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269336

Sigma-Aldrich

Peracetic acid solution

32 wt. % in dilute acetic acid

Sinónimos:

Peroxyacetic acid

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About This Item

Fórmula lineal:
CH3CO3H
Número de CAS:
79-21-0
Peso molecular:
76.05
Beilstein/REAXYS Number:
1098464
MDL number:
MFCD00002128
UNSPSC Code:
12352106
PubChem Substance ID:
329752891

vapor pressure

20 mmHg ( 25 °C)

Quality Level

100

form

liquid

composition

acetic acid, 40-45%

reaction suitability

reagent type: oxidant

concentration

29.0-35% (by sodium thiosulfate, titration)
32 wt. % in dilute acetic acid

impurities

<6.0% hydrogen peroxide

refractive index

n20/D 1.3876

pH

<1

density

1.13 g/mL at 25 °C

shipped in

wet ice

storage temp.

2-8°C

SMILES string

CC(=O)OO

InChI

1S/C2H4O3/c1-2(3)5-4/h4H,1H3

InChI key

KFSLWBXXFJQRDL-UHFFFAOYSA-N

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General description

Peracetic acid (PAA) is a peroxy acid that is commonly used as an excellent oxidizing agent in organic synthesis. It is also used as a bleaching and sterilizing agent.

Application

Peracetic acid solution (32 wt. % in dilute acetic acid) can be used as an oxidant for the selective epoxidation of aliphatic terminal alkenes in the presence of manganese(II) perchlorate as the catalyst at ambient temperature. It is also used to oxidize sulfides, selenides, and amines.

Features and Benefits

  • Easily synthesized
  • Environmentally benign reagent

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Org. Perox. D - Skin Corr. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

5.2 - Organic peroxides and self-reacting hazardous materials

wgk_germany

WGK 2

flash_point_f

132.8 °F

flash_point_c

56 °C

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Ultrasound-assisted MnO2 catalyzed homolysis of peracetic acid for phenol degradation: The assessment of process chemistry and kinetics.
Rokhina EV, et al.
Chemical Engineering Journal, 276, 91-96 (2015)
Eagleson M.
Concise Encyclopedia Chemistry, 894-894 (1994)
Mi Li et al.
Biotechnology for biofuels, 10, 237-237 (2017-12-08)
Hydrothermal pretreatment using liquid hot water (LHW) is capable of substantially reducing the cell wall recalcitrance of lignocellulosic biomass. It enhances the saccharification of polysaccharides, particularly cellulose, into glucose with relatively low capital required. Due to the close association with
Hyeonjun Hong et al.
Materials science & engineering. C, Materials for biological applications, 103, 109837-109837 (2019-07-28)
Compressed collagen is a promising scaffold for corneal stroma analogue due to its facile incorporation of keratocytes while mimicking the mechanical niche of a native cornea with dense collagen fibrillar structures. However, it does not offer the sufficient biochemical niche
Xinqiang Xie et al.
Nucleic acids research, 40(18), 9115-9124 (2012-07-10)
Diverse bacteria contain DNA with sulfur incorporated stereo-specifically into their DNA backbone at specific sequences (phosphorothioation). We found that in vitro oxidation of phosphorothioate (PT) DNA by hydrogen peroxide (H(2)O(2)) or peracetic acid has two possible outcomes: DNA backbone cleavage
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