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2C-T-7 The Drug Enforcement Administration's Special Testing and Research Laboratory generated this monograph using structurally confirmed reference material. Page 1 of 5 SWGDRUG.org/monographs.htm Latest Revision: 12/05/2014 O O S CH 3 CH 3 C H 3 NH 2 1. GENERAL INFORMATION IUPAC Name: 2-[2,5-dimethoxy-4-(propylsulfanyl)phenyl]ethanamine CAS#: 207740-26-9 Synonyms: 2,5-dimethoxy-4-n-propylthio-beta-phenethylamine Source: DEA Reference Material Collection Appearance: Off-white powder (HCl) UV max (nm): Not Determined 2. CHEMICAL AND PHYSICAL DATA 2.1 CHEMICAL DATA Form Chemical Formula Molecular Weight Melting Point ( o C) Base C 13 H 21 NO 2 S 255 Not Determined HCl C 13 H 21 NO 2 S . HCl 291 Not Determined

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2C-T-7

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  • 2C-T-7The Drug Enforcement Administration's Special Testing and Research Laboratory

    generated this monograph using structurally confirmed reference material.

    Page 1 of 5SWGDRUG.org/monographs.htmLatest Revision: 12/05/2014

    O

    OS

    CH3

    CH3

    CH3

    NH2

    1. GENERAL INFORMATION

    IUPAC Name: 2-[2,5-dimethoxy-4-(propylsulfanyl)phenyl]ethanamine

    CAS#: 207740-26-9

    Synonyms: 2,5-dimethoxy-4-n-propylthio-beta-phenethylamine

    Source: DEA Reference Material Collection

    Appearance: Off-white powder (HCl)

    UVmax(nm): Not Determined

    2. CHEMICAL AND PHYSICAL DATA

    2.1 CHEMICAL DATA

    Form Chemical Formula Molecular Weight Melting Point (oC)

    Base C13H21NO2S 255 Not Determined

    HCl C13H21NO2S. HCl 291 Not Determined

  • 2C-T-7The Drug Enforcement Administration's Special Testing and Research Laboratory

    generated this monograph using structurally confirmed reference material.

    Page 2 of 5SWGDRUG.org/monographs.htmLatest Revision: 12/05/2014

    3. QUALITATIVE DATA

    3.1 NUCLEAR MAGNETIC RESONANCE

    Sample Preparation: Dilute analyte to ~10 mg/mL inCD3OD containing TMS for 0 ppm reference andmaleic acid as quantitative internal standard.

    Instrument: 400 MHz NMR spectrometerParameters: Spectral width: at least containing -3 ppm through 13 ppm

    Pulse angle: 90o

    Delay between pulses: 45 seconds1H NMR: 2C-T-7 HCl Lot # 2TDM-198-01; CD3OD; 400MHz

    7 6 5 4 3 2 1 0

    0

    1

    2

    3

    4

    5

    6

    7

    8

    9

    10

    323252

    Maleic Acid

    from CD3OD

    TMS

    from CD3OD

    3.150

    2

    1.025

    3

    1.650 1.600

    2

    2.95 2.90 2.85

    3

    3.84 3.82

    5

    6.900 6.850

    2

    6 4

    6 42 2

  • 2C-T-7The Drug Enforcement Administration's Special Testing and Research Laboratory

    generated this monograph using structurally confirmed reference material.

    Page 3 of 5SWGDRUG.org/monographs.htmLatest Revision: 12/05/2014

    3.2 GAS CHROMATOGRAPHY/MASS SPECTROMETRY

    Sample Preparation: Dilute analyte ~1 mg/mL in chloroform.

    Instrument: Agilent gas chromatograph operated in split mode with MS detectorColumn: DB-1 MS (or equivalent); 30m x 0.25 mm x 0.25 mmCarrier Gas: Helium at 1 mL/minTemperatures: Injector: 280oC

    MSD transfer line: 280oCMS Source: 230oCMS Quad: 150oCOven program:

    1) 100oC initial temperature for 1.0 min2) Ramp to 300oC at 12 oC/min3) Hold final temperature for 9.0 min

    Injection Parameters: Split Ratio = 20:1, 1 mL injectedMS Parameters: Mass scan range: 30-550 amu

    Threshold: 100Tune file: stune.uAcquisition mode: scan

    Retention Time: 11.057 minEI Mass Spectrum: 2C-T-7 HCl Lot # 2TDM-198-01

    m/z240220200180160140120100806040

    [x 1

    05]

    Inte

    nsity

    0.1

    0.2

    0.3

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    0.5

    0.6

    0.7

    0.8

    414141 4141414141 4141414141 4141414141 41414141

    535353 5353535353 5353535353 5353535353 53535353 656565 6565656565 6565656565 6565656565 65656565

    777777 7777777777 7777777777 7777777777 77777777858585 8585858585 8585858585 8585858585 85858585

    919191 9191919191 9191919191 9191919191 91919191979797 9797979797 9797979797 9797979797 97979797

    110

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    EI+

  • 1700 1600 1500 1400 1300 1200 1100 1000 900 800 700 Wavenumber (cm-1) Latest Revision: 12/05/2014 SWGDRUG.org/monographs.htm Page 4 of 5

    3.3 INFRARED SPECTROSCOPY (FTIR)

    Insrument: FTIR with diamond ATR attachment (3 bounce)Scan Parameters: Number of scans: 32

    Number of background scans: 32Resolution: 4 cm-1

    Sample gain: 8Aperture: 150

    FTIR ATR (Diamond, 3 Bounce): 2C-T-7 HCl Lot # 2TDM-198-01

    Wavenumber (cm-1)3500 3000 2500 2000 1500

    %Tr

    ansm

    ittan

    ce

    20

    30

    40

    50

    60

    440440440440440440440440440440440440440440440440440440440440440440737

    737737737737737737737737737737737737737737737737737737737737737789

    789789789789789789789789789789789789789789789789789789789789789812

    812812812812812812812812812812812812812812812812812812812812812

    823823823823823823823823823823823823823823823823823823823823823823850

    850850850850850850850850850850850850850850850850850850850850850

    951951951951951951951951951951951951951951951951951951951951951951

    1038103810381038103810381038103810381038103810381038103810381038103810381038103810381038

    1057105710571057105710571057105710571057105710571057105710571057105710571057105710571057

    1117111711171117111711171117111711171117111711171117111711171117111711171117111711171117

    1186118611861186118611861186118611861186118611861186118611861186118611861186118611861186

    1205120512051205120512051205120512051205120512051205120512051205120512051205120512051205

    1309130913091309130913091309130913091309130913091309130913091309130913091309130913091309

    1392139213921392139213921392139213921392139213921392139213921392139213921392139213921392

    14641464146414641464146414641464146414641464146414641464146414641464146414641464146414641489

    1489148914891489148914891489148914891489148914891489148914891489148914891489148914891498149814981498149814981498149814981498149814981498149814981498149814981498149814981498

    1603160316031603160316031603160316031603160316031603160316031603160316031603160316031603

    20462046204620462046204620462046204620462046204620462046204620462046204620462046204620462659

    265926592659265926592659265926592659265926592659265926592659265926592659265926592659

    2754275427542754275427542754275427542754275427542754275427542754275427542754275427542754

    2846284628462846284628462846284628462846284628462846284628462846284628462846284628462846

    2893289328932893289328932893289328932893289328932893289328932893289328932893289328932893

    %Tr

    ansm

    ittan

    ce

    20

    30

    40

    50

    60

    440440440440440440440440440440440440440440440440440440440440440440737

    737737737737737737737737737737737737737737737737737737737737737789

    789789789789789789789789789789789789789789789789789789789789789812

    812812812812812812812812812812812812812812812812812812812812812

    823823823823823823823823823823823823823823823823823823823823823823850

    850850850850850850850850850850850850850850850850850850850850850

    951951951951951951951951951951951951951951951951951951951951951951

    1038103810381038103810381038103810381038103810381038103810381038103810381038103810381038

    1057105710571057105710571057105710571057105710571057105710571057105710571057105710571057

    11171117111711171117111711171117111711171117111711171117111711171117111711171117111711171155

    115511551155115511551155115511551155115511551155115511551155115511551155115511551155

    1186118611861186118611861186118611861186118611861186118611861186118611861186118611861186

    1205120512051205120512051205120512051205120512051205120512051205120512051205120512051205

    1309130913091309130913091309130913091309130913091309130913091309130913091309130913091309

    1392139213921392139213921392139213921392139213921392139213921392139213921392139213921392

    14641464146414641464146414641464146414641464146414641464146414641464146414641464146414641489

    1489148914891489148914891489148914891489148914891489148914891489148914891489148914891498149814981498149814981498149814981498149814981498149814981498149814981498149814981498

    1603160316031603160316031603160316031603160316031603160316031603160316031603160316031603

    2C-T-7The Drug Enforcement Administration's Special Testing and Research Laboratory

    generated this monograph using structurally confirmed reference material.

  • Page 5 of 5SWGDRUG.org/monographs.htmLatest Revision: 12/05/2014

    http://forendex.southernforensic.org/index.php/detail/index/469

    http://en.wikipedia.org/wiki/2C-T-7

    4. ADDITIONAL RESOURCES

    Forendex

    Wikipedia

    2C-T-7The Drug Enforcement Administration's Special Testing and Research Laboratory

    generated this monograph using structurally confirmed reference material.