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902160

Sigma-Aldrich

Phosphorus pentoxide

anhydrous, free-flowing, Redi-Dri, ReagentPlus®, 99%

Sinonimo/i:

Phosphoric anhydride, Phosphorus(V) oxide

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About This Item

Formula condensata:
P2O5
Numero CAS:
Peso molecolare:
141.94
Numero MDL:
Codice UNSPSC:
12352303
ID PubChem:
NACRES:
NA.21

Grado

anhydrous

Densità del vapore

4.9 (vs air)

Tensione di vapore

1 mmHg ( 384 °C)
10 mmHg ( 238 °C)

Nome Commerciale

ReagentPlus®
Redi-Dri

Saggio

99%

Stato

powder

Qualità

free-flowing

pH

1.5 (20 °C, 10 g/L)

Punto di fusione

340 °C (lit.)

Densità

2.3 g/mL at 25 °C (lit.)

Cationi in tracce

As: ≤100 mg/kg
Fe: ≤100 mg/kg
heavy metals (as Pb): ≤0.02%

Stringa SMILE

O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3

InChI

1S/O10P4/c1-11-5-12(2)8-13(3,6-11)10-14(4,7-11)9-12
YWEUIGNSBFLMFL-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Phosphorus pentoxide is a deliquescent compound prepared by reacting phosphorus with air. It is a commonly used as dehydrating and condensing agent in organic synthesis.

Applicazioni

Dehydrating agent used for halogenation with tetrabutylammonium halides.

Process for Producing Halogenated Heteroaryl Compounds
Phosphorus pentachloride has been used for the vaccum distillation of 1-methyl-2-pyrrolidinone (NMP), which was employed as mobile phase in a chromatographic analysis.

It may be used as one of the reaction components in the synthesis of dichlorine heptoxide (Cl2O7) and transition-metal phosphides (Ni2P, Co2P and MoP). P2O5 supported on alumina can be used for the solvent-free and microwave-assisted preparation of 1, 5-benzodiazepine analogs. P2O5/KX (X = Br, I) reagent system may be used for the transformation of alcohols into the corresponding alkyl iodides and bromides.
Phosphorus pentoxide/methanesulfonic acid (PPMA) may be used as a condensing agent and solvent for the synthesis of:
  • High molecular weight poly(benzoxazole)s via direct polycondensation of aromatic dicarboxylic acids containing phenyl ether structure with 3,3′-dihydroxybenzidine dihydrochloride.
  • Aromatic poly(phenylene ether ether ketone)s via direct self-polycondensation of 4-(4′-phenoxyphenoxy)benzoic acids.
  • 1,3-1H-dibenzimidazole-benzene by the reaction of isophthalic acid with 1,2-diaminobenzene.

Note legali

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

Pittogrammi

Corrosion

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Eye Dam. 1 - Skin Corr. 1A

Rischi supp

Codice della classe di stoccaggio

8B - Non-combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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An efficient and selective method for the iodination and bromination of alcohols under mild conditions.
Khazdooz L, et al.
Tetrahedron Letters, 57(2), 168-171 (2016)
Kinetics of melting and crystallization of phosphorus pentoxide.
Cormia RL, et al.
Journal of Applied Physics, 34(8), 2239-2244 (1963)
Synthesis of aromatic poly (ether ketone) s in phosphorus pentoxide/methanesulfonic acid.
Ueda M and Oda M.
Polymer Journal, 21(9), 673-679 (1989)
Mechanical mixtures of metal oxides and phosphorus pentoxide as novel precursors for the synthesis of transition-metal phosphides.
Guo L, et al.
Dalton Transactions, 45(3), 1225-1232 (2016)
Sulfonated polysulfone with 1, 3-1H-dibenzimidazole-benzene additive as a membrane for direct methanol fuel cells.
Fu Y, et al.
Journal of Membrane Science, 310(1), 262-267 (2008)

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