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    Methiopropamine molecular structure

    Methiopropamine Stats & Data

    Mpa Blow
    NPS DataHub
    MW155.26
    FormulaC8H13NS
    CAS801156-47-8
    IUPACN-methyl-1-thiophen-2-ylpropan-2-amine
    SMILESCNC(C)Cc1cccs1
    InChIKeyHPHUWHKFQXTZPS-UHFFFAOYSA-N
    Phenethylamines; Arylalkylamines; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Psychoactive Class Stimulant

    Interaction Warnings

    stimulants

    MPA can be potentially dangerous in combination with other stimulants as it can increase one's heart rate and blood pressure to dangerous levels.

    mdma

    The neurotoxic effects of MDMA may be increased when combined with amphetamine and other stimulants.

    cocaine

    This combination may increase strain on the heart.

    Receptor Profile

    Receptor Actions

    Inhibitors
    Norepinephrine-dopamine reuptake inhibitor (NDRI)
    Other
    approximately 1.85 times more selective for norepinephrine than dopamine

    Receptor Binding

    norepinephrine reuptake inhibitor
    dopamine reuptake inhibitor

    History & Culture

    1942–present

    Methiopropamine was first synthesized and reported in 1942. The work was primarily conducted at the University of Michigan, with limited pharmacological evaluation carried out at Parke Davis pharmaceutical company. This early research demonstrated that the compound possessed substantial pressor (blood pressure-increasing) activity. Following its initial characterization, the substance remained largely obscure for several decades with no significant research attention or recreational interest.

    2010–present

    Methiopropamine appeared for public sale in the United Kingdom in December 2010, marketed as a "research chemical" or "legal high" and sold in both powder and pill form. One of its earliest brand names was "Blow." The compound's structural resemblance to methamphetamine initially led vendors and users to anticipate stronger recreational properties than the substance could actually deliver. Throughout the 2010s, MPA was marketed under numerous brand names including Ivory Dove Ultra, China White, Walter White, Quick Silver Ultra, Bullet, Mind Melt, Pink Panthers, Poke, Rush, and Snow White. Products labeled as "Synthacaine" contributed to some users expecting cocaine-like effects, though these products were often found to contain additional substances beyond MPA alone. MPA was frequently combined with other novel psychoactive substances and sold as branded blends. Notable products included Sparkle-E (combining MPA with MDAI, later reformulated with 5-MeO-DALT), Pink Panther (MPA with MDAI and other compounds), Green Beans and M&M (both containing MPA with NM2AI), and GoGaine (MPA with MDAI, later reformulated with ephedrine). These formulations evolved over time as manufacturers adjusted their compositions in response to market conditions and regulatory changes. In Scotland, MPA gained particular traction among people who inject drugs, reportedly replacing ethylphenidate as a preferred substance within certain user communities following controls placed on methylphenidate-based novel psychoactive substances.

    Subjective Effect Notes

    physical: The physical effects of methiopropamine can be broken down into several components which progressively intensify proportional to dosage.

    cognitive: The cognitive effects of methiopropamine can be broken down into several components which progressively intensify proportional to dosage. It contains a large number of typical stimulant cognitive effects. Although negative side effects are usually mild at low to moderate doses, they become increasingly likely to manifest themselves with higher amounts or extended usage. This particularly holds true during the offset of the experience.

    Effect Profile

    Curated + 28 Reports
    Stimulant 8.8

    Strong stimulation, euphoria, focus, and anxiety/jitters

    Stimulation / Energy×3
    1010
    Euphoria / Mood Lift×2
    109.6
    Focus / Productivity×2
    1010
    Anxiety / Jitters×1
    1010
    Catalog Erowid

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

    Full tolerance 1d Half tolerance 10d Baseline ~18d

    Experience Report Analysis

    Erowid
    28 Reports
    2011–2017 Date Range
    26 With Age Data
    21 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 28 experience reports (28 Erowid)

    28 Reports
    21 Effects Detected
    9 Positive
    9 Adverse
    3 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 9

    Stimulation 71.4% 70%
    Euphoria 64.3% 70%
    Focus Enhancement 53.6% 70%
    Empathy 42.9% 70%
    Music Enhancement 35.7% 70%
    Tactile Enhancement 25.0% 70%
    Body High 21.4% 70%
    Color Enhancement 14.3% 70%
    Creativity Enhancement 10.7% 70%

    Adverse Effects 9

    Anxiety 42.9% 70%
    Jaw Clenching 25.0% 70%
    Pupil Dilation 25.0% 70%
    Increased Heart Rate 25.0% 70%
    Confusion 21.4% 70%
    Nausea 17.9% 70%
    Headache 17.9% 70%
    Sweating 14.3% 70%
    Appetite Suppression 10.7% 70%

    Real-World Dose Distribution

    62K Doses

    From 33 individual dose entries

    Insufflated (n=16)

    Median: 27.5mg 25th: 22.5mg 75th: 75.0mg 90th: 100.0mg
    mg/kg median: 0.668 mg/kg 75th: 1.169

    Oral (n=10)

    Median: 30.0mg 25th: 26.25mg 75th: 57.5mg 90th: 90.0mg
    mg/kg median: 0.436 mg/kg 75th: 0.75

    Common Combinations

    Most co-occurring substances in experience reports

    Form / Preparation

    Most common forms and preparations reported

    Body-Weight Dosing

    Dose relative to body weight from reports with weight data

    Median: 0.498 mg/kg IQR: 0.38–0.668 mg/kg n=6

    Redose Patterns

    Redosing behavior across 23 reports

    30.4% Redosed
    1.8 Avg Doses
    68m Median Interval

    Legal Status

    Country Status Notes
    Australia Uncontrolled As of 2018, not specifically scheduled under federal legislation. May still be subject to analog provisions in some states.
    Austria Illegal (SMG) Controlled under the Suchtmittelgesetz (Narcotics Act) since June 26, 2019. Possession, production, and sale are prohibited.
    Canada Potentially controlled (analog provisions) Not specifically scheduled, but may be considered an illicit analog under the Controlled Drugs and Substances Act due to structural similarity to methamphetamine.
    China Controlled substance Added to the list of controlled substances by the China Food and Drug Administration effective October 1, 2015.
    Finland Illegal Classified as an illegal substance under Finnish drug legislation.
    France Stupéfiant Classified as a stupéfiant, the French designation for recognized drugs of abuse with the highest level of control. Possession, purchase, sale, and manufacture are illegal.
    Germany Anlage I BtMG Controlled under Anlage I of the Betäubungsmittelgesetz (Narcotics Act) since July 17, 2013. Manufacturing, possession, import, export, purchase, sale, procurement, and dispensing without a license are prohibited.
    Switzerland Verzeichnis D Specifically named as a controlled substance under Verzeichnis D of Swiss narcotics regulations.
    United Kingdom Class B Initially placed under a Temporary Class Drug Order on November 27, 2015, following recommendation by the Advisory Council on the Misuse of Drugs. After the TCDO demonstrated effectiveness in reducing availability and harm indicators, MPA was permanently added to the Misuse of Drugs Act 1971 as a Class B substance on November 27, 2017.
    United States Unscheduled (Federal Analogue Act may apply) Not scheduled at the federal level. However, the DEA has noted it is a 2-thienyl analog of the Schedule II substance methamphetamine, and prosecution under the Federal Analogue Act is possible if sold for human consumption. The structural differences from methamphetamine (five-member sulfur-containing ring versus benzene ring) make analogue status legally uncertain. State-level controls exist in Florida (Schedule I since December 2012) and Arizona (listed as a dangerous drug since April 2014).
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