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.

6-(6-Amino-Hexyldisulfanyl)-Hexylamine Hydrochloride CAS NO 118077-46-6

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CAS No.:118077-46-6

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Content:99.90%

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Bis(1-Thio-2-Amino-3-Phenylpropane) CAS NO 118433-74-2

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CAS No.:118433-74-2

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2-Thiazolethiol, 4,5-Dimethyl- CAS NO 118090-07-6

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CAS No.:118090-07-6

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2-Benzoxazolethiol CAS NO 118090-08-7

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CAS No.:118090-08-7

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Carbaphethiol CAS NO 118104-82-8

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CAS No.:118104-82-8

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1-Methylthio-2-Butyne CAS NO 118891-26-2

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CAS No.:118891-26-2

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Content:99.90%

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Bis(2-Methylpropyl) (2S,3R)-2,3-Bis-Sulfanylbutanedioate CAS NO 118908-62-6

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CAS No.:118908-62-6

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Content:99.90%

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1-Ethylsulfanyl-2-Methylsulfanyl-Ethanone CAS NO 119152-81-7

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CAS No.:119152-81-7

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Content:99.90%

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