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.

5-Chloro-2-Mercaptoaniline Hydrochloride CAS NO 615-48-5

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CAS No.:615-48-5

Grade:Pharmacy Grade

Content:99.90%

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Pentane-3-Thiol CAS NO 616-31-9

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CAS No.:616-31-9

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1,4-Benzenedithiol CAS NO 624-39-5

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CAS No.:624-39-5

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1,3-Benzenedithiol CAS NO 626-04-0

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CAS No.:626-04-0

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2,2-Dimethylthiopropionamide CAS NO 630-22-8

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CAS No.:630-22-8

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4-Mercaptophenol CAS NO 637-89-8

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CAS No.:637-89-8

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4-Methyl-6-Mercapto-2-Pyrimidinol CAS NO 638-13-1

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CAS No.:638-13-1

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4-Trifluoromethyl-2,3,5,6-Tetrafluorothiophenol CAS NO 651-84-3

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CAS No.:651-84-3

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Content:99.90%

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