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3-[4-(3-chlorophenyl)piperazin-1-yl]propan-1-ol, commonly known as mCPP, is a psychoactive drug that belongs to the phenylpiperazine class. It is characterized by its ability to act as a serotonin and norepinephrine reuptake inhibitor, which disrupts the normal reabsorption of these neurotransmitters by nerve cells, leading to elevated levels of serotonin and norepinephrine in the brain. This results in a range of psychological and physiological effects, such as mood changes, anxiety, agitation, and increased heart rate. Due to its psychoactive properties, mCPP has been associated with drug abuse and overdose incidents, and is subject to regulation in certain countries.

32229-98-4

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32229-98-4 Usage

Uses

Used in Scientific Research:
3-[4-(3-chlorophenyl)piperazin-1-yl]propan-1-ol is used as a research tool for studying the effects of psychoactive substances on the central nervous system. Its action as a serotonin and norepinephrine reuptake inhibitor allows researchers to investigate the role of these neurotransmitters in various psychological and physiological processes.
Used in Pharmaceutical Development:
mCPP is utilized in the development of pharmaceuticals targeting the serotonin and norepinephrine systems. Its mechanism of action provides insights into the potential therapeutic effects of drugs that modulate these neurotransmitters, which can be beneficial in treating conditions such as depression, anxiety, and other mood disorders.
Used in Drug Abuse and Overdose Studies:
3-[4-(3-chlorophenyl)piperazin-1-yl]propan-1-ol is employed in research aimed at understanding the risks and consequences of drug abuse and overdose involving psychoactive substances. Studying mCPP's effects can contribute to the development of prevention strategies, treatment protocols, and public health policies to address substance misuse.
Used in Regulatory and Forensic Analysis:
mCPP is used in regulatory and forensic analysis to detect and monitor the presence of this psychoactive drug in cases of drug abuse, overdose, and illegal distribution. Its identification in biological samples can provide crucial evidence for legal proceedings and support efforts to enforce drug control regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 32229-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,2 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32229-98:
(7*3)+(6*2)+(5*2)+(4*2)+(3*9)+(2*9)+(1*8)=104
104 % 10 = 4
So 32229-98-4 is a valid CAS Registry Number.

32229-98-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[4-(3-chlorophenyl)piperazin-1-yl]propan-1-ol

1.2 Other means of identification

Product number -
Other names 3-[4-(3-chloro-phenyl)-1-piperazinyl]propanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:32229-98-4 SDS

32229-98-4Relevant academic research and scientific papers

N-Aryl-N-phenoxy-alkyl-piperazine compounds useful in decreasing intracranial pressure

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, (2008/06/13)

A piperazine derivative of the formula: STR1 wherein R1 is hydrogen, alkyl (C1-8), alkyl (C1-4)-sulfonyl or an acyl group of the formula: R3 CO--(wherein R3 is hydrogen, alkyl (C1-7), halogenoalkyl (C1-4), alkoxy (C1-4)-carbonyl-alkyl (C1-4), cycloalkyl (C3-6), alkenyl (C2-5), alkoxy (C1-4), amino, alkyl (C1-4)-amino or anilino), R2 is hydrogen, alkyl (C1-4), alkoxy (C1-4)-carbonyl-alkyl (C1-4), carboxy-alkyl (C1-4), alkenyl (C2-5) or alkyl (C1-4)-sulfonyl, or R1 and R2 are combined together to form succinyl group, Ring A is phenyl, alkyl (C1-4)-phenyl or halogenophenyl, and n is an integer of 2 to 6, or a pharmaceutically acceptable acid addition salt thereof. The piperazine derivative (I) has an intracranial pressure-lowering activity. Said derivative also has a depressing effect on central nervous system.

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