Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-013044 |
CAS: 1346597-90-7 |
Molecular Formula: C15H19D3N2O |
Molecular Weight: 249.37 |
Chemical Structure |
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Description | Mepivacaine-[d3] is the labelled analogue of Mepivacaine, which is an analgesic and anti-inflammatory agent. |
Synonyms | Mepivacaine D3; N-(2,6-Dimethylphenyl)-1-methyl-2-piperidinecarboxamide-d3; (±)-Mepivacaine-d3; 1-Methyl-2',6'-pipecoloxylidide-d3; APF 135-d3; Carbocain-d3; Carbocaine-d3; Carbocaine-V-d3; DL-Mepivacaine-d3; MepiSV-d3; Mepicaine-d3; Scandicain-d3; Scandicaine-d3; Tevacaine-d3 |
IUPAC Name | N-(2,6-dimethylphenyl)-1-(trideuteriomethyl)piperidine-2-carboxamide |
Related CAS | 96-88-8 (unlabelled) 1722-62-9 (unlabelled hydrochloride) |
Canonical SMILES | CC1=C(C(=CC=C1)C)NC(=O)C2CCCCN2C |
InChI | InChI=1S/C15H22N2O/c1-11-7-6-8-12(2)14(11)16-15(18)13-9-4-5-10-17(13)3/h6-8,13H,4-5,9-10H2,1-3H3,(H,16,18)/i3D3 |
InChI Key | INWLQCZOYSRPNW-HPRDVNIFSA-N |
Melting Point | 148-151°C |
Purity | 95% by HPLC; 98% atom D |
Solubility | Soluble in Chloroform (Slightly), Methanol (Slightly) |
Appearance | White to Pale Yellow Solid |
Storage | Store at 2-8°C |
Mepivacaine-[d3], a deuterated variant of the local anesthetic mepivacaine, finds widespread use in both preclinical and research environments. Here are the key applications of Mepivacaine-[d3]:
Pharmacokinetic Studies: Delving into the world of pharmacokinetics, Mepivacaine-[d3] serves as a valuable tool for exploring the absorption, distribution, metabolism, and excretion (ADME) of mepivacaine. The deuterated nature of this compound enables more precise tracing and differentiation within biological samples, aiding researchers in refining dosing strategies and enhancing safety profiles.
Metabolic Pathway Elucidation: By harnessing the power of Mepivacaine-[d3], scientists can unravel the intricate metabolic pathways and enzymatic transformations that govern its fate within the body. The incorporation of deuterium elevates the sensitivity of mass spectrometry for detecting metabolites, shedding light on how the drug undergoes processing and unveiling potential metabolites with therapeutic or toxic implications.
Analytical Method Development: The versatility of Mepivacaine-[d3] extends to the realm of analytical method development, playing a pivotal role in crafting and validating assays for drug analysis. Its stable isotope labeling facilitates the creation of highly sensitive and specific detection methods, crucial for clinical diagnostics and forensic investigations. This capability ensures the accurate quantification and monitoring of drugs in a variety of biological matrices, underpinning reliable results and insights.
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