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So as you can see, Dibutylone has similar effects to party drugs such as MDMA. Please note however, that the effects you experience will depends greatly on you as an individual and the dosage you took, as always it’s best to start a low dosage and build up so you understand your tolerance of the drug. Also remember that taking the drug orally will results in a longer high but will also take longer to get started; it’s best not to re-dose even if you feel that the drug hasn’t affected you.
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- Stimulation – Dichloropane is usually considered to be energetic and stimulating in a fashion that is comparatively weaker than cocaine, but stronger than that of modafinil, caffeine, and methylphenidate. The particular style of stimulation which dichloropane presents can be described as encouraged at low to moderate dosages but forced at higher dosages. This means that at certain dosages, it becomes difficult or impossible to keep still as jaw clenching, involuntarily bodily shakes and vibrations become present, resulting in extreme shaking of the entire body, unsteadiness of the hands, and a general lack of fine motor control. This effect is replaced with moderate fatigue and general exhaustion during the offset of the experience.
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Ethylone is also known as 3, 4-methylenedioxy-N-ethylcathinone, MDEC and βk-MDEA. It belongs to the family of phenethylamine, amphetamine and cathinone class of drugs. It is also related to Methylone drug having structural similarities. Ethylone has stimulant nature as it acts on the central nervous system of the body in order to produce euphoric effects.
It is recommended that the drug may be kept in cool and humid less atmosphere. High storage temperature or humidity can affect the condition of the drug. Measures should be taken in order to keep the drug from mixing with impurities.
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Ethylphenidate was recently reported as a novel drug metabolite in two overdose fatalities where there was evidence of methylphenidate and ethanol coingestion. This study explores the pharmacokinetics of ethylphenidate relative to methylphenidate and the major metabolite ritalinic acid, in six healthy subjects who received methylphenidate and ethanol under controlled conditions. Subjects (three males, three females) received a single oral dose of methylphenidate (20 mg; two 10-mg tablets) followed by consumption of ethanol (0.6 g/kg) 30 min later. Methylphenidate, ritalinic acid, and ethylphenidate were quantified using liquid chromatography-tandem mass spectrometry. Ethylphenidate was detectable in the plasma and urine of all subjects after ethanol ingestion. The mean (±S.D.) area under the concentration versus time curve for ethylphenidate was 1.2 ± 0.7 ng/ml/h, representing 2.3 ± 1.3% that of methylphenidate (48 ± 12 ng/ml/h). A significant correlation was observed between the area under the concentration versus time curve of methylphenidate and that of ethylphenidate. In view of the known dopaminergic activity of racemic ethylphenidate, it remains possible that under certain circumstances of higher level dosing, e.g., in the abuse of methylphenidate and ethanol, the metabolite ethylphenidate may contribute to drug effects.
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Etizolam is a thienodiazepine which is chemically related to benzodiazepine (BDZ) drug class; it differs from BDZs in having a benzene ring replaced with a thiophene ring. It is an agonist at GABA-A receptors and possesses amnesic, anxiolytic, anticonvulsant, hypnotic, sedative and skeletal muscle relaxant properties. Initially introduced in 1983 in Japan as treatment for neurological conditions such as anxiety and sleep disorders, etizolam is marketed in Japan, Italy and India. It is not approved for use by FDA in the US; however it remains unscheduled in several states and is legal for research purposes.
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While transdermal patches of Fentanyl in gel form (e.g. original Duragesic) is a bad idea, non-clinical injection of the drug is even worse. The medication is 50–100x stronger than other opioids even morphine, from which the drug is derived.
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Flubromazepam is likely much stronger than regular pharmaceutical benzos because it is still being studied and developed for prescription use. Recreational users might not be aware of the strength of the medication and end up taking too much without realizing. The drug can also take time to reach its full effect which could potentially lead to overdose if users become impatient and start taking more of the drug.
Flubromazepam also has a long half-life and the effects of the drug can last almost the entire day making it the type of medication that the brain gets adjusted to. When this happens it can potentially lead to a serious addiction because the brain gets used to functioning with the effect of benzodiazepine all the time.
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Gamma-butyrolactone (GBL) is a precursor in the manufacture of gamma-hydroxybutyric acid (GHB). In
aqueous solution, GBL undergoes a hydrolysis reaction and exists in equilibrium with GHB. This solution
chemistry is strongly dependent upon solution pH, as well as other factors, and is discussed in detail in the GHB
Relatively pure samples of GBL produce a blue phase below the red reagent solution, which slowly dissipates
as GBL dissolves into solution. Other organic liquids (e.g., ethanol, acetone) may also produce a blue color, but
appear differently as the entire solution develops blue. 1,4-Butanediol, as well as aqueous solutions of GBL,
fail to produce a color change. An alternative procedure entailing a toluene extraction has been developed for
aqueous solutions of GBL (Morris, 1999), but may be difficult to interpret. Recently the hydroxamic acid test
has been reported as an effective presumptive test for GBL with less false positives (Morris, 2005).
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N-ethyl-nor-hexedrone (Hexen) is a stimulant in the cathinone class. It’s only been on the market since ~2015 and little more than anecdotal reports exist about its activity.
It’s become somewhat popular due to its recreational potential. People have turned to the drug as an alternative to methamphetamine, cocaine, alpha-PHP, and alpha-PVP, among other recreational stimulants. It’s most often used via fast-acting routes of administration (e.g. intranasal and inhalation) to maximize its recreational effects.
Though most people are pursuing euphoria when using it, the drug may be used as a productive stimulant at low to common doses.
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Meclonazepam is a benzodiazepine derivative similar in structure to clonazepam, but was never used as medicine and instead appeared on the illicit drug market as a designer drug. A certified Snap-N-Spike® solution suitable for use as starting material in calibrators and controls for meclonazepam LC/MS or GC/MS testing methods in clinical toxicology, urine drug testing or forensic analysis applications.
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Mephedrone: A new psychoactive substance
Public health officials are concerned about synthetic cathinones and other types of “new psychoactive substances” (NPS), or “legal highs.”
An NPS is an unregulated substance that mimics existing drugs. They often have altered chemical structures that help them avoid becoming illegal.
They are sometimes called legal highs because the change in chemical means they are no longer illegal. Some countries have adapted their drug laws and made such drugs illegal, regardless of their exact chemical content.
It can come in the form of tablets, capsules, or white powder. Users may swallow, snort, or inject mephedrone, but snorting is the most common way of taking the drug.
- Highly addictive: the quick-lasting high leads to increased frequency and quantity of dosing. Addiction is more strongly associated with snorting, due to the near-instant high. Oral consumption is the safest way to use.
- Fiending: it is easy to use up your entire supply in 1 session. It’s hard to stop using in any given session. Buy in only small quantities and limit the amount you use in 1 night
- Panic attacks, paranoia and hallucinations in heavy use
- Hard Crash: depression, difficulties concentrating, anxiety and insomnia can last 3-4 days after you come down
- Nasal douche with warm water to flush out powder residue