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Pentaerythritol tetrakis(3-mercaptopropionate) is a common thiol monomer reacted with alkenes in the thiol-ene reaction to form polymeric networks. [3] Being functionalized with four thiol groups, it can react with multifunctional alkenes to form thiol-ene networks.
3-Mercaptopropionic acid (3-MPA) is an organosulfur compound with the formula HSCH 2 CH 2 CO 2 H. It is a bifunctional molecule, containing both carboxylic acid and thiol groups. It is a colorless oil.
3-Mercaptopropionitrile is the organosulfur compound with the formula HSCH 2 CH 2 CN. [1] Containing both thiol and nitrile functional groups , it is a bifunctional compound . A colorless liquid, the compound has found some use as a masked form of thiolate.
Multifunctional thiols such as pentaerythritol tetrakis(3-mercaptopropionate) can react with multifunctional enes such as norbornene-functionalized monomers, by photopolymerization to form cross-linked polymer networks. These thiol-ene networks are advantageous over traditional networks in that they form rapidly and quantitatively under ...
Pentaerythritol was first reported in 1891 by German chemist Bernhard Tollens and his student P. Wigand. [5] It may be prepared via a base-catalyzed multiple-addition reaction between acetaldehyde and 3 equivalents of formaldehyde to give pentaerythrose (CAS: 3818-32-4), followed by a Cannizzaro reaction with a fourth equivalent of formaldehyde to give the final product plus formate ion.
This category has the following 3 subcategories, out of 3 total. C. Carboxylic acid-based monomers ... (3-mercaptopropionate) P-Phenylenediamine; Polymerisation ...
pentaerythritol tetrakis(3-mercaptopropionate) 7575-23-7 C 17 H 29 NO 3 S: sethoxydim: 74051-80-2 C 17 H 30: cyclopentylbicyclohexyl: 26447-22-3 C 17 H 30 N 2: tributylmethyl pyrazine: 116660-18-5 C 17 H 30 O 2: geranyl heptanoate: 73019-15-5 C 17 H 31 Cl 3 O 2: pentadecyl trichloroacetate: 74339-53-0 C 17 H 32 O: cycloheptadecanone: 3661-77-6 ...
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