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.

Ethanone, 1-(5-Mercapto-1-Methyl-1H-Pyrazol-4-Yl)- (9Ci) CAS NO 111493-63-1

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CAS No.:111493-63-1

Grade:Pharmacy Grade

Content:99.90%

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A-D-Mannopyranoside, Phenyl 2,3,4,6-Tetrakis-o-(Phenylmethyl)-1-Thio- CAS NO 116501-53-2

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CAS No.:116501-53-2

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Content:99.90%

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S-2-(3-Methylaminopropylamino)Ethanethiol CAS NO 117062-90-5

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CAS No.:117062-90-5

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Content:99.90%

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1-(3-Mercapto-1-Oxopropoxy)-2,5-Pyrrolidinedione CAS NO 117235-10-6

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CAS No.:117235-10-6

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Content:99.90%

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Ethanethiol, 2-[(2-Methylcyclopentyl)Oxy]-, trans- (9Ci) CAS NO 117391-09-0

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CAS No.:117391-09-0

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Content:99.90%

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4-tert-Butyl-1,2-Dimercaptobenzene CAS NO 117526-80-4

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CAS No.:117526-80-4

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Content:99.90%

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2-Thioxo-1-Pyrrolidinethioacetamide CAS NO 117947-07-6

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CAS No.:117947-07-6

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Content:99.90%

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Diisopropyl 2,3-Dimercaptosuccinate CAS NO 118311-05-0

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CAS No.:118311-05-0

Grade:Pharmacy Grade

Content:99.90%

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