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2-(3-Ethoxy-4-methoxyphenyl)ethylamine-[d7] Hydrochloride

General Information
Catalog: BLP-006361
CAS: 1398065-60-5
Molecular Formula: C11H10D7NO2.HCl
Molecular Weight: 238.76
Chemical Structure
2-(3-Ethoxy-4-methoxyphenyl)ethylamine-[d7] Hydrochloride
Synonyms 2-(3-Ethoxy-4-methoxy-d3-phenyl)ethyl-1,1,2,2-d4-amine HCl; 3-Ethoxy-4-Methoxyphenethylamine-d7 Hydrochloride; 2-(3-Ethoxy-4-Methoxyphenyl)Ethan-1-Amine-d7 Hydrochloride
IUPAC Name 1,1,2,2-tetradeuterio-2-[3-ethoxy-4-(trideuteriomethoxy)phenyl]ethanamine;hydrochloride
Related CAS 403842-03-5 (unlabelled) 86456-97-5 (unlabelled free base)
Canonical SMILES CCOC1=C(C=CC(=C1)CCN)OC.Cl
InChI InChI=1S/C11H17NO2.ClH/c1-3-14-11-8-9(6-7-12)4-5-10(11)13-2;/h4-5,8H,3,6-7,12H2,1-2H3;1H/i2D3,6D2,7D2;
InChI Key YXLSDLKSKODYFG-VPTCIXLOSA-N
Purity 98%

2-(3-Ethoxy-4-methoxyphenyl)ethylamine-[d7] Hydrochloride, a labeled chemical compound, finds diverse scientific and analytical applications. Here are key applications presented with a high degree of perplexity and burstiness:

Pharmacokinetic Studies: In the realm of pharmacokinetics, this isotopically labeled compound plays a vital role in tracking and quantifying the biodistribution of drugs within the body. By utilizing its stable isotope-labeled counterpart, researchers can delve into the absorption, distribution, metabolism, and excretion profiles of drugs. Such intricate analyses aid in refining drug dosing regimens and enhancing therapeutic outcomes through meticulous assessment of drug behavior in vivo.

Metabolomics Research: Within the field of metabolomics, 2-(3-Ethoxy-4-methoxyphenyl)ethylamine-[d7] Hydrochloride acts as a stalwart internal standard for both qualitative and quantitative analysis of metabolites. It ensures unwavering precision and consistency in detection and measurement processes, particularly when employing mass spectrometry techniques. This application stands as a cornerstone for pinpointing biomarkers and unraveling the intricate metabolic shifts linked to various diseases, painting a detailed portrait of physiological processes at play.

Chemical Synthesis: Serving as a linchpin in chemical synthesis endeavors, this compound emerges as a pivotal precursor or reference material in the creation of elaborate molecular structures. Its intricate isotopic labeling scheme permits precise and controlled chemical reactions, facilitating explorations in synthetic chemistry and materials science. Researchers harness the power of the labeled form to map out reaction pathways and validate synthetic methodologies, paving the way for advancements in molecular design and innovation.

Analytical Method Development: 2-(3-Ethoxy-4-methoxyphenyl)ethylamine-[d7] Hydrochloride assumes a crucial role in the development and validation of analytical methods, particularly in the domains of spectroscopy and chromatography. It acts as a linchpin in fine-tuning equipment settings and calibration procedures necessary for accurate and reliable analyses in laboratory settings. This application stands as a cornerstone in upholding the integrity and repeatability of scientific measurements, laying a robust foundation for rigorous scientific inquiry and experimentation.

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