باب
Levothyroxine
رقم CAS
51-24-1
الصيغة الجزيئية
C14H9I3O4
وزن جزيئي
621.90 g/mol
مرادف

Triiodothyroacetic Acid (EP);Levothyroxine T3-Acetic Acid (USP);[4-(4-Hydroxy-3-iodophenoxy)-3,5-diiodophenyl]acetic acid; 2-(4-(4-Hydroxy-3-iodophenoxy)-3,5-diiodophenyl)acetic Acid;4-(4-Hydroxy-3-iodophenoxy)-3,5-diiodobenzeneacetic Acid; Nidolin; Tiratricol; Triacana

الكلمات الرئيسية
Fine Chemicals
Aromatics
Pharmaceutical Standards
Impurities
Drug Analogs
Intermediates
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.

Levothyroxine EP Impurity C is a specified related substance listed in the European Pharmacopoeia for levothyroxine. It represents a minor degradation or synthetic impurity of the API, and its level must be controlled and measured using validated methods, such as HPLC, to ensure the purity, quality, and safety of levothyroxine products.