organic synthesis. It is particularly valuable for introducing acetyl groups to primary amine functionalities, such as lysine residues or N-terminal amines in peptides, proteins, and other biomolecules, under mild aqueous conditions. This modification helps block reactive amines, enhance protein stability, reduce immunogenicity, or prepare acetylated derivatives for biochemical and pharmaceutical research. It is also employed in the synthesis of modified antibodies, therapeutic proteins, and in applications related to drug delivery and diagnostic development.

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