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Not to be confused with Lisdexamfetamine.
Stereo, Kekulé, skeletal formula of levoamphetamine
Systematic IUPAC name
156-34-3 YesY
ChEBI CHEBI:42724 YesY
ChemSpider 30477 YesY
EC Number 205-850-8
Jmol 3D model Interactive image
Interactive image
PubChem 32893
Molar mass 135.2062 g mol−1
log P 1.789
Legal status
Oral (as part of Adderall, Evekeo, and generic amphetamine sulfate[2][3])
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Levoamphetamine, also known as levamfetamine (INN),[4] (R)-amphetamine,[4] and (−)-amphetamine),[4] is a central nervous system (CNS) stimulant known to increase wakefulness and concentration in association with decreased appetite and fatigue. Pharmaceuticals that contain levoamphetamine are currently indicated and prescribed for the treatment of attention deficit hyperactivity disorder (ADHD), obesity, and narcolepsy in some countries.

Levoamphetamine is the levorotatory stereoisomer of the amphetamine molecule.


Levoamphetamine is the levorotary stereoisomer of the amphetamine molecule. Racemic amphetamine contains two optical isomers, dextroamphetamine and levoamphetamine.[5]


L-amphetamine-succinate: base content 22,3% It was a medicine in Hungary between 1952-1955, it's branmd name was Cydril.

Racemic amphetamine[edit]

The first patented amphetamine brand, Benzedrine, was a racemic (i.e., equal parts) mixture of the freebases or sulfate salts of both amphetamine enantiomers (levoamphetamine and dextroamphetamine) that was introduced in the United States in 1934 as an inhaler for treating nasal congestion.[2] It was later realized that the amphetamine enantiomers could treat obesity, narcolepsy, and ADHD.[2][3] The Benzedrine brand is no longer marketed;[6] however, racemic (50:50) amphetamine sulfate is still prescribed under other brand names (e.g. Evekeo) and as their generic equivalents.[3][7]


Adderall is an amphetamine pharmaceutical that contains 25% levoamphetamine salts and 75% dextroamphetamine salts.[5]

See also[edit]


  1. ^ "Amphetamine - PubChem Public Chemical Project". The PubChem Project. USA: National Center for Biotechnology Information. 8 August 2005. Descriptors Computed from Structure. Retrieved 26 September 2011. 
  2. ^ a b c Heal DJ, Smith SL, Gosden J, Nutt DJ (June 2013). "Amphetamine, past and present – a pharmacological and clinical perspective". J. Psychopharmacol. 27 (6): 479–496. doi:10.1177/0269881113482532. PMC: 3666194. PMID 23539642. 
  3. ^ a b c "Evekeo prescribing information" (PDF). Arbor Pharmaceuticals LLC. April 2014. pp. 1–2. Retrieved 11 August 2015. 
  4. ^ a b c "R(-)amphetamine". IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved 30 March 2016. 
  5. ^ a b "Adderall XR Prescribing Information" (PDF). United States Food and Drug Administration. December 2013. Retrieved 30 December 2013. 
  6. ^ "Benzedrine". United States Food and Drug Administration. Retrieved 4 September 2015. 
  7. ^ "Evekeo". United States Food and Drug Administration. Retrieved 11 August 2015.