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8.07471

Sigma-Aldrich

Polyphosphoric acid

for synthesis

Sinonimo/i:

Polyphosphoric acid, PPA

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About This Item

Formula condensata:
HO[P(OH)(O)O](n)H
Numero CAS:
Numero MDL:
Codice UNSPSC:
12352301
Numero indice EU:
232-417-0
NACRES:
NA.22

Tensione di vapore

2 hPa ( 20 °C)

Livello qualitativo

Saggio

83-87% P2O5 basis (acidimetric)

Forma fisica

viscous liquid

P. eboll.

530 °C/1013 hPa

Punto di fusione

-20 °C

Densità

2.06 g/cm3 at 20 °C

Temperatura di conservazione

2-30°C

InChI

1S/O5P2.H3O4P/c1-2-7-4-3-6(1)5-7;1-5(2,3)4/h;(H3,1,2,3,4)
FVYIVXLIMHNYTD-UHFFFAOYSA-N

Descrizione generale

Polyphosphoric acid (PPA) is a strong mineral acid that combines orthophosphoric acid and linear phosphoric acids. It is widely used in organic synthesis because of its powerful dehydrating properties, low nucleophilicity of the phosphoric acid media, good solvation power, relatively mild acidity, and low oxidation potential. Even though PPA is a significantly weaker acid than H2SO4, it demonstrates 100% dehydration rate.

Applicazioni

Polyphosphoric acid (PPA) can be used as a reagent:
  • In acylation and alkylation reactions.
  • To synthesize cyclic aromatic compounds via cyclization of aromatic acids, esters, ketones, aldehydes, acetals, alcohols, and alkenes.
  • In Bischler−Napieralski reaction to construct isoquinoline ring system from phenethylformamides.
  • To prepare substituted indoles at position-2 from hydrazones via Fisher indole synthesis.
  • For the conversion of oximes into amides via Beckmann rearrangement.

PPA can also be used as a catalyst to synthesize:
  • Aniline derivatives by Lossen rearrangement of aromatic carboxylic acids with nitromethane.
  • Amides by hydrolysis nitriles.
  • Dimethyl carbonate (DMC) from urea and methanol.
  • Benzofurans by cyclization of α-phenoxy ketones.

PPA is also used with other reagents for various organic transformations. For example:
  • PPA/Ethanethiol mixture can be used to selectively open one epoxide in bis-epoxy steroid.
  • PPA/POCl3 catalytic mixture used to convert tertiary alcohols into corresponding chlorides.
  • PPA/acetic acid is used to synthesize nonenolizable β-diketones.
  • PPA/potassium iodide mixture used to convert primary methyl ether to a primary alkyl iodide.
  • PPA/nitric acid catalytic combination used for nitration reactions which is less hazardous than Ac2O/HNO3 mixtures.

Risultati analitici

Assay (acidimetric, calc. as P₂O₅): 83.0 - 87.0 %
Due to its specific melting range the product may be solid, liquid, a solidified melt or a supercooled melt.

Pittogrammi

Corrosion

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Codice della classe di stoccaggio

8B - Non-combustible, corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

does not flash

Punto d’infiammabilità (°C)

does not flash


Certificati d'analisi (COA)

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I clienti hanno visto anche

Synthesis of dimethyl carbonate from urea and methanol using polyphosphoric acid as catalyst
Sun Jianjun, et al.
J. Mol. Catal. A: Chem., 239(1-2), 82-86 (2005)
Polyphosphoric Acid
Dodd, John H
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)

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