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Isoxsuprine-[d6] hydrochloride

General Information
Catalog: BLP-013970
Molecular Formula: C13H13D6ClNO3
Molecular Weight: 343.88
Chemical Structure
Isoxsuprine-[d6] hydrochloride
Description Isoxsuprine-[d6] HCl is an isotope labelled derivative of Isoxsuprine. Isoxsuprine is a β2 adrenoreceptor agonist and can be used as a vasodilator in humans and equines.
Synonyms Isoxsuprine-d6 HCl (3-phenoxy-2-propyl-1,1,1,2,3,3-d6-amine) (mixture of diastereomers); 3-Phenoxy-2-propyl-1,1,1,2,3,3,3-d6-amine Hydrochloride (mixture of diastereomers); 4-Hydroxy-α-[1-[(1-methyl-2-phenoxyethyl)amino]ethyl]benzenemethanol Hydrochloride-D6; p-Hydroxy-α-[1-[(1-methyl-2-phenoxyethyl)amino]ethyl]benzyl Alcohol Hydrochloride-D6
Related CAS 579-56-6 (unlabelled)
Melting Point 180-183°C
Purity 95% by HPLC; 98% atom D
Solubility Soluble in DMSO (Slightly), Methanol (Slightly), Water (Slightly)
Appearance White to Off-white Solid
Storage Store at -20°C

Isoxsuprine-[d6] hydrochloride, a deuterated derivative of isoxsuprine hydrochloride, is renowned for its effects on muscle relaxation and enhancement of blood flow. Here are the crucial applications of isoxsuprine-[d6] hydrochloride:

Pharmacokinetic Studies: Utilizing isoxsuprine-[d6] hydrochloride in pharmacokinetic investigations allows researchers to meticulously track and comprehend the metabolic processes and biotransformation of isoxsuprine within the body. The deuterated nature of this compound enables clear differentiation between the drug, endogenous compounds, and its non-deuterated version. This isotope-labeled compound plays a pivotal role in achieving precise pharmacokinetic profiling.

Analytical Method Development: In the realm of analytical chemistry, isoxsuprine-[d6] hydrochloride shines as an internal standard indispensable for formulating and validating analytical methodologies spanning mass spectrometry and high-performance liquid chromatography (HPLC). Its incorporation ensures heightened accuracy and precision in the quantification of isoxsuprine across various biological samples, thereby guaranteeing the reliability and reproducibility of analytical outcomes.

Toxicological Studies: In toxicological investigations, isoxsuprine-[d6] hydrochloride finds critical application in assessing the potential toxic impacts of isoxsuprine and its metabolites. The deuterated formulation acts as a reliable tracer, facilitating the tracing of metabolic pathways and identification of toxicological endpoints. This data is instrumental in establishing a comprehensive safety profile for the drug under varying conditions, ensuring informed decision-making regarding its usage.

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