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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:
36-40% (by Na2S2O3, redox titration), 36-40 wt. % in acetic acid
Form:
liquid
InChI
1S/C2H4O3/c1-2(3)5-4/h4H,1H3
SMILES string
CC(=O)OO
InChI key
KFSLWBXXFJQRDL-UHFFFAOYSA-N
form
liquid
reaction suitability
reagent type: oxidant
availability
available only in EU
concentration
36-40% (by Na2S2O3, redox titration), 36-40 wt. % in acetic acid
density
1.13 g/cm3
storage temp.
2-8°C
Quality Level
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Application
Peracetic acid solution may be used as a reaction media to transform phenyldimethylsilyl group to hydroxyl group attached to carbon.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - 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
The Role of Peracetic Acid in Bloodmeal Decoloring.
Hicks TM, et al.
Journal of the American Oil Chemists' Society, 90(10), 1577-1587 (2013)
Peracetic acid oxidation as an alternative pre-treatment for the anaerobic digestion of waste activated sludge.
Appels L, et al.
Bioresource Technology, 102(5), 4124-4130 (2011)
A one-pot conversion of the phenyldimethylsilyl group into a hydroxyl group.
Fleming I and Sanderson PEJ.
Tetrahedron Letters, 28(26), 4229-4232 (1987)
Alberto Baggioli et al.
Physical chemistry chemical physics : PCCP, 15(4), 1130-1140 (2012-12-12)
We examine several computational strategies for the prediction of the (17)O-NMR shielding constants for a selection of organic acids and peracids in aqueous solution. In particular, we consider water (the solvent and reference for the chemical shifts), hydrogen peroxide, acetic
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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