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D/L-AMPHETAMINE HYDROCHLORIDE

D/L-AMPHETAMINE HYDROCHLORIDE Structure
CAS No.
300-62-9
Chemical Name:
D/L-AMPHETAMINE HYDROCHLORIDE
Synonyms
amfetamine;1-phenylpropan-2-amine;Benzedrine;alpha-methylphenethylamine;Phenamine;Amphetamine (Narcotics);Finam;Isomyn;Adipan;C07514
CBNumber:
CB4716187
Molecular Formula:
C9H13N
Molecular Weight:
135.21
MOL File:
300-62-9.mol
Modify Date:
2024/3/14 15:18:26

D/L-AMPHETAMINE HYDROCHLORIDE Properties

Melting point 146 °C
Boiling point bp760 200-203°; bp13 82-85°
Density d425 0.913
vapor density 4.65
refractive index 1.5180 (estimate)
Flash point 9℃
storage temp. -20°C
solubility Chloroform (Slightly)
pka 9.94±0.10(Predicted)
form Liquid or oil
EPA Substance Registry System Amphetamine (300-62-9)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS06,GHS08
Signal word  Danger
Hazard statements  H225-H301+H311+H331-H370
Precautionary statements  P210-P260-P280-P301+P310-P311
Hazard Codes  F,T
Risk Statements  11-23/24/25-39/23/24/25
Safety Statements  16-36/37-45-7
RIDADR  1851
WGK Germany  1
HazardClass  6.1(a)
PackingGroup  II
Toxicity LD50 in rats (mg/kg): 180 s.c. (Warren, Werner)
NFPA 704
1
3 0

D/L-AMPHETAMINE HYDROCHLORIDE Chemical Properties,Uses,Production

Chemical Properties

Colorless, volatile liquid; characteristic strong odor; slight burning taste. Soluble in alcohol and ether; slightly soluble in water.

Uses

Stimulant (central).

World Health Organization (WHO)

Amfetamine and its derivatives are potent central stimulants. Use of amfetamines has widely been discouraged due to abuse of their euphoric effect and their limited field of usefulness. Amfetamines have a place in the treatment of narcolepsy and in hyperkinetic syndrome in children. However, they are no longer recommended for use in obesity or depressive illness. Amfetamine is controlled under Schedule II of the 1971 Convention on Psychotropic Substances. (Reference: (UNCPS2) United Nations Convention on Psychotropic Substances (II), , , 1971)

General Description

Colored liquid with an amine odor. Used as a pharmaceutical, a central nervous system stimulant.

Reactivity Profile

Amines, such as D/L-AMPHETAMINE HYDROCHLORIDE, are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.

Hazard

Flammable, moderate fire risk. Basis of a group of hallucinogenic (habit-forming) drugs that affect the central nervous system. Sale and use restricted to physicians. Production limited by law.

Health Hazard

D/L-AMPHETAMINE HYDROCHLORIDE is classified as extremely hazardous. Probable lethal dose in humans is 5-50 mg/kg or 7 drops to 1 teaspoon for a 70 kg (150 lb.) person. Habit forming drug which affects the central nervous system. Excessive use may lead to tolerance and physical dependence. Death is possible.

Fire Hazard

Dangerous when exposed to heat or flames. Upon decomposition, nitrogen oxides are emitted. Can react with oxidizing materials.

Safety Profile

A deadly human poison by an unspecified route. An experimental poison by ingestion, subcutaneous, intraperitoneal, and intravenous routes. Experimental reproductive effects. Mutation data reported. A central nervous system stimulant. Overdoses cause hyperactivity, restlessness, insomnia, rapid pulse, rise in blood pressure, dilated pupils, dryness of the throat. Combustible when exposed to heat, flame, or oxidizers. When heated to decomposition it emits toxic fumes of NO,. To fight fire, use CO2, dry chemical, alcohol foam, water mist, fog. See other benzedrine entries.

Potential Exposure

Amphetamine is used as a pharmaceutical. It is a CNS stimulant.

Environmental Fate

Amphetamines are indirect acting sympathomimetics, producing their effects by inhibiting the transporters of dopamine, norepinephrine, and serotonin at the presynaptic nerve terminal. This increases the release of norepinephrine, dopamine, and serotonin and increased norepinephrine levels at central synapses, which further stimulates alpha and beta receptors. Some amphetamines also inhibit monoamine oxidase, preventing the breakdownof catecholamines. Thesemechanisms combine to produce the sympathomimetic and central nervous system (CNS) effects seen with amphetamine abuse.

Shipping

UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.

Waste Disposal

It is inappropriate and possibly dangerous to the environment to dispose of expired or waste pharmaceuticals by flushing them down the toilet or discarding them to the trash. Household quantities of expired or waste pharmaceuticals may be mixed with wet cat litter or coffee grounds, double-bagged in plastic, discard in trash. Larger quantities shall carefully take into consideration applicable DEA, EPA, and FDA regulations. If possible return the pharmaceutical to the manufacturer for proper disposal being careful to properly label and securely package the material. Alternatively, the waste pharmaceutical shall be labeled, securely packaged and transported by a state licensed medical waste contractor to dispose by burial in a licensed hazardous or toxic waste landfill or incinerator Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

D/L-AMPHETAMINE HYDROCHLORIDE Preparation Products And Raw materials

)-beta-Phenylisopropylamine )-Desoxynorephedrine 1-Benzylethyla-mine 1-Methyl-2-phenylethylamine -Aminopropylbenzene Anorexide Anorexine Benzebar Benzeneethanamine, alpha-methyl-, (± Benzeneethanamine, alpha-methyl-, (.+/-.)- Benzolone beta-Aminopropylbenzene beta-phenylisopropylamin beta-phenylisopropylamine deoxy-norephedrin desoxynorephedrine dl-1-Phenyl-2-aminopropane DL-alpha-Methylphenethylamine dl-Benzedrine Elastonon Fenamin Fenylo-izopropylaminyl Finam Isoamycin Isoamyne Isomyn (±)-Amphetamine solution D/L-AMPHETAMINE HYDROCHLORIDE Mecodrin -Methylbenzeneethana-mine Norephedrane Norephedrine, deoxy- Novydrine Oktedrin Ortedrine Phenedrine Phenethylamine, alpha-methyl-, (± Phenethylamine, alpha-methyl-, (.+/-.)- Profamina Propisamine Psychedrine racemic-Desoxynor-ephedrine racemicdesoxy-nor-ephedrine Raphetamine Rhinalator Simpatedrin Simpatina Sympamine Sympatedrine Weckamine (.+/-.)-alpha-Methylphenethylamine (.+/-.)-alpha-Methylphenylethylamine (.+/-.)-Benzedrine (.+/-.)-beta-Phenylisopropylamine (.+/-.)-Desoxynorephedrine (+-)-alpha-methylbenzeneethanamine 1-phenyl-2-amino-propan 1-Phenyl-2-aminopropane