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线性分子式:
CH3CO3H
化学文摘社编号:
分子量:
76.05
UNSPSC Code:
12352106
NACRES:
NA.21
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1098464
Concentration:
38.5-41.5% (iodometric, redox titration), ~39% in acetic acid (RT)
Form:
liquid
InChI key
KFSLWBXXFJQRDL-UHFFFAOYSA-N
SMILES string
CC(=O)OO
InChI
1S/C2H4O3/c1-2(3)5-4/h4H,1H3
grade
purum
form
liquid
shelf life
limited shelf life, expiry date on the label
reaction suitability
reagent type: oxidant
concentration
38.5-41.5% (iodometric, redox titration), ~39% in acetic acid (RT)
impurities
≤6% H2O2, ~45% acetic acid
refractive index
n20/D 1.391
density
1.15 g/mL at 20 °C
storage temp.
2-8°C
Quality Level
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General description
本品为乙酸中过氧乙酸的 39% 溶液。过氧乙酸具有抗菌、抗真菌和杀菌的特性,因此被广泛用于污水消毒。
Application
过氧乙酸可通过 Prilezhaev 反应合成环氧乙烷(环氧化物)。
Disclaimer
The product is not intended for use as a biocide under global biocide regulations, including but not limited to US EPA′s Federal Insecticide Fungicide and Rodenticide Act, European Biocidal Products Regulation, Canada’s Pest Management Regulatory Agency, Turkey’s Biocidal Products Regulation, Korea’s Consumer Chemical Products and Biocide Safety Management Act (K-BPR) and others.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 3 - Org. Perox. D - Skin Corr. 1A - STOT SE 3
target_organs
Respiratory system
存储类别
5.2 - Organic peroxides and self-reacting hazardous materials
wgk
WGK 2
flash_point_f
132.8 °F - closed cup
flash_point_c
56 °C - closed cup
法规信息
新产品
此项目有
Mehmet Kitis
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Eagleson M.
Concise Encyclopedia Chemistry, 743-743 (1994)
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Journal of endodontics, 38(9), 1197-1201 (2012-08-16)
The goal of this study was to evaluate the efficiencies of different irrigation solutions in the removal of calcium hydroxide (CH). Forty-eight maxillary central incisor teeth were used. Root canals were prepared with the ProTaper system (Dentsply Maillefer, Baillagues, Switzerland).
Anabella Ivancich et al.
Biochemistry, 52(41), 7271-7282 (2013-09-21)
Catalase-peroxidases or KatGs can utilize organic peroxyacids and peroxides instead of hydrogen peroxide to generate the high-valent ferryl-oxo intermediates involved in the catalase and peroxidase reactions. In the absence of peroxidatic one-electron donors, the ferryl intermediates generated with a low
Arnaud Bridier et al.
PloS one, 7(9), e44506-e44506 (2012-09-14)
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