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Культура Документы
NH2
O
H 3C
CH3
H 3C
1. GENERAL INFORMATION
IUPAC Name:
1-(3,4-dimethoxyphenyl)propan-2-amine
CAS#:
120-26-3
Synonyms:
3,4-DMA
Source:
Appearance:
UVmax (nm):
Not Determined
Form
Chemical Formula
Molecular Weight
Base
C11H17NO2
195
Not Determined
HCl
C11H17NO2 . HCl
231
151.1
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3,4-Dimethoxyamphetamine
The Drug Enforcement Administration's Special Testing and Research Laboratory
generated this monograph using structurally confirmed reference material.
3. QUALITATIVE DATA
3.1 NUCLEAR MAGNETIC RESONANCE
Method NMR D 2O
Sample Preparation: Dilute analyte to ~10 mg/mL in D2O containing TSP for 0 ppm reference and maleic
acid as quantitative internal standard.
Instrument:
Parameters:
3.5
3.0
2.5
Maleic Acid
2.0
1.5
1.0
TSP
0.5
solvent impurity
0
111
8
6 1
6
0.4
3
2
1.0
0.3
0.2
0.5
0.1
0
0
1
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3
Chemical Shift (ppm)
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3,4-Dimethoxyamphetamine
The Drug Enforcement Administration's Special Testing and Research Laboratory
generated this monograph using structurally confirmed reference material.
3.2 Gas Chromatography/Mass Spectrometry
Sample Preparation: Dilute analyte ~1 mg/mL base extracted into chloroform.
Instrument:
Column:
Carrier Gas:
Helium at 1 mL/min
Injector: 280oC
MSD transfer line: 280oC
MS Source: 230 oC
MS Quad: 150oC
Oven program:
1) 100oC initial temperature for 1.0 min
2) Ramp to 300 oC at 12 oC/min
3) Hold final temperature for 9.0 min
Split Ratio = 20:1, 1 L injected
Temperatures:
Injection Parameters:
MS Parameters:
Retention Time:
5
Intensity [x 10 ]
44
160
180
195
179
180
164
137
140
200 m/z
195
179
180
164
152
121
107
120
137
107
91
100
91
80
77
65
60
51
44
40
77
51
EI+
3
Intensity [x 10 ]
65
121
152
EI+
40
60
80
100
120
140
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160
180
200 m/z
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3,4-Dimethoxyamphetamine
The Drug Enforcement Administration's Special Testing and Research Laboratory
generated this monograph using structurally confirmed reference material.
3.3 INFRARED SPECTROSCOPY (FTIR)
Insrument:
Scan Parameters:
461
563
768
795
850
1011
440
625
739
930
1120
1024
1144
1232
30
1153
1508
1267
40
1043
1338
1429 1443
1466
2833
50
1599
2908
60
2939
2974
3163
70
2509
2573
2590
2605
2700
%Transmittance
20
1500
Wavenumber (cm-1)
600
461
625
563
1011
768
795
850
440
739
804
1043
1024
1144
1232
1508
30
1153
1267
40
1120
50
2000
1203
1599
60
2500
893
916
930
958
989
70
3000
1338
1363
1371
1389 1417
1429 1443
1452
1466
%Transmittance
3500
20
1700
1600
1500
1400
1300
1200
1100
1000
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900
800
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3,4-Dimethoxyamphetamine
The Drug Enforcement Administration's Special Testing and Research Laboratory
generated this monograph using structurally confirmed reference material.
4. ADDITIONAL RESOURCES
Wikipedia
http://en.wikipedia.org/wiki/Dimethoxyamphetamine
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