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About This Item
Linear Formula:
CH3CO3H
CAS Number:
Molecular Weight:
76.05
PubChem Substance ID:
UNSPSC Code:
12352106
Beilstein/REAXYS Number:
1098464
MDL number:
Concentration:
29.0-35% (by sodium thiosulfate, titration), 32 wt. % in dilute acetic acid
Form:
liquid
vapor pressure
20 mmHg ( 25 °C)
Quality Level
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
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
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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
WGK 2
flash_point_f
132.8 °F
flash_point_c
56 °C
Regulatory Information
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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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 269336-100ML | 04061826135044 |
| 269336-500ML | 04061826135051 |
| 269336-5ML | 04061826135068 |



