باب
Amitriptyline
رقم CAS
72-69-5
الصيغة الجزيئية
C19H21N
وزن جزيئي
263.4 g/mol
مرادف

N-methyl-3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,11,13-hexaenylidene)propan-1-amine; 3-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-ylidene)-N-methylpropan-1-amine; Sesaval; Noramitriptyline; Ateben; Avantyl; Aventyl; Demethylamitriptyline; Desitriptilina; Desmethylamitriptyline; 3-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-1-propanamine; 10,11-Dihydro-5-(3-methylaminopropylidene)-5H-dibenzo[a,d][1,4]cycloheptene; 10,11-Dihydro-N-methyl-5H-dibenzo[a,d]cycloheptane-Δγpropylamine; 3-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methylpropylamine; 5-(3-Methylaminopropylidene)-10,11-dihydro-5H-dibenzo[a,d]cycloheptene; 3-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-ylidene)-N-methylpropan-1-amine; Nortriptyline (USP)

الكلمات الرئيسية
Intermediates
Impurities
Metabolites.
Pharmaceutical Standards
Fine Chemicals
slide.1
Purity:

Above - 95.0%

Technical Data:

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Amitriptyline EP Impurity C is a designated impurity defined in the European Pharmacopoeia for amitriptyline, controlled within specified limits to maintain the drug’s quality, safety, and purity.