Skip to Content
Merck
All Photos(4)

Key Documents

298220

Sigma-Aldrich

Phosphorus pentoxide

powder, ACS reagent, ≥98.0%

Synonym(s):

Phosphoric anhydride, Phosphorus(V) oxide

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
P2O5
CAS Number:
Molecular Weight:
141.94
EC Number:
UNSPSC Code:
12352303
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

vapor density

4.9 (vs air)

vapor pressure

1 mmHg ( 384 °C)
10 mmHg ( 238 °C)

Assay

≥98.0%

form

powder

impurities

P2O3, passes test (lim. ~0.02%)
≤0.02% insolubles

pH

1.5 (20 °C, 10 g/L)

mp

340 °C (lit.)

density

2.3 g/mL at 25 °C (lit.)

cation traces

NH4+: ≤0.01%
heavy metals (as Pb): ≤0.01%

SMILES string

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

InChI key

YWEUIGNSBFLMFL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

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

Application

Phosphorus pentoxide may be used for the vacuum 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.P8}
  • 1,3-1H-dibenzimidazole-benzene by the reaction of isophthalic acid with 1,2-diaminobenzene.

recommended

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1A

Supplementary Hazards

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals
Royal Society of Chemistry null
Synthesis of poly (benzoxazole) s by direct polycondensation of dicarboxylic acids with 3, 3??dihydroxybenzidine dihydrochloride using phosphorus pentoxide/methanesulfonic acid as condensing agent and solvent.
Ueda M, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 24(5), 1019-1026 (1986)
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)
Kinetics of melting and crystallization of phosphorus pentoxide.
Cormia RL, et al.
Journal of Applied Physics, 34(8), 2239-2244 (1963)
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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service