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Gabapentin-lactam

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Gabapentin-lactam Basic information

Product Name:
Gabapentin-lactam
Synonyms:
  • 2-AZA-SPIRO[4.5]DECAN-3-ONE
  • Gabapentin-lactam
  • 3-AZASPIRO[4.5]DECAN-2-ONE
  • 4,4-PENTAMETHYLENE-2-PYRROLIDINONE
  • 3,3'-PENTAMETHYLENE-4-BUTYROLACTAM
  • 3,3-PENTAMETHYLENE-4-BUTYROLACTAM
  • beta,beta-pentamethylen-gamma-butyrolactam
  • 3,3-Pentamethylene glutarimide (CDI) or 2-Azaspiro{4,5} decan-3-one
CAS:
64744-50-9
MF:
C9H15NO
MW:
153.22
EINECS:
451-630-1
Product Categories:
  • Building Blocks
  • C4 to C10
  • (intermediate of gabapentin)
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Pyrrolidines
  • INTERMEDIATESOFGABAPENTIN
  • Heterocyclic Compounds
  • Intermediates & Fine Chemicals
  • Neurochemicals
  • Pharmaceuticals
Mol File:
64744-50-9.mol
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Gabapentin-lactam Chemical Properties

Melting point:
84-89 °C(lit.)
Boiling point:
181 °C / 13mmHg
Density 
1.05±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Soluble in DMSO (up to 40 mg/ml)
pka
16.39±0.20(Predicted)
color 
White
Stability:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months.
InChIKey
JAWPQJDOQPSNIQ-UHFFFAOYSA-N
CAS DataBase Reference
64744-50-9(CAS DataBase Reference)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
RTECS 
CM0120000
HazardClass 
IRRITANT
HS Code 
29337900

MSDS

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Gabapentin-lactam Usage And Synthesis

Description

Gabapentin lactam (CAS 64744-50-9) reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington’s disease.1 Displays neurotrophic effects, enhancing the formation of dendritic filopodia and inducing a network of F-actin-containing neurites in cultured hippocampal neurons.2 Promotes the survival of cultured central nervous system neurons possibly by opening mitochondrial KATP channels.3 Displays neuroprotective effects in a rat model of acute retinal ischemia.4

Chemical Properties

Gabapentin-lactam is White Solid

Uses

Gabapentin-lactam reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington’s disease. It opens mitochondrial ATP-dependent potassium channels.

Uses

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Uses

Gabapentin Lactam reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington disease. It opens mitochondrial ATP-dependent potassium channels

Definition

ChEBI: 2-Azaspiro[4.5]decan-3-one is an azaspiro compound.

General Description

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

References

1) Zucker et al. (2004), Gabapentin-lactam, but not gabapentin, reduces protein aggregates and improves motor performance in transgenic mouse model of huntington’s disease; Nauyn Schmiedebergs Arch. Pharmacol., 370 131 2) Henle et al. (2006), Gabapentin-lactam induces dendritic filopodia and motility in cultured hippocampal neurons; J. Pharmacol. Exp. Ther., 319 181 3) Pielen et al. (2004), Retinal ganglion cell survival is enhanced by gabapentin-lactam in vitro: evidence for involvement of mitochondrial KATP channels; Graefes Arch. Clin. Exp. Ophthalmol., 242 240 4) Lagreze et al. (2001), The neuroprotective properties of gabapentin-lactam; Graefes Arch. Clin. Exp. Ophthalmol., 239 845

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