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Merck
모든 사진(5)

문서

P45907

Sigma-Aldrich

Piperazine

ReagentPlus®, 99%

동의어(들):

1,4-Diazacyclohexane, Diethylenediamine

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About This Item

실험식(Hill 표기법):
C4H10N2
CAS Number:
Molecular Weight:
86.14
Beilstein:
102555
EC Number:
MDL number:
UNSPSC 코드:
12352100
eCl@ss:
39160301
PubChem Substance ID:
NACRES:
NA.21

vapor pressure

0.8 mmHg ( 20 °C)

Quality Level

제품 라인

ReagentPlus®

분석

99%

형태

solid

expl. lim.

14 %

불순물

<1% water

pH

10.8-11.8 (100 g/L)

bp

145-146 °C (lit.)

mp

109-112 °C (lit.)

solubility

H2O: 0.9 g/L at 20 °C

SMILES string

C1CNCCN1

InChI

1S/C4H10N2/c1-2-6-4-3-5-1/h5-6H,1-4H2

InChI key

GLUUGHFHXGJENI-UHFFFAOYSA-N

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관련 카테고리

일반 설명

Piperazine (PZ) is an amine solvent. The ability of aqueous PZ to absorb carbon dioxide (CO2) has been assessed. It is reported to cause paralysis in Ascaris worms. The analysis of the crystal structure of PZ at 150K shows the presence of layered structure with NH...N hydrogen-bonded chains.

애플리케이션

Intermediate for a wide range of pharmaceuticals, polymers, dyes, corrosion inhibitors, rubber accelerators and surfactants.
Piperazine may be used in the preparation of N-(hetero)arylpiperazines.

법적 정보

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

픽토그램

FlameHealth hazardCorrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Dam. 1 - Flam. Sol. 1 - Repr. 2 - Resp. Sens. 1B - Skin Corr. 1B - Skin Sens. 1B

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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이미 열람한 고객

Carbon dioxide capture with concentrated, aqueous piperazine.
Freeman SA, et al.
International Journal of Greenhouse Gas Control, 4(2), 119-124 (2010)
Investigations on the action of piperazine on Ascaris lumbricoides.
Norton S and De Beer EJ.
The American Journal of Tropical Medicine and Hygiene, 6(5), 898-905 (1957)
Synthesis of N-arylpiperazines from aryl halides and piperazine under a palladium tri-tert-butylphosphine catalyst.
Nishiyama M, et al.
Tetrahedron Letters, 39(7), 617-620 (1998)
Absorption of carbon dioxide into aqueous piperazine: reaction kinetics, mass transfer and solubility.
Bishnoi S and Rochelle GT.
Chemical Engineering Science, 55(22), 5531-5543 (2000)
Andrew Parkin et al.
Acta crystallographica. Section B, Structural science, 60(Pt 2), 219-227 (2004-03-16)
The crystal structures of piperazine, piperidine and morpholine have been determined at 150 K. All three structures are characterized by the formation of NH...N hydrogen-bonded chains. In piperazine these are linked to form sheets, but the chains are shifted so

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