Product Detail
Amitriptyline N-Oxide-13C3
Metabolite
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category
Metabolite
API Family
--
Storage
Refer MSDS for complete information.
Hazard Information
Refer MSDS for complete information.
Amitriptyline N-Oxide-13C3 Product Information
Amitriptyline N-Oxide-13C3 is listed under Metabolite. 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-100841.
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
Amitriptyline N-Oxide-13C3
CAS No.
-
CAT No.
CS-T-100841
Molecular Formula
C17¹³C3H23NO
Molecular Weight
296.38
Category
Storage Condition
Refer MSDS for complete information.
SMILES
[13CH3][N+]([13CH3])([13CH2]CC=C1C2=CC=CC=C2CCC3=CC=CC=C31)[O-]
IUPAC Name
N,N-di((113C)methyl)-3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,11,13-hexaenylidene)(113C)propan-1-amine oxide
Hazard Compound
Refer MSDS for complete information.
Description
Overview
Amitriptyline N-Oxide13C3 is an isotope analog of Amitriptyline N-Oxide (A633355). Amitriptyline N-oxide is used in biological studies to metabolize drugs by fungi colonizing cadavers using LC-ESI-MS/MS and GC-MS. This compound is also used in the development of antidepressant drugs.
Synonyms
"3-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N,N-dimethyl-1-propanamine N-Oxide-13C3; 10,11-Dihydro-N,N-dimethyl-5H-Dibenzo[a,d]cycloheptene-?5,?-propylamine N-Oxide-13C3; Amitriptyline Oxide-13C3; Amitriptylinoxide-13C3; Equilibrin-13C3"
Application Notes
Amitriptyline N-Oxide13C3 is an isotope analog of Amitriptyline N-Oxide (A633355). Amitriptyline N-oxide is used in biological studies to metabolize drugs by fungi colonizing cadavers using LC-ESI-MS/MS and GC-MS. This compound is also used in the development of antidepressant drugs.
References
"Martinez-Ramirez, J.A., et al.: Anal. Bioanal. Chem., 404, 1339 (2013); Wissenbach, D.K., et al.: Anal. Bioanal. Chem., 400, 79 (2011)"
