298220
Phosphorus pentoxide
powder, ACS reagent, ≥98.0%
Synonym(s):
Phosphoric anhydride, Phosphorus(V) oxide
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About This Item
Linear Formula:
P2O5
CAS Number:
Molecular Weight:
141.94
EC Number:
MDL number:
UNSPSC Code:
12352303
PubChem Substance ID:
NACRES:
NA.21
Assay:
≥98.0%
Grade:
ACS reagent
Form:
powder
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
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.
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.
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1A
Supplementary Hazards
Storage Class Code
8A - 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
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