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Details

Stereochemistry ACHIRAL
Molecular Formula C18H28N2
Molecular Weight 272.4283
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIBUTYLTRYPTAMINE

SMILES

CCCCN(CCCC)CCC1=CNC2=C1C=CC=C2

InChI

InChIKey=LZLJUZWFWYEQLY-UHFFFAOYSA-N
InChI=1S/C18H28N2/c1-3-5-12-20(13-6-4-2)14-11-16-15-19-18-10-8-7-9-17(16)18/h7-10,15,19H,3-6,11-14H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C18H28N2
Molecular Weight 272.4283
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:59:48 GMT 2023
Edited
by admin
on Sat Dec 16 16:59:48 GMT 2023
Record UNII
QFE8WT8WCW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIBUTYLTRYPTAMINE
Common Name English
DBT
Common Name English
N,N-DIBUTYLTRYPTAMINE
Common Name English
1H-INDOLE-3-ETHANAMINE, N,N-DIBUTYL-
Common Name English
N-BUTYL-N-(2-(1H-INDOL-3-YL)ETHYL)BUTAN-1-AMINE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA TiHKAL
Created by admin on Sat Dec 16 16:59:48 GMT 2023 , Edited by admin on Sat Dec 16 16:59:48 GMT 2023
Code System Code Type Description
FDA UNII
QFE8WT8WCW
Created by admin on Sat Dec 16 16:59:48 GMT 2023 , Edited by admin on Sat Dec 16 16:59:48 GMT 2023
PRIMARY
PUBCHEM
27848
Created by admin on Sat Dec 16 16:59:48 GMT 2023 , Edited by admin on Sat Dec 16 16:59:48 GMT 2023
PRIMARY
WIKIPEDIA
Dibutyltryptamine
Created by admin on Sat Dec 16 16:59:48 GMT 2023 , Edited by admin on Sat Dec 16 16:59:48 GMT 2023
PRIMARY
EPA CompTox
DTXSID40166255
Created by admin on Sat Dec 16 16:59:48 GMT 2023 , Edited by admin on Sat Dec 16 16:59:48 GMT 2023
PRIMARY
CAS
15741-77-2
Created by admin on Sat Dec 16 16:59:48 GMT 2023 , Edited by admin on Sat Dec 16 16:59:48 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY
Has been sold as a "research chemical" and has been confirmed to be an active hallucinogen although somewhat weaker than other similar tryptamine derivatives.