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Rufinamide

Rufinamide Structure
CAS No.
106308-44-5
Chemical Name:
Rufinamide
Synonyms
1-(2,6-Difluorobenzyl)-1H-1,2,3-triazole-4-carboxamide;E 2080;RUF 331;CS-1133;Inovelon;CGP 33101;Rufinamide;Rufinamide>Rufinamide, >=99%;Rufinamide(E 2080
CBNumber:
CB5972298
Molecular Formula:
C10H8F2N4O
Molecular Weight:
238.19
MOL File:
106308-44-5.mol
MSDS File:
SDS
Modify Date:
2024/7/29 17:07:33

Rufinamide Properties

Melting point 232-234?C
Boiling point 473.8±55.0 °C(Predicted)
Density 1.52±0.1 g/cm3(Predicted)
Flash point 2℃
storage temp. -20°C
solubility DMSO: soluble9mg/mL
pka 14.37±0.50(Predicted)
form powder
color white
Merck 14,8293
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 1 month.

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Warning
Hazard statements  H336-H351-H361fd
Precautionary statements  P201-P202-P261-P271-P280-P308+P313
Hazard Codes  F,T
Risk Statements  11-23/24/25-39/23/24/25-48-41-38-28
Safety Statements  7-16-36/37-45-36/37/39-28-26-24/25
RIDADR  UN 1648 3 / PGII
WGK Germany  3
HS Code  29339900

Rufinamide price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) R8404 Rufinamide ≥98% (HPLC), powder 106308-44-5 10MG ₹13780.23 2022-06-14 Buy
Sigma-Aldrich(India) R8404 Rufinamide ≥98% (HPLC), powder 106308-44-5 50MG ₹61962.3 2022-06-14 Buy
Sigma-Aldrich(India) R-023 Rufinamide solution 1.0?mg/mL in acetonitrile: water (9:1), certified reference material, Cerilliant? 106308-44-5 1ML ₹18300.8 2022-06-14 Buy
Sigma-Aldrich(India) PHR1625 Rufinamide Pharmaceutical Secondary Standard; Certified Reference Material 106308-44-5 500MG ₹16540.6 2022-06-14 Buy
TCI Chemicals (India) R0143 Rufinamide 106308-44-5 25MG ₹2300 2022-05-26 Buy
Product number Packaging Price Buy
R8404 10MG ₹13780.23 Buy
R8404 50MG ₹61962.3 Buy
R-023 1ML ₹18300.8 Buy
PHR1625 500MG ₹16540.6 Buy
R0143 25MG ₹2300 Buy

Rufinamide Chemical Properties,Uses,Production

Description

Approximately 2.5 million people worldwide are afflicted with epilepsy, a devastating neurological disorder diagnosed by the tendency toward recurrent, unprovoked seizures, often of unknown etiology. Rufinamide has been launched primarily as adjunctive therapy of LGS. Its proposed mechanism of action involves the limitation of firing of sodium-dependent action potentials. The ultimate result is membrane stabilization. Since it does not exhibit measurable binding to monoamine, acetylcholine, histamine, glycine, AMPA/kainate, NMDA, or GABA receptors or systems, these receptor-mediated pathways are not anticipated to be involved in the exertion of rufinamide’s effects. Rufinamide displayed efficacy in several electrical and chemical animal seizure models.

Chemical Properties

White Solid

Uses

Labelled Rufinamide (R701552). Antiepileptic triazole derivative which decreases firing by neurons at sodium channels. Anticonvulsant.

General Description

An antiepileptic drug and anticonvulsant, Rufinamide is approved for the treatment of partial seizures associated with Lennox-Gastaut syndrome in adults and children 4 years and older. Rufinamide is marketed as Banzel® in the US and Inovelon® in the EU.

Biological Activity

Board spectrum anticonvulsant. Prolongs the inactivation of sodium channels and limits the frequency of action potential firing in cultured and acutely isolated neurons. Displays anticonvulsive activity in a range of animal seizure models.

Side effects

Rufinamide was well tolerated with the most common adverse events including fatigue, somnolence, tremors, mild-to-moderate dizziness, nausea, headache, and diplopia. Since rufinamide is not metabolized by the CYP450 system, it is anticipated to have a low potential for interaction with drugs metabolized by the CYP isozymes. Rufinamide, however, does exhibit clinically relevant interactions with other antiepileptic drugs; concomitant treatment with valproate results in a reduction in rufinamide clearance while concomitant treatment with phenytoin, primidone, phenobarbital, carbamazepine, or vigabatrin causes an increase in rufinamide clearance. In these situations, rufinamide dosage adjustment may be required.

Rufinamide Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 289)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Jigs Chemical ltd +919099003427 Gujarat, India 239 58 Inquiry
Lupin Ltd +91-8019896181 +91-8019896181 Maharashtra, India 93 58 Inquiry
Glenmark Pharmaceuticals Limited +912240189999 Maharashtra, India 93 58 Inquiry
Hetero Drugs Limited +91-4023704923 +91-4023704923 Telangana, India 296 58 Inquiry
AKASH PHARMA EXPORTS +91-9388123451 +91-9846039283 Kerela, India 470 58 Inquiry
Manus Aktteva Biopharma LLP 08048250218Ext 800 Ahmedabad, India 655 58 Inquiry
MSN LIFE SCIENCES PRIVATE LTD +91 84523 34200 New Delhi, India 104 58 Inquiry
MSN LABORATORIES PRIVATE LTD +91 40 30438600 New Delhi, India 230 58 Inquiry
GLENMARK LIFE SCIENCES LTD +91 22 4018 9999 New Delhi, India 103 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry

Rufinamide Spectrum

1H-1,2,3-TRIAZOLE-4-CARBOXAMIDE, 1-[(2,6-DIFLUOROPHENYL)METHYL]- Rufinamide Rufinamide (200 mg) RufinaMide(Banzel) CGP 33101 E 2080 Inovelon RUF 331 Rufinamide solution Rufinamide, >=99% Rufinamide, 98%, a sodium channel blocker 1-[(2,6-difluorophenyl)methyl]-4-triazolecarboxamide CS-1133 Rufinamide(E 2080 CGP 33101; E 2080; INOVELON; RUF 331; BANZEL;E2080 Rufinamide> Rufinamide USP/EP/BP Rufinamide (CGP 33101 RufinamideQ: What is Rufinamide Q: What is the CAS Number of Rufinamide Q: What is the storage condition of Rufinamide Q: What are the applications of Rufinamide TIANFU CHEM- Rufinamide Rufinamide (1606401) 5R)-Rosuvastatin Lactone 1-(2,6-Difluorobenzyl)-1H-1,2,3-triazole-4-carboxamide Rufinamide/E2080/CGP33101/RUF331 CGP 33101|||E 2080|||RUF 331 106308-44-5 C10H6D2F2N4O C10H6D2F2N315NO Inhibitors Banzel Pharmaceuticals Isotope Labelled Compounds Amines Aromatics Bases & Related Reagents Heterocycles Intermediates & Fine Chemicals Nucleotides