باب
Amitriptyline
رقم CAS
1210-35-1
الصيغة الجزيئية
C15H12O
وزن جزيئي
208.26 g/mol
مرادف

tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,11,13-hexaen-2-one; 5H-Dibenzo[a,d]cyclohepten-5-one, 10,11-dihydro-; 10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-one; 10,11-Dihydro-5H-dibenzo[a,d][7]annulen-5-one; Dibenzocycloheptenone; Dibenzo[a,d]cyclohepten-5-one; Dibenzosuberone; 10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-one; Amitriptyline Related Compound A (USP); 10,11-Dihydro-5H-dibenzo[a,d][7]annulen-5-one

الكلمات الرئيسية
Impurities
Metabolites.
Pharmaceutical Standards
Intermediates
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 A is a controlled chemical byproduct in amitriptyline, monitored to ensure drug purity and safety.