Tropina, 98 %, Thermo Scientific Chemicals
Tropina, 98 %, Thermo Scientific Chemicals
Tropina, 98 %, Thermo Scientific Chemicals
Tropina, 98 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Tropina, 98 %, Thermo Scientific Chemicals

CAS: 120-29-6 | C8H15NO | 141.214 g/mol
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Cantidad:
10 g
50 g
Número de catálogo L02332.09
también denominado L02332-09
Precio (EUR)
41,00
Each
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Cantidad:
10 g
Pedido a granel o personalizado
Precio (EUR)
41,00
Each
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Identificadores químicos
CAS120-29-6
IUPAC Name8-methyl-8-azabicyclo[3.2.1]octan-3-ol
Molecular FormulaC8H15NO
InChI KeyCYHOMWAPJJPNMW-UHFFFAOYNA-N
SMILESCN1C2CCC1CC(O)C2
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EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)White to pale cream
FormCrystalline powder
Assay (GC)> 97.5%
Water Content (Karl Fischer Titration)< 3.0%
Assay (Non-aqueous acid-base Titration)>97.5 to <102.5% (dry wt. basis)
Tropine as an oxidative product of Tropane, used to synthesize alkaloid derivatives. Benzatropine and etybenzatropine are derivatives of tropine. It is also a building block of atropine, an anticholinergic drug prototypical of the muscarinic antagonist class.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
El tropina se utiliza como producto oxidativo del tropane para sintetizar derivados de alcaloides. Benzatropina y etibenzatropina son derivados de tropina. También es un compuesto básico de la atropina, un fármaco anticolinérgico prototípico de la clase de antagonistas muscarínicos.

Solubilidad
Soluble en agua. (100 g/l) a 20 °C.

Notas
Higroscópico. Almacenar a 4 °C. Incompatible con ácidos fuertes y agentes oxidantes.
RUO – Research Use Only

General References:

  1. Muriel E. Farquharson and R. G. Johnston. Antagonism Of The Effects Of Tremorine By Tropine Derivatives.British Journal of Pharmacology and Chemotherapy.1959, 14 559-566.
  2. Edward. Leete. The Stereospecific Incorporation of Ornithine into the Tropine Moiety of Hyoscyamine.J. Am. Chem. Soc.1962, 84 (1), 55-57.