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Home > Products >  99%min Oxcarbazepine Manufacturer For Neurological Medication

99%min Oxcarbazepine Manufacturer For Neurological Medication CAS NO.28721-07-5

  • Min.Order: 10 Gram
  • Payment Terms: T/T,MoneyGram
  • Product Details

Keywords

  • 99%min Oxcarbazepine
  • For Neurological Medication
  • Oxcarbazepine Manufacturer

Quick Details

  • ProName: 99%min Oxcarbazepine Manufacturer For ...
  • CasNo: 28721-07-5
  • Molecular Formula: C15H12N2O2
  • Appearance: White Powder
  • Application: It Can Be Used As Pharmaceutical Inte...
  • DeliveryTime: 2-4 days after confirming your payment...
  • PackAge: 100g/ bag, 2 kg/ bag, 25kg/ carton or ...
  • Port: Wuhan
  • ProductionCapacity: 10000 Metric Ton/Month
  • Purity: 99%
  • Storage: Store in sealed containers at cool & d...
  • Transportation: By DHL, TNT, FedEx, HKEMS, UPS, Etc
  • LimitNum: 10 Gram

Superiority

 

Advantages:
 
Hubei XinRunde Chemical Co., Ltd is a renowned pharmaceutical manufacturer. We can offer high quality products at competitive price in quick delivery with 100% custom pass guaranteed. Never stop striving to offer our best service is our philosophy. We have Flexible and Untraceable payment terms. As a leading manufacture, our products have been exported to Germany, Norway, Poland, Finland, Spain, UK, France, Russia, USA, Brazil, Mexico, Australia, Japan, Korea, Thailand, Indonesia, Uruguay and many other countries.

 

1. Quality.Every batch of steroid powders have tobetested by our QC(quality control) before they are allowed to sell.


2. Delivery We have stock, so we can delivery quickly at the very day when receive the payment. Within 24 hours after receiving the payment Lead time 4 or 7 days.


3. Discreet package Safelyand Professionally Disguised Package Guaranteed. For your safety and to insure delivery all products will be packed in a discreet way to prevent any suspicions, no steroids related name will appear on the parcels. high successful delivery rate.


4. Warm after-sale service Any of your question would be solved for the first as soon as possible.

 

Details

Oxcarbazepine Basic information
Product Name: Oxcarbazepine
Synonyms: 10,11-DIHYDRO-10-OXO-5H-DIBENZ[B,F]AZEPINE-5-CARBOXAMIDE;10,11-DIHDYRO-10-OXO-5H-DIBENZ[B,F]AZEPINE-5-CARBOXAMIDE;5H-DIBENZ[B,F]AZEPINE-5-CARBOXAMIDE, 10,11-DIHYDRO-10-OXO-;TRILEPTAL;f)azepine-5-carboxamide,10,11-dihydro-10-oxo-5h-dibenz(;gp47680;OXCARBAMAZEPINE;OXCARBAZEPINE
CAS: 28721-07-5
MF: C15H12N2O2
MW: 252.27
EINECS: 249-188-8
Product Categories: Heterocyclic Compounds;APIs;Intermediates & Fine Chemicals;Pharmaceuticals;Chiral Reagents;Heterocycles;Metabolites & Impurities;Pharmaceutical raw material;Chiral Reagents, Heterocycles, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals;COREG;Other APIs
Mol File: 28721-07-5.mol
Oxcarbazepine Structure
 
Oxcarbazepine Chemical Properties
Melting point  215-216°C
Fp  2℃
storage temp.  Store at RT
solubility  DMSO: ~9 mg/mL
form  solid
color  white
Water Solubility  Soluble in DMSO, methanol, water, ethanol and acetone.
Merck  14,6929
CAS DataBase Reference 28721-07-5(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xn,F
Risk Statements  22-36-20/21/22-11
Safety Statements  16-36/37
RIDADR  UN 1648 3 / PGII
WGK Germany  3
RTECS  HN8445000
Hazardous Substances Data 28721-07-5(Hazardous Substances Data)
 
 
Oxcarbazepine Usage And Synthesis
Chemical Properties Pale Yellow Powder
Uses A metabolite of Eslicarbazepine acetate, (BIA 2-093), a novel central nervous system drug.
Uses beta-adrenergic blocker
Uses The keto derivative of Carbamazepine. Used as an anticonvulsant
Definition ChEBI: A dibenzoazepine derivative, having a carbamoyl group at the ring nitrogen, substituted with an oxo group at C-4 of the azepeine ring which is also hydrogenated at C-4 and C-5. It is a anticholinergic anticonvulsant and mood stabilizing drug, used primaril in the treatment of epilepsy.
Biological Activity Anticonvulsant; protects mice and rats against generalized tonic-clonic seizures induced by electroshock. Thought to act via inhibition of sodium channel activity.

 

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