2950-45-0

  • Product Name:2,2,4,4,6,6,8,8-octachloro-2,2,4,4,6,6,8,8-octahydro-1,3,5,7,2,4,6,8-tetraazatetraphosphocine
  • Molecular Formula:Cl8N4 P4
  • Molecular Weight:463.546
Inquiry

Product Details

pd_meltingpoint:123-124 °C

Purity:99%

Quality manufacturer supply 2,2,4,4,6,6,8,8-octachloro-2,2,4,4,6,6,8,8-octahydro-1,3,5,7,2,4,6,8-tetraazatetraphosphocine 2950-45-0 in stock with high standard

  • Molecular Formula:Cl8N4 P4
  • Molecular Weight:463.546
  • Melting Point:123-124 °C 
  • Refractive Index:1.797 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:88.68000 
  • Density:2.58g/cm3 
  • LogP:7.43760 

2,2,4,4,6,6,8,8-octachloro-2,2,4,4,6,6,8,8-octahydro-1,3,5,7,2,4,6,8-tetraazatetraphosphocine(Cas 2950-45-0) Usage

General Description

2,2,4,4,6,6,8,8-octachloro-2,2,4,4,6,6,8,8-octahydro-1,3,5,7,2,4,6,8-tetraazatetraphosphocine is a compound with a highly complex and specific chemical structure. It contains eight chlorine atoms and eight hydrogen atoms attached to a central core made up of four nitrogen and four phosphorus atoms. 2,2,4,4,6,6,8,8-octachloro-2,2,4,4,6,6,8,8-octahydro-1,3,5,7,2,4,6,8-tetraazatetraphosphocine is highly toxic and is not naturally occurring in the environment. Its chemical structure makes it extremely stable and difficult to break down, presenting significant environmental and health risks if released into the environment. Due to its toxic nature, it is not commonly used and is strictly controlled and regulated.

InChI:InChI=1/Cl8H8N4P4/c1-13(2)9-14(3,4)11-16(7,8)12-15(5,6)10-13/h9-16H

2950-45-0 Relevant articles

ALLYL-PHENOXY-CYCLOPHOSPHAZENE COMPOUND, AND PRODUCTION METHOD THEREFOR

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Paragraph 0217, (2018/06/15)

An object of the present invention is to...

Octa-(1,2-dyhydroxyl-2-methoxyl)tetra-polyphosphazene

-

Paragraph 0022; 0023, (2017/01/02)

The invention discloses octa-(1,2-dyhydr...

Structure and conformation of the medium-sized chlorophosphazene rings

Bowers, David J.,Wright, Brian D.,Scionti, Vincenzo,Schultz, Anthony,Panzner, Matthew J.,Twum, Eric B.,Li, Lin-Lin,Katzenmeyer, Bryan C.,Thome, Benjamin S.,Rinaldi, Peter L.,Wesdemiotis, Chrys,Youngs, Wiley J.,Tessier, Claire A.

, p. 8874 - 8886 (2014/12/09)

Medium-sized cyclic oligomeric phosphaze...

Probing the mechanism of the PCl5-initiated living cationic polymerization of the phosphoranimine Cl3P=NSiMe3 using model compound chemistry

Blackstone, Vivienne,Lough, Alan J.,Murray, Martin,Manners, Ian

, p. 3658 - 3667 (2009/09/24)

New insight into the mechanism of the am...

2950-45-0 Process route

ammonium chloride

ammonium chloride

chlorine
7782-50-5

chlorine

phosphorus trichloride
7719-12-2,52843-90-0

phosphorus trichloride

hydrogenchloride
7647-01-0,15364-23-5

hydrogenchloride

2,2,4,4,6,6-hexachloro-1,3,5-triaza-2,4,6-triphosphorine
940-71-6,16422-79-0

2,2,4,4,6,6-hexachloro-1,3,5-triaza-2,4,6-triphosphorine

cyclic polyphosphorus nitride dichloride

cyclic polyphosphorus nitride dichloride

octachlorocyclotetraphosphazene
2950-45-0

octachlorocyclotetraphosphazene

Conditions
Conditions Yield
In further solvent(s); dissolving PCl3 distd. under N2 in (CHCl2)2 distd. under N2; addn. of NH4Cl dryed in vac. and passing in the corresponding amount of Cl2; heating in a stream of N2 at 130 °C; removal of formed HCl by a stream of N2;; filtration, distg. off the solvent at 40 °C and 0.5 Torr; recrystn. from petroleum ether; products (NPCl2)3, (NPCl2)4 and a small amount of oily polymers;;
In chlorobenzene; dissolving PCl3 distd. under N2 in C6H5Cl distd. under N2; addn. of NH4Cl dryed in vac. and passing in the corresponding amount of Cl2; heating in a stream of N2 at 130 °C; removal of formed HCl by a stream of N2;; filtration, distg. off the solvent at 40 °C and 0.5 Torr; recrystn. from petroleum ether; product contains small amounts of higher polymers;;
In further solvent(s); dissolving PCl3 distd. under N2 in (CHCl2)2 distd. under N2; addn. of NH4Cl dryed in vac. and passing in the corresponding amount of Cl2; heating in a stream of N2 at 130 °C; removal of formed HCl by a stream of N2;; filtration, distg. off the solvent at 40 °C and 0.5 Torr; recrystn. from petroleum ether; yield 35-40 %, product contains small amounts of higher polymers;;
35-40
In chlorobenzene;
P<sub>3</sub>N<sub>7</sub>H<sub>12</sub>

P3N7H12

phosphorus trichloride
7719-12-2,52843-90-0

phosphorus trichloride

hydrogenchloride
7647-01-0,15364-23-5

hydrogenchloride

octachlorocyclotetraphosphazene
2950-45-0

octachlorocyclotetraphosphazene

Conditions
Conditions Yield
In not given; reaction with an equimolar amount of PCl3 under formation of P4N4Cl8 and evolution of 2 mol HCl;;
In not given; reaction with an equimolar amount of PCl3 under formation of P4N4Cl8 and evolution of 2 mol HCl;;

2950-45-0 Upstream products

  • 10026-13-8
    10026-13-8

    phosphorus pentachloride

  • 7664-41-7
    7664-41-7

    ammonia

  • 7782-50-5
    7782-50-5

    chlorine

  • 7719-12-2
    7719-12-2

    phosphorus trichloride

2950-45-0 Downstream products

  • 7647-01-0
    7647-01-0

    hydrogenchloride

  • 14700-00-6
    14700-00-6

    octafluorophosphazene

  • 7446-09-5
    7446-09-5

    sulfur dioxide

  • 6710-61-8
    6710-61-8

    2,2,4,4,6,6,8,8-octaisothiocyanato-1,3,5,7-tetraza-2λ5,4λ5,6λ5,8λ5-tetraphosphacycloocta-1,3,5,7-tetraene

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