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Key Documents

73659

Sigma-Aldrich

1-(4-Chlorophenyl)piperazine

≥98.0% (GC)

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About This Item

Empirical Formula (Hill Notation):
C10H13ClN2
CAS Number:
Molecular Weight:
196.68
Beilstein/REAXYS Number:
150981
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥98.0% (GC)

form

crystals

mp

76-79 °C

functional group

chloro

SMILES string

Clc1ccc(cc1)N2CCNCC2

InChI

1S/C10H13ClN2/c11-9-1-3-10(4-2-9)13-7-5-12-6-8-13/h1-4,12H,5-8H2

InChI key

UNEIHNMKASENIG-UHFFFAOYSA-N

Gene Information

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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R W Fuller et al.
Research communications in chemical pathology and pharmacology, 29(1), 201-204 (1980-07-01)
1-(p-Chlorophenyl)piperazine (PCPP), a structural analog of p-chloroamphetamine (PCA), increased serotonin and decreased 5-hydroxyindoleacetic acid (5-HIAA) concentration in rat brain at 6 hours. At one day and one week, serotonin and 5-HIAA concentrations were normal. In contrast, PCA lowered serotonin and
J Maj et al.
Polish journal of pharmacology and pharmacy, 32(4), 495-504 (1980-07-01)
Studies of 1-(m-chlorophenyl)-piperazine (m-CPP), 1-(p-chlorophenyl)-piperazine (p-CPP) and 1-phenylpiperazine (PP) were carried out on rats, mice and rabbits in order to assess their stimulatory effect on the central serotonin system. It was found out that m-CPP and p-CPP evoked a characteristic
Piotr Cysewski
Journal of molecular modeling, 23(4), 136-136 (2017-03-30)
In silico screening was performed to search for binary solids in which a phenylpiperazine-derivative drug was cocrystallized with a dicarboxylic acid. The phenylpiperazine derivative could be any of 61 such drugs, while the dicarboxylic acid could be any of nine

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