Propylhexedrine

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Propylhexedrine
Systematic (IUPAC) name
N,α-dimethyl-cyclohexylethylamine
Identifiers
CAS number 3595-11-7
ATC code ??  ?
PubChem 7558
DrugBank ?
Chemical data
Formula C10H21N 
Mol. mass 155.29 g/mol
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.

C

Legal status

Unscheduled (US Federal)
Schedule varies (US States)
Schedule V (Canada Exempted from the application of the CDSA

Routes Nasal inhaler

Propylhexedrine, also known as hexahydrodesoxyephedrine or dimethylcyclohexaneethanamine, is a sympathomimetic with varied medicinal uses, is an adrenergic compound used mainly to provide temporary symptomatic relief of nasal congestion due to colds, allergies and allergic rhinitis. Being a vasoconstrictor used to decongest nasal mucosa, it is administered by inhalation. Propylhexedrine is most commonly found in over the counter Benzedrex inhalers and is similar to norepinephrine and epinephrine [1]. Benzedrex was first manufactured by Smith, Kline and French after the Benzedrine inhaler which contained amphetamine, became unavailable after the placement of amphetamines on Schedule II status (highest abuse potential of all legal drugs).

Contents

[edit] Recreational use

These inhalers have been occasionally used by people for their stimulant effects which are believed by some to be similar to methamphetamine. This is done by removing the cotton rod from the inhaler and performing a cold-water extraction, or just mixing it with soda, though occasionally some swallow it. Each cotton contains 250 mg (quarter-gram) of propylhexedrine. An equally potent alternate method is soaking the cotton rod in mild solution of ascorbic acid, otherwise known as Vitamin C, or citric acid, thereby forming a solution of active propylhexderine salt (for e.g. propylhexedrine citrate). Among users, the substance, particularly in pill form, is sometimes referred to as Glow.

Propylhexedrine is of significantly less risk of being used recreationally than amphetamines. This is primarily because propylhexedrine has limited methods of use, unlike amphetamines. The abuse potential is low enough that neither the DEA nor the WHO consider it a drug of concern, unlike ephedrine or its salts. However, attempts to extract the drug from the nasal inhaler and then inject it have been known. Abuse by injection is dangerous and could result in death, which has been recorded.[1] [2]

As with similar drugs, using propylhexedrine to keep oneself awake for extended amounts of time can lead to a temporary state of sleep deprivation psychosis during which an individual may experience hallucinations of all kinds as well as extreme paranoia, all common effects associated with sleep deprivation. The most sought-after effect is a general state of well-being and happiness associated with stimulants. However, this effect is not as pronounced as that delivered by more commonly abused stimulants such as methamphetamine or cocaine.

The effects vary from person to person. Many people suffer adverse effects after using the drug, feeling sick and nauseated. It is a vasoconstrictor, so ingestion can cause nausea and serious gastrointestinal issues, though the majority of the adverse effects are assumed to occur due to the cotton and what users call 'menthol burps'. As with similar stimulants, it is possible to overdose on the substance and extremely unwise to combine with any other drug that raises blood pressure.

Eating cotton for any reason is not at all a healthy practice, and though not necessarily fatal, can still lead to severe gastrointestinal problems, which may require medical attention. Gastric blockages and even internal infection can occur if too much cotton is routinely ingested in a short space of time.

[edit] Chemistry

Propylhexedrine is structurally similar to methamphetamine. The only difference is that the phenyl group of the methamphetamine molecule is swapped with a cyclohexyl group. It is because of this that propylhexedrine is not an amphetamine, nor even a phenethylamine. It is most like methamphetamine in terms that it contains a methyl (CH3) group in positions Rα and RN.

[edit] See also

[edit] Notes

  1. ^ "Proposed Rules" . Federal Register 50 (10): 2226 – 2227. 
  2. ^ Prince v. Ascher, 90 P.3d 1020 (2004).
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