S-Acetylthioglycolic acid N-hydroxysuccinimide ester

>94.0%(GC)

Reagent Code: #121500
label
Alias N-S-acetylmercaptoglycol succinate, N-succinimidyl-S-acetylthioacetate, succinimidyl S-acetylthioacetate, SATA
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CAS Number 76931-93-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.23 g/mol
Formula C₈H₉NO₅S
badge Registry Numbers
MDL Number MFCD00036891
thermostat Physical Properties
Melting Point 97°C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

S-Acetylthioglycolic acid N-hydroxysuccinimide ester is widely used in bioconjugation chemistry for modifying biomolecules. It serves as a key reagent in the preparation of thiol-reactive crosslinkers, enabling the attachment of peptides, proteins, or antibodies to various surfaces or other molecules. Its acetyl group provides stability, preventing premature reactions, while the N-hydroxysuccinimide ester facilitates efficient coupling with primary amines. This compound is particularly valuable in the development of diagnostic assays, targeted drug delivery systems, and functionalized nanoparticles. Its ability to introduce thiol groups into biomolecules makes it essential for creating stable and site-specific conjugates in biochemical research and therapeutic applications.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to light yellow powder to crystal
Purity (GC) 94-100
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days Ft30,928.32
inventory 500mg
10-20 days Ft102,540.86
inventory 1g
10-20 days Ft147,376.55
S-Acetylthioglycolic acid N-hydroxysuccinimide ester
S-Acetylthioglycolic acid N-hydroxysuccinimide ester is widely used in bioconjugation chemistry for modifying biomolecules. It serves as a key reagent in the preparation of thiol-reactive crosslinkers, enabling the attachment of peptides, proteins, or antibodies to various surfaces or other molecules. Its acetyl group provides stability, preventing premature reactions, while the N-hydroxysuccinimide ester facilitates efficient coupling with primary amines. This compound is particularly valuable in the development of diagnostic assays, targeted drug delivery systems, and functionalized nanoparticles. Its ability to introduce thiol groups into biomolecules makes it essential for creating stable and site-specific conjugates in biochemical research and therapeutic applications.
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