Product Detail
2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one-d6
Stable Isotopes
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category
Stable Isotopes
API Family
--
Storage
Refer MSDS for complete information.
Hazard Information
Refer MSDS for complete information.
2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one-d6 Product Information
2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one-d6 is listed under Stable Isotopes. It is associated with - and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-T-99919.
Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight, stock enquiry details and supporting documentation.
Technical Data
Product Name
2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one-d6
CAS No.
-
CAT No.
CS-T-99919
Molecular Formula
C13H15D6NO2
Molecular Weight
229.35
Category
API Family
Storage Condition
Refer MSDS for complete information.
SMILES
O=C1N(CCC(C)=O)CC2(CC([2H])([2H])C([2H])([2H])C([2H])([2H])C2)C1
IUPAC Name
2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one-d6
Hazard Compound
Refer MSDS for complete information.
Description
Overview
2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one-d6 is the isotope labelled analog of 2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one (O848400); a derivative of Gabapentin Lactam (G117275) which is a compound that reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington’s disease. Gabapentin Lactam also opens mitochondrial ATP-dependent potassium channels.
Synonyms
2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one-d6
Application Notes
2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one-d6 is the isotope labelled analog of 2-(3-Oxobutyl)-2-azaspiro[4.5]decan-3-one (O848400); a derivative of Gabapentin Lactam (G117275) which is a compound that reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington’s disease. Gabapentin Lactam also opens mitochondrial ATP-dependent potassium channels.
References
"Zucker, B.,et al.: Naunyn Schmiedebergs Arch. Pharmacol., 370, 131 (2004)"
![Dibenzo[a,e]pyrene-D14 chemical structure](https://structures.clearsynth.com/CS-T-103893.PNG)
