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230286

Sigma-Aldrich

Phosphonitrilic chloride trimer

99%

Synonym(s):

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

Linear Formula:
(NPCl2)3
CAS Number:
940-71-6
Molecular Weight:
347.66
EC Number:
213-376-8
MDL number:
MFCD00006474
UNSPSC Code:
12162002
PubChem Substance ID:
24853791
NACRES:
NA.23

Assay

99%

form

solid

mp

112-115 °C (lit.)

density

1.98 g/mL at 25 °C (lit.)

SMILES string

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

InChI key

UBIJTWDKTYCPMQ-UHFFFAOYSA-N

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Application

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.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Supplementary Hazards

EUH014

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
David K Y Lee et al.
Dalton transactions (Cambridge, England : 2003), 39(22), 5341-5348 (2010-05-05)
Two novel cyclic phosphazenes with asymmetric spiro rings were synthesized via reactions of hexachlorocyclotriphosphazene with chiral amino alcohol residues. The reactions showed preferential formation of the cis isomer possibly due to the delocalization of the lone pair electrons of the
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
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