Fenethylline
- Product Name
- Fenethylline
- CAS No.
- 3736-08-1
- Chemical Name
- Fenethylline
- Synonyms
- H-814;R-720/11;Amfetylline;Theophyllineethylamphetamine;1,3-dimethyl-7-(2-((1-phenylpropan-2-yl)amino)ethyl)-1H-purine-2,6(3H,7H)-dione;1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-7-[2-[(1-methyl-2-phenylethyl)amino]ethyl]-
- CBNumber
- CB21178722
- Molecular Formula
- C18H23N5O2
- Formula Weight
- 341.41
- MOL File
- 3736-08-1.mol
Fenethylline Property
- Boiling point:
- 563.8±60.0 °C(Predicted)
- Density
- 1.26±0.1 g/cm3(Predicted)
- pka
- 9.39±0.28(Predicted)
Safety
- Hazardous Substances Data
- 3736-08-1(Hazardous Substances Data)
- Toxicity
- LD50 oral in rat: 100mg/kg
- DEA Controlled Substances
- CSCN: 1503
CSA SCH: Schedule I
NARC: No
N-Bromosuccinimide Price
- Product number
- F-7691
- Product name
- FenethyllineHCl
- Packaging
- 10mg
- Price
- $1200
- Updated
- 2021/12/16
Fenethylline Chemical Properties,Usage,Production
Originator
Captagon,Homburg,W. Germany,1961
Definition
ChEBI: Fenetylline is an oxopurine.
Manufacturing Process
1 mol of 7-(β-chloroethyl)-theophylline and 2? mols of α-methyl-β-phenyl
ethylamine are heated for 6 hours in an oil bath, if necessary with addition of
alcohol or toluene. The reaction mixture is diluted with alcohol and acidified
with alcoholic hydrochloric acid. The crystalline mass formed is filtered with
suction and extracted by boiling with alcohol. A product having a melting point
of 237°C to 239°C is formed. With prolonged extraction by boiling with
alcohol, the melting point of the mass falls, preferably due to a change in
modification, to 227°C to 229°C. However, analysis shows that both products
are the pure condensation product.
Instead of the chloroethyl theophylline, it is also possible to use the
corresponding bromine derivative. It was found that in this way the process is
facilitated and the yield is improved
brand name
Biocapton;Captagon cpr nsfp.
Therapeutic Function
Central stimulant
World Health Organization (WHO)
Fenetylline, a theophylline derivative of amfetamine, was introduced in 1966 as a central nervous stimulant. It is subject to abuse and is therefore controlled under Schedule II of the 1971 Convention on Psychotropic Substances. Fenetylline is not widely marketed. (Reference: (UNCPS2) United Nations Convention on Psychotropic Substances (II), , , 1971)