Category
Trihexyphenidyl
CAS Number
52-49-3
Alternate CAS Number
144-11-6(Freebase)
Molecular Formula
C₂₀H₃₂ClNO
Molecular Weight
337.92 g/mol
Synonym

Trihexyphenidyl Hydrochloride; D,L-Trihexyphenidyl Hydrochloride; α-Cyclohexyl-α-phenyl-1-piperidinepropanol Hydrochloride; (±)-Trihexyphenidyl Hydrochloride; 1-Phenyl-1-cyclohexyl-3-piperidyl-1-propanol Hydrochloride; 3-(1-Piperidyl)-1-cyclohexyl-1-phenyl-1-propanol Hydrochloride; 3-(1-​Piperidyl)-1-phenyl-1-cyclohexyl-1-propanol Hydrochloride; Alpha-cyclohexyl-alpha-phenyl-1-piperidinepropanol Hydrochloride; Antitrem; Aparkane; Artane; Artane Hydrochloride; Benzhexol Chloride; Benzhexol Hydrochloride; Broflex; Cyclodol; Pacitane; Paralest; Parcopane; Pargitan; Parkidyl; Parkinane; Parkinol; Parkinsan; Parkisan; Parkopan; Partigan; Peragit; Pipanol (USP)

Keywords
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.

Achieve superior assay precision and accelerate your commercial release timelines with our premium Trihexyphenidyl Hydrochloride Reference Standard (Chemical Name: 1-cyclohexyl-1-phenyl-3-(piperidin-1-yl)propan-1-ol hydrochloride; CAS: 52-49-3). As a specialized, certified pharmaceutical-grade reference material, this salt-form compound is an absolute necessity for verifying the quantitative potency, dissolution profiles, and therapeutic efficacy of anti-Parkinsonian medicinal dosage forms. Featuring a molecular formula of C₂₀H₃₂ClNO and a molecular weight of 337.92 g/mol, our high-purity reference standard seamlessly aligns with the most stringent USP and EP pharmacopeial monograph specifications. Backed by Manasa Life Sciences’ industry-leading synthesis expertise, each batch undergoes exhaustive LC-MS and NMR fingerprinting to provide the fully traceable, GDP-compliant distribution data necessary to confidently support your USFDA submissions and EMA drug product marketing authorizations.