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D-AMPHETAMINE HYDROCHLORIDE

D-AMPHETAMINE HYDROCHLORIDE Basic information
Product Name:D-AMPHETAMINE HYDROCHLORIDE
Synonyms:DEXTRO-AMPHETAMINE;D-AMPHETAMINE HYDROCHLORIDE;C07884;S(+)-Amphetamine, 1.0 mg/mL;(aS)-a-Methyl-benzeneethanamine;d-a-Methylphenethylamine;DELTA-AMPHETAMINE;S(+)-Amphetamine (dextro-Amphetamine)
CAS:51-64-9
MF:C9H13N
MW:135.21
EINECS:200-112-1
Product Categories:Amines;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:51-64-9.mol
D-AMPHETAMINE HYDROCHLORIDE Structure
D-AMPHETAMINE HYDROCHLORIDE Chemical Properties
Melting point 25°C
Boiling point 208.93°C (estimate)
density 0.9354 (estimate)
refractive index 1.5087 (estimate)
Fp 9℃
storage temp. -20°C
pkapKa 9.90 (Uncertain)
color Oil
EPA Substance Registry SystemDextroamphetamine (51-64-9)
Safety Information
Hazard Codes F,T
Risk Statements 11-23/24/25-39/23/24/25
Safety Statements 16-36/37-45
RIDADR 3249
WGK Germany 1
HazardClass 6.1(a)
PackingGroup II
Hazardous Substances Data51-64-9(Hazardous Substances Data)
ToxicityLD50 orl-rat: 38 mg/kg TXAPA9 18,185,71
MSDS Information
D-AMPHETAMINE HYDROCHLORIDE Usage And Synthesis
UsesCNS stimulant; anorexic. More active isomer of Amphetamine. Induces release of catecholamines and serotonin by displacing the monoamines from their vesicular storage sites; blocks catecholamine reuptake. Controlled substance (stimulant)
DefinitionChEBI: A 1-phenylpropan-2-amine that has S configuration.
Brand nameDexampex (Teva); Dexedrine (GlaxoSmithKline); Dextrostat (Shire); Ferndex (Ferndale);Adiparthrol;Afatin;Amfe-dyn;Amphaetex;Bipheramine;Curban;D-amfetasul;Dexadrine;Dexamed;Dexedrina;Dexten;Dextro-profetamine;Drinamyl;Durophet-m;Maxiton;Mephadexamine-r;Mephadexamin-r;Obetrol;Obotan;Proptan;Robese;Simpamina d;Steladex;Stil-2;Synatan.
World Health Organization (WHO)Schedule II of the 1971 Convention on Psychotropic Substances. See WHO comment for amfetamine. (Reference: (UNCPS2) United Nations Convention on Psychotropic Substances (II), , , 1971)
Safety ProfilePoison by ingestion, subcutaneous, intravenous, and intraperitoneal routes. Experimental reproductive effects. Chronic exposure causes central nervous system damage and blood-pressure effects. When heated to decomposition it emits toxic NOx. See other amphetamine entries.
SynthesisThe compound can be prepared by optical resolution of amphetamineor directly from (-)-norephedrine by conversion to the (+)-chloroamine followed by catalytic hydrogenation .
Synthesis_51-64-9
D-AMPHETAMINE HYDROCHLORIDE Preparation Products And Raw materials
Tag:D-AMPHETAMINE HYDROCHLORIDE(51-64-9) Related Product Information
N-[2-Cyanoethyl] amphetamine, hydrochloride N-(2-NORBORNYL)-(+)-AMPHETAMINE HYDROCHLORIDE L-AMPHETAMINE HYDROCHLORIDE METHYLENEDIOXY-3,4-AMPHETAMINE HYDROCHLORIDE CI (25 MG) (AS) (MDA) (RS)-A-METHYL-2-CARBOXYPH ENYLGLYCINE (RS-MCPG) (+/-)-3,4-METHYLENEDIOXY-AMPHETAMINE HYDROCHLORIDE D/L-AMPHETAMINE HYDROCHLORIDE