214701

Phosphorus pentoxide

ReagentPlus^®, 99%

• Synonyme(s) : Phosphoric anhydride, Phosphorus(V) oxide
• Formule linéaire : P₂O₅
• Numéro CAS: 1314-56-3
• Poids moléculaire : 141.94
• Numéro CE : 215-236-1
• Code UNSPSC : 12352303
• ID de substance PubChem : 24852847
• Nomenclature NACRES : NA.21

Propriétés

• Densité de vapeur: 4.9 (vs air)
• Niveau de qualité: 100
• Pression de vapeur: 1 mmHg ( 384 °C); 10 mmHg ( 238 °C)
• Gamme de produits: ReagentPlus^®
• Pureté: 99%
• Forme: powder
• pH: 1.5 (20 °C, 10 g/L)
• Pf: 340 °C (lit.)
• Densité: 2.3 g/mL at 25 °C (lit.)
• Traces de cations: As: ≤100 mg/kg; Fe: ≤100 mg/kg; heavy metals (as Pb): ≤0.02%
• Chaîne SMILES: 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
• Clé InChI: YWEUIGNSBFLMFL-UHFFFAOYSA-N

Description

Description générale

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.

Application

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.

Informations légales

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Informations sur la sécurité

• Pictogrammes: GHS05
• Mention d'avertissement: Danger
• Mentions de danger: H314
• Conseils de prudence: P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363
• Classification des risques: Eye Dam. 1 - Skin Corr. 1A
• Risques supp: EUH014
• Code de la classe de stockage: 8A - Combustible corrosive hazardous materials
• Classe de danger pour l'eau (WGK): WGK 1
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges