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Chemical Structure| 1130-32-1 Chemical Structure| 1130-32-1
Chemical Structure| 1130-32-1

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Product Details of Gabapentin Impurity 3

CAS No. :1130-32-1
Formula : C10H15NO2
M.W : 181.23
SMILES Code : O=C1CC2(CC(=O)N1)CCCCC2
MDL No. :MFCD00023872
InChI Key :FNIPRNMPSXNBDI-UHFFFAOYSA-N
Pubchem ID :14324

Safety of Gabapentin Impurity 3

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Gabapentin Impurity 3

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1130-32-1 ]

[ 1130-32-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1130-32-1 ]
  • [ 99189-60-3 ]
YieldReaction ConditionsOperation in experiment
Synthesis of 1.1-cvclohexane diacetic acid monoamide25.7 kg (19.3 1) of electrolytic soda were charged in reactor C by means of meteringpump.The temperature was brought to about 95°C and it was maintained until the completedissolution of the solid, then the mixture was brought to reflux (101-105°C).Reflux was maintained for about six hours, then the reaction check was carried outAt the completion of the reaction, the solution was cooled to about 20°C withprecipitation of a solid white flocculate, then, at temperature 45.0 kg (57.3) ofisopropanol were charged and subsequently in about one hour, maintainingtemperature below 25°C, about 125 kg (107.7 1) of synthetic hydrochloric acid werecharged until reaching a pH of 6.5 +/- 0.2, measured with pH meter.Once the desired pH was reached, the suspension was heated to 35-40°C and it wasmaintained at this temperature until dissolution of the solid.At the completion of the dissolution, the solution was transferred into reactor E andsubsequently 20 kg of demineralised water were charged in the reactor.The washing was kept under stirring for 5-10 minutes, then it was transferred intoreactor E.The internal temperature of reactor E was regulated to about 35-40°C then, maintaining temperature, 40 kg (34.5 1) of synthetic hydrochloric acid were added in about one hour until reaching a pH of 4.0-4.5, measured with paper. The pH of the suspension was checked to be stable for at least 10-15 minutes, then the internal temperature of reactor E was brought to about 50°C and it was maintained for about 30 minutes.In about one and one half hours the suspension was cooled to about 15-20°C andafter about one hour several centrifuging operations were carried out. The panel waswashed twice with a mixture formed by isopropanol and water.In total, 23.6 kg (30 k) of isopropanol and 30 kg of demineralised water were used.After one washing with the alcoholic mixture, the panel was subjected to sixwashings with water.In total, 270 kg of demineralised water were indicatively used.78.0 kg of humid product were obtained, which after drying at about 50°C undervacuum yield about 59.0 kg of the desired dry product.
Example 8; Synthesis of cyclohexanediacetic acid monoamide (V); 9g of 2, 4-dioxo-3-azaspiro [5,5] undecane and 30 g of 10percent NaOH are placed in a 250 ml flask equipped with mechanical agitator, thermometer and condenser. The mixture is heated under reflux for 1 hour, cooled to 25°C and acidified with 36percent HCI to pH 5. The precipitate formed is filtered off, washed with water and dried under vacuum. 6.4 g of cyclohexanediacetic acid monoamide are obtained.
 

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