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3-(1-Methylpyrrolidin-2-yl)-piperidine, also known as MPPP, is a chemical compound belonging to the class of piperidines. It is a derivative of the synthetic opioid drug pethidine and exhibits potent narcotic analgesic properties. MPPP shares similar effects with other opioids, such as providing pain relief and inducing feelings of euphoria. However, it also possesses a high potential for abuse and dependence, leading to its classification as a Schedule I controlled substance in the United States due to its lack of accepted medical use and high abuse potential.

5337-62-2

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5337-62-2 Usage

Uses

Used in Pharmaceutical Industry:
3-(1-Methylpyrrolidin-2-yl)-piperidine is used as a potent narcotic analgesic for its ability to provide pain relief and induce feelings of euphoria. Its opioid-like effects make it a potential candidate for the development of pain management medications, although its high potential for abuse and dependence must be carefully considered.
Used in Research and Development:
MPPP is utilized in scientific research to study the effects of opioids on the human body and to develop new medications with reduced potential for abuse and dependence. Its chemical structure and properties provide valuable insights into the development of safer and more effective pain management therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 5337-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5337-62:
(6*5)+(5*3)+(4*3)+(3*7)+(2*6)+(1*2)=92
92 % 10 = 2
So 5337-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H20N2/c1-12-7-3-5-10(12)9-4-2-6-11-8-9/h9-11H,2-8H2,1H3

5337-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-METHYL-2-PYRROLIDINYL)PIPERIDINE

1.2 Other means of identification

Product number -
Other names 3-(1-Methylpyrrolidin-2-yl)-piperidine

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:5337-62-2 SDS

5337-62-2Downstream Products

5337-62-2Relevant academic research and scientific papers

A new approach to nicotine: Symmetry consideration for synthesis design

Ho, Tse-Lok,Kuzakov, Eugene V.

, p. 2712 - 2716 (2007/10/03)

A synthesis of nicotyrine (9), and hence formally racemic nicotine, was carried out by elaboration of the 1:1 adduct 2 of cycloocta-1,5-diene and chlorosulfonyl isocyanate (CISO2-NCO). Transformation of adduct 2 into carbamate 4 was followed by ozonolysis, tosylation, and NaH treatment, which led to pyrrolidinylpiperidinone 6. LiAIH4 Reduction, debenzylation, and aromatization yielded 2.

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