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-[2-(p-Tolyloxy)Butyl]Aminoethanethiol Sulfate CAS NO 19143-03-4

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CAS No.:19143-03-4

Grade:Pharmacy Grade

Content:99.90%

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(R)-2-Hydroxyethyl-L-Cysteine CAS NO 19179-73-8

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CAS No.:19179-73-8

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Content:99.90%

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.Beta.-D-Glucopyranose, 1-Thio-, 2,3,4,6-Tetraacetate 1-(Dimethylcarbamodithioate) CAS NO 19200-24-9

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CAS No.:19200-24-9

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Content:99.90%

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2,3,6,2',3',4',6'-Hepta-o-Acetyl-1-Thio-Β-D-Lactose 1-(Dimethylcarbamodithioate) CAS NO 19200-34-1

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CAS No.:19200-34-1

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Carbonic Acid, Dithio-, S-(2-Aminoethyl) Ester, S-Ester With 5-Mercapt Ovaleric Acid, Hydrochloride CAS NO 19213-26-4

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CAS No.:19213-26-4

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Benzoic Acid, 2-Mercapto-, Disodium Salt CAS NO 19296-18-5

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CAS No.:19296-18-5

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Content:99.90%

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4,4'-Thiodibenzenethiol CAS NO 19362-77-7

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CAS No.:19362-77-7

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2-Amino-4-(Trifluoromethyl)Thiophenol3-Amino-4-Mercaptobenzotrifluoride CAS NO 19406-49-6

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CAS No.:19406-49-6

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Content:99.90%

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