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Structure of 7634-96-0
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This thiol-functional molecule features two reactive sulfhydryl groups in proximity, enabling efficient conjugation in bioconjugation and surface modification workflows. The carboxylic acid moiety provides additional anchoring capability for coupling to amine-containing substrates or biomolecules under standard conditions.
3-Mercapto-2-(mercaptomethyl)propanoic acid serves as a versatile bifunctional thiol building block, enabling efficient conjugation and disulfide bridge formation in peptide synthesis and protein engineering. Its dual thiol functionality enhances reactivity in copper-catalyzed click chemistry and facilitates site-specific bioconjugation. The molecule exhibits good bench stability and simplifies purification due to its high polarity, making it well-suited for scalable applications in medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2928
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Class : 6.1,8
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Packing Group : Ⅱ
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Hazard Statements : H301-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: