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PIPERAZINE-2,5-DICARBOXYLIC ACID, also known as lysipamide, is a versatile chemical compound that serves as a crucial intermediate in the pharmaceutical industry for the synthesis of various drugs, such as antihistamines and antipsychotics. As a derivative of piperazine, it features a heterocyclic organic structure with a six-membered ring containing two nitrogen atoms. Its ability to form stable salts with a range of drugs makes it an indispensable building block in pharmaceutical production. Beyond its pharmaceutical applications, PIPERAZINE-2,5-DICARBOXYLIC ACID also exhibits utility as a corrosion inhibitor in cooling water systems, where it chelates metal ions to prevent precipitation. Furthermore, it plays a role in the production of plasticizers, surfactants, and as a precursor in the synthesis of pesticides and dyes.

89601-10-5

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89601-10-5 Usage

Uses

Used in Pharmaceutical Industry:
PIPERAZINE-2,5-DICARBOXYLIC ACID is used as a key intermediate for the synthesis of various drugs, including antihistamines and antipsychotics, due to its ability to form stable salts with a variety of drugs.
Used in Cooling Water Systems:
PIPERAZINE-2,5-DICARBOXYLIC ACID is used as a corrosion inhibitor for its ability to chelate metal ions and prevent their precipitation, thereby protecting cooling water systems from corrosion.
Used in Chemical Production:
PIPERAZINE-2,5-DICARBOXYLIC ACID is used as a precursor in the synthesis of pesticides and dyes, contributing to the development of these chemical products.
Used in Plasticizer and Surfactant Production:
PIPERAZINE-2,5-DICARBOXYLIC ACID is used as a building block in the production of plasticizers and surfactants, enhancing their performance and utility in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 89601-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,0 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89601-10:
(7*8)+(6*9)+(5*6)+(4*0)+(3*1)+(2*1)+(1*0)=145
145 % 10 = 5
So 89601-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O4/c9-5(10)3-1-7-4(2-8-3)6(11)12/h3-4,7-8H,1-2H2,(H,9,10)(H,11,12)

89601-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name PIPERAZINE-2,5-DICARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names Piperazin-2,5-dicarbonsaeure

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:89601-10-5 SDS

89601-10-5Downstream Products

89601-10-5Relevant academic research and scientific papers

SUBSTITUTED PIPERAZINE COMPOUND, AND ABSORBENT AND LIQUID ABSORBENT FOR ACIDIC GAS

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Paragraph 0031; 0034, (2018/10/19)

PROBLEM TO BE SOLVED: To provide a substituted piperazine compound that can suppress composition change when used by preparing a liquid absorbent, to provide an absorbent containing the substituted piperazine compound as an active ingredient and to provide a liquid absorbent for the treatment of an acidic gas such as carbon dioxide or the like that is prepared by using the substituted piperazine compound. SOLUTION: The substituted piperazine compound is represented by the following general formula. The liquid absorbent for absorption treatment of an acidic gas such as carbon dioxide or the like is prepared by using the absorbent containing the substituted piperazine compound as an active ingredient and water. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2018,JPOandINPIT

Hydroformylation of olefins using azoxy-dentated ligands

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, (2008/06/13)

At a temperature in the range 100° C to 225° C the destructive dissociation of cobalt carbonyl compounds to cobalt metal and residue is inhibited by the action of one or more azoxy-dentated chelation ligands.

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