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Piperazine

pharmaceutical raw materials
Piperazine structure

Piperazine 

structure
  • CAS No:

    110-85-0

  • Formula:

    C4H10N2

  • Chemical Name:

    Piperazine

  • Synonyms:

    Piperazine;Antiren;1,4-Diazacyclohexane;Diethylenediamine;Dispermine;Hexahydropyrazine;Lumbrical;Piperazidine;Pyrazine,hexahydro-;Pyrazine hexahydride;Pipersol;1,4-Piperazine;Wurmirazin;Worm-A-Ton;Eraverm;Uvilon;Vermex;NSC 474;Tetrahydro-1,4-diazine;8017-90-1;8027-81-4;81546-15-8;854880-15-2;861800-35-3

  • Categories:

    Active Pharmaceutical Ingredients  >  Antiparasitic Drugs

Description

HYGROSCOPIC COLOURLESS CRYSTALS OR WHITE FLAKES WITH PUNGENT ODOUR.

Piperazine Basic Attributes

86.14

86.14

102555

203-808-3

2933599090

Characteristics

24.1

-1.17

White to slightly yellow Crystalline Flakes

1.1 g/cm3

106 °C

146 °C @ Press: 760 Torr

65 °C

1.424

H2O: 150 g/L (20 ºC)

Store in dark!

0.8 mm Hg ( 20 °C)

Relative vapour density (air = 1): 3

Oral-rat LD50: 1900 mg/kg; Oral-Mouse LD50: 600 mg/kg

Combustible; decomposes toxic nitrogen oxide gas in case of heat

14%

Typical amine odor

Salty taste

pH = 10.8-11.8 (10% aqueous solution)

9.73None

Safety Information

III

8

UN 2579 8/PG 3

1

34-42/43-52/53-62-52-63

22-26-36/37/39-45-61

TK7800000

C,Xn

Treasury is ventilated, low temperature and dry; stored separately from acid

Harmful/Corrosive

Explosive when mixed with air

Stable. Hygroscopic. Light sensitive. Flammable. Incompatible with strong oxidizing agents.

P261-P280-P305 + P351 + P338-P310

H314-H317-H334-H361fd

Toxicity

moderately toxic

Piperazine Use and Manufacturing

Methods of Manufacturing

The preparation method is based on chloroethanol as the raw material, and is obtained through amination and cyclization. The process is to heat chloroethanol and ammonium hydroxide in an autoclave to an ammonia pressure of 441 kPa, stir the reaction for 5 hours, and recover excess ammonium hydroxide at normal pressure to obtain an aminoethanol aqueous solution. Add quantitative hydrochloric acid and stir, concentrate under reduced pressure to a semi-paste-like ethanolamine hydrochloride concentrate, warm up to 150°C, add paraffin wax that has been melted in advance, continue to heat up to 260°C, and maintain (260±2)°C for 12h , Filtration and removal of paraffin wax to obtain piperazine hydrochloride. Piperazine hydrochloride, solid sodium hydroxide, and water were added to the reaction kettle, stirred for 1.5h, and the ammonia was discharged. Then, the temperature was raised to 130-140°C, the piperazine hexahydrate solution was distilled off, the residue was filtered off, and the piperazine hexahydrate solution was frozen to At 8 ℃, centrifugal spin filtration to obtain piperazine hexahydrate, piperazine hexahydrate dehydration to obtain the finished piperazine. The reaction equation is as follows: ClCH2CH2OH+NH4OH→NH2CH2CH2OH·HCl+H2O

Uses

keratolytic, antiseborheic

Computed Properties

Molecular Weight:86.14
XLogP3:-1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Exact Mass:86.084398327
Monoisotopic Mass:86.084398327
Topological Polar Surface Area:24.1
Heavy Atom Count:6
Complexity:26.5
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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