Category
Trihexyphenidyl
CAS Number
144-11-6
Alternate CAS Number
52-49-3(HCl Salt)
Molecular Formula
C₂₀H₃₁NO
Molecular Weight
301.47 g/mol
Synonym

Trihexyphenidyl; 1-Cyclohexyl-1-phenyl-3-(piperidin-1-yl)propan-1-ol; 1-Piperidinepropanol, α-cyclohexyl-α-phenyl-; 1-Piperidinepropanol, α-cyclohexyl-α-phenyl-; (±)-Benzhexol; (±)-Trihexyphenidyl; (±)-Triphenidyl; 1-Cyclohexyl-1-phenyl-3-(piperidin-1-yl)propan-1-ol; 1-Cyclohexyl-1-phenyl-3-piperidin-1-ylpropan-1-ol; Benzhexol

Keywords
Impurities
Metabolites.
Pharmaceutical Standards
Intermediates
Fine Chemicals
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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.

Manasa Life Sciences, a premier global manufacturer and commercial supplier, offers the high-purity Trihexyphenidyl Base Reference Standard (Chemical Name: 1-Cyclohexyl-1-phenyl-3-(piperidin-1-yl)propan-1-ol; CAS: 144-11-6), a vital antimuscarinic agent used for the therapeutic management of Parkinson’s disease and drug-induced extrapyramidal symptoms. Synthesized specifically for pharmaceutical analytical method development and rigorous quality control (QC) validation, this premium-grade material features a molecular formula of C₂₀H₃₁NO and a molecular weight of 301.47 g/mol. To ensure the highest level of data integrity for your regulatory filings, every single batch is strictly manufactured under current GMP conditions and meticulously characterized using state-of-the-art HPLC, LC-MS, NMR, and IR spectroscopy. Each shipment is backed by comprehensive, lot-specific CoA (Certificate of Analysis) and MSDS documentation, empowering your laboratory to maintain flawless compliance with USP, EP, USFDA, EMA, and ICH guidelines for stability testing and global active pharmaceutical ingredient (API) profiling.