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73659

Sigma-Aldrich

1-(4-Chlorophenyl)piperazine

≥98.0% (GC)

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About This Item

Empirical Formula (Hill Notation):
C10H13ClN2
CAS Number:
38212-33-8
Molecular Weight:
196.68
Beilstein:
150981
MDL number:
MFCD00044823
UNSPSC Code:
12352100
PubChem Substance ID:
57652448
NACRES:
NA.22

Assay

≥98.0% (GC)

form

crystals

mp

76-79 °C

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

rat ... Htr3a(79246)

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

73659-5G-F:
73659-1G:
73659-VAR-F:
73659-BULK-F:
73659-1G-F:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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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