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A5880

Sigma-Aldrich

D-Amphetamine hemisulfate salt

Synonym(s):

(+)-α-Methylphenethylamine hemisulfate salt, Dextroamphetamine hemisulfate salt

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About This Item

Empirical Formula (Hill Notation):
C9H13N · 0.5 H2SO4
CAS Number:
51-63-8
Molecular Weight:
184.25
EC Number:
200-111-6
MDL number:
MFCD00069209
UNSPSC Code:
12352116
PubChem Substance ID:
24891028
NACRES:
NA.77

form

powder

drug control

USDEA Schedule II; Home Office Schedule 2; stupéfiant (France); kontrollierte Droge in Deutschland; regulated under CDSA - not available from Sigma-Aldrich Canada

solubility

H2O: soluble
ethanol: soluble

application(s)

forensics and toxicology

SMILES string

OS(O)(=O)=O.CC(N)Cc1ccccc1.CC(N)Cc2ccccc2

InChI

1S/2C9H13N.H2O4S/c2*1-8(10)7-9-5-3-2-4-6-9;1-5(2,3)4/h2*2-6,8H,7,10H2,1H3;(H2,1,2,3,4)/t2*8-;/m00./s1

InChI key

PYHRZPFZZDCOPH-QXGOIDDHSA-N

Gene Information

human ... SLC18A2(6571)

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Application

D-Amphetamine hemisulfate salt has been used in oxidative fermentative (OF) test, and exploratory test.

Biochem/physiol Actions

D-Amphetamine is an active isomer of amphetamine. It induces release of catecholamines and serotonin by displacing the monoamines from their vesicular storage sites, which blocks catecholamine reuptake.

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Opioid addiction has been declared a public health emergency, with fatal overdoses following relapse reaching epidemic proportions and disease-associated costs continuing to escalate. Relapse is often triggered by re-exposure to drug-associated cues, and though the neural substrates responsible for relapse
J Cartmell et al.
The Journal of pharmacology and experimental therapeutics, 291(1), 161-170 (1999-09-22)
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A M Barr et al.
Pharmacology, biochemistry, and behavior, 64(3), 597-604 (1999-11-05)
The present study sought to determine the effect of withdrawal from an escalating dose schedule of d-amphetamine on sexual behavior in male rats. Tests were conducted every 5 days until stable levels of sexual behavior were obtained. With repeated testing
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