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-010841 |
CAS: 120404-22-0 |
Molecular Formula: C3D6Br2 |
Molecular Weight: 207.92 |
Chemical Structure |
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Description | 1,3-Dibromopropane-[d6] is the labelled analogue of 1,3-Dibromopropane. |
Synonyms | 1,3-Dibromopropane-d6; Propane-1,1,2,2,3,3-d6, 1,3-dibromo- (9CI) |
IUPAC Name | 1,3-dibromo-1,1,2,2,3,3-hexadeuteriopropane |
Related CAS | 109-64-8 (unlabelled) |
Isomeric SMILES | [2H]C([2H])(C([2H])([2H])Br)C([2H])([2H])Br |
Canonical SMILES | C(CBr)CBr |
InChI | InChI=1S/C3H6Br2/c4-2-1-3-5/h1-3H2/i1D2,2D2,3D2 |
InChI Key | VEFLKXRACNJHOV-NMFSSPJFSA-N |
Boiling Point | 167°C (lit.) |
Melting Point | -34°C (lit.) |
Purity | 99% by CP; 99% atom D |
Density | 2.047 g/cm3 at 25°C |
Storage | Store at RT |
1,3-Dibromopropane-[d6], a deuterated organic compound, finds diverse applications in research and industrial settings. Below are key applications intricately presented with high perplexity and burstiness:
Nuclear Magnetic Resonance (NMR) Studies: In the realm of NMR spectroscopy, 1,3-Dibromopropane-[d6] emerges as a pivotal player, serving either as a solvent or an internal standard. Its deuterated nature minimizes interference in proton NMR signals, allowing researchers to delve deep into the chemical structures and dynamics of organic molecules. This application plays a critical role in unraveling reaction mechanisms and validating compound purity through meticulous analysis.
Synthetic Chemistry: Positioned at the heart of organic synthesis, this compound acts as a crucial intermediate, particularly in reactions necessitating heavy isotopic labeling. Chemists harness the power of 1,3-Dibromopropane-[d6] to incorporate deuterium atoms into target molecules, offering invaluable insights for mechanistic studies and the development of pharmaceuticals with modified metabolic properties. This enables the tracing of intricate reaction pathways and the fine-tuning of synthesis conditions for optimal outcomes.
Environmental Tracing: With its labeled hydrogen atoms, 1,3-Dibromopropane-[d6] emerges as a potent tracer in environmental investigations. Researchers meticulously track its movement and degradation across various ecosystems, shedding light on pollutant pathways and evaluating environmental exposure risks. This application plays a pivotal role in shaping strategies for environmental monitoring and bolstering efforts in pollution control, safeguarding our delicate ecosystems.
Isotopic Labeling: Stepping into the realm of biochemistry, 1,3-Dibromopropane-[d6] assumes the role of an indispensable tool for isotopic labeling of biomolecules. This labeling aids in tracking molecular interactions and pathways, offering unique signatures in mass spectrometry for precise identification and quantification of metabolites. Such detailed information proves critical for advancing metabolic research and propelling drug development, paving the way for groundbreaking discoveries in the pharmaceutical landscape.
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