Amerigo Scientific

Amerigo Scientific logo

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.

Company Website

Product Listing

Tetramethylthiourea Inquiry  | >98%

Amerigo Scientific

Tetramethylthiourea molecule shows crystallographic two-fold symmetry with weak hydrogen bond packing, which connects the molecules to form layers.

More Information Supplier Page

Tetratetracontane Inquiry  | >99%

Amerigo Scientific

Tetratetracontane is a long chain alkane. It is the main constituents of essential oils from Euphorbia macroclada. Coadsorption of tetratetracontane and [Na(H2O)P5W30O110] results in single, isolated surfactant-encapsulated clusters on a buffer layer of tetratetracontane, which was determined by scanning tunneling microscopy. Thermooxidative degradation of tetratetracontane has been reported.

More Information Supplier Page

Tetrathiafulvalene Inquiry  | >97%

Amerigo Scientific

Tetrathiafulvalene (TTF) is an electron-donor which consists of oligomers, dendrimers and polymers which can be used in the formation of redox macromolecules.

More Information Supplier Page

Thianaphthene-2-carboxylic acid Inquiry  | >98%

Amerigo Scientific

Thianaphthene-2-carboxylic acid, a benzothiophene, is a heterocyclic sulfur compound. It undergoes degradation (23%) by employing a mixture of washed cells of Rhodococcus erythropolis DS-3 and Gordonia sp. C-6.

More Information Supplier Page

Thianaphthene-3-carboxaldehyde Inquiry  | >95%

Amerigo Scientific

Thianaphthene-3-carboxaldehyde, also known as benzo[b]thiophene-3-carboxaldehyde, can be synthesized from 3-methyl-benzo[b]thiophene. It undergoes phosphine-free palladium coupling with aryl halides to form 2-arylbenzo[b]thiophenes.

More Information Supplier Page

Thianthrene Inquiry  | >97%

Amerigo Scientific

Thianthrene undergoes liquid phase tert-butylation in the presence of large pore zeolites and mesoporous aluminosilicates catalyst to yield tert-butyl derivatives. Thianthrene on oxidation in the presence of hydrogen peroxide and ligninase as catalyst from Phanerochaete chrysosporium yields thianthrene monosulfoxide.

More Information Supplier Page

Thiazolidine-2-carboxylic acid Inquiry  | >97%

Amerigo Scientific

Thiazolidine-2-carboxylic acid (β-thiaproline) is a proline analog. It is an important building block of β-lactam antibiotics. Its X-ray photoelectron spectra has been investigated. It has been reported as a physiological substrate of hog kidney D-amino acid oxidase. Thiazolidine-2-carboxylic acid can be synthesized from cysteamine and glyoxylate.

More Information Supplier Page

Thieno[3,2-b]thiophene Inquiry  | >95%

Amerigo Scientific

Thieno(3,2-b)thiophene (TT) is an electron rich conjugated polymer that has a quinoidal structure with a narrow band gap. It facilitates a strong intermolecular networking.

More Information Supplier Page

Thieno[3,2-b]thiophene-2,5-diboronic acid bis(pinacol ester) Inquiry  | >99%

Amerigo Scientific

Thieno[3,2-b]thiophene-2,5-diboronic acid bis(pinacol ester) is a charge transport material commonly used in thin film transistors. They have very high carrier mobility because of the conjugation of the fused ring system and also due to the high concentration of sulphur atoms. The boronic acid ester group improves the solubility and also enhances the charge transport properties.

More Information Supplier Page

Thioacetamide Inquiry  | >98%

Amerigo Scientific

Thioacetamide is a thiocarbonyl compound. It undergoes deuterium exchange reaction with D2O to afford N-dideuterated thioacetamide. Infrared spectral investigations of thioacetamide and its deuterated derivative (N-dideuterated thioacetamide) have been reported.

More Information Supplier Page

Thioacetamide Inquiry  | >99%

Amerigo Scientific

Thioacetamide is a thiocarbonyl compound. It undergoes deuterium exchange reaction with D2O to afford N-dideuterated thioacetamide. Infrared spectral investigations of thioacetamide and its deuterated derivative (N-dideuterated thioacetamide) have been reported.

More Information Supplier Page