Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C13H19NO2 |
| Molecular Weight | 221.2955 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCNC(C)CC1=CC=C2OCOC2=C1
InChI
InChIKey=LBXMQBTXOLBCCA-UHFFFAOYSA-N
InChI=1S/C13H19NO2/c1-3-6-14-10(2)7-11-4-5-12-13(8-11)16-9-15-12/h4-5,8,10,14H,3,6-7,9H2,1-2H3
| Molecular Formula | C13H19NO2 |
| Molecular Weight | 221.2955 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Detection of 3-methylmethcathinone and its metabolites 3-methylephedrine and 3-methylnorephedrine in pubic hair samples by liquid chromatography-high resolution/high accuracy Orbitrap mass spectrometry. | 2016-08 |
|
| Ultra-high-pressure liquid chromatography tandem mass spectrometry determination of hallucinogenic drugs in hair of psychedelic plants and mushrooms consumers. | 2014-11 |
|
| Mixed-mode solid-phase extraction procedures for the determination of MDMA and metabolites in urine using LC-MS, LC-UV, or GC-NPD. | 2004-02-28 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:14:38 GMT 2025
by
admin
on
Mon Mar 31 23:14:38 GMT 2025
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| Record UNII |
B4W69BKX3L
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| Record Status |
Validated (UNII)
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| Record Version |
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WIKIPEDIA |
PiHKAL
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admin on Mon Mar 31 23:14:38 GMT 2025 , Edited by admin on Mon Mar 31 23:14:38 GMT 2025
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559375
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3,4-Methylenedioxy-N-propylamphetamine
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B4W69BKX3L
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DTXSID50339877
Created by
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74698-36-5
Created by
admin on Mon Mar 31 23:14:38 GMT 2025 , Edited by admin on Mon Mar 31 23:14:38 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE |
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SALT/SOLVATE -> PARENT |
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ENANTIOMER -> RACEMATE |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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