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1,4-Dipropionylpiperazine, also known as 1,4-DPPP or Tripip, is a synthetic designer drug that belongs to the piperazine class. It is structurally similar to other piperazine-based compounds, such as 1-benzylpiperazine (BZP) and 1-(3-trifluoromethylphenyl)piperazine (TFMPP), and is known for its stimulant and entactogenic effects. 1,4-DPPP was first synthesized in the 1970s and has been used recreationally for its psychoactive properties, which include increased energy, euphoria, and empathogenic sensations. However, due to its potential for abuse and health risks, 1,4-DPPP has been classified as a controlled substance in several countries, and its use is discouraged due to the lack of comprehensive research on its long-term effects and safety.

5436-89-5

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5436-89-5 Usage

Chemical class

Piperazine derivatives

Common use

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Enzymatic reactions

Acts as a substrate for various enzymatic reactions

Utilization

Often utilized in research and development of new drugs

Application

Used as a reagent in organic chemistry

Pharmacological properties

Studied for its potential pharmacological properties

Toxicity

Has potential toxicity

Environmental concerns

Raises environmental concerns

Regulation and monitoring

Use and handling should be carefully regulated and monitored

Check Digit Verification of cas no

The CAS Registry Mumber 5436-89-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5436-89:
(6*5)+(5*4)+(4*3)+(3*6)+(2*8)+(1*9)=105
105 % 10 = 5
So 5436-89-5 is a valid CAS Registry Number.

5436-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-dipropionyl piperazine

1.2 Other means of identification

Product number -
Other names 1,4-Dipropionylpiperazine

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:5436-89-5 SDS

5436-89-5Downstream Products

5436-89-5Relevant academic research and scientific papers

Design, synthesis and nootropic activity of new analogues of sunifiram and sapunifiram, two potent cognition-enhancers

Martini, Elisabetta,Salvicchi, Alberto,Ghelardini, Carla,Manetti, Dina,Dei, Silvia,Guandalini, Luca,Martelli, Cecilia,Melchiorre, Michele,Cellai, Cristina,Scapecchi, Serena,Teodori, Elisabetta,Romanelli, Maria Novella

experimental part, p. 7606 - 7614 (2011/02/24)

A series of amides and sulfonamides, structurally related to DM235 (sunifiram) and MN19 (sapunifram), derived by ring expansion or contraction, or by inversion of the exocyclic amide function, have been syn-thesized and tested for cognition-enhancing acti

Process for one-step synthesis of amides

-

, (2008/06/13)

A N-alkyl amide derivative is synthesized in one-step by reacting an olefin, nitrogen-containing compound and carbon monoxide with a catalyst comprising a rhodium-containing compound in the presence of water at a pressure of at least 500 psi and a temperature of at least 50° C.

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