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Merck
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Documenti

230286

Sigma-Aldrich

Phosphonitrilic chloride trimer

99%

Sinonimo/i:

1,3,5,2,4,6-Triazatriphosphorine-2,2,4,4,6,6-hexachloride, 1,3,5-Triaza-2,4,6-triphosphorin-2,2,4,4,6,6-hexachloride, Hexachlorocyclotriphosphazene

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About This Item

Formula condensata:
(NPCl2)3
Numero CAS:
940-71-6
Peso molecolare:
347.66
Numero CE:
213-376-8
Numero MDL:
MFCD00006474
Codice UNSPSC:
12162002
ID PubChem:
24853791
NACRES:
NA.23

Saggio

99%

Forma fisica

solid

Punto di fusione

112-115 °C (lit.)

Densità

1.98 g/mL at 25 °C (lit.)

Stringa SMILE

Clp1(Cl)np(Cl)(Cl)np(Cl)(Cl)n1

InChI

1S/Cl6N3P3/c1-10(2)7-11(3,4)9-12(5,6)8-10
UBIJTWDKTYCPMQ-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

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.

Pittogrammi

Corrosion
GHS05

Avvertenze

Danger

Indicazioni di pericolo

H314

Classi di pericolo

Skin Corr. 1B

Rischi supp

EUH014

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

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Ji-Yeon Seong et al.
International journal of pharmaceutics, 314(1), 90-96 (2006-03-22)
Biocompatible and thermosensitive poly(organophosphazenes) with a lower critical solution temperature (LCST) below body temperature have been designed with the aim for the local delivery of peptide and protein drugs. These polymers could be synthesized by introducing short chain tri- or
Studies on the reaction of hexachlorocyclotriphosphazene and 2-hydroxyethyl methacrylate and on the physical properties of its polymer.
M Anzai et al.
The Journal of Nihon University School of Dentistry, 26(2), 109-118 (1984-06-01)
Tam T T Bui et al.
Chirality, 17(8), 438-443 (2005-08-13)
The gem-disubstituted cyclotriphosphazene 1 reacted with piperazine (pip) to give the piperazine-bridged derivative 2, which is expected to exist in meso and racemic forms because the two PCl (pip) groups are stereogenic. The proton-decoupled (31)P NMR spectrum of 2 gave
S Paasch et al.
Solid state nuclear magnetic resonance, 4(5), 267-280 (1995-07-01)
The present study deals with solid-state nuclear magnetic resonance (NMR) investigations on hexachlorocyclotriphosphazene (N3P3Cl6) and T and K form of octachlorocyclotetraphosphazene (N4P4Cl8). Using 31P NMR we have recorded spectra of different magic-angle spinning (MAS) frequencies and static powder spectra. By
Hiroyoshi Kawakami et al.
Artificial organs, 26(10), 883-890 (2002-09-26)
We investigated biodegradation and biocompatibility of poly(organophosphazenes). We prepared poly(organophosphazenes) having different side chain groups. The blood compatibility of poly(organophosphazenes) containing fluorinated side groups, poly(bis[trifluoroethoxy]phosphazene) (PbFP) and poly([trifluoroethoxy][ethyl glycinate]phosphazene) (PFGP), without heparinization were evaluated in vitro. The deformation and aggregation
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