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.

N,n-Bis(2-Mercaptoethyl)-N'',N''-Diethylethylenediamine CAS NO 93798-62-0

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CAS No.:93798-62-0

Grade:Pharmacy Grade

Content:99.90%

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(1-Phenyl-1H-Benzoimidazol-2-Ylsulfanyl)-Acetic Acid CAS NO 93866-15-0

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CAS No.:93866-15-0

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2-Amino-4-Bromobenzenethiol CAS NO 93933-49-4

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CAS No.:93933-49-4

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(2-Mercaptoethyl)Ammonium Hydrogen Maleate CAS NO 93965-19-6

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CAS No.:93965-19-6

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2,2,2-Trifluoro-n-(4-Mercaptophenyl)Acetamide CAS NO 94006-35-6

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CAS No.:94006-35-6

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Methyl Alpha-Mercaptofuran-2-Butyrate CAS NO 94042-80-5

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CAS No.:94042-80-5

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1-(2'-Thienyl)Ethylmercaptan CAS NO 94089-02-8

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CAS No.:94089-02-8

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1-Methoxyundecane-3-Thiol CAS NO 94201-22-6

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CAS No.:94201-22-6

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