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Details

Stereochemistry RACEMIC
Molecular Formula C9H12ClN
Molecular Weight 169.651
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-CHLOROAMPHETAMINE

SMILES

CC(N)CC1=CC=C(Cl)C=C1

InChI

InChIKey=WWPITPSIWMXDPE-UHFFFAOYSA-N
InChI=1S/C9H12ClN/c1-7(11)6-8-2-4-9(10)5-3-8/h2-5,7H,6,11H2,1H3

HIDE SMILES / InChI

Molecular Formula C9H12ClN
Molecular Weight 169.651
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Metabolic activation of the serotonergic neurotoxin para-chloroamphetamine to chemically reactive intermediates by hepatic and brain microsomal preparations.
1986 May 15
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:51:52 GMT 2023
Edited
by admin
on Sat Dec 16 09:51:52 GMT 2023
Record UNII
897NVD4A52
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-CHLOROAMPHETAMINE
Common Name English
DL-CHLOROAMPHETAMINE
Common Name English
(±)-PCA
Common Name English
(±)-1-METHYL-2-(4-CHLOROPHENYL)ETHYLAMINE
Systematic Name English
NSC-287208
Code English
(±)-P-CHLOROAMPHETAMINE
Common Name English
4-CHLOROAMPHETAMINE
Systematic Name English
4-CA
Common Name English
PHENETHYLAMINE, P-CHLORO-.ALPHA.-METHYL-
Common Name English
PARA-CHLOROAMPHETAMINE
Systematic Name English
(±)-4-CHLOROAMPHETAMINE
Common Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-4-CA
Created by admin on Sat Dec 16 09:51:52 GMT 2023 , Edited by admin on Sat Dec 16 09:51:52 GMT 2023
Code System Code Type Description
WIKIPEDIA
PARA-CHLOROAMPHETAMINE
Created by admin on Sat Dec 16 09:51:52 GMT 2023 , Edited by admin on Sat Dec 16 09:51:52 GMT 2023
PRIMARY para-Chloroamphetamine (PCA), also known as 4-chloroamphetamine (4-CA), is an amphetamine derivative and monoamine releaser similar to MDMA, but with substantially higher neurotoxicity, thought to be due to the unrestrained release of both serotonin and dopamine by a metabolite. It is used as a neurotoxin by neurobiologists to selectively kill serotonergic neurons for research purposes, in the same way that 6-hydroxydopamine is used to kill dopaminergic neurons. However, the effects of the compound on experimental animals appear less encouraging.[6] It has been detected as an apparent designer drug, along with the related 3-chloroamphetamine, which is even more potent as a releaser of dopamine and serotonin but slightly less neurotoxic.
FDA UNII
897NVD4A52
Created by admin on Sat Dec 16 09:51:52 GMT 2023 , Edited by admin on Sat Dec 16 09:51:52 GMT 2023
PRIMARY
PUBCHEM
3127
Created by admin on Sat Dec 16 09:51:52 GMT 2023 , Edited by admin on Sat Dec 16 09:51:52 GMT 2023
PRIMARY
NSC
287208
Created by admin on Sat Dec 16 09:51:52 GMT 2023 , Edited by admin on Sat Dec 16 09:51:52 GMT 2023
PRIMARY
EPA CompTox
DTXSID90897229
Created by admin on Sat Dec 16 09:51:52 GMT 2023 , Edited by admin on Sat Dec 16 09:51:52 GMT 2023
PRIMARY
CAS
64-12-0
Created by admin on Sat Dec 16 09:51:52 GMT 2023 , Edited by admin on Sat Dec 16 09:51:52 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY