Piperazine
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Piperazine
structure -
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CAS No:
110-85-0
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Formula:
C4H10N2
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Chemical Name:
Piperazine
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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
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CAS No:
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
Piperazine Use and 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
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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