2,2,4,4,6,6-hexaamino-2,2,4,4,6,6-hexahydro-1,3,5,2,4,6-triazatriphosphorine

Q: What is the CAS number for 2,2,4,4,6,6-hexaamino-2,2,4,4,6,6-hexahydro-1,3,5,2,4,6-triazatriphosphorine?

The CAS number of 2,2,4,4,6,6-hexaamino-2,2,4,4,6,6-hexahydro-1,3,5,2,4,6-triazatriphosphorine is 13597-92-7.

Factory Sells Best Quality 2,2,4,4,6,6-hexaamino-2,2,4,4,6,6-hexahydro-1,3,5,2,4,6-triazatriphosphorine 13597-92-7 with ISO standards

Molecular Formula:H12N9 P3
Molecular Weight:231.077
PKA:0.01±0.50(Predicted)
PSA：222.63000
Density:3.83g/cm³
LogP:2.09940

2,2,4,4,6,6-hexaamino-2,2,4,4,6,6-hexahydro-1,3,5,2,4,6-triazatriphosphorine(Cas 13597-92-7) Usage

General Description

2,2,4,4,6,6-hexaamino-2,2,4,4,6,6-hexahydro-1,3,5,2,4,6-triazatriphosphorine, also known as HAPT, is a chemical compound with the molecular formula C6H24N6P3. It is a nitrogen and phosphorus-containing compound that has potential application as a flame retardant. HAPT has been studied for its ability to reduce the flammability and smoke generation of various polymers, making it a promising candidate for use in the construction, transportation, and electronics industries. Additionally, it has been investigated for its potential use in the development of environmentally friendly flame retardants due to its low toxicity and potential for biodegradation. Overall, HAPT shows promise as a novel flame retardant with potential benefits for a range of industries.

InChI:InChI=1/H12N9P3/c1-10(2)7-11(3,4)9-12(5,6)8-10/h1-6H2

13597-92-7 Relevant articles

X-ray crystal structures and DFT calculations of differently charged aminocyclophosphazenes

Vorontsov, Ivan I.,Tur, Dzidra R.,Papkov, Vladimir S.,Antipin, Mikhail Yu.

, p. 1 - 11 (2009)

Molecular structures of hexakis(amino)cy...

Phosphazene compound, composite containing phosphazene compound, flame retardant containing composite and application

-

Paragraph 0364-0365; 0368; 0369, (2019/01/23)

The invention relates to a phosphazene c...

Nitrido-Sodalites. II. Synthesis, Crystal Structure, and Properties of M(6+(y/2)-x)H(2x)[P12N24]Z(y) with M=Fe, Co, Ni, Mn; Z=Cl, Br, I; 0<=x<=4; y<=2

Schnick, W.,Stock, N.,Luecke, J.,Volkmann, M.,Jansen, M.

, (2008/10/08)

The nitrido sodalites M(6+(y/2)-x)H(2x)[...

Hydrolysis pathways for aminophosphazenes

Allcock,Fuller,Matsumura

, p. 515 - 521 (2008/10/08)

The hydrolysis behavior of the aminocycl...

13597-92-7 Process route

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

: 7664-41-7
ammonia

: 13597-92-7
hexaaminocyclotriphosphazene

Conditions

Conditions	Yield

In neat (no solvent); react. of liquid NH3 with (PNCl2)3;;
In not given; react. of NH3 with (PNCl)3 in an organic solvent;;
In not given; react. of liquid NH3 with (PNCl2)3;;
In not given; react. of NH3 with (PNCl)3 in an organic solvent;;
In neat (no solvent); react. of liquid NH3 with (PNCl2)3;;
In diethyl ether; according to D.B.Sowerby, L.F.Audrieth, Chem. Ber. 94 (1961) 2670; addn.soln. of (PNCl2)3 to liquid NH3 at -40°C;;
In neat (no solvent, solid phase); N3P3Cl6 reacted with liq. NH3, held at -33°C for 24 h; NH3 decanted, residue washed with MeOH, dried at 75°C in vac. 1.38 Pa; elem. anal.;
In tetrahydrofuran; methanol; at 0 - 5 ℃; for 20h; Inert atmosphere;

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

: 7664-41-7
ammonia

: 13597-92-7
hexaaminocyclotriphosphazene

: ammonium chloride

Conditions

Conditions	Yield
In neat (no solvent); direct react. of (PNCl2)3 with a large excess of liquid NH3 under pressure; react. completed after 48 h;;	36%
In neat (no solvent); direct react. of (PNCl2)3 with a large excess of liquid NH3 under pressure; react. completed after 48 h;;	36%
In benzene; passing gaseous NH3 in a soln. of (NPCl2)3 in C6H6 for a longer period of time; formation of a mixt. of P3N3(NH2)6 and NH4Cl;;
In diethyl ether; addn. of a soln. of (PNCl2)3 in ether to an excess of liquid NH3; stirring the formed soln. at ambient temp. for some h;; removal of by-product NH4Cl by extraction with liquid NH3 or on heating the react. product in CHCl3 with diethylamine;;
In diethyl ether; addn. of a soln. of (PNCl2)3 in ether to an excess of liquid NH3; stirring the formed soln. at ambient temp. for some h;; removal of by-product NH4Cl by extraction with liquid NH3 or on heating the react. product in CHCl3 with diethylamine;;
In benzene; passing gaseous NH3 in a soln. of (NPCl2)3 in C6H6 for a longer period of time; formation of a mixt. of P3N3(NH2)6 and NH4Cl;;