Piperazine compounds

Piperazine compound refers to compound with its structure containing the piperazine structure. Such compound belongs to an important class of pharmaceutical intermediates and is mainly used for the production of anthelmintic piperazine phosphate, piperazine citrate and fluphenazine, bucinnazine and rifampicin. It can also be used for the production of surfactants products such as wetting agents, emulsifying agents and dispersing agents as well as the production of antioxidants, preservatives, stabilizers and other kinds of plastic processing aids and rubber additives.

Piperazine is also known as hexahydropyrazino and diethylene diamine. Piperazine precipitate from ethanol appears as white orthorhombic leaf-shaped crystals with a mild amine odor, salty taste and is hygroscopic. It has its relative density being 0.876, melting point of 106.6 ℃ and the boiling point of 146 ℃. It is easily soluble in water and glycerol, slightly soluble in ethanol and insoluble in ether. It exhibits strong alkalinity with the pH of its 10% aqueous solution being 10.8 to 11.8. It can absorb the carbon dioxide in the air and is irritating to eyes and skin. It can have typical secondary amine reaction. It can be made through the reaction between ethylene diamine and 1, 2-dichloroethane or obtained by the dimerization of amino-ethanol at high temperatures. Its inorganic acid and organic acid salts can be used as human and animal anthelmintics, being effective drugs to get rid of roundworm, pinworm and can also be used in organic synthesis.

Piperazine has a strong effect on roundworm and pinworm and can cause muscle relaxation paralysis of roundworm so that the roundworm can’t reverse the peristalsis movement and can be excreted. There is no excitement phenomenon before the parasite paralysis phenomenon, thereby it is safe. It can be applied to the treatment of incomplete intestinal obstruction caused by roundworm and can be used for treating biliary ascariasis as well as being used in patients with ulcer disease. The curing rate in general dose can be up to 70% to 80% without continuous medication for two days being able to further increases the curing rate. For the treatment of pinworm, the patients need to be subject to continuous medication for 7 to 10 days. The drug has a low toxicity with nausea, vomiting and urticaria occasionally happening upon the amount of treatment.

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Structure Chemical Name CAS MF
1-(1-HEPTYL)-PIPERAZINE 1-(1-HEPTYL)-PIPERAZINE 82502-77-0 C11H24N2
4-PIPERAZIN-1-YL-PHENYLAMINE 4-PIPERAZIN-1-YL-PHENYLAMINE 67455-41-8 C10H15N3
1-(4-CHLORO-3-TRIFLUOROMETHYLPHENYL)PIPERAZINE 1-(4-CHLORO-3-TRIFLUOROMETHYLPHENYL)PIPERAZINE 41213-04-1 C11H12ClF3N2
N-Isopropylpiperazine N-Isopropylpiperazine 137186-14-2 C7H17ClN2
Acefylline piperazinate Acefylline piperazinate 18833-13-1 C13H20N6O4
1-INDAN-1-YL-PIPERAZINE 1-INDAN-1-YL-PIPERAZINE 185678-56-2 C13H18N2
2-Piperazinecarboxamide 2-Piperazinecarboxamide 84501-64-4 C5H11N3O
Double sodiuM piperazine Double sodiuM piperazine
difluanazine difluanazine 5522-39-4 C28H33F2N3
piperazine-1,4-dipropiononitrile piperazine-1,4-dipropiononitrile 4159-11-9 C10H16N4
Hydroxyethyl piperazine Hydroxyethyl piperazine C6H14N2O
Tolnapersine Tolnapersine 70312-00-4 C21H26N2O
1-Piperazinepropanoicacid,methylester(9CI) 1-Piperazinepropanoicacid,methylester(9CI) 43032-40-2 C8H16N2O2
2-Piperazinemethanol 2-Piperazinemethanol 28795-50-8 C5H12N2O
ETHYL-2-PIPERAZINECARBOXYLATE ETHYL-2-PIPERAZINECARBOXYLATE 89941-07-1 C7H14N2O2
1-BENZYLPIPERAZINE 1-BENZYLPIPERAZINE 2759-17-3 C17H18N4S
2,6-Dichloropiperazine 2,6-Dichloropiperazine 89007-51-2 C4H8Cl2N2
Piperazine, 1-(trifluoroacetyl)- (7CI,8CI,9CI) Piperazine, 1-(trifluoroacetyl)- (7CI,8CI,9CI) 6511-88-2 C6H9F3N2O
1-[3-(Methylsulfonyl)propyl]-piperazine2HCl 1-[3-(Methylsulfonyl)propyl]-piperazine2HCl 910572-80-4 C8H18N2O2S
2-Piperazinamine(9CI) 2-Piperazinamine(9CI) 471925-18-5 C4H11N3
2-Cyanopiperazine 2-Cyanopiperazine 187589-36-2 C5H9N3
Piperazine, 2-(bromomethyl)- (9CI) Piperazine, 2-(bromomethyl)- (9CI) 804425-48-7 C5H11BrN2
1,3-DIMETHYL-PIPERAZINE 1,3-DIMETHYL-PIPERAZINE 22317-01-7 C6H14N2
N-(n-butoxycarbonyl)piperazine N-(n-butoxycarbonyl)piperazine 50606-32-1 C9H18N2O2
piperazine-1-methylamine piperazine-1-methylamine 18190-85-7 C5H13N3
Piperazine, 1-(2,2-dimethylpropyl)- (9CI) Piperazine, 1-(2,2-dimethylpropyl)- (9CI) 57184-50-6 C9H20N2
2-Piperazinecarboxaldehyde 2-Piperazinecarboxaldehyde 773866-77-6 C5H10N2O
PIPERAZINE-1-CARBOXYLIC ACID AMIDE HCL PIPERAZINE-1-CARBOXYLIC ACID AMIDE HCL 474711-89-2 C5H12ClN3O
1-CYCLOOCTYLPIPERAZINE 1-CYCLOOCTYLPIPERAZINE 21043-43-6 C12H24N2
1-(DIBENZOSUBERYL)PIPERAZINE 1-(DIBENZOSUBERYL)PIPERAZINE 69159-50-8 C19H22N2
4-PIPERAZINYL BENZENESULFONAMIDE 4-PIPERAZINYL BENZENESULFONAMIDE 121278-31-7 C10H15N3O2S
3'H-CYCLOPROPA[1,2]PREGNA-1,4,6-TRIENE-3,20-DIONE 3'H-CYCLOPROPA[1,2]PREGNA-1,4,6-TRIENE-3,20-DIONE 17092-31-8 C24H27ClF2O4
1-piperazinecarboxaldehyde 1-piperazinecarboxaldehyde C5H10N2O
1-CINNAMOYL-PIPERAZINE 1-CINNAMOYL-PIPERAZINE 55486-27-6 C13H16N2O
Ethyl 1,4-diazepane-1-carboxylate ,97% Ethyl 1,4-diazepane-1-carboxylate ,97% 18739-39-4 C8H16N2O2
TRANS-1-CINNAMYLPIPERAZINE TRANS-1-CINNAMYLPIPERAZINE 18903-01-0 C13H18N2
2-Piperazinecarboxylicacid,1,1-dimethylethylester(9CI) 2-Piperazinecarboxylicacid,1,1-dimethylethylester(9CI) 146398-94-9 C9H18N2O2
NICLOSAMIDE PIPERAZINE SALT NICLOSAMIDE PIPERAZINE SALT 34892-17-6 C17H18Cl2N4O4
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