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.

Dichloromethanedisulfenyl Chloride CAS NO 17494-65-4

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CAS No.:17494-65-4

Grade:Pharmacy Grade

Content:99.90%

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1H-Imidazole-5-Methanethiol CAS NO 17496-21-8

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CAS No.:17496-21-8

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Content:99.90%

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1,1'-Dithiobis(3,5,7,10,10-Pentamethyl-2,4,6,8-Tetrathiaadamantane) CAS NO 17525-43-8

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CAS No.:17525-43-8

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3-Pyridinemethanethiol(6Ci,7Ci,8Ci,9Ci) CAS NO 17617-05-9

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CAS No.:17617-05-9

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6-Mercaptonicotinic Acid CAS NO 17624-07-6

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CAS No.:17624-07-6

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1-Benzyl-2-Pyrrolidinethione CAS NO 17642-88-5

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CAS No.:17642-88-5

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5-Carboxy-1-Pentanethiol CAS NO 17689-17-7

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CAS No.:17689-17-7

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3-(Triethylsilyl)-1-Propanethiol CAS NO 17877-45-1

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CAS No.:17877-45-1

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Content:99.90%

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