S-Acetylthioglycolic acid N-hydroxysuccinimide ester
>94.0%(GC)
Reagent
Code: #121500
Alias
N-S-acetylmercaptoglycol succinate, N-succinimidyl-S-acetylthioacetate, succinimidyl S-acetylthioacetate, SATA
CAS Number
76931-93-6
blur_circular Chemical Specifications
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Molecular Information
Weight
231.23 g/mol
Formula
C₈H₉NO₅S
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Registry Numbers
MDL Number
MFCD00036891
thermostat
Physical Properties
Melting Point
97°C
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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
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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