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Merck
CN

191337

1-(4-氟苯基)哌嗪

98%

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经验公式(希尔记法):
C10H13FN2
化学文摘社编号:
分子量:
180.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
218-846-6
MDL number:
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产品名称

1-(4-氟苯基)哌嗪, 98%

InChI key

AVJKDKWRVSSJPK-UHFFFAOYSA-N

InChI

1S/C10H13FN2/c11-9-1-3-10(4-2-9)13-7-5-12-6-8-13/h1-4,12H,5-8H2

SMILES string

Fc1ccc(cc1)N2CCNCC2

assay

98%

form

solid

drug control

Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet
kontrollierte Droge in Deutschland

Quality Level

Gene Information

rat ... Chrnb2(54239)

bp

118-123 °C/0.1 mmHg (lit.)

mp

30-33 °C (lit.)

Application

1-(4-Fluorophenyl)piperazine was used in the synthesis of N,N-disubstituted piperazine.

Legal Information

German
Dieses Produkt fällt unter das Betäubungsmittelgesetz (BtMG). Für eine Bestellung dieses Produktes ist eine Erlaubnis nach § 3 BtMG zwingend erforderlich, es sei denn, es greift eine Ausnahme von der Erlaubnispflicht nach § 4 oder § 26 BtMG.

English
This product is subject to the German Narcotics Act. A permit under Section 3 of the German Narcotics Act is mandatory for ordering this product unless an exemption from the permit requirement under Section 4 or Section 26 of the German Narcotics Act applies.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

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Craig A Stockmeier et al.
Journal of psychiatric research, 43(10), 887-894 (2009-02-14)
Serotonin-1A receptors may play a role in the pathophysiology of depression and suicide. In postmortem brain tissue, agonist binding to serotonin-1A receptors is reportedly increased or unchanged in depression or suicide, while neuroimaging studies report a decrease in antagonist binding
Rapid synthesis of N, N'-disubstituted piperazines. Application to the preparation of No carrier added 1-(4-[18F] fluorophenyl) piperazine and of an [18F]-selective ligand of serotoninergic receptors (5HT2 antagonist).
Collins M, et al.
Journal of the Chemical Society. Perkin Transactions 1, 23, 3185-3188 (1992)
P E Keane et al.
Neuropharmacology, 21(2), 163-169 (1982-02-01)
Niaprazine (60 mg/kg i.p.) increased rat brain 5-hydroxyindole acetic acid (5-HIAA) concentrations 30 min after treatment, and reduced them at 3-8 hr after treatment. Rat brain 5-hydroxytryptamine (5-HT) levels were unchanged. Niaprazine also produced a short-lasting depletion of rat brain
Camilla Montesano et al.
Drug testing and analysis, 9(5), 798-807 (2016-07-28)
In this paper, an analytical method has been developed and validated for the analysis of new psychoactive substances (NPS) and metabolites in hair samples. The method was based on pressurized liquid extraction (PLE) followed by solid-phase extraction (SPE) clean-up and

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