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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3-Mercaptophenol Inquiry  | >96%

Amerigo Scientific

3-mercaptophenol coated cantilevers can be used as formaldehyde sensors since it is highly selective towards formaldehyde and can show highest downward deflection on coming in contact with it.

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3-Methoxy-1-propanol Inquiry  | Purity Not Available

Amerigo Scientific

3-Methoxy-1-propanol is a primary alcohol. Kinetics of the reactions of 3-methoxy-1-propanol with phenyl isocyanate in the presence of metal catalysts has been reported. Selective synthesis of 3-methoxy-1-propanol from methanol and allyl alcohol with metal oxides and zeolites catalysts in the liquid phase has been studied.

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3-Methoxy-2-naphthoic acid Inquiry  | Purity Not Available

Amerigo Scientific

3-Methoxy-2-naphthoic acid is a naphthoic acid derivative. 3-Methoxy-2-naphthoic acid can be prepared from 3-hydroxy-2-naphthoic acid, via methylation. It undergoes reduction under the following reaction conditions:in the presence of Li and NH4Cl to afford 1,2,3,4-tetrahydro-2-naphthoic acidby using Li, NH4Cl and anhydrous FeCl3 to afford 3-methoxy-1, 2-dihydro-2-naphthoic acidin anhydrous ether, liquid ammonia, lithium wire and anhydrous ethanol […]

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3-Methoxy-2-nitrobenzaldehyde Inquiry  | >97%

Amerigo Scientific

3-Methoxy-2-nitrobenzaldehyde undergoes 1,4-diazabicyclo[2. 2. 2]octane-catalyzed reaction with methyl vinyl ketone (MVK) to afford normal Baylis-Hillman adduct, the MVK dimer and a pair of diastereomeric bis-(MVK)Baylis-Hillman adducts.

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3-Methoxy-3-methyl-1-butanol Inquiry  | >98%

Amerigo Scientific

3-Methoxy-3-methyl-1-butanol is widely used as solvent for paints, inks, and fragrances. Kinetics of the reaction of 3-methoxy-3-methyl-1-butanol with OH radicals using a relative rate method has been reported. It has been identified as oxidation products of dyes such as methyl yellow, methyl red and methyl orange.

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