Anodyne

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Amphetamine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
[]
Chlorphenoxyacetate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Sulfate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Aspartate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Adipate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Tartrate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Phosphate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Saccharate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Succinate
Generated by the Chemistry Development Kit (http://github.com/cdk)
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]
Toxicity
[]
Rat:
- intraperitoneal: 23 mg/kg
- intravenous: 20 mg/kg
Dog:
- subcutaneous: 20 mg/kg
Monkey:
- subcutaneous: 20 mg/kg
Rabbit:
- subcutaneous: 20 mg/kg
- intravenous: 25 mg/kg
Guinea pig:
- oral: 200 mg/kg
- subcutaneous: 20 mg/kg
- parenteral: 20 mg/kg
Rat:
- oral: 30 mg/kg
- subcutaneous: 180 mg/kg
Mouse:
- oral: 21 mg/kg
- intraperitoneal: 5500 μg/kg
- subcutaneous: 15 mg/kg
- intravenous: 15 mg/kg
Mammal (species unspecified):
- oral: 135 mg/kg
- intraperitoneal: 65 mg/kg

Amphetamine

(Redirected from levoamphetamine)

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

Chemistry

Salts []

Amphetamine is typically found in the form of its chlorphenoxyacetate, sulfate, hydrochloride, aspartate, adipate, tartrate, phosphate, saccharate and succinate salts.

 []

Amphetamine is a racemic mixture of the

Stereoisomers
LevoamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
DextroamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects []

Anodyne Usernotes
[]
0xea / Amphetamine[freebase][sulfate][hydrochloride] via Oral, Insufflated, Intrarectal, Subcutaneous, Intramuscular, Intravenous, Inhaled, Vaporized and SublingualModerate ; Moderate ; Strong ; Practical via Intravenous Injection, 1 minute comeup 3-4 hour duration; Practical via Subcutaneous Injection 25 minute comeup

Experience reports []

There are currently 6 experience reports involving amphetamine on OpenErowid:

See also []

  • Substituted amphetamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 3007, Amphetamine. Accessed August 7, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/3007

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Amphetamine. UNII: CK833KGX7E. Global Substance Registration System. Accessed August 7, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/CK833KGX7E