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Table of content
- Structure and Analog Relationship
- Stereochemistry
- Physical Properties
- Stimulation
- Spontaneous Bodily Sensations
- Physical Euphoria
- Other Physical Effects
- Enhancements
- Suppressions and Distortions
How to get 3-MMC
In recent years, a surge in interest and availability of novel psychoactive substances has captured the attention of both researchers and recreational drug users alike. Among these emerging compounds is 3-MMC, or 3-Methylmethcathinone, a synthetic stimulant that has gained popularity within various circles. Despite its growing recognition, the accessibility of 3-MMC remains a subject of concern due to its potential health risks and legal ambiguities. As scientists and medical professionals strive to comprehend the intricacies of this compound, it becomes essential to delve into its History, effects, dosages, legal Status, pharmacology, and chemistry.
Introduction to 3-Methylmethcathinone (3-MMC)
3-Methylmethcathinone, commonly referred to as 3-MMC or metaphedrone, is a novel stimulant and entactogen that belongs to the cathinone class of substances. It was developed as a structural analog of mephedrone (4-MMC) and emerged after 4-MMC was banned, serving as a legal alternative in various markets. While the exact mechanism of action of 3-MMC has not been fully explored, it is believed to act on the brain by affecting dopamine, serotonin, and norepinephrine levels, similar to other substances in the stimulant category.
The compound first appeared in the online research chemical market in Europe around 2012, shortly after the prohibition of mephedrone. 3-MMC exemplifies the phenomenon of designer drugs, which are synthesized to mimic or replace previously controlled substances while circumventing legal restrictions.
Subjective Effects of 3-MMC
The effects of 3-MMC are reported to be similar to those of its chemical predecessor, mephedrone, though with some nuanced differences. Users describe a range of subjective effects, including:
- Stimulation
- Anxiety suppression
- Disinhibition
- Enhanced empathy and sociability
- Relaxation
- Increased libido
- Euphoria
Many individuals compare the effects of 3-MMC to a combination of MDMA (ecstasy) and cocaine, producing both empathogenic (emotionally connected) and stimulant effects. However, 3-MMC is said to be slightly less entactogenic (lacking some emotional warmth) but more stimulating than mephedrone, and in some cases, users report experiencing more side effects.
Similar to other potent stimulants like mephedrone and cocaine, 3-MMC is often associated with compulsive redosing due to its intense but short-lived euphoric effects. The most common methods of administration include insufflation (snorting), though oral and injection routes have also been observed.
Risks and Side Effects of 3-MMC
Although research into the pharmacological properties, metabolism, and toxicity of 3-MMC is limited, early evidence indicates that chronic use of the substance may present significant health risks. High doses and frequent use over extended periods are associated with neurotoxic and cardiotoxic effects, though more research is needed to fully confirm these risks.
One commonly reported consequence of excessive use is serotonin depletion, which can manifest in mood disturbances, cognitive impairments, and emotional instability. Given its potential for abuse due to its euphoric effects, 3-MMC carries the risk of compulsive use, similar to other stimulant drugs
Chemistry of 3-MMC
3-Methylmethcathinone belongs to the cathinone class, which is a subgroup of synthetic amphetamines. Cathinones are chemically characterized by their core amphetamine structure, consisting of a phenyl ring bound to an amino group via an ethyl chain. What differentiates cathinones from traditional amphetamines is the presence of a ketone group on the beta carbon of the structure, hence the term β-keto-amphetamines.
Structure and Analog Relationship
3-MMC is structurally similar to mephedrone (4-MMC), with the key difference being the placement of the methyl group on the phenyl ring. In 3-MMC, the methyl group is located at the R3 position, while in mephedrone, it is positioned at R4. This small structural modification results in a compound that shares many of mephedrone's effects but with slight alterations in potency and subjective experience.
Stereochemistry
3-MMC is a chiral molecule, meaning it exists in two enantiomeric forms, R-3-MMC and S-3-MMC. These enantiomers are mirror images of each other and may differ in potency and effect. Based on similarities to other cathinones, the S-enantiomer is believed to be the more potent of the two, though no definitive studies have confirmed this assumption.
Physical Properties
In its most common form, 3-MMC is available as a white crystalline powder. It is often found in its hydrochloride salt form, which has specific physical properties:
- Melting Point: 193.2 ± 0.2°C (hydrochloride salt)
- Boiling Point: 280.5 ± 23.0°C at 760 mm Hg
- Solubility: Sparingly soluble in phosphate-buffered saline (PBS), and slightly soluble in ethanol, dimethyl sulfoxide (DMSO), and dimethylformamide (DMF).
Pharmacology of 3-MMC
Due to limited scientific research on 3-MMC, most pharmacological insights are derived from its structural similarity to other well-known entactogens and stimulants like mephedrone, amphetamine, and 2-FMA.
It is believed that 3-MMC functions primarily as a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI). This mechanism of action increases the availability of the monoamine neurotransmitters—serotonin, norepinephrine, and dopamine—by inhibiting their reabsorption back into neurons. The resulting accumulation of these neurotransmitters in the brain's synaptic clefts leads to the compound's characteristic stimulant and euphoric effects.
Despite its presumed mode of action, the full pharmacological profile of 3-MMC, including its interaction with various receptors and enzymes, remains underexplored. This lack of data emphasizes the need for further study to understand its long-term impact on human health, particularly its potential for addiction and neurotoxicity.