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N-Methylnorfentanyl The Drug Enforcement Administration's Special Testing and Research Laboratory generated this monograph using structurally confirmed reference material. Latest Revision: 9/26/2018 Page 1 of 4 SWGDRUG.org/monographs.htm 1. GENERAL INFORMATION IUPAC Name: CAS#: Synonyms: Source: Appearance: UV max (nm): 2. CHEMICAL AND PHYSICAL DATA 2.1 CHEMICAL DATA Form Chemical Formula Molecular Weight Melting Point ( o C) Base C 15 H 22 N 2 O 246.35 Not Determined HCl C 15 H 22 N 2 O HCl 282.81 Not Determined N N O CH 3 CH 3 N-(1-methylpiperidin-4-yl)-N-phenylpropionamide NA NA DEA Reference Material Collection Beige powder Not determined
4

O CH3 - SWGDRUGswgdrug.org/Monographs/N-methylnorfentanyl.pdf · 2018-10-01 · N-Methylnorfentanyl The Drug Enforcement Administration's Special Testing and Research Laboratory generated

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Page 1: O CH3 - SWGDRUGswgdrug.org/Monographs/N-methylnorfentanyl.pdf · 2018-10-01 · N-Methylnorfentanyl The Drug Enforcement Administration's Special Testing and Research Laboratory generated

N-MethylnorfentanylThe Drug Enforcement Administration's Special Testing and Research Laboratory

generated this monograph using structurally confirmed reference material.

Latest Revision: 9/26/2018 Page 1 of 4SWGDRUG.org/monographs.htm

1. GENERAL INFORMATION

IUPAC Name:

CAS#:

Synonyms:

Source:

Appearance:

UVmax(nm):

2. CHEMICAL AND PHYSICAL DATA

2.1 CHEMICAL DATA

Form Chemical Formula Molecular Weight Melting Point (oC)

Base C15H22N2O 246.35 Not Determined

HCl C15H22N2O HCl 282.81 Not Determined

N

N

O

CH3

CH3

N-(1-methylpiperidin-4-yl)-N-phenylpropionamide

NA

NA

DEA Reference Material Collection

Beige powder

Not determined

Page 2: O CH3 - SWGDRUGswgdrug.org/Monographs/N-methylnorfentanyl.pdf · 2018-10-01 · N-Methylnorfentanyl The Drug Enforcement Administration's Special Testing and Research Laboratory generated

N-MethylnorfentanylThe Drug Enforcement Administration's Special Testing and Research Laboratory

generated this monograph using structurally confirmed reference material.

Latest Revision: 9/26/2018 Page 2 of 4SWGDRUG.org/monographs.htm

3. QUALITATIVEDATA

3.1 NUCLEAR MAGNETIC RESONANCE

Sample Preparation: Dilute analyte to ~16 mg/mL in methanol-d4 containing TMS for 0 ppm reference and dimethylfumarate 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 seconds

1HNMR: N-Methylnorfentanyl HCl; Lot # N18-P78C; CD3OD; 400MHz

7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0

3222322123

dimethylfumarate

methanol-d4

methanol-d4

TMS

7.525 7.475

3

7.250

2

4.854.804.75

1

3.525

2

3.20

2

2.81

3

2.1 2.0

22

1.75 1.65

2

1.000

3

CD3OD

Page 3: O CH3 - SWGDRUGswgdrug.org/Monographs/N-methylnorfentanyl.pdf · 2018-10-01 · N-Methylnorfentanyl The Drug Enforcement Administration's Special Testing and Research Laboratory generated

N-MethylnorfentanylThe Drug Enforcement Administration's Special Testing and Research Laboratory

generated this monograph using structurally confirmed reference material.

Latest Revision: 9/26/2018 Page 3 of 4SWGDRUG.org/monographs.htm

3.2 GAS CHROMATOGRAPHY/MASS SPECTROMETRY

Sample Preparation: Dilute analyte ~8 mg/2 mL in CHCl3/MeOH

Instrument: Agilent gas chromatograph operated in split mode with MS detectorColumn: HP-5 MS (or equivalent); 30m x 0.25 mm x 0.25 mCarrier Gas: Helium at 1.5 mL/minTemperatures: Injector: 280oC MSD transfer line: 280oC

MS Source: 230oC MS Quad: 150oCOven program:

1) 100oC initial temperature for 1.0 min2) Ramp to 280oC at 12 oC/min3) Hold final temperature for 9.0 min

Injection Parameters: Split Ratio = 25:1, 1 L injectedMS Parameters: Mass scan range: 30-550 amu

Tune file: stune.u Threshold: 250 Acquisition mode: scan

Retention Time: 11.178 min

EI Mass Spectrum: N-Methylnorfentanyl HCl; Lot # N18-P78C

m/z240220200180160140120100806040

[x 1

06 ]In

tens

ity

0

0.5

1.0

1.5

42424242424242424242424242424242424242424242

444444444444444444444444444444444444444444445555555555555555555555555555555555555555555557575757575757575757575757575757575757575757

68686868686868686868686868686868686868686868

70707070707070707070707070707070707070707070

77777777777777777777777777777777777777777777

82828282828282828282828282828282828282828282

96969696969696969696969696969696969696969696

97979797979797979797979797979797979797979797

98989898989898989898989898989898989898989898

104104104104104104104104104104104104104104104104104104104104104104118118118118118118118118118118118118118118118118118118118118118118

130130130130130130130130130130130130130130130130130130130130130130132

146146146146146146146146146146146146146146146146146146146146146146

158158158158158158158158158158158158158158158158158158158158158158

173173173173173173173173173173173173173173173173173173173173173173

189189189189189189189189189189189189189189189189189189189189189189

190190190190190190190190190190190190190190190190190190190190190190

217217217217217217217217217217217217217217217217217217217217217217246

247247247247247247247247247247247247247247247247247247247247247247

Page 4: O CH3 - SWGDRUGswgdrug.org/Monographs/N-methylnorfentanyl.pdf · 2018-10-01 · N-Methylnorfentanyl The Drug Enforcement Administration's Special Testing and Research Laboratory generated

N-MethylnorfentanylThe Drug Enforcement Administration's Special Testing and Research Laboratory

generated this monograph using structurally confirmed reference material.

Latest Revision: 9/26/2018 Page 4 of 4SWGDRUG.org/monographs.htm

3.3 INFRARED SPECTROSCOPY (FTIR)

Instrument: FTIR with diamond ATR attachment (1 bounce)Scan Parameters: Number of scans: 32

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

Sample gain: 1Aperture: 150

FTIR ATR (Diamond 1 Bounce): N-Methylnorfentanyl HCl; Lot # N18-P78C

Wavenumber (cm-1)3500 3000 2500 2000 1500 1000

%Tr

ansm

ittan

ce

32

40

48

56

64

72

405405405405405405405405405405405405405405405405405405405405405405

551551551551551551551551551551551551551551551551551551551551551551

698698698698698698698698698698698698698698698698698698698698698698709

709709709709709709709709709709709709709709709709709709709709709

963963963963963963963963963963963963963963963963963963963963963963

1044104410441044104410441044104410441044104410441044104410441044104410441044104410441044

1266126612661266126612661266126612661266126612661266126612661266126612661266126612661266

1377137713771377137713771377137713771377137713771377137713771377137713771377137713771377

1396139613961396139613961396139613961396139613961396139613961396139613961396139613961396

1644164416441644164416441644164416441644164416441644164416441644164416441644164416441644

2525252525252525252525252525252525252525252525252525252525252525252525252525252525252525

2641264126412641264126412641264126412641264126412641264126412641264126412641264126412641

2666266626662666266626662666266626662666266626662666266626662666266626662666266626662666

2939293929392939293929392939293929392939293929392939293929392939293929392939293929392939

2978297829782978297829782978297829782978297829782978297829782978297829782978297829782978

31653165316531653165316531653165316531653165316531653165316531653165316531653165316531653427

342734273427342734273427342734273427342734273427342734273427342734273427342734273427

Wavenumber (cm-1)1900 1800 1700 1600 1500 1400 1300 1200 1100 1000 900 800 700

%Tr

ansm

ittan

ce

32

40

48

56

64

72

405405405405405405405405405405405405405405405405405405405405405405

453453453453453453453453453453453453453453453453453453453453453453486

486486486486486486486486486486486486486486486486486486486486486

551551551551551551551551551551551551551551551551551551551551551551

575575575575575575575575575575575575575575575575575575575575575575

621621621621621621621621621621621621621621621621621621621621621621666

666666666666666666666666666666666666666666666666666666666666666

698698698698698698698698698698698698698698698698698698698698698698709

709709709709709709709709709709709709709709709709709709709709709

745745745745745745745745745745745745745745745745745745745745745745

776776776776776776776776776776776776776776776776776776776776776776

791791791791791791791791791791791791791791791791791791791791791791809809809809809809809809809809809809809809809809809809809809809809

855855855855855855855855855855855855855855855855855855855855855855

941941941941941941941941941941941941941941941941941941941941941941

963963963963963963963963963963963963963963963963963963963963963963

10061006100610061006100610061006100610061006100610061006100610061006100610061006100610061022102210221022102210221022102210221022102210221022102210221022102210221022102210221022

1044104410441044104410441044104410441044104410441044104410441044104410441044104410441044

1074107410741074107410741074107410741074107410741074107410741074107410741074107410741074

11051105110511051105110511051105110511051105110511051105110511051105110511051105110511051176

117611761176117611761176117611761176117611761176117611761176117611761176117611761176

1248124812481248124812481248124812481248124812481248124812481248124812481248124812481248

1266126612661266126612661266126612661266126612661266126612661266126612661266126612661266

1319131913191319131913191319131913191319131913191319131913191319131913191319131913191319

1377137713771377137713771377137713771377137713771377137713771377137713771377137713771377

1396139613961396139613961396139613961396139613961396139613961396139613961396139613961396

14521452145214521452145214521452145214521452145214521452145214521452145214521452145214521472

1472147214721472147214721472147214721472147214721472147214721472147214721472147214721494

149414941494149414941494149414941494149414941494149414941494149414941494149414941494

1594159415941594159415941594159415941594159415941594159415941594159415941594159415941594

1644164416441644164416441644164416441644164416441644164416441644164416441644164416441644