Substance
ID:179871
Names and Identifiers
Synonyms
D-安非他明 半硫酸盐Dextroamphetamine hemisulfate saltD-Amphetamine hemisulfate salt(+)-α-Methylphenethylamine hemisulfate salt
IUPAC name
bis((2S)-1-phenylpropan-2-amine); sulfuric acid
IUPAC Traditional name
bis(amphetamine); sulfuric acid
Properties
Safety Information
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Packing Group
2
European Hazard Symbols
Toxic (T)UN Number
2811
RTECS
SI1400000
GHS Signal Word
Danger
GHS Hazard statements
H300
Personal Protective Equipment
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS Precautionary statements
P264-P301+P310
RID/ADR
UN 2811 6.1/PG 2
Drug Control
USDEA Schedule II; Home Office Schedule 2; stupéfiant; kontrollierte Droge in Deutschland; regulated under CDSA - not available from Sigma-Aldrich Canada
Risk Statements
25
Safety Statements
45
Hazard Class
6.1
German water hazard class
3
Physical Property
Solubility
H2O: soluble
ethanol: soluble
Molecule Details
Other Notes
More active isomer of amphetamine
Application
D-Amphetamine induces the release of catecholamines and blocks catecholamine reuptake. D-Amphetamine has also been used to study the extinction of cued fear, as well as the therapeutic implications for learned phobias and post-traumatic stress disorder.
Biochem/physiol Actions
Induces release of catecholamines and serotonin by displacing the monoamines from their vesicular storage sites; blocks catecholamine reuptake.
More active isomer of amphetamine
Application
D-Amphetamine induces the release of catecholamines and blocks catecholamine reuptake. D-Amphetamine has also been used to study the extinction of cued fear, as well as the therapeutic implications for learned phobias and post-traumatic stress disorder.
Biochem/physiol Actions
Induces release of catecholamines and serotonin by displacing the monoamines from their vesicular storage sites; blocks catecholamine reuptake.
Molecular Spectra
No Data Available
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References
No Data Available
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