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    2C-T-7 molecular structure

    2C-T-7 Stats & Data

    T7 Beautiful 7th heaven Blue mystic 2ct7
    NPS DataHub
    MW255.38
    FormulaC13H21NO2S
    CAS207740-26-9
    IUPAC2-(2,5-dimethoxy-4-propylsulfanylphenyl)ethanamine
    SMILESCCCSc1cc(OC)c(CCN)cc1OC
    InChIKeyOLEVEPDJOFPJTF-UHFFFAOYSA-N
    Phenethylamines; 2020/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2021/1. Von 2-Phenethylamin abgeleitete Verbindungen; 2022/1. Von 2-Phenethylamin abgeleitete Verbindungen
    Chemical Class Phenethylamine
    Psychoactive Class Psychedelic
    Half-Life Unknown in humans (no reliable PK published); do not equate psychoactive duration with elimination half‑life.

    Pharmacology

    DrugBank

    Mechanism of Action

    Studies involving a bromine-substituted analogue, 2C-B (4-bromo-2,5- dimethoxyphenethylamine), have shown it to be a partial agonist for 5-HT2 (5-HT2A and 5-HT2C) serotonergic receptors and 1-adrenergic receptors. At 10-6 M, 2C-B also acted as a competitive 5-HT antagonist, but, at higher concentrations (2.8 x 10-5M), it acted as a non-competitive 5-HT antagonist. ... As 2C-T-7 is phenethylamine based, it is possible that it may have serotonergic receptor affinity similar to 2C-B (i.e. binding t

    Metabolism

    ... it is likely that its metabolism may proceed via similar pathways as 2C-B, possibly with additional metabolic reactions.

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (partial)
    Inhibitors
    Monoamine oxidase-A inhibitor (reversible, theoretical)

    History & Culture

    1980–1991

    2C-T-7 was developed around 1980 by Alexander Shulgin and Peyton Jacob III as part of Shulgin's extensive research program into substituted phenethylamines. The compound was first described in scientific literature by Myron Stolaroff by 1990, with more detailed characterization published by Shulgin and colleagues the following year. The compound was subsequently included in Shulgin's influential 1991 text PiHKAL (Phenethylamines I Have Known and Loved), where it holds a distinguished position among his self-designated "magical half-dozen"—the six phenethylamine compounds Shulgin considered most significant from his research. This group comprises mescaline, DOM, 2C-B, 2C-E, 2C-T-2, and 2C-T-7, with mescaline being the only member that Shulgin did not personally design and synthesize.

    1991–2002

    Following its publication in PiHKAL, 2C-T-7 remained relatively obscure through the 1990s, produced primarily in underground college laboratories and by small commercial research operations. Around the year 2000, availability expanded significantly as grey-market commercial vendors began supplying the compound, and it transitioned from an obscure research chemical to a recreational substance appearing at parties and clubs across North America and Europe. During this period, 2C-T-7 was sold openly in Dutch and Japanese smartshops as well as through online retailers. In the Netherlands, the compound briefly appeared on the market after 2C-T-2 had been prohibited, filling the resulting commercial gap before being banned in turn.

    2002–present

    In January 2002, Rolling Stone magazine published "The New (legal) Killer Drug," an article that brought substantial public attention to 2C-T-7. While the piece suggested the substance was legal, its status under United States law was actually ambiguous at the time due to the Federal Analogue Act. The accuracy of the Rolling Stone coverage was subsequently challenged in a detailed response published on the website disinfo.com. As of August 2007, at least three deaths had been reported in association with 2C-T-7 use. These fatalities involved either insufflated doses of 30 milligrams or greater, or occurred when the compound was combined with stimulants such as MDMA. The deaths and heightened media scrutiny contributed to rapid regulatory responses in multiple jurisdictions.

    Subjective Effect Notes

    cognitive: The head space of 2C-T-7 is described by many as one which is both insightful and relatively normal in its thought processes even at moderate to high dosages.

    Effect Profile

    Curated + 257 Reports
    Psychedelic 8.8

    Strong visuals, headspace, auditory effects, and body load

    Visual Intensity×3
    10104.0
    Headspace Depth×3
    107.61.7
    Auditory Effects×1
    10101.6
    Body Load / Somatic Effects×1
    10105.8
    Catalog Erowid BlueLight
    Empathogen 7.7

    Strong stimulation, sensory enhancement, and euphoria with moderate empathy

    Empathy / Social Openness×3
    66.11.7
    Euphoria / Mood Elevation×2
    86.03.7
    Stimulation×1
    105.53.1
    Sensory Enhancement×1
    10102.3
    Catalog Erowid BlueLight

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    19 minutes - 2.33 hours
    10-30 minutes
    3-6 hours
    2-4 hours
    4-12 hours
    Total: 5-10 hours
    Insufflated
    4-19 minutes
    19 minutes - 1.0 hours
    1-2 hours
    1-2 hours
    4-12 hours
    Total: 3-7 hours
    Rectal
    10-30 minutes
    15-45 minutes
    2-4 hours
    1-3 hours
    4-12 hours

    Community Effects

    TripSit
    Negative
    nausea

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans (no reliable PK published); do not equate psychoactive duration with elimination half‑life.
    Addiction Potential
    Low physical dependence; limited compulsive use potential. Psychological reinforcement possible due to euphoria and novelty, but rapid tolerance and long duration disincentivize frequent use.

    Tolerance Decay

    Full tolerance 1d Half tolerance 5d Baseline ~10d

    Pattern inferred from general serotonergic psychedelic tolerance behavior; empirical decay to baseline typically takes 10–14 days. Users often report diminished effects if re-dosing within one week.

    Cross-Tolerances

    LSD
    60% ●○○
    Psilocybin
    60% ●○○
    Other serotonergic phenethylamines (e.g., 2C‑B/2C‑E)
    50% ●○○

    Experience Report Analysis

    Erowid BlueLight
    206 Reports
    1997–2024 Date Range
    15 With Age Data
    33 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 256 experience reports (206 Erowid + 51 Bluelight)

    256 Reports
    150 Effects Detected
    72 Positive
    51 Adverse
    27 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 72

    Color Enhancement 49.6% 89%
    Visual Trails 36.0% 86%
    Music Enhancement 35.5% 86%
    Stimulation 34.4% 84%
    Euphoria 33.2% 90%
    Patterning 30.0% 86%
    Melting/flowing 28.0% 86%
    Tactile Enhancement 27.3% 82%
    Empathy 26.2% 82%
    Surface Breathing 24.0% 83%
    Joy 22.0% 87%
    Awe 22.0% 84%
    Focus Enhancement 19.5% 75%
    Introspection 17.6% 81%
    Sociability Enhancement 16.0% 84%
    Morphing 16.0% 85%
    Body High 15.3% 86%
    Geometric Imagery 14.0% 86%
    Insight 12.0% 82%
    Contentment 12.0% 85%

    Adverse Effects 51

    Nausea 54.3% 90%
    Body Load 42.0% 84%
    Anxiety 34.4% 84%
    Confusion 27.8% 83%
    Vomiting 22.0% 90%
    Fear 22.0% 86%
    Muscle Tension 19.1% 90%
    Thought Disorganization 14.0% 81%
    Paranoia 14.0% 81%
    Depersonalization 12.0% 85%
    Ataxia 10.0% 82%
    Memory Suppression 9.4% 88%
    Headache 8.6% 89%
    Focus Suppression 8.0% 78%
    Stomach Cramps 8.0% 81%
    Insomnia 8.0% 80%
    Disrupted Sleep Architecture 8.0% 76%
    Pupil Dilation 7.8% 88%
    Motor Impairment 7.4% 88%
    Increased Heart Rate 6.3% 70%

    Dose-Response Correlation

    How effect frequency changes across dose levels

    Insufflated

    View data table
    Effect Common (n=11) Strong (n=12) Heavy (n=23)
    Visual Distortions 90.9% 83.3% 82.6%
    Nausea 63.6% 66.7% 69.6%
    Color Enhancement 63.6% 58.3% 39.1%
    Music Enhancement 45.5% 25.0% 39.1%
    Stimulation 45.5% 0% 34.8%
    Tactile Enhancement 45.5% 0% 34.8%
    Euphoria 45.5% 41.7% 43.5%
    Confusion 18.2% 25.0% 43.5%
    Anxiety 36.4% 16.7% 39.1%
    Closed-Eye Visuals 36.4% 0% 0%
    Empathy 36.4% 33.3% 30.4%
    Focus Enhancement 18.2% 33.3% 8.7%
    Auditory Effects 0% 25.0% 30.4%
    Hospital 0% 0% 26.1%
    Introspection 18.2% 25.0% 17.4%

    Oral

    View data table
    Effect Light (n=14) Common (n=16) Strong (n=50) Heavy (n=24)
    Visual Distortions 92.9% 93.8% 82.0% 83.3%
    Nausea 57.1% 56.2% 58.0% 62.5%
    Auditory Effects 0% 25.0% 24.0% 58.3%
    Stimulation 57.1% 31.2% 48.0% 41.7%
    Color Enhancement 50.0% 56.2% 44.0% 54.2%
    Empathy 50.0% 25.0% 38.0% 16.7%
    Tactile Enhancement 35.7% 37.5% 30.0% 50.0%
    Confusion 28.6% 31.2% 32.0% 50.0%
    Anxiety 21.4% 50.0% 36.0% 41.7%
    Music Enhancement 28.6% 37.5% 46.0% 37.5%
    Closed-Eye Visuals 35.7% 12.5% 22.0% 20.8%
    Euphoria 35.7% 25.0% 34.0% 33.3%
    Muscle Tension 35.7% 31.2% 26.0% 29.2%
    Focus Enhancement 28.6% 31.2% 24.0% 20.8%
    Sedation 21.4% 31.2% 28.0% 25.0%

    Subjective Effect Ontology

    Experience Reports

    Structured effect tags extracted from 257 Erowid & Bluelight experience reports using a controlled vocabulary of 220+ canonical effects across 15 domains.

    Gastrointestinal

    nausea 139 54.2%

    Visual

    visual distortions 173 67.3% color enhancement 127 49.7%

    3 unique effects extracted · Derived from Erowid & Bluelight reports

    Dose–Effect Mapping

    Experience Reports

    How reported effects shift across dose tiers, based on 206 experience reports.

    Insufflated dose range: 8.0–25.0 mg (median 11.0 mg)
    Effect Common (n=11) Strong (n=12) Heavy (n=23)
    visual distortions
    91%
    83%
    83%
    nausea
    64%
    67%
    70%
    color enhancement
    64%
    58%
    39%
    music enhancement
    46%
    25%
    39%
    stimulation
    46%
    35%
    tactile enhancement
    46%
    35%
    euphoria
    46%
    42%
    44%
    confusion
    18%
    25%
    44%
    anxiety
    36%
    17%
    39%
    closed-eye visuals
    36%
    empathy
    36%
    33%
    30%
    focus enhancement
    18%
    33%
    9%
    auditory effects
    25%
    30%
    hospital
    26%
    introspection
    18%
    25%
    17%
    body high
    18%
    9%
    time distortion
    18%
    17%
    pupil dilation
    18%
    open-eye visuals
    18%
    13%
    headache
    18%

    Showing top 20 of 29 effects

    Oral dose range: 20.0–37.0 mg (median 30.0 mg)
    Effect Light (n=14) Common (n=16) Strong (n=50) Heavy (n=24)
    visual distortions
    93%
    94%
    82%
    83%
    nausea
    57%
    56%
    58%
    62%
    auditory effects
    25%
    24%
    58%
    stimulation
    57%
    31%
    48%
    42%
    color enhancement
    50%
    56%
    44%
    54%
    empathy
    50%
    25%
    38%
    17%
    tactile enhancement
    36%
    38%
    30%
    50%
    confusion
    29%
    31%
    32%
    50%
    anxiety
    21%
    50%
    36%
    42%
    music enhancement
    29%
    38%
    46%
    38%
    closed-eye visuals
    36%
    12%
    22%
    21%
    euphoria
    36%
    25%
    34%
    33%
    muscle tension
    36%
    31%
    26%
    29%
    focus enhancement
    29%
    31%
    24%
    21%
    sedation
    21%
    31%
    28%
    25%
    memory suppression
    21%
    8%
    25%
    introspection
    25%
    20%
    12%
    dissociation
    19%
    22%
    25%
    open-eye visuals
    12%
    25%
    body high
    21%
    19%
    12%
    21%

    Showing top 20 of 33 effects

    Risk Escalation

    Sentiment Analysis

    Average frequency of positive vs adverse effects across dose tiers (Insufflated)

    Common n=11
    9 positive 37.4% 6 adverse 28.8%
    Strong n=12
    7 positive 33.3% 5 adverse 28.4%
    Heavy n=23
    9 positive 28.5% 7 adverse 29.2%
    View effect breakdown

    Adverse Effects

    Effect Common (n=11) Strong (n=12) Heavy (n=23) Change
    Nausea
    64%
    67%
    70%
    9%
    Confusion
    18%
    25%
    44%
    +139%
    Anxiety
    36%
    17%
    39%
    7%
    Pupil Dilation
    18%
    0%
    Headache
    18%
    0%
    Increased Heart Rate
    18%
    13%
    -28%
    Motor Impairment
    17%
    0%
    Muscle Tension
    17%
    13%
    -22%
    Memory Suppression
    17%
    0%
    Thought Loops
    9%
    0%

    Positive Effects

    Effect Common (n=11) Strong (n=12) Heavy (n=23) Change
    Color Enhancement
    64%
    58%
    39%
    -38%
    Music Enhancement
    46%
    25%
    39%
    -14%
    Stimulation
    46%
    35%
    -23%
    Tactile Enhancement
    46%
    35%
    -23%
    Euphoria
    46%
    42%
    44%
    -4%
    Empathy
    36%
    33%
    30%
    -16%
    Focus Enhancement
    18%
    33%
    9%
    -52%
    Introspection
    18%
    25%
    17%
    -4%
    Body High
    18%
    9%
    -52%
    Pain Relief
    17%
    0%

    Risk Escalation

    Sentiment Analysis

    Average frequency of positive vs adverse effects across dose tiers (Oral)

    Light n=14
    8 positive 38.4% 5 adverse 32.8%
    Common n=16
    10 positive 30.0% 9 adverse 27.8%
    Strong n=50
    11 positive 27.6% 11 adverse 18.5%
    Heavy n=24
    10 positive 29.6% 9 adverse 27.8%
    View effect breakdown

    Adverse Effects

    Effect Light (n=14) Common (n=16) Strong (n=50) Heavy (n=24) Change
    Nausea
    57%
    56%
    58%
    62%
    9%
    Confusion
    29%
    31%
    32%
    50%
    +74%
    Anxiety
    21%
    50%
    36%
    42%
    +94%
    Muscle Tension
    36%
    31%
    26%
    29%
    -18%
    Memory Suppression
    21%
    8%
    25%
    +16%
    Sweating
    19%
    4%
    12%
    -33%
    Pupil Dilation
    19%
    0%
    Motor Impairment
    19%
    8%
    -55%
    Headache
    18%
    0%
    Increased Heart Rate
    12%
    6%
    -52%
    Jaw Clenching
    12%
    4%
    -68%
    Psychosis
    8%
    12%
    +56%
    Thought Loops
    4%
    8%
    +107%

    Positive Effects

    Effect Light (n=14) Common (n=16) Strong (n=50) Heavy (n=24) Change
    Stimulation
    57%
    31%
    48%
    42%
    -26%
    Color Enhancement
    50%
    56%
    44%
    54%
    8%
    Empathy
    50%
    25%
    38%
    17%
    -66%
    Tactile Enhancement
    36%
    38%
    30%
    50%
    +40%
    Music Enhancement
    29%
    38%
    46%
    38%
    +31%
    Euphoria
    36%
    25%
    34%
    33%
    -6%
    Focus Enhancement
    29%
    31%
    24%
    21%
    -27%
    Introspection
    25%
    20%
    12%
    -50%
    Body High
    21%
    19%
    12%
    21%
    -2%
    Creativity Enhancement
    12%
    4%
    8%
    -33%
    Pain Relief
    4%
    0%

    Dosage Distribution

    Dose distribution from experience reports

    Insufflated

    Median: 11.0 mg IQR: 8.0–25.0 mg n=50

    Oral

    Median: 30.0 mg IQR: 20.0–37.0 mg n=103

    Real-World Dose Distribution

    62K Doses

    From 268 individual dose entries

    Insufflated (n=81)

    Median: 10.0mg 25th: 6.0mg 75th: 17.0mg 90th: 30.0mg
    mg/kg median: 0.125 mg/kg 75th: 0.22

    Oral (n=158)

    Median: 25.0mg 25th: 15.0mg 75th: 35.0mg 90th: 50.0mg
    mg/kg median: 0.344 mg/kg 75th: 0.45

    Smoked (n=10)

    Median: 3.75mg 25th: 3.0mg 75th: 9.0mg 90th: 12.0mg
    mg/kg median: 0.059 mg/kg 75th: 0.147

    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

    Insufflated

    Median: 0.163 mg/kg IQR: 0.106–0.263 mg/kg n=45

    Oral

    Median: 0.38 mg/kg IQR: 0.257–0.49 mg/kg n=99

    Smoked

    Median: 0.136 mg/kg IQR: 0.045–0.157 mg/kg n=6

    Redose Patterns

    Redosing behavior across 179 reports

    15.6% Redosed
    1.2 Avg Doses
    30m Median Interval

    Legal Status

    European Council Decision (November 2003) - Member states required to implement control measures and criminal penalties within three months
    Country Status Notes
    Australia Schedule 9 Covered by analogue drug laws and formally added to Schedule 9 (the most restrictive category) by the National Drugs and Poisons Schedule Committee in 2005.
    Austria Illegal Prohibited under the Suchtmittelgesetz (SMG). Possession, production, and sale are illegal.
    Belgium Controlled Added to the list of illegal psychotropic substances on November 8, 2004.
    Brazil Controlled Possession, production, and sale are illegal. Listed on Portaria SVS/MS nº 344 as of February 18, 2014.
    Canada Schedule III Controlled as of October 31, 2016 as a derivative of 2,5-dimethoxyphenethylamine under the 2C-phenethylamine catch-all provision.
    China Category I psychotropic substance Controlled substance as of October 2015. Illegal to sell, buy, import, export, and manufacture.
    Denmark Category B Added to category B of the controlled substances list on August 23, 2003.
    Estonia Schedule I Added to Schedule I in February 2011 alongside several other novel psychoactive substances.
    Finland Controlled Scheduled under the government decree on substances, preparations, and plants considered to be narcotic drugs.
    Germany Anlage I BtMG Controlled under Anlage I of the Betäubungsmittelgesetz (Narcotics Act) as of July 1, 2001. Manufacturing, possession, import, export, purchase, sale, procurement, and dispensing are illegal without a license.
    Greece Controlled Became a controlled substance on February 18, 2003.
    Italy Tabella I Added to Tabella I (list of prohibited plants and substances) by Ministry of Health statement on January 11, 2005.
    Latvia Schedule I Classified as a Schedule I controlled substance. Possession, production, and distribution are prohibited.
    Netherlands List I (Opiumwet) The first country to ban 2C-T-7 after brief availability in smartshops. Following the ban on 2C-T-2, 2C-T-7 appeared on the market but was quickly prohibited under List I of the Opium Law.
    Poland Schedule I (I-P) Reported as a Schedule I controlled substance. Possession, production, and distribution are prohibited.
    Portugal Controlled Legislation enacted in January 2005 to control 2C-T-7 alongside 2C-I, 2C-T-2, and TMA-2.
    Slovakia Grade 2 Added to Grade 2 (equivalent to Schedule II under the 1971 UN Convention on Psychotropic Substances) in October 2009.
    Sweden Schedule I First classified as a health hazard under the Act on the Prohibition of Certain Goods Dangerous to Health (SFS 1999:58) as of April 1, 1999, making it illegal to sell or possess. Subsequently added to Schedule I as of March 16, 2004.
    Switzerland Controlled (Verzeichnis D) Specifically named as a controlled substance under Verzeichnis D of Swiss narcotics legislation.
    United Kingdom Class A Controlled as a Class A substance under the Misuse of Drugs Act 1971 as a result of the phenethylamine catch-all clause. In 1999, the Home Office effectively placed all compounds listed in PiHKAL into Class A.
    United States Schedule I Classified as Schedule I by emergency DEA ruling on September 20, 2002. Permanently placed in Schedule I on March 18, 2004 when the DEA published a Final Rule in the Federal Register (69 FR 12794). Manufacturing, buying, possessing, or distributing without a DEA license is illegal.

    Harm Reduction

    drugs.wiki

    Evidence-based harm-reduction points and corrections: 1) Insufflation carries disproportionate risk: at least two deaths followed nasal doses around 30–35 mg, and users frequently report burning pain, vomiting, and delirium; therefore nasal use is strongly discouraged in favor of oral titration. Source: Erowid dosage/effects pages and death summaries; EU risk communication. 2) Onset is often delayed (60–150 min, sometimes longer), which tempts premature redosing; waiting a full 3 hours before any adjustment is a practical guardrail. Source: Erowid basics/effects. 3) Likely MAO‑A involvement: sulfur‑substituted phenethylamines in this family have shown selective, reversible MAO‑A inhibition in vitro; in practice, combining 2C‑T‑7 with MAOIs (including linezolid/harmalas) or strongly serotonergic agents (MDMA, DXM, tramadol, meperidine) increases serotonin‑toxicity risk; avoid. Source: summary of Monte et al. reported on Drugs‑Forum; NCBI/StatPearls MAOI interaction guidance; Erowid deprenyl case notes. 4) Documented fatalities: at least three publicly reported deaths (two insufflated, one oral with MDMA). The prior claim of “eight deaths” is not supported by the curated sources below, so the figure is corrected to “at least three.” Source: Erowid death summaries. 5) Reagent testing: Marquis typically gives salmon orange/red with 2C‑T‑7. Use multiple reagents and beware mis-sold phenethylamines/NBOMe analogs; always test each batch. Source: Erowid Marquis chart and history notes. 6) Set, setting, sitter: high-dose reactions may include dissociation, agitation, or delirium; vomiting plus confusion increases aspiration risk; a sober sitter and calm environment reduce danger; seek emergency care for persistent chest pain, high temperature, seizures, cyanosis, or uncontrolled agitation; medical benzodiazepines are standard for severe agitation. Source: Erowid effects/overdose narratives. 7) Route cautions: IM/IV/injection has been associated with severe adverse events and is further discouraged; rectal use is less characterized—dose reductions versus oral are prudent. Source: Erowid surveys/pharmacology article. 8) Tolerance: acute tolerance emerges after one session and decays over about 10–14 days, with cross‑tolerance to serotonergic psychedelics (LSD, psilocybin). Source: TripSit general psychedelic tolerance guidance; community reports; Erowid survey patterns. 9) Street names and recognition: “T7,” “Blue Mystic,” “Beautiful,” and “Tripstasy/7‑Up” have appeared in historical markets; knowing aliases helps with test‑kit interpretation and avoiding misrepresented pills. Source: Erowid vault and East Bay Express article mirrored at Erowid. 10) Pharmacokinetics are not characterized in humans; no reliable elimination half‑life is published in the curated literature below. Duration of effects should not be conflated with half‑life. Source: Erowid basics notes “Pharmacology Summary Needed.”

    References

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