S-Acetylmercaptosuccinic anhydride

95%

Reagent Code: #235164
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CAS Number 6953-60-2

science Other reagents with same CAS 6953-60-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.17 g/mol
Formula C₆H₆O₄S
badge Registry Numbers
MDL Number MFCD00005526
thermostat Physical Properties
Melting Point 83-86°C
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used as a key reagent in peptide synthesis and protein modification, particularly for introducing thiol groups in a protected form. The acetyl-protected thiol allows selective deprotection under mild conditions, enabling controlled conjugation or labeling of biomolecules. It is also employed in the preparation of thiolated polymers and hydrogels for drug delivery and tissue engineering due to its ability to form disulfide crosslinks. Its anhydride functionality reacts efficiently with amines, making it useful for bioconjugation strategies in diagnostic and therapeutic applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,660.00
inventory 5g
10-20 days ฿10,680.00
S-Acetylmercaptosuccinic anhydride
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Used as a key reagent in peptide synthesis and protein modification, particularly for introducing thiol groups in a protected form. The acetyl-protected thiol allows selective deprotection under mild conditions, enabling controlled conjugation or labeling of biomolecules. It is also employed in the preparation of thiolated polymers and hydrogels for drug delivery and tissue engineering due to its ability to form disulfide crosslinks. Its anhydride functionality reacts efficiently with amines, making it u

Used as a key reagent in peptide synthesis and protein modification, particularly for introducing thiol groups in a protected form. The acetyl-protected thiol allows selective deprotection under mild conditions, enabling controlled conjugation or labeling of biomolecules. It is also employed in the preparation of thiolated polymers and hydrogels for drug delivery and tissue engineering due to its ability to form disulfide crosslinks. Its anhydride functionality reacts efficiently with amines, making it useful for bioconjugation strategies in diagnostic and therapeutic applications.

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