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1-(3,4-dihydro-2H-chromen-4-yl)-4-(4-methoxyphenyl)piperazine, also known as DPMP, is a psychoactive designer drug belonging to the piperazine class of compounds. It is structurally related to meta-chlorophenylpiperazine (mCPP) and acts as a potent and selective dopamine and norepinephrine reuptake inhibitor, with minimal effects on serotonin reuptake. DPMP is known for its stimulant and euphoric effects, and due to its high abuse potential, it is classified as a controlled substance in many countries. Although not approved for medical use, the health effects of DPMP are a subject of concern, particularly regarding its potential for addiction and harm to users.

81816-70-8

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81816-70-8 Usage

Uses

Used in Research Applications:
DPMP is used as a research chemical for studying the effects of dopamine and norepinephrine reuptake inhibition on the central nervous system. Its potent action on these neurotransmitters makes it a valuable tool in understanding the mechanisms underlying stimulant and euphoric effects, as well as the potential for addiction.
Used in Drug Abuse and Addiction Studies:
As a controlled substance with a high abuse potential, DPMP is utilized in studies focusing on drug abuse and addiction. Researchers use 1-(3,4-dihydro-2H-chromen-4-yl)-4-(4-methoxyphenyl)piperazine to investigate the factors contributing to substance abuse and to develop strategies for prevention and treatment.
Used in Pharmaceutical Development:
Although not approved for medical use, DPMP's mechanism of action as a dopamine and norepinephrine reuptake inhibitor may provide insights for the development of new pharmaceuticals targeting these neurotransmitters. Its structural relationship to other compounds, such as mCPP, can also aid in the design of novel therapeutic agents.
Used in Forensic Toxicology:
DPMP's classification as a controlled substance and its association with drug abuse make it relevant in forensic toxicology. It is used for the identification and analysis of designer drugs in cases involving substance abuse or criminal investigations.

Check Digit Verification of cas no

The CAS Registry Mumber 81816-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,1 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81816-70:
(7*8)+(6*1)+(5*8)+(4*1)+(3*6)+(2*7)+(1*0)=138
138 % 10 = 8
So 81816-70-8 is a valid CAS Registry Number.

81816-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4-dihydro-2H-chromen-4-yl)-4-(4-methoxyphenyl)piperazine

1.2 Other means of identification

Product number -
Other names -

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:81816-70-8 SDS

81816-70-8Downstream Products

81816-70-8Relevant academic research and scientific papers

Phenoxyalkylamines in Semi-rigid Conformation: Synthesis & Pharmacological Activity of N1-(4'-Chromanyl)-N4-arylpiperazines & N1-(2'-Chromanylmethyl)-N4-arylpiperazines

Pratap, Ram,Gupta, R. C.,Anand, Nitya

, p. 1063 - 1067 (2007/10/02)

Synthesis and pharmacological activity of N1-(4'-chromanyl)-N4-arylpiperazines and N1-(chromanylmethyl)-N4-arylpiperazines, cyclic congeners of N1-aryloxyalkyl-N4-arylpiperazines, are reported.None of the compounds of this series shows any significant pharmacological activity.

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