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Organometallic compounds contain direct bonds between carbon atoms and metal atoms/ions and play roles as homogeneous catalysts and stoichiometric reagents in reactions; available in various chemical compositions, quantities, purities, and reagent grades.
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Triphenyltin chloride-d15 is the deuterium-labeled analogue of triphenyltin chloride supplied as a high-purity reference standard for research and analytical use. It is intended for use as an internal standard in mass spectrometry, isotopic tracing, and labeling studies, and is provided in small, laboratory-scale quantities.
Deuterium-labeled (D15) isotopologue for accurate mass spectrometry quantitation.
High purity suitable for reference standard and analytical use.
Small-scale quantities for laboratory research and method development.
Useful for isotopic tracing and labeling experiments.
Provided as a solid with defined molecular weight and CAS registry number.
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Triphenyltin chloride-d15 is the deuterium-labeled analogue of triphenyltin chloride used as a stable isotope reference standard and research reagent for analytical chemistry, mass spectrometry, and isotopic labeling studies. It is supplied as a powder and characterized by high isotopic enrichment and chemical purity.
Deuterium-labeled standard for analytical and mass spectrometry applications.
High chemical purity and isotopic enrichment for accurate quantitation.
Supplied as a stable powder with defined storage conditions.
Useful as an internal standard and reference material in method development.
Characterized by molecular formula C18D15ClSn and molecular weight 400.57 g/mol.
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Obidoxime dichloride is a non-full spectrum oxime agent used as an antidote for organophosphate nerve agent poisoning. It reactivates sarin-inhibited acetylcholinesterase (AChE) and reduces the acute toxicity of sarin. It is for research use only and not sold to patients. In vivo, obidoxime dichloride (intramuscular injection; 10 mg/kg; after 60 mins) exhibits an LD50 of 57.7 mg/kg after administration of sarin, and it reduces the acute toxicity of sarin.
Used as an antidote for organophosphate nerve agent poisoning
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ABT-639 is a novel, peripherally acting, selective T-type Ca2+ channel blocker. It effectively blocks recombinant human T-type (Cav3.2) Ca2+ channels and attenuates low voltage-activated currents in rat DRG neurons. With high oral bioavailability and low brain:plasma ratio, it demonstrates dose-dependent antinociception in models of knee joint pain and increases tactile allodynia thresholds in neuropathic pain models.
Selective T-type Ca2+ channel blocker
High oral bioavailability
Low protein binding
Low brain:plasma ratio
Produces antinociception in knee joint pain models
Increases tactile allodynia thresholds in neuropathic pain models
Does not significantly alter hemodynamic or psychomotor function at higher doses
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Also available in 1 mg, 2 mg, 5 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. ABT-639 is a potent and selective T-type calcium channel blocker.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More