Amerigo Scientific

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With years of experience in the life sciences, Amerigo Scientific has integrated global cutting-edge technology resources to provide the latest technological equipment, instruments, biological products, and custom services for research institutions and enterprises in the biological, chemical, pharmaceutical, medical, and other industries.

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Dimethyl 2-oxoglutarate Inquiry  | >96%

Amerigo Scientific

Dimethyl 2-oxoglutarate is a key intermediate formed during the Krebs cycle and an important nitrogen transporter in the biological metabolic pathways. The electrochemical behavior of dimethyl-2-oxoglutarate has been investigated by cyclic voltammetry, square wave voltammetry and differential pulse voltammetry using a glassy carbon electrode.

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Dimethyl 2-thioxo-1,3-dithiole-4,5-dicarboxylate Inquiry  | Purity Not Available

Amerigo Scientific

Dimethyl 2-thioxo-1,3-dithiole-4,5-dicarboxylate is a sulphur-containing heterocyclic building block. It has been reported to be formed during the reaction of 1,3-dithiolan-2-thiones with dimethyl acetylenedicarboxylate. It is formed as major product during the reaction of ethylene trithiocarbonate with dimethyl acetylenedicarboxylate.

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Dimethyl 2,6-dibromoheptanedioate Inquiry  | >97%

Amerigo Scientific

Dimethyl 2,6-dibromoheptanedioate acts as a bifunctional initiator in various polymerization reactions. Its electrochemical cyclization affords high yields of three- to six-membered dimethyl 1,2-cycloalkanedicarboxylates.

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Dimethyl 2,6-pyridinedicarboxylate Inquiry  | >99%

Amerigo Scientific

The standard molar enthalpy of formation for dimethyl 2,6-pyridinedicarboxylate (dimethylpyridine-2,6-dicarboxylate) has been calculated from the standard molar enthalpy of combustion, which was measured by a static bomb calorimeter.

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Dimethyl 3-hydroxyglutarate Inquiry  | Purity Not Available

Amerigo Scientific

Enantioselective hydrolysis and ammonolysis of dimethyl-3-hydroxyglutarate has been studied using immobilized lipase B isolated from Candida antarctica.

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Dimethyl 5-hydroxyisophthalate Inquiry  | >98%

Amerigo Scientific

Dimethyl 5-hydroxyisophthalate undergoes a base-catalyzed nucleophilic oxirane ring-opening addition reaction with allyl glycidyl ether, to afford 5-substituted derivatives of isophthalic acid. Influence of third component, i. e. a series of 1,ω-alkanediols on the copolymerization reaction of dimethyl 5-hydroxyisophthalate with poly(ethylene glycol) has been studied. Lipase-catalyzed condensation polymerization of dimethyl 5-hydroxyisophthalate with polyethylene glycol is reported.

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Dimethyl acetylsuccinate Inquiry  | Purity Not Available

Amerigo Scientific

Dimethyl acetylsuccinate undergoes sulfuric acid catalyzed Pechmann condensation with the corresponding resorcinol derivative to give 7-hydroxycoumarins.

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