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Key Documents

8.22287

Sigma-Aldrich

Hydrogen peroxide solution

30%, (stabilized) for synthesis

Synonym(s):

Hydrogen peroxide solution, Perhydrol

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About This Item

Empirical Formula (Hill Notation):
H2O2
CAS Number:
Molecular Weight:
34.01
Beilstein:
3587191
MDL number:
UNSPSC Code:
12352304
NACRES:
NA.22

product name

Hydrogen peroxide 30%, (stabilized) for synthesis

vapor pressure

18 hPa ( 20 °C)
23.3 mmHg ( 30 °C)

Quality Level

form

liquid

reaction suitability

reagent type: oxidant

pH

2-4 (20 °C in H2O)

bp

107 °C/1013 hPa

mp

-26 °C

density

1.11 g/cm3 at 20 °C

storage temp.

2-25°C

SMILES string

OO

InChI

1S/H2O2/c1-2/h1-2H

InChI key

MHAJPDPJQMAIIY-UHFFFAOYSA-N

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Application

Hydrogen peroxide 30% can be used as an oxidizing agent:
  • To synthesize 5-bromo-2-nitropyridine from 5-bromo-2-aminopyridine in the presence of H2SO4.
  • For the oxidation of aromatic and aliphatic sulfides to sulfoxides or sulfones.
  • For the epoxidation of terminal olefins using a mixture of Na2WO4 dihydrate, (aminomethyl)phosphonic acid, and methyltrin-octylammonium hydrogensulfate.
  • To prepare adipic acid via oxidation of cyclohexanone and cyclohexanol in the presence of H2WO4 as a catalyst.
  • To convert cyclopentanone to δ-valerolactone via Baeyer−Villiger-oxidation in the presence of a solid acid catalyst.

Analysis Note

Assay (manganometric): 29.0 - 31.0 %
Density (d 20/4): 1.11 - 1.12 g/cm³

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Dam. 1

Storage Class Code

5.1B - Oxidizing hazardous materials

WGK

WGK 1

Flash Point(F)

not combustible

Flash Point(C)

not combustible


Certificates of Analysis (COA)

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Baeyer-Villiger-oxidation of cyclopentanone with aqueous hydrogen peroxide by acid heterogeneous catalysis
Fischer J and Holderich WF
Applied Catalysis A: General, 180(1-2), 435-443 (1999)
A green method of adipic acid synthesis: organic solvent-and halide-free oxidation of cycloalkanones with 30% hydrogen peroxide
Usui Y and Sato K
Green Chemistry, 5(4), 373-375 (2003)

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