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-010189 |
CAS: 126840-15-1 |
Molecular Formula: C8H6D4O2 |
Molecular Weight: 142.19 |
Chemical Structure |
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Description | 1,2-Dimethoxybenzene-[3,4,5,6-d4] is a labelled analogue of 1,2-Dimethoxybenzene. 1,2-Dimethoxybenzene is a common reagent in the synthesis. |
Synonyms | o-Dimethoxybenzene-3,4,5,6-d4; Veratrole-3,4,5,6-d4; Catechol Dimethyl Ether-3,4,5,6-d4; Pyrocathecol Dimethyl Ether-3,4,5,6-d4 |
IUPAC Name | 1,2,3,4-tetradeuterio-5,6-dimethoxybenzene |
Related CAS | 91-16-7 (unlabelled) |
Canonical SMILES | COC1=CC=CC=C1OC |
InChI | InChI=1S/C8H10O2/c1-9-7-5-3-4-6-8(7)10-2/h3-6H,1-2H3/i3D,4D,5D,6D |
InChI Key | ABDKAPXRBAPSQN-LNFUJOGGSA-N |
Boiling Point | 206.3±8.0°C at 760 mmHg |
Purity | 98 atom % D |
Density | 1.0±0.1 g/cm3 |
1,2-Dimethoxybenzene-[3,4,5,6-d4] is a deuterium-labeled chemical compound that serves various applications in scientific research and industry. Here are some key applications of 1,2-Dimethoxybenzene-[3,4,5,6-d4]:
Nuclear Magnetic Resonance (NMR) Spectroscopy: 1,2-Dimethoxybenzene-[3,4,5,6-d4] is commonly used as a reference or standard compound in NMR spectroscopy. The deuterium labeling provides distinct spectral patterns that help in the precise identification and analysis of other compounds in mixtures. Researchers can trace molecular structures and interactions with high accuracy due to these stable isotopic labels.
Metabolic Studies: This compound is utilized in metabolic pathway studies involving organisms or cells. Using the deuterium-labeled version of dimethoxybenzene allows researchers to track metabolic transformations and pathways with enhanced sensitivity. This can lead to deeper insights into metabolic processes and the development of improved biochemical models.
Chemical Synthesis: In synthetic chemistry, 1,2-Dimethoxybenzene-[3,4,5,6-d4] is used as a labeled precursor or reagent. Its isotopic labeling can help study reaction mechanisms by providing a clear distinction between starting materials and products. This assists chemists in fine-tuning synthesis processes and developing novel compounds with desired properties.
Environmental Analysis: The deuterated version of dimethoxybenzene can be employed in environmental studies to trace the fate and transport of organic compounds. By analyzing isotopic signatures, scientists can better understand the degradation pathways and persistence of pollutants in various ecosystems. This technique is crucial in assessing environmental impacts and developing strategies for pollution management.
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