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.

14-Mercaptotetradecanoic Acid CAS NO 184639-68-7

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CAS No.:184639-68-7

Grade:Pharmacy Grade

Content:99.90%

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(S)-4-Mercapto-2-Pyrrolidinone CAS NO 184759-58-8

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CAS No.:184759-58-8

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2-Diethylamino Ethanethiol Hcl CAS NO 185463-71-2

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CAS No.:185463-71-2

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L-Arabinopyranoside, Methyl 1-Thio-, Triacetate CAS NO 185549-85-3

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CAS No.:185549-85-3

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2-Benzothiazoleaceticacid,6-Mercapto-(9Ci) CAS NO 185805-00-9

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CAS No.:185805-00-9

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Benzamide, 4-Mercapto-n-Methyl- CAS NO 187160-34-5

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CAS No.:187160-34-5

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2-Pyrrolidinethione, 1-Acetyl-5-Phenyl- (9Ci) CAS NO 187276-87-5

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CAS No.:187276-87-5

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n-(2-Acetyl-5-tert-Butyl-Thiophen-3-Yl)-Succinamic Acid CAS NO 187334-30-1

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CAS No.:187334-30-1

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