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Structure of 98486-87-4
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S-(6-Aminohexyl) ethanethioate hydrochloride features a primary amine at one terminus and a thiol group at the other, enabling dual conjugation chemistry. The hydrochloride salt enhances solubility and stability in aqueous buffers, facilitating efficient coupling to maleimides, gold surfaces, or cysteine residues under mild conditions. This bifunctional reagent streamlines site-specific bioconjugation workflows.
S-(6-Aminohexyl) ethanethioate hydrochloride serves as a versatile bifunctional building block for conjugation and polymer synthesis. The primary amine enables efficient coupling reactions, while the thiol group facilitates site-specific attachment via Michael addition or gold-catalyzed thiol-ene chemistry. Its hydrochloride salt form enhances solubility and stability in aqueous and protic media, simplifying handling and purification in synthetic workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H312-H315-H318-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: