$125.00 – $5,000.00
Product name: 2F-VIMINOL
Molar mass: 362.94 g/mol
Boiling point: 732.2°F (389°C)
ChemSpider ID: 59125
Elimination half-life: 1 – 3 hours
PubChem CID: 65697
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What is 2F-VIMINOL POWDER ?
2F-VIMINOL is an opioid analgesic developed by the pharmaceutical company Zambon in the 1960s based on the structure of α-pyrryl-2-aminoethanloa, originally developed as a cough medicine.
2F-VIMINOL is a new designer drug,a strong opioid analgesic that has legal status in many countries in Europe and the world.
2F-VIMINOL has both antitussive (cough suppressing) and analgesic (pain reducing) effects. Viminol has additional effects similar to other opioids including sedation and euphoria.It has six different stereoisomers which have varying properties. Four are inactive, but the 1S-(R,R)-disecbutyl isomer is a μ-opioid full agonist around 5.5 times more potent than morphine and the 1S-(S,S)-disecbutyl isomer is an antagonist. Since vimonol is supplied as a racemic mixture of isomers, the overall effect is a mixed agonist–antagonist profile similar to that of opioids such as pentazocine, although with somewhat fewer side effects.
Side effects 2F-VIMINOL POWDER
- Respiratory depression – At low to moderate doses, this effect results in the sensation that the breath is slowed down mildly to moderately, but does not cause noticeable impairment. At high doses and overdoses, opioid-induced respiratory depression can result in a shortness of breath, abnormal breathing patterns, semi-consciousness, or unconsciousness. Severe overdoses can result in a coma or death without immediate medical attention.
- Pain relief
- Cough suppression
- Decreased libido
- Difficulty urinating
- Stomach cramps
- Pupil constriction
- Orgasm suppression
Later work showed that replacing the chlorine atom with an fluorine atom (2F-Viminol) or with a trifluoromethyl group produced a compound with twice the potency and half the acute toxicity. A later team at Zambon found that one isomer of a pyrrolidone analog is 318 times as potent as morphine in its analgesic activity in animal studies. A number of related compounds were also found to be active, allowing a QSAR model to be constructed.
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