Thiols/Thiophenols

Thiols/Thiophenols

Thiols and thiophenols are sulfur-containing organic reagents with strong nucleophilicity and characteristic odor. They participate in thiol-ene reactions, nucleophilic substitution, oxidation, metal binding, and polymer modification. Thiols are essential in bioconjugation, peptide chemistry, and redox biology due to their ability to form disulfide bonds. Thiophenols are used in pharmaceuticals, agrochemicals, and materials synthesis, particularly in forming thioethers and sulfur-functionalized aromatic compounds. Their metal-chelating ability supports catalyst formation and surface modification. Thiols also play roles in polymer crosslinking, vulcanization, and antioxidant chemistry. Their rich reactivity and biological relevance make thiols indispensable across chemical, biochemical, and materials science fields.

(±)-2-Butanethiol CAS NO 91840-99-2

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CAS No.:91840-99-2

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Content:99.90%

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1-p-Tolyl-1H-Benzoimidazole-2-Thiol CAS NO 92149-91-2

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CAS No.:92149-91-2

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cis-4,5,9-Trithiadodeca-1,6,11-Triene-9- CAS NO 92285-01-3

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CAS No.:92285-01-3

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1-(3-Phenoxycarbamidophenyl)-5-Mercaptotetrazole CAS NO 92339-43-0

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CAS No.:92339-43-0

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D-Isovaline, 3-Mercapto-3-Methyl- (9Ci) CAS NO 92462-77-6

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CAS No.:92462-77-6

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2,6-Naphthalenecarbodithioic Acid CAS NO 92827-62-8

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CAS No.:92827-62-8

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3-Aminopropyl Methanethiosulfonate, Hydrobromide CAS NO 92953-13-4

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CAS No.:92953-13-4

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2,2,4,6,6-Pentamethylheptane-4-Thiol CAS NO 93002-38-1

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CAS No.:93002-38-1

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