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modified on 8 July 2009 at 20:22 ••• 11,363 views

Mdpv

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MDPV is a smartdrug, meaning it is legal in some countries. MDPV stands for Methylenedioxypyrovalerone and is also known as MDPK.


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}} }} }} }} {{#ifeq: | combo | | {{#ifeq: | vaccine | | | bgcolor="#ddeeff" | Mol. mass || bgcolor="#eeeeee" | {{#if:275.35 g/mol | 275.35 g/mol | ? }} }} }} {{#ifeq: | combo | | {{#ifeq: | vaccine | | {{#if: | {{#ifeq: | combo | | {{#ifeq: | vaccine | | {{#if: | {{#ifeq: | combo | | {{#ifeq: | vaccine | | {{#if: | | colspan="2" bgcolor="#dddddd" | Physical data | {{#if: | | colspan="2" bgcolor="#dddddd" | Physical data | {{#if: | | colspan="2" bgcolor="#dddddd" | Physical data | {{#if: | | colspan="2" bgcolor="#dddddd" | Physical data | {{#if: | | colspan="2" bgcolor="#dddddd" | Physical data | {{#if: | | colspan="2" bgcolor="#dddddd" | Physical data }} }} }} }} }} }} }} }} {{#ifeq: | combo | | {{#ifeq: | vaccine | | {{#if: | {{#ifeq: | combo | | {{#ifeq: | vaccine | | {{#if: | {{#ifeq: | combo | | {{#ifeq: | vaccine | | {{#if: | {{#ifeq: | combo | | {{#ifeq: | vaccine | | {{#if: | {{#ifeq: | combo | | {{#ifeq: | vaccine | | {{#if: | {{#ifeq: | combo | | {{#ifeq: | vaccine | | {{#if: | {{#ifeq: | combo | | {{#ifeq: | vaccine | | | colspan="2" bgcolor="#dddddd" | Pharmacokinetic data }} }} {{#ifeq: | combo | | {{#ifeq: | vaccine | | | bgcolor="#ddeeff" style="vertical-align: top;" | Bioavailability || bgcolor="#eeeeee" | {{#if: | | ? 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[[Image:{{{image2}}} | {{#if: | px }} {{#if:150 150 | 150px }} 220 | 220px }}
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Chemical structure of Mdpv|{{#ifeq: | mab | | {{#ifeq: | combo | | {{#ifeq: | | }}}}}} }} }}
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Mdpv }}{{#ifeq: | mab | ?}}
align="center" colspan="2" bgcolor="#dddddd" | Vaccine description align="center" colspan="2" bgcolor="#dddddd" | Combination of align="center" colspan="2" bgcolor="#dddddd" | Therapeutic monoclonal antibody align="center" colspan="2" bgcolor="#dddddd" | Systematic (IUPAC) name }}
killed |Inactivated |inactivated = Killed/Inactivated attenuated = Attenuated virus live = Live bacteria toxoid = Toxoid subunit = Subunit protein subunit |Protein |protein = Protein subunit conjugate=Conjugate vaccine recombinant = Recombinant Vector dna = DNA vaccination  ? }} }}
?  ? Class

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Identifiers
CAS number {{#if:687603-66-3 | 687603-66-3 | ? }} {{#if:{{#ifeq:24622-62-6|24622-62-6|24622-62-6 | 24622-62-6}} (Hydrochloride) | {{#ifeq:24622-62-6|24622-62-6|24622-62-6 | 24622-62-6}} (Hydrochloride) }}
ATC code {{#if: | [[ATC_code_|]]{{#if: | [1] }} | ? }}
PubChem {{#if:20111961 | 20111961 | ? }}

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DrugBank [2]

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ChemSpider {{{ChemSpiderID}}}

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SMILES eMolecules & PubChem

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Synonyms {{{synonyms}}}

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Density {{{density}}} g/cm³

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Melt. point {{{melting_point}}}{{#if:| –{{{melting_high}}}}} °C ({{#expr: ( {{{melting_point}}} * 9 / 5 ) + 32 round 0 }}{{#if:| –{{#expr: ( {{{melting_high}}} * 9 / 5 ) + 32 round 0 }} }} °F)

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Boiling point {{{boiling_point}}} °C ({{#expr: ( {{{boiling_point}}} * 9 / 5 ) + 32 round 0 }} °F)

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Solubility in water {{{solubility}}} mg/mL (20 °C)

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Spec. rot {{{specific_rotation}}}

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SEC Combust {{{sec_combustion}}}

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Protein binding {{{protein_bound}}}

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Therapeutic considerations
Pregnancy cat.

{{#if: |

 {{#switch:  
A = A B1 = B1 B2 = B2 B3 = B3 B = B? C = C D = D X = X  ?
 }}(AU) 

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 {{#switch:  
A = A B = B C = C D = D X = X  ?
}}(US) 

}}{{#if: | | {{#if: | | {{#if: | | ? }} }} }}

Legal status

{{#if: |

 {{#switch: 
Unscheduled = Unscheduled | S2 | Schedule 2 = Pharmacy Only (S2) S3 | Schedule 3 = Pharmacist Only (S3) S4 | Schedule 4 = Prescription Only (S4) S5 | Schedule 5 = Caution (S5) S6 | Schedule 6 = Poison (S6) S7 | Schedule 7 = Dangerous Poison (S7) S8 | Schedule 8 = Controlled (S8) S9 | Schedule 9 = Prohibited (S9)  ?
 }}(AU) 

}}{{#if: |

  {{#switch: 
Schedule I = Schedule I Schedule II = Schedule II Schedule III = Schedule III Schedule IV = Schedule IV Schedule V = Schedule V Schedule VI = Schedule VI Schedule VII = Schedule VII Schedule VIII= Schedule VIII  ?
 }}(CA) 

}}{{#if: |

 {{#switch: 
GSL = GSL P =P POM = POM CD =CD Class A = Class A Class B = Class B Class C = Class C  ?
 }}(UK) 

}}{{#if: |

 {{#switch: 
OTC = OTC Template:Unicode-only | Template:Unicode | rx | Rx | rx-only | Rx-only = [[Prescription drug|Template:Unicode-only]] Schedule I = Schedule I Schedule II = Schedule II Schedule III = Schedule III Schedule IV = Schedule IV Schedule V = Schedule V  ?
 }}(US) 

}}{{#if:unscheduled (illegal in Denmark) |

 {{#switch: unscheduled (illegal in Denmark)
RX | Rx | rx-only | Rx-only = Template:Unicode Prescription only unscheduled (illegal in Denmark)
 }}

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Dependence Liability {{{dependency_liability}}}

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Routes {{#if:oral, insufflation, intravenous | oral, insufflation, intravenous | ? }}

{{#if: | |}}

Subjective effects include CNS stimulation, euphoria, hypersexuality, agitation/anxiety and insomnia, with a duration of three to six hours. High doses have been observed to cause intense, prolonged anxiety attacks in stimulant-intolerant users, and there are anecdotal reports of addiction at higher doses or more frequent dosing intervals. MDPV has been remarked about more than once for its powers as an aphrodisiac, which have been said to rival those of methamphetamine when dosed correctly. However, it is apparently not as powerful as meth as far as general effects go, and may be safer (there have been no reports of death or disability as a result of abuse posted on "research chemical" related internet forums, and these tend to surface rapidly when a substance poses immediate dangers).

MDPV is the 3,4-methylenedioxy ring-substituted analogue of the appetite suppressant pyrovalerone, however despite its apparent structural similarity to the untrained eye, the effects of MDPV bear little resemblance to other methylenedioxyphenylalkylamine derivatives such as MDMA and methylone, instead producing purely stimulant effects with no empathogenic qualities. Extended binges on MDPV have also been reported to produce severe come-down syndrome similar to that of methamphetamine and characterised by depression, lethargy and headache.

MDPV is only listed as a ilegal drug in Denmark so far, but its structural similarity to illegal drugs of abuse makes it likely that it would be considered a controlled substance analogue in several countries such as the USA, Australia and New Zealand. Other analogues derived from alpha-pyrrolidinopropiophenone include the 4-methyl analogue pyrovalerone, as well as analogues with no substitution on the aromatic ring, and analogues with between 3 and 6 carbons on the alkyl chain. These compounds have been reported as stimulants of abuse mainly in Germany and other european countries since the early 2000s, but they have remained little known and rarely used or encountered by law enforcement. MDPV was never sold online in large quantities.


  • Swedish flag.gif Om MDPV på Svenska