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.

4-Mercapto-4-Methylvaleric Acid CAS NO 140231-31-8

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CAS No.:140231-31-8

Grade:Pharmacy Grade

Content:99.90%

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2-Pyrimidinethiol, 1,4-Dihydro-4-Imino- (9Ci) CAS NO 140907-24-0

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CAS No.:140907-24-0

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3-(4-Fluorophenyl)Thiophenol CAS NO 141106-53-8

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CAS No.:141106-53-8

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n-Butyl 2-Imidazolyl Disulfide CAS NO 141400-57-9

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CAS No.:141400-57-9

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(S)-2-Benzyl-2-n-Bocamino-Ethyl Thiol CAS NO 141437-85-6

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CAS No.:141437-85-6

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n-Octylpyridine-4-Thione CAS NO 141537-35-1

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CAS No.:141537-35-1

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(Z)-1-Methoxy-2-Thiomethoxy-3,3-Dimethylbutene CAS NO 141739-68-6

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CAS No.:141739-68-6

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S,O,O'-Tripropyryl-1-Thioglycerol CAS NO 141923-05-9

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CAS No.:141923-05-9

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Content:99.90%

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