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Merck
CN

8.22287

Hydrogen peroxide solution

30%, (stabilized) for synthesis

别名:

Hydrogen peroxide solution, Perhydrol

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经验公式(希尔记法):
H2O2
化学文摘社编号:
分子量:
34.01
NACRES:
NA.22
UNSPSC Code:
12352304
MDL number:
Beilstein/REAXYS Number:
3587191
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产品名称

过氧化氢 溶液, (stabilized) for synthesis

InChI

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

SMILES string

OO

InChI key

MHAJPDPJQMAIIY-UHFFFAOYSA-N

grade

synthesis grade

vapor pressure

18 hPa ( 20 °C)
23.3 mmHg ( 30 °C)

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

Quality Level

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Analysis Note

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

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.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1

存储类别

5.1B - Oxidizing hazardous materials

wgk

WGK 1

flash_point_f

not combustible

flash_point_c

not combustible

法规信息

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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)
Oxidation of sulfides to sulfoxides and sulfones with 30% hydrogen peroxide under organic solvent-and halogen-free conditions
Sato K, et al.
Tetrahedron, 57(13), 2469-2476 (2001)
Handling hydrogen peroxide oxidations on a Large Scale: synthesis of 5-bromo-2-nitropyridine
Agosti A, et al.
Organic Process Research & Development, 21(3), 451-459 (2017)
A Practical Method for Epoxidation of Terminal Olefins with 30 Hydrogen Peroxide under Halide-Free Conditions.
Kazuhiko Sato et al.
The Journal of organic chemistry, 61(23), 8310-8311 (1996-11-15)

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