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3-(DIPHENYLMETHOXY)PIPERIDINE, also known as D2PM, is a psychoactive chemical compound belonging to the class of piperidine derivatives. It is recognized for its stimulant and hallucinogenic effects, often sought after for recreational use. D2PM functions as a serotonin and dopamine releasing agent, which leads to heightened levels of these neurotransmitters in the brain, inducing sensations of euphoria, increased energy, and altered perception. Despite its psychoactive properties, D2PM poses significant health risks, including cardiotoxicity, neurotoxicity, and the potential for addiction and overdose. Due to its abuse potential and associated health hazards, it is classified as a controlled substance in many jurisdictions.

78503-38-5

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78503-38-5 Usage

Uses

Used in Pharmaceutical Research:
3-(DIPHENYLMETHOXY)PIPERIDINE is used as a research chemical for studying the effects of psychoactive substances on the central nervous system. Its action as a serotonin and dopamine releasing agent makes it a valuable tool in understanding the mechanisms of mood, perception, and potential therapeutic applications for neurological disorders.
Used in Recreational Substances:
3-(DIPHENYLMETHOXY)PIPERIDINE is used as a recreational substance for its stimulant and hallucinogenic effects, providing users with feelings of euphoria, increased energy, and altered perception. However, its use in this context is fraught with health risks and legal restrictions due to its potential for abuse and associated hazards.
Used in Toxicological Studies:
3-(DIPHENYLMETHOXY)PIPERIDINE is used as a subject in toxicological studies to investigate the cardiotoxic and neurotoxic effects associated with its use. Understanding these risks is crucial for developing potential treatments and preventive measures against the substance's adverse health effects.
Used in Addiction Research:
3-(DIPHENYLMETHOXY)PIPERIDINE is used in addiction research to explore the potential for substance abuse and the development of addiction. Studying its effects on the brain can provide insights into the neurobiological basis of addiction and inform the development of interventions and treatments for substance use disorders.
Used in Regulatory and Forensic Analysis:
3-(DIPHENYLMETHOXY)PIPERIDINE is used in regulatory and forensic analysis to detect and monitor the presence of this controlled substance in various contexts, such as drug enforcement and public health surveillance. This helps in the enforcement of laws and regulations surrounding its use and distribution.

Check Digit Verification of cas no

The CAS Registry Mumber 78503-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,0 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78503-38:
(7*7)+(6*8)+(5*5)+(4*0)+(3*3)+(2*3)+(1*8)=145
145 % 10 = 5
So 78503-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H21NO/c1-3-8-15(9-4-1)18(16-10-5-2-6-11-16)20-17-12-7-13-19-14-17/h1-6,8-11,17-19H,7,12-14H2

78503-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzhydryloxypiperidine

1.2 Other means of identification

Product number -
Other names Piperidin-3-yl-benzhydryl-aether

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:78503-38-5 SDS

78503-38-5Relevant academic research and scientific papers

GABA uptake inhibitors. Syntheses and structure-activity studies on GABA analogues containing diarylbutenyl and diarylmethoxyalkyl N-substituents

Falch,Krogsgaard-Larsen

, p. 69 - 77 (2007/10/02)

A number of analogues of GABA or β-alanine containing 4,4-diphenyl-3-butenyl (DPB), benzhydryl ethyl ether (BEE), or benzhydryl propyl ether N-substituents have been synthesized and tested as inhibitors of synaptosomal GABA uptake. Whereas the N-DPB and N

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