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Phosphonitrilic chloride trimer

Basic information Safety Supplier Related

Phosphonitrilic chloride trimer Basic information

Product Name:
Phosphonitrilic chloride trimer
Synonyms:
  • PPZ
  • AKOS BBS-00002918
  • 1,3,5-TRIAZA-2,4,6-TRIPHOSPHORIN-2,2,4,4,6,6-HEXACHLORIDE
  • 1,3,5,2,4,6-TRIAZATRIPHOSPHORINE-2,2,4,4,6,6-HEXACHLORIDE
  • 1,3,5,2,4,6-TRIAZATRIPHOSPHORINE,2,2,4,4,6,6-HEXACHLORO-2,2,4,4,6,6-HEXAHYDRO-
  • 2,2,4,4,6,6-HEXACHLORO-1,3,5,2LAMBDA5,4LAMBDA5,6LAMBDA5-TRIAZATRIPHOSPHININE
  • AURORA KA-1096
  • CYCLIC PHOSPHONITRILIC CHLORIDE TRIMER
CAS:
940-71-6
MF:
Cl6N3P3
MW:
347.66
EINECS:
213-376-8
Product Categories:
  • organophosphorus compound
  • API intermediates
Mol File:
940-71-6.mol
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Phosphonitrilic chloride trimer Chemical Properties

Melting point:
112-115 °C(lit.)
Boiling point:
127 °C (13 mmHg)
Density 
1.98 g/mL at 25 °C(lit.)
Water Solubility 
Insoluble in water
solubility 
reacts with H2O
form 
crystal
pka
-12.98±0.10(Predicted)
Specific Gravity
1.98
color 
white
Sensitive 
Moisture Sensitive
CAS DataBase Reference
940-71-6(CAS DataBase Reference)
NIST Chemistry Reference
1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexachloro-2,2,4,4,6,6-hexahydro-(940-71-6)
EPA Substance Registry System
1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexachloro-2,2,4,4,6,6-hexahydro- (940-71-6)
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Safety Information

Hazard Codes 
C
Risk Statements 
14-34-20/21/22
Safety Statements 
26-36/37/39-45-7/8-41
RIDADR 
UN 3260 8/PG 2
WGK Germany 
3
21
TSCA 
Yes
HazardClass 
8
PackingGroup 
II
HS Code 
28530090

MSDS

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Phosphonitrilic chloride trimer Usage And Synthesis

Chemical Properties

white crystalline powder

Uses

Reagent for the synthesis of ″dandelion″ (spherical) dendrimers. Ring-opening polymerization, ligand and/or ligand precursor for transition metals, and the study of P-Cl bond substitution reactions are among the interesting uses for this product.

Preparation

Hexachlorocyclotriphosphazene (PNCl2)3 (mp114 ℃, bp 256℃), which is produced on an industrial scale as the starting material for the manufacture of organosubstituted polyphosphazenes. It forms an almost planar six-membered ring with equal P?N bond lengths.

Purification Methods

Purify it by zone melting, by crystallisation from pet.ether, n-hexane or *benzene, and by sublimation. [van der Huizen et al. J Chem Soc, Dalton Trans 1311 1986, Meirovitch et al. J Phys Chem 88 1522 1984, Alcock et al. J Am Chem Soc 106 5561 1984; Winter & van de Grampel J Chem Soc, Dalton Trans 1269 1986.] Phosphoric acid [7664 -38 -2] M 98.0, m 42.3o, pK 1 2.15, pK 2 7.21, pK 3 12.37. Pyrophosphate can be removed from phosphoric acid by diluting with distilled H2O and refluxing overnight. By cooling to 11o and seeding with crystals obtained by cooling a few millilitres in a Dry-ice/acetone bath, 85% orthophosphoric acid crystallises as H3PO4.H2O. The crystals are collected on a sintered glass filter. [Weber & King Inorg Synth I 101 1939.]

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