Category
Baclofen
Baclofen
CAS Number
1134-47-0
Molecular Formula
C₁₀H₁₂ClNO₂
Molecular Weight
213.66 g/mol
Synonym

Baclofen - API ; β-(Aminomethyl)-4-chloro-benzenepropanoic Acid; β-(Aminomethyl)-p-chlorohydrocinnamic Acid; β-(4-Chlorophenyl)-GABA; Baclon; Clofen; Lioresal; Butanoic acid, 4-amino-3-(4-chlorophenyl)-; β-(Aminomethyl)-p-chlorohydrocinnamic acid (USP);

Keywords
Pharmaceutical Standards
Amines
Aromatics
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.

Baclofen Standard (CAS No. 1134-47-0) with molecular formula C₁₀H₁₂ClNO₂ and molecular weight 213.66 g/mol is a high-purity pharmaceutical reference standard widely utilized for impurity profiling, analytical method development, validation, and quality control of Baclofen in bulk drugs and finished formulations. As a centrally acting antispastic agent used in the management of muscle spasticity associated with multiple sclerosis, spinal cord injuries, and neurological disorders, Baclofen requires precise analytical evaluation in regulated environments. This reference material is extensively applied in advanced techniques such as HPLC, LC-MS/MS, GC-MS, NMR, and IR spectroscopy to ensure accurate identification, quantification, and stability assessment in compliance with global regulatory frameworks including ICH guidelines, EMA, US FDA, USP, and European Pharmacopoeia (EP) standards. Manasa Life Sciences, Hyderabad, India, is a trusted global manufacturer and supplier of Baclofen Standard, delivering high-quality reference materials with complete documentation support including COA, GMP compliance, GDP standards, MSDS, and SDS, ensuring reliability for pharmaceutical research, regulatory submissions, and GMP-certified quality control laboratories worldwide.