Category
Amidotrizoic acid
CAS Number
NA
Molecular Formula
C₁₁H₈I₄N₂O₄
Molecular Weight
739.8 g/mol
Synonym

3-(Acetylamino)-5-[(iodoacetyl)amino]-2,4,6-triiodobenzoic acid (as per EP);
3-Acetamido-2,4,6-triiodo-5-(2-iodoacetamido)benzoic Acid;

Keywords
Fine Chemicals
Aromatics
Amines
Pharmaceutical Standards
Intermediates
High-Quality Pharmaceutical Reference Standards
Impurities Manufacturer in India
Impurities manufacturer and Suppliers in Hyderabad india
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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.

Amidotrizoic Acid EP Impurity D (molecular formula C₁₁H₈I₄N₂O₄; molecular weight 739.8) is an Amidotrizoic acid pharmaceutical impurity reference material intended for analytical research, impurity profiling, HPLC analysis, related-substance testing, method development, validation, and pharmaceutical quality control. Manasa Life Sciences, India, manufactures and supplies analytical pharmaceutical impurities with comprehensive documentation to support laboratory, quality-control, research, and regulatory requirements. Applicable quality frameworks may include European Pharmacopoeia (EP), USP, EMA, and ICH guidelines, particularly guidance relating to impurity control, analytical validation, specifications, and pharmaceutical quality.  Supporting documentation may include Certificate of Analysis (COA), potency/assay information, analytical data, chromatograms, characterization data, specifications, and applicable GLP/GDP documentation, depending on the material and batch.