1-phenyl-N-propylpropan-2-amine

Names

[ CAS No. ]:
51799-32-7

[ Name ]:
1-phenyl-N-propylpropan-2-amine

[Synonym ]:
1-Phenyl-2-n-propylamino-propan [German]
1-Phenyl-2-n-propylamino-propane
1-Phenyl-2-propylaminopropane
d-N-Propylamphetamine

Chemical & Physical Properties

[ Density]:
0.897g/cm3

[ Boiling Point ]:
254.4ºC at 760mmHg

[ Molecular Formula ]:
C12H19N

[ Molecular Weight ]:
177.28600

[ Flash Point ]:
103.6ºC

[ Exact Mass ]:
177.15200

[ PSA ]:
12.03000

[ LogP ]:
3.00810

Safety Information

[ Symbol ]:

GHS02, GHS06, GHS08

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225-H301 + H311 + H331-H370

[ Precautionary Statements ]:
P210-P260-P280-P301 + P310-P311

[ RIDADR ]:
UN1230 - class 3 - PG 2 - Methanol, solution

[ HS Code ]:
2921499090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Propylamine
  • Phenylacetone
  • 1-Iodopropane
  • Benzeneethanamine, a-methyl-
  • N,N-di-n-propylamphetamine
  • N-Propyl-Methylamphetamine

DownStream

Customs

[ HS Code ]: 2921499090

[ Summary ]:
2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

A convenient derivatization method for gas chromatography/mass spectrometric determination of phenmetrazine in urine using 2,2,2-trichloroethyl chloroformate.

J. Forensic Sci. 43(3) , 630-5, (1998)

Phenmetrazine is a central nervous system stimulant currently used as an anorectic agent. The drug is abused and is reported to cause death from overdose. We describe a new derivatization method for p...

Amphetamine in rat brain after intraperitoneal injection of N-alkylated analogues.

Prog. Neuropsychopharmacol. Biol. Psychiatry 7(4-6) , 813-6, (1983)

Three N-alkylated analogues of amphetamine were administered intraperitoneally to male Sprague-Dawley rats and whole brain levels of amphetamine (AM) and the N-alkyl analogue were determined one hour ...

In vivo and in vitro o-methylation of 1-(3,4-dihydroxyphenyl)-2-(n-propyl-amino) propane - an intermediate in N-(N-propyl) amphetamine metabolism.

Res. Commun. Chem. Pathol. Pharmacol. 36(1) , 173-6, (1982)

In vitro metabolism of 1-(3,4-dihydroxyphenyl)-2-(n-propylamino)-propane (Id) by rat liver cytosol in the presence of S-adenosyl-L-methyl-methionine produced almost quantitatively the corresponding 3-...


More Articles

Related Compounds

  • 2-methyl-1-phenyl-N-propylpropan-2-amine
  • 1-phenyl-N-propylpropan-2-amine,hydrochloride
  • 1-phenyl-N-propylpentan-2-amine
  • 1-phenyl-N-(2-phenylethyl)pyrrolidin-3-amine,hydrochloride
  • 1-phenyl-N-[2-(9H-thioxanthen-9-yl)ethyl]propan-2-amine
  • 1-phenyl-N-[2-[2-[(1-phenyltetrazol-5-yl)amino]ethyldisulfanyl]ethyl]tetrazol-5-amine
  • 3-(1-Methylpiperidin-2-yl)propan-1-amine
  • 1-(4,4-Dimethylcyclohexyl)ethan-1-ol
  • 2-Bromomethyl-6-(cyclopropanecarbonyl-amino)-benzoic acid methyl ester
  • 1-(2-methylpentyl)-1H-imidazol-2-amine
  • 1-(1-Cyclopropyl-4-hydroxy-1H-pyrazol-3-yl)ethan-1-one
  • 1H-Benzimidazole-5-carboxylic acid, 2,7-dimethyl-
  • 2-(Methylamino)cyclopentane-1-carboxylic acid
  • Ethyl 2-(4-amino-2-fluorophenoxy)propanoate
  • 2,6-Dichloro-1-phenylindole-3-carboxylic acid
  • ethyl 7-methoxy-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-5-carboxylate
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