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Amphetamine

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Amphetamine
Molecular structure via molpic based on CDK
Physical properties
[]
135.21 g/mol [1]
Density0.913 at 77 °F (EPA, 1998) - Less dense than water; will float g/cm3 [1]
AppearanceMobile liquid [1]
OdorAmine odor [1]
TasteAcrid, burning taste [1]
Melting point25 °C [1]
Boiling point392 to 397 °F at 760 mmHg (EPA, 1998) [1]
DecompositionWhen heated to decomposition it emits toxic fumes of nitroxides. [1]
SolubilityModerate solubility [1]
1.8 [1]
Structural Identifiers
[]
C9H13N [1]
1-phenylpropan-2-amine [1]
CC(CC1=CC=CC=C1)N [1]
InChI=1S/C9H13N/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3 [1]
InChIKeyKWTSXDURSIMDCE-UHFFFAOYSA-N [1]
Pharmacokinetics[]
Duration of actionImmediate release dosing: 3 – 6 hours Extended release dosing: 8 – 12 hours
Dosing[]
Insufflated
[]
Light≤ 13.2 mg(518x - 25.4%)
Common13.2 - 20 mg(635x - 31.2%)
Strong20 - 30 mg(449x - 22%)
Heavy30 - 44 mg(233x - 11.4%)
Extreme44 mg +(202x - 9.9%)
Intravenous
[]
Light≤ 25 mg(430x - 46.7%)
Common25 - 30 mg(178x - 19.3%)
Strong30 - 35 mg(165x - 17.9%)
Heavy35 - 40 mg(75x - 8.1%)
Extreme40 mg +(73x - 7.9%)
Sublingual
[]
Light≤ 13.9 mg(2x - 40%)
Common13.9 - 15 mg(1x - 20%)
Strong15 - 37.5 mg(1x - 20%)
Heavy37.5 - 45 mg
Extreme45 mg +(1x - 20%)
Oral
[]
Light≤ 17 mg(374x - 25.9%)
Common17 - 30 mg(446x - 30.8%)
Strong30 - 50 mg(305x - 21.1%)
Heavy50 - 97 mg(178x - 12.3%)
Extreme97 mg +(143x - 9.9%)
Intrarectal
[]
Light≤ 40.7 mg(19x - 33.9%)
Common40.7 - 70 mg(11x - 19.6%)
Strong70 - 100 mg(15x - 26.8%)
Heavy100 - 162.5 mg(5x - 8.9%)
Extreme162.5 mg +(6x - 10.7%)
Statistically derived dosages via DBI-IGS
We do not take any responsibility for medical complications or loss of life sustained by following these dosages blindly.

Amphetamine (also known as Amfetamine, 1-Phenyl-2-aminopropane, Desoxynorephedrine, Norephedrane, Elastonon, Fenopromin, Phenedrine, β-Aminopropylbenzene, Propisamine or Psychedrine) is a stimulant substance of the amphetamine class.

Chemistry

 []

Amphetamine is a racemic mixture of the .

LevoamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
DextroamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
Stereoisomer enumberation with rdkit

Amphetamine matches Lipinski's rule of five.

Pharmacology

In the () amphetamine acts as a stimulant (), sympathomimetic () and psychoanaleptic ().[1]

Subjective effects []

class / Stimulant
Mere / Amphetamine []
magnus / Amphetamine []
Routes:
  • Oral
  • Insufflation
Salts:
  • Sulfate
Effects:
ninerik / Amphetamine []
Source:
  • DNM: Speed (pink discoleration)
Effects:
alina / Amphetamine []
Routes:
  • Insufflated (10.0mg)
bonzi / Amphetamine []
x86pup / Amphetamine []
Routes:
  • Oral
Pilz / Amphetamine []
Routes:
  • Oral (3 - 20mg)
  • Insufflated (8 - 46mg)
Salts:
  • Sulfate
Indication:Effects:Notes:
  • Consumed close to daliy since 11-2025, helps against ADHD
emily / Amphetamine []
Routes:
  • Insufflated (9 - 51mg)
  • Oral (10 - 20mg)
0xea / Amphetamine []
Routes:
  • Oral (10 - 50mg)
    Onset: 20 - 35 m
    Duration: 4 - 6 h
  • Insufflated (30 - 60mg)
  • Intrarectal (30 - 90mg)
  • Subcutaneous
    Onset: 25 m
    Duration: 3 - 5 h
  • Intramuscular (10 - 35mg)
  • Intravenous (15 - 50mg)
    Onset: 1 m
    Duration: 3 - 4 h
  • Inhaled
  • Vaporized (5mg)
  • Sublingual (5mg)
Salts:
  • Sulfate
  • Hydrochloride
Source:
  • Amphetamine Sulfate: DNM Germany
  • Speed paste: Goerlitzer park
  • Speed paste: Drug taxi
  • Speed: Warschauer
Indication:Effects:After Effects:Odor:
  • freebase smells strongly of rotten fish
  • pristine sulfate is practically odorless
Notes:

 []

  • Australia: Amphetamine is a Schedule 8 substance.
  • Brazil: Amphetamine is a A3 substance.
  • Canada: Amphetamine is a Schedule I substance.
  • Germany: Amphetamine is a Anlage III substance.
  • New Zealand: Amphetamine is a Class B substance.
  • United Kingdom: Amphetamine is a Class B substance.
  • United States: Amphetamine is a List of Schedule II controlled substances (U.S.)|Schedule II substance.[2]
  • United Nations: Amphetamine is a Schedule II substance.

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 3007, Amphetamine. Accessed June 17, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/3007

  2. Ingersoll J. Amphetamine, Methamphetamine, and Optical Isomers. Bureau of Narcotics and Dangerous Drugs}. July 7, 1971. Accessed June 17, 2026. https://archives.federalregister.gov/issue_slice/1971/7/7/12730-12734.pdf

  3. Adderall- dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate tablet. Teva Pharmaceuticals USA, Inc.. November 8, 2019. Accessed June 17, 2026. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f22635fe-821d-4cde-aa12-419f8b53db81