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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4-Aminophenol Inquiry  | >98%

Amerigo Scientific

4-Aminophenol (4-Hydroxyaniline) is an organic building block. Its quantification in water samples upto the detection limit of 8×10-10mol l-1 has been proposed by employing single-wall carbon nanotubes (SWNT)-nafion film coated glassy carbon electrodes. It is present as the main contaminant in pharmaceutical formulations of paracetamol. High-performance liquid chromatographic (HPLC) method with amperometric detection has been […]

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4-Aminopyridine Inquiry  | >99%

Amerigo Scientific

4-Aminopyridine (4-AP) blocks the voltage-dependent potassium channels in other nerve membranes. 4-AP is a K+ channel blocker and causes epileptiform activity in in vitro preparations and is a potent convulsant in animals and man.

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4-Aminoresorcinol hydrochloride Inquiry  | >96%

Amerigo Scientific

Electrochemical oxidation of 4-aminoresorcinol hydrochloride (2,4-dihydroxyaniline hydrochloride) has been studied using a boron-doped diamond electrode as anode. It is an inhibitor of meta-cleavage dioxygenase enzyme isolated from cell extracts of Bordetella sp. strain 10d.

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4-Aminothiophenol Inquiry  | >97%

Amerigo Scientific

4-Aminothiophenol (p-aminothiophenol, PATP) is an aromatic thiol. The self-assembly of silver and gold nano particles which are interconnected with 4-ATP to form metal-molecule-metal sandwich architecture has been characterized by surface enhanced Raman scattering (SERS) using an off-surface plasmon resonance condition. Chemical transformation of PATP to 4,4-dimercaptoazobenzene (DMAB) has been extensively studied.

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4-Azatricyclo[4.3.1.13,8]undecan-5-one Inquiry  | Purity Not Available

Amerigo Scientific

4-Azatricyclo[4. 3. 1. 1]undecan-5-one is formed during the Beckman rearrangement of adamantanone oxime. Crystal structure of 4-azatricyclo[4. 3. 1. 1]undecan-5-one (homoazaadamantanone) has been studied.

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