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Bupivacaine-d9

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    Bupivacaine-d<sub>9</sub>
  • Bupivacaine-d<sub>9</sub>
Cat No: 18246
Biochemicals - Ion Channel Modulation
Cayman

Bupivacaine-d9 is intended for use as an internal standard for the quantification of bupivacaine (Item No. 16618) by GC- or LC-MS. Bupivacaine is a sodium channel blocker and local anesthetic.{49026,49029} It inhibits sodium currents in rat dorsal hor...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 1-(butyl-d9)-N-(2,6-dimethylphenyl)-2-piperidinecarboxamide
Correlated keywords:
  • 2180-92-9 deuterated deuterium GCMS LCMS NA+ K+ MK801
Product Overview:
Bupivacaine-d9 is intended for use as an internal standard for the quantification of bupivacaine (Item No. 16618) by GC- or LC-MS. Bupivacaine is a sodium channel blocker and local anesthetic.{49026,49029} It inhibits sodium currents in rat dorsal horn neurons in a concentration-dependent manner and inhibits synaptic transmission in rat sympathetic ganglia, increasing the firing threshold when used at a concentration of 200 nM.{49030,49027} Bupivacaine (10 µM) blocks cardiac sodium channels in a use-dependent manner and inhibits respiration in cardiac cell mitochondria when palmitoyl-carnitine or acetyl-carnitine are used as substrates (IC50s = 0.78 and 0.37 mM, respectively).{49026,49028} It also reduces thermal hyperplasia in a rat model of sciatic ligation injury when 0.6 ml of a 0.5% solution is administered into the perinerve space, and the duration of this effect is extended by co-administration of the NMDA receptor antagonist MK-801 (Item No. 10009019).{49029} Formulations containing bupivacaine have been used as local anesthetics for surgery, oral surgery, and dental procedures and for anesthetic purposes in research studies using animals.
Size 500 µg
Shipping dry ice
CAS Number 474668-57-0
Molecular Formula C18H19D9N2O
SMILES CC1=CC=CC(C)=C1NC(C2N(C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])CCCC2)=O
Molecular Weight 297,5
Formulation A solid
Purity ≥99% deuterated forms (d1-d9)
Custom Code 3822.19
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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