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110-85-0

  • Product Name:68 Piperazine
  • Molecular Formula:C4H10N2
  • Molecular Weight:86.1368
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Product Details

Detail

  • Cas No： 110-85-0
  • Molecular Formula： C4H10N2
  • Appearance： needle-like white or colorless crystals
  • Purity： 99%
Product Name Piperazine
Alias 1,4-Diazacyclohexane
English
Molecular formula C4H10N2
Molecular weight 86.13
CAS No 110-85-0
EINECS 203-808-3
Specification

Appearance:  whitecrystal

Assay:99.5% min

Water:0.50%max

Chromaticity:30 max
Appearance traits
Use Used as pharmaceutical Intermediates, mainly for piperazine phosphate,fluphenazine, rifampicin, norfloxacin, flame retardants, desulfurization, decarburization,etc., also used for wetting agents, emulsifiers, dispersants, antioxidants, etc.
Package 50kg/drum
Other product information

RIDADR:UN 2579 8/PG 3

HS CODE:2933599090

Molecular Structure

Factory supply 68 Piperazine  110-85-0 (Piperazine Anhydrous)  with low price

  • Molecular Formula:C4H10N2
  • Molecular Weight:86.1368
  • Appearance/Colour:needle-like white or colorless crystals 
  • Vapor Pressure:4.049mmHg at 25°C 
  • Melting Point:109-112 °C(lit.) 
  • Refractive Index:1.424 
  • Boiling Point:149.324 °C at 760 mmHg 
  • PKA:9.55±0.10(Predicted) 
  • Flash Point:49.726 °C 
  • PSA：24.06000 
  • Density:0.874 g/cm3 
  • LogP:-0.16320 

1,4-Diazacyclohexane(Cas 110-85-0) Usage

General Description

1,4-Diazacyclohexane, also known as piperazine, is a chemical compound with the molecular formula C4H10N2. It is a heterocyclic organic compound containing two nitrogen atoms in a six-membered ring. Piperazine is commonly used as a pharmaceutical intermediate in the production of various medications, including antihistamines, anthelmintics, and antipsychotics. It is also utilized as a corrosion inhibitor, a precursor for rubber additives, and a component in some specialty solvents. Piperazine has also been studied for its potential use as a carbon dioxide absorbent in gas separation processes. Overall, 1,4-Diazacyclohexane has a wide range of industrial and pharmaceutical applications due to its versatile chemical properties.

InChI:InChI=1/C4H10N2/c1-2-6-4-3-5-1/h5-6H,1-4H2

Our main markets are China, the United States, Europe, Korea, and Japan. The main business scope includes electronic chemicals, liquid crystal intermediates, high-purity metal compounds, pharmaceutical intermediates, special chemicals, and so on.

110-85-0 Relevant articles

Axial ligation of iron(III) porphyrin with a series of aliphatic bases: Piperazine, piperidine and pyrrolidine

Saffari,Khorasani-Motlagh,Noroozifar

, p. 128 - 132 (2012)

The binding of a series of nitrogen dono...

Putrescine Transaminases for the Synthesis of Saturated Nitrogen Heterocycles from Polyamines

Slabu, Iustina,Galman, James L.,Weise, Nicholas J.,Lloyd, Richard C.,Turner, Nicholas J.

, p. 1038 - 1042 (2016)

Putrescine transaminase (pATA; EC 2.6.1....

Cobalt-bridged secondary building units in a titanium metal-organic framework catalyze cascade reduction of N-heteroarenes

Feng, Xuanyu,Song, Yang,Chen, Justin S.,Li, Zhe,Chen, Emily Y.,Kaufmann, Michael,Wang, Cheng,Lin, Wenbin

, p. 2193 - 2198 (2019)

We report here a novel Ti3-BPDC metal-or...

Chemical equilibrium constants for the formation of carbamates in (carbon dioxide + piperazine + water) from 1H-NMR-spectroscopy

Ermatchkov, Viktor,Perez-Salado Kamps, Alvaro,Maurer, Gerd

, p. 1277 - 1289 (2003)

H-NMR spectroscopic investigations were ...

Intermolecular condensation of ethylenediamine to 1,4-diazabicyclo[2,2,2]octane over TS-1 catalysts

Wang, Yong,Liu, Yueming,Li, Xiaohong,Wu, Haihong,He, Mingyuan,Wu, Peng

, p. 258 - 267 (2009)

The intermolecular condensation of ethyl...

Intermolecular condensation of ethylenediamine to 1,4-diazabicyclo(2,2,2)octane over H-ZSM-5 catalysts: Effects of Si/Al ratio and crystal size

Wang, Yong,Guo, Lifang,Ling, Yun,Liu, Yueming,Li, Xiaohong,Wu, Haihong,Wu, Peng

, p. 45 - 53 (2010)

The intermolecular condensation of ethyl...

Gas-phase pyrolysis in organic synthesis: A route for synthesis of cyanamides

Al-Awadi, Nouria A.,Abdelkhalik, Mervat Mohammed,El-Dusouqui, Osman M. E.,Elnagdia, Mohammad H.

, p. 207 - 209 (2010)

(Chemical Equation Presented) Pyrolysis ...

Facile hydrogenation of N-heteroarenes by magnetic nanoparticle-supported sub-nanometric Rh catalysts in aqueous medium

Nasiruzzaman Shaikh,Aziz, Md. Abdul,Kalanthoden, Abdul Nasar,Helal, Aasif,Hakeem, Abbas S.,Bououdina, Mohamed

, p. 4709 - 4717 (2018)

The hydrogenation of nitrogen-containing...

-

Avar,Kisch

, p. 89,91,95 (1978)

-

-

Martin,Martell

, p. 1817 (1948)

-

Reactivity of borohydride incorporated in coordination polymers toward carbon dioxide

Kadota, Kentaro,Sivaniah, Easan,Horike, Satoshi

, p. 5111 - 5114 (2020)

Borohydride (BH4-)-containing coordinati...

Magnesium borohydride confined in a metal-organic framework: A preorganized system for facile arene hydroboration

Ingleson, Michael J.,Barrio, Jorge Perez,Bacsa, John,Steiner, Alexander,Darling, George R.,Jones, James T. A.,Khimyak, Yaroslav Z.,Rosseinsky, Matthew J.

, p. 2012 - 2016 (2009)

(Chemical Equation Presented) In close q...

Palladium supported on magnesium hydroxyl fluoride: An effective acid catalyst for the hydrogenation of imines and N-heterocycles

Agbossou-Niedercorn, Francine,Corre, Yann,Dongare, Mohan K.,Kemnitz, Erhard,Kokane, Reshma,Michon, Christophe,Umbarkar, Shubhangi B.

supporting information, p. 19572 - 19583 (2021/11/04)

Palladium catalysts supported on acidic ...

METHOD FOR PRODUCING ETHANOLAMINES AND/OR ETHYLENEAMINES

-

Paragraph 0250-0257, (2020/04/09)

The present invention relates to a proce...

METHOD FOR THE PRODUCTION OF ETHYLENEAMINES

-

Paragraph 0336-0352, (2020/05/14)

The present invention relates to a proce...

One-pot dual catalysis for the hydrogenation of heteroarenes and arenes

Chatterjee, Basujit,Kalsi, Deepti,Kaithal, Akash,Bordet, Alexis,Leitner, Walter,Gunanathan, Chidambaram

, p. 5163 - 5170 (2020/09/07)

A simple dinuclear monohydrido bridged r...

110-85-0 Process route

glycerol
56-81-5,25618-55-7,64333-26-2,8013-25-0

glycerol

piperazine
110-85-0

piperazine

N-(1-aminomethyl-2-hydroxyethyl)amine
2811-20-3

N-(1-aminomethyl-2-hydroxyethyl)amine

1,2,3-triaminopropane
21291-99-6

1,2,3-triaminopropane

(RS)-2-methylpiperazine
109-07-9

(RS)-2-methylpiperazine

ethylenediamine
107-15-3,85404-18-8

ethylenediamine

1,2-diaminopropan
78-90-0,10424-38-1

1,2-diaminopropan

3,5-dimethylpiperazine
108-49-6

3,5-dimethylpiperazine

Conditions
Conditions Yield
With ammonia; hydrogen; Raney nickel; In water; at 200 ℃; under 15001.5 - 150015 Torr; Product distribution / selectivity; Autoclave;
 
glycerol
56-81-5,25618-55-7,64333-26-2,8013-25-0

glycerol

piperazine
110-85-0

piperazine

propylamine
107-10-8,42939-71-9

propylamine

2-Amino-1-propanol
6168-72-5

2-Amino-1-propanol

N-(1-aminomethyl-2-hydroxyethyl)amine
2811-20-3

N-(1-aminomethyl-2-hydroxyethyl)amine

(RS)-2-methylpiperazine
109-07-9

(RS)-2-methylpiperazine

ethylamine
75-04-7,85404-22-4

ethylamine

isopropylamine
75-31-0

isopropylamine

1,2-diaminopropan
78-90-0,10424-38-1

1,2-diaminopropan

3-amino-2-propanol
78-96-6,1674-56-2

3-amino-2-propanol

methylamine
74-89-5

methylamine

Conditions
Conditions Yield
With ammonia; hydrogen; catalyst obtained by prereduction from precursor whose catalytically active composition before the reduction with hydrogen comprised 13% by weight of Cu, calculated as CuO, 28% by weight of NI, calculated as NiO, 28% by weight of Co, calculated as CoO and 31% by weight of Zr, calculated as ZrO2; In water; at 250 ℃; under 37503.8 - 225023 Torr; Product distribution / selectivity; Autoclave;
 

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