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Modafinil

Modafinil Structure
CAS No.
68693-11-8
Chemical Name:
Modafinil
Synonyms
Provigi;Modiodal;CEP 1538;DEP 1538;MODAFINIL;CRC 40476;CRL-40476;Modaphonil;F9Modafinil;Modafinilrac
CBNumber:
CB5223833
Molecular Formula:
C15H15NO2S
Molecular Weight:
273.35
MOL File:
68693-11-8.mol
Modify Date:
2023/6/30 15:45:59

Modafinil Properties

Melting point 164-166°C
Boiling point 559.1±50.0 °C(Predicted)
Density 1.283±0.06 g/cm3(Predicted)
Flash point 2℃
storage temp. Store at +4°C
solubility DMSO: 18 mg/mL, soluble
form white solid
pka 14.88±0.40(Predicted)
color white
BCS Class 4
CAS DataBase Reference 68693-11-8(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Warning
Hazard statements  H302-H361d
Precautionary statements  P202-P264-P270-P280-P301+P312-P308+P313
Hazard Codes  T+,Xn,F
Risk Statements  26/27/28-36-20/21/22-11
Safety Statements  24/25-45-36/37/39-22-36/37-16
RIDADR  UN 1648 3 / PGII
WGK Germany  3
HS Code  29309090
NFPA 704
0
3 0

Modafinil Chemical Properties,Uses,Production

Description

Modafinil, a centrally active α1-adrenergic agonist, was marketed in France as a psychostimulant for the treatment of narcolepsy and idiopathic hypersomnia including Gelineau's syndrome. In monkeys, modafinil was found to induce potent behavioral stimulation and awakening without stereotyped behavior. In narcoleptic patients, modafinil reduces the daily number of sleep attacks significantly and markedly improves performance. The mechanism of action for its locomotor effects was reported to be due to the stimulation of the central α1-adrenergic system, opposite to amphetamine and methylphenidate, which act mainly by dopaminergic mechanisms. Modafinil has been reported to exhibit minimal peripheral side effects at therapeutic doses and appears to have low abuse potential. The use of modafinil in the treatment of cerebral infarction and ischemia has been claimed.

Chemical Properties

Crystalline Solid

Uses

Modafinil is an α-1-adrenergic agonist. Modafinil is a CNS stimulant; psychostimulant that displays neuroprotective and antiparkinsonian activity in a primate model of Parkinson's disease.

General Description

Modafinil (Provigil) has overall wakefulness-promotingproperties similar to those of central sympathomimetics. It isconsidered an atypical α1-norepinephrine (NE) receptorstimulant and is used to treat daytime sleepiness in narcolepsypatients. Adverse reactions at therapeutic doses arereportedly not severe and may include nervousness, anxiety,and insomnia. Modafinil is used by oral administration.

Biological Activity

Psychostimulant that displays neuroprotective and antiparkinsonian activity in a primate model of Parkinson's disease. Promotes vigilence and wakefulness without the central and peripheral side effects associated with conventional dopaminergic psychostimulants. Mechanism of action is not fully understood, possibly via modulation of catecholamine/GABAergic neurotransmission.

Modafinil Preparation Products And Raw materials

MODAFINIL Acetamide, 2-[(diphenylmethyl)sulfinyl]- Modiodal (Benzhydrylsulfinyl)acetamide Modafinilrac 2-[di(phenyl)methylsulfinyl]ethanamide Modafinil,2-[(Diphenylmethyl)sulfinyl]-acetamide Modafinil CIV (200 mg)F0D3510.997mg/mg(ai) Modafinil CIV (200 mg) F9Modafinil 2-[(R)-(diphenylMethane)sulfinyl]acetaMide CEP 1538 CRC 40476 DEP 1538 Modaphonil (±)-Modafinil-d10 MODAFINIL-DEA SCHEDULE IV 2-(BENZHYDRYLSULFINYL)ACETAMIDE 2-[(DIPHENYLMETHYL)SULFINYL]ACETAMIDE AKOS BC-1794 Modafinil,MODAFINIL CRL-40476 Provigi MODAFINIL INTERMEDIATE:DIPHENYL METHANESULFONYLACETAMIDE Modafinil solution Armodafinil Racemic Mixture( Modafinil) Modafinil (1.0 mg/mL in Acetonitrile) Modafinil CRS Modafinil for system suitability CRS Modafinil USP/EP/BP ModafinilQ: What is Modafinil Q: What is the CAS Number of Modafinil Q: What is the storage condition of Modafinil Q: What are the applications of Modafinil Modafinil CIV (1445404) *Barbital Impurity 1 (Cyclobarbital) 68693-11-8 C15H15NO2S LOTENSIN Active Pharmaceutical Ingredients Intermediates & Fine Chemicals Neurochemicals Pharmaceuticals