10,11-DIHYDRO-10-HYDROXYCARBAZEPINE
10,11-DIHYDRO-10-HYDROXYCARBAZEPINE Basic information
- Product Name:
- 10,11-DIHYDRO-10-HYDROXYCARBAZEPINE
- Synonyms:
-
- Oxcarbazepine Hydroxy Impurity
- 5-Carbamoyl-10,11-dihydro-5H-dibenzo[b,f]azepine-10-ol
- 6-hydroxy-5,6-dihydrobenzo[b][1]benzazepine-11-carboxamide
- 10,11-Dihydro-10-hydroxy-5H-dibenz(Z)[b,f]azepin-5-carboxamide
- 10-hydroxy-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxaMide
- 10,11-Dihydro-10-hydroxy
- (±)-10-Hydroxy-10,11-dihydro-5H-dibenz[b,f]azepine-5-carboxaMide
- 5H-Dibenz[b,f]azepine-5-carboxaMide,10,11-dihydro-10-hydroxy-
- CAS:
- 29331-92-8
- MF:
- C15H14N2O2
- MW:
- 254.28
- Product Categories:
-
- Intermediates & Fine Chemicals
- Metabolites & Impurities
- Pharmaceuticals
- Isotope Labeled Compounds
- Mol File:
- 29331-92-8.mol
10,11-DIHYDRO-10-HYDROXYCARBAZEPINE Chemical Properties
- Melting point:
- 186-189°C
- Boiling point:
- 431.3±55.0 °C(Predicted)
- Density
- 1.336
- Flash point:
- 2℃
- storage temp.
- -20°C
- solubility
- Soluble to 100 mM in DMSO and to 50 mM in ethanol
- form
- Solid
- pka
- 13.75±0.20(Predicted)
- color
- White to off-white
- BRN
- 1540211
- InChIKey
- BMPDWHIDQYTSHX-UHFFFAOYSA-N
- CAS DataBase Reference
- 29331-92-8
Safety Information
- Hazard Codes
- N,Xn,F
- Risk Statements
- 51/53-36-20/21/22-11
- Safety Statements
- 61-36/37-26-16
- RIDADR
- UN 3077 9 / PGIII
- WGK Germany
- 3
10,11-DIHYDRO-10-HYDROXYCARBAZEPINE Usage And Synthesis
Chemical Properties
White Solid
Uses
A metabolite of Oxcarbazepine
Uses
A labelled metabolite of Oxcarbazepine
Uses
10,11-dihydro-10-hydroxy Carbamazepinee is the active metabolite of oxcarbazepine . Oxcarbazepine is rapidly and almost completely converted to 10,11-dihydro-10-hydroxycarbamazepine, which then demonstrates anticonvulsant efficacy by modulating several ion channels and receptors. ?10,11-dihydro-10-hydroxy Carbamazepine is reported to inhibit both voltage-gated Na+ and Ca2+ channels, to potentiate voltage-gated K+ channels, to antagonize adenosine A1 receptors, to increase dopaminergic transmission, and to inhibit glutamate release.
Definition
ChEBI: A dibenzoazepine that is 5H-dibenzo[b,f]azepine, reduced across the C-10,11 positions and carrying a carbamoyl substituent at the azepine nitrogen and a hydroxy function at C-10. A voltage-gated sodium channel b ocker with anticonvulsant and mood-stabilizing effects, it is related to oxcarbazepine and is an active metabolite of oxcarbazepine.
storage
Store at RT
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