214701

Phosphorus pentoxide

ReagentPlus^®, 99%

• Sinónimos: Phosphoric anhydride, Phosphorus(V) oxide
• Fórmula lineal: P₂O₅
• Número de CAS: 1314-56-3
• Peso molecular: 141.94
• Número CE: 215-236-1
• Número MDL: MFCD00148880
• Código UNSPSC: 12352303
• ID de la sustancia en PubChem: 24852847
• NACRES: NA.21
• Ensayo: 99%
• Formulario: powder

Propiedades

• densidad de vapor: 4.9 (vs air)
• Nivel de calidad: 100
• presión de vapor: 1 mmHg ( 384 °C); 10 mmHg ( 238 °C)
• Línea del producto: ReagentPlus^®
• Ensayo: 99%
• Formulario: powder
• pH: 1.5 (20 °C, 10 g/L)
• mp: 340 °C (lit.)
• densidad: 2.3 g/mL at 25 °C (lit.)
• trazas de catión: As: ≤100 mg/kg; Fe: ≤100 mg/kg; heavy metals (as Pb): ≤0.02%
• cadena 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
• Clave InChI: YWEUIGNSBFLMFL-UHFFFAOYSA-N

Descripción

Descripción general

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.

Aplicación

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.

Información legal

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

Información de seguridad

• Pictogramas: GHS05
• Palabra de señalización: Danger
• Frases de peligro: H314
• Consejos de prudencia: P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363
• Clasificaciones de peligro: Eye Dam. 1 - Skin Corr. 1A
• Riesgos supl.: EUH014
• Código de clase de almacenamiento: 8A - Combustible corrosive hazardous materials
• Clase de riesgo para el agua (WGK): WGK 1
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges