Peroxyacetic acid supplier

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Name
Peroxyacetic acid
EINECS 201-186-8
CAS No. 79-21-0
Article Data221
CAS DataBase
Density 1.216 g/cm³
Solubility soluble in water, ethanol, ethyl ether, sulfuric acid
Melting Point - 44 °C
Formula C₂H₄O₃
Boiling Point 119.123 °C at 760 mmHg
Molecular Weight 76.052
Flash Point 54.931 °C
Transport Information UN 3109 5.2
Appearance colourless liquid with an acrid odour
Safety 26-36/37/39-45-61-3/7-23-14-60-9
Risk Codes 7-20/21/22-35-50-10
Molecular Structure
Hazard Symbols O,C,N
Synonyms Percidin 535;Perethanoic acid;Proxitane 12A;Proxitane 15;Proxitane 4002;Steridial P;Tsunami 100;Acetic peroxide;Agrosteril 110;Estosteril;LCAP;Osbon AC;Oxigreen010;Ozonit;Peraclean Ocean;
PSA 46.53000
LogP 0.02250

Synthetic route

: 64-19-7
acetic acid

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With KU-2 cation exchanger; dihydrogen peroxide In 1,4-dioxane at 30℃; for 3h;	99.3%
With Pyridine-2,6-dicarboxylic acid; phosphoric acid; dihydrogen peroxide In Isopropyl acetate; 1-Propyl acetate at 80℃; under 675.068 Torr; for 5h; Catalytic behavior; Reagent/catalyst; Temperature; Solvent; Pressure;	93%
With sulfuric acid; dihydrogen peroxide at 25 - 30℃; for 24h;	60%

: 75-07-0
acetaldehyde

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With iron(III)-acetylacetonate; oxygen In acetone at 60℃; under 2250.23 Torr;	84%
Bei der Autoxydation in Gegenwart oder Abwesenheit von Katalysatoren;
With oxygen

: 108-24-7
acetic anhydride

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With sulfuric acid; dihydrogen peroxide In water at 30 - 70℃; for 0.0533333h; Flow reactor;	76.7%
With dihydrogen peroxide; acetic acid at 35 - 40℃;
With dihydrogen peroxide

: 142-92-7
1-hexyl acetate

A: 79-21-0
peracetic acid

B: 111-27-3
hexan-1-ol

Conditions

Conditions	Yield
With dihydrogen peroxide; cation exchanger KU-2 x 8 In 1,4-dioxane at 29.9℃; Rate constant; Kinetics; Equilibrium constant; other temperature, other ratio;	A 72% B n/a

: 628-63-7
1-pentyl acetate

A: 79-21-0
peracetic acid

B: 71-41-0
pentan-1-ol

Conditions

Conditions	Yield
With dihydrogen peroxide; cation exchanger KU-2 x 8 In 1,4-dioxane at 29.9℃; Rate constant; Kinetics; Equilibrium constant; other temperature, other ratio;	A 68% B n/a

: 123-86-4
acetic acid butyl ester

A: 79-21-0
peracetic acid

B: 71-36-3
butan-1-ol

Conditions

Conditions	Yield
With dihydrogen peroxide; cation exchanger KU-2 x 8 In 1,4-dioxane at 29.9℃; Rate constant; Kinetics; Equilibrium constant; other temperature, other ratio;	A 65% B n/a

: 109-60-4
1-Propyl acetate

A: 71-23-8
propan-1-ol

B: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With dihydrogen peroxide; cation exchanger KU-2 x 8 In 1,4-dioxane at 29.9℃; Rate constant; Kinetics; Equilibrium constant; other temperature, other ratio;	A n/a B 63%

: 141-78-6
ethyl acetate

A: 79-21-0
peracetic acid

B: 64-17-5
ethanol

Conditions

Conditions	Yield
With dihydrogen peroxide; cation exchanger KU-2 x 8 In 1,4-dioxane at 29.9℃; Rate constant; Kinetics; Equilibrium constant; other temperature, other ratio;	A 61% B n/a
With Pseudomonas fluorescens esterase; dihydrogen peroxide In aq. buffer pH=6.5; Kinetics; Reagent/catalyst; Enzymatic reaction;

: 10543-57-4
N,N,N',N'-tetraacetylethylenediamine

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With dihydrogen peroxide; sodium carbonate; sodium hydroxide In water	52.56%
With dihydrogen peroxide In water

: 79-20-9
acetic acid methyl ester

A: 67-56-1
methanol

B: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With dihydrogen peroxide; cation exchanger KU-2 x 8 In 1,4-dioxane at 29.9℃; Rate constant; Kinetics; Equilibrium constant; other temperature, other ratio;	A n/a B 48%
With pseudomonas fluorescens esterase L29P-PFE; dihydrogen peroxide; sodium bromide at 23℃; pH=6.5; Kinetics; Concentration; Reagent/catalyst; Enzymatic reaction;

: 74-84-0
ethane

A: 79-21-0
peracetic acid

B: 3031-73-0
methyl hydroperoxide

C: 3031-74-1
ethyl hydroperoxide

D: 15932-89-5
hydroxymethylhydroperoxide

Conditions

Conditions	Yield
With nitrogen; oxygen; chlorine at 24.85℃; under 760 Torr; for 0.5h; Kinetics; Oxidation; Photolysis;	A 2% B 6.2% C 10.2% D 0.4%

...Expand

: 74-98-6
propane

A: 79-21-0
peracetic acid

B: 3031-73-0
methyl hydroperoxide

C: 3031-74-1
ethyl hydroperoxide

D: 15932-89-5
hydroxymethylhydroperoxide

Conditions

Conditions	Yield
With nitrogen; oxygen; chlorine at 24.85℃; under 760 Torr; for 0.333333h; Kinetics; Oxidation; Photolysis;	A 0.1% B 3.39% C 0.61% D 0.14%

...Expand

: 591-49-1
1-methylcyclohex-1-ene

A: 79-21-0
peracetic acid

B: 3031-73-0
methyl hydroperoxide

C: 15932-89-5
hydroxymethylhydroperoxide

Conditions

Conditions	Yield
With ozone under 787.563 Torr; Product distribution; Criegee cleavage;	A 0.19% B 0.95% C 0.007%

...Expand

: 80-56-8, 177698-18-9
Pinene

A: 79-21-0
peracetic acid

B: 3031-73-0
methyl hydroperoxide

C: 15932-89-5
hydroxymethylhydroperoxide

Conditions

Conditions	Yield
With ozone under 787.563 Torr; Product distribution; Criegee cleavage;	A 0.39% B 0.71% C 0.089%

...Expand

: 110-86-1
pyridine

: 7416-48-0
1-hydroxyethyl ethaneperoxoate

: 71-43-2
benzene

A: 79-21-0
peracetic acid

B: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
at 25℃; under 110 Torr;

...Expand

: 463-51-4
Ketene

A: 79-21-0
peracetic acid

B: 110-22-5
diacetyl peroxide

Conditions

Conditions	Yield
With dihydrogen peroxide

: 110-22-5
diacetyl peroxide

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With dihydrogen peroxide
With water Hydrolysis;
With dihydrogen peroxide In water at 25℃; Rate constant; carbonate, borate and phosphate buffers;

: 644-31-5
acetyl benzoyl peroxide

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With water

: 108-24-7
acetic anhydride

: 64-19-7
acetic acid

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With sulfuric acid; dihydrogen peroxide at 35 - 40℃;

: 75-07-0
acetaldehyde

A: 79-21-0
peracetic acid

B: 64-19-7
acetic acid

Conditions

Conditions	Yield
With water; oxygen; cobalt ions at 25 - 35℃; Mechanism; other concentration of water, other temperature;
With oxygen at 15℃; under 759811 Torr; Product distribution; Rate constant; study of the effects of ultrasound intensity, external pressure, and temperature on the oxidation of acetaldehyde under cavitation conditions;
With tetrachloromethane; ozone at -20℃;
With tetrachloromethane; ozone at -30℃;
With ozone at -10℃;

: 75-36-5
acetyl chloride

A: 79-21-0
peracetic acid

B: 110-22-5
diacetyl peroxide

Conditions

Conditions	Yield
With dihydrogen peroxide

: 123-86-4
acetic acid butyl ester

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With sulfuric acid; dihydrogen peroxide In 1,4-dioxane; nitrobenzene at 50℃; for 9h; Thermodynamic data; Kinetics; different mixtures of solvents, 20 - 40 deg C, ΔH(excit.),ΔS(excit.), ΔG(excit.);

: 10543-57-4
N,N,N',N'-tetraacetylethylenediamine

A: 79-21-0
peracetic acid

B: 137706-80-0
N,Ν,Ν'-triacetylenediamine

Conditions

Conditions	Yield
With 1,2-ethanediylbistetraphosphonic acid; dihydrogen peroxide at 25℃; Rate constant; pH 9.60 (carbonate buffer);

: 137706-80-0
N,Ν,Ν'-triacetylenediamine

A: 79-21-0
peracetic acid

B: 871-78-3
N,N'-diacetylethylenediamine

Conditions

Conditions	Yield
With 1,2-ethanediylbistetraphosphonic acid; dihydrogen peroxide at 25℃; Kinetics; Thermodynamic data; various pH values (carbonate buffer), other temperatures; ΔH(excit.), ΔS(excit.);

: 90584-32-0
1,1-Dichloroethyl hydroperoxide

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With water In chloroform-d1 at 0℃; for 0.166667h; Mechanism; Dioxane-d8, -10 deg C;

: 75-07-0
acetaldehyde

A: 79-21-0
peracetic acid

B: 34557-54-5
methane

C: 124-38-9
carbon dioxide

D: 201230-82-2
carbon monoxide

E: 64-19-7
acetic acid

Conditions

Conditions	Yield
With oxygen In water Rate constant; accelerated by ultrasound;

...Expand

: 141-78-6
ethyl acetate

A: 79-21-0
peracetic acid

B: 108-24-7
acetic anhydride

C: 75-07-0
acetaldehyde

D: 64-19-7
acetic acid

E: α-Acetoxy-α-hydroperoxyethanol

Conditions

Conditions	Yield
With air at 120℃; under 10500.8 Torr; Product distribution; Mechanism; Other temperature;

...Expand

: 75-36-5
acetyl chloride

: 79-21-0
peracetic acid

Conditions

Conditions	Yield
With peroxide anion In 1,4-dioxane; water at 22℃; Rate constant; pH=12.7; different reagent concentrations;

: 78-93-3
butanone

A: 79-21-0
peracetic acid

B: 18428-20-1
3-hydroperoxy-butan-2-one

C: 513-86-0, 52217-02-4
3-hydroxy-2-butanon

D: 75-07-0
acetaldehyde

E: 64-19-7
acetic acid

F: 431-03-8
dimethylglyoxal

Conditions

Conditions	Yield
With air at 123℃; under 11025.9 Torr; for 0.583333h; Product distribution;

...Expand

: 79-21-0
peracetic acid

: 407-25-0
trifluoroacetic anhydride

: acetylperfluoroacetyl peroxide

Conditions

Conditions	Yield
In dichloromethane at -20℃;	100%

: 79-21-0
peracetic acid

: 1345824-05-6
dimethyl 2,2'-((2-iodo-5-1,3-phenylene)bis(oxy))diacetate

: 1345824-00-1
C16H19IO10

Conditions

Conditions	Yield
In acetic acid at 20℃; for 24h;	100%

: 79-21-0
peracetic acid

: 64-19-7
acetic acid

: 2,2’-diiodo-4,4’,6,6’-tetramethylbiphenyl

: 1257076-22-4
1,3,9,11-tetramethyl-5λ3,7λ3-dibenzo[d,f][1,3,2]diiodaoxepine-5,7-diyl diacetate

Conditions

Conditions	Yield
In acetonitrile at 20℃;	100%

...Expand

: 79-21-0
peracetic acid

: 496-78-6
2,4,5-trimethylphenol

A: 13038-87-4
2,3,5-trimethyl-1,6-benzoquinone

B: 69305-42-6
1-acetoxy-2,4,5-trimethylbenzene

C: 4537-09-1
1,4-dimethoxy-2,3,5-trimethyl-benzene

D: 21573-38-6
1-methoxy-2,4,5-trimethylbenzene

: 5-acetoxy-2,4-dihydroxy-2,4,5-trimethyl-3,6-lacto-1-hexanoic acid

Conditions

Conditions	Yield
sulfuric acid at 50℃; for 0.5h; Mechanism; Thermodynamic data; effect of catalysts;	A n/a B 0.03% C 0.07% D 0.07% E 99.76%

...Expand

: 79-21-0
peracetic acid

: 2416-94-6
2,3,6-trimethylphenol

A: 935-92-2
2,3,5-Trimethyl-1,4-benzoquinone

B: 527-17-3, 70128-24-4
Duroquinone

C: 700-13-0
Trimethylhydroquinone

D: 2819-86-5
pentamethylphenol

E: 21573-36-4
1-methoxy-2,3,6-trimethylbenzene

F: 62687-45-0
2,3,6-trimethylphenyl acetate

Conditions

Conditions	Yield
sulfuric acid at 50℃; for 0.5h; Mechanism; Thermodynamic data; effect of catalysts;	A 99.7% B 0.04% C 0.01% D 0.01% E 0.03% F 0.04%

...Expand

: 79-21-0
peracetic acid

: 700-13-0
Trimethylhydroquinone

A: 935-92-2
2,3,5-Trimethyl-1,4-benzoquinone

B: 4537-09-1
1,4-dimethoxy-2,3,5-trimethyl-benzene

C: 7479-28-9
2,3,5-trimethyl-1,4-hydroquinone diacetate

D: 36592-62-8
4-acetoxy-2,3,5-trimethylphenol

E: 130422-86-5
4-methoxy-2,3,5-trimethylphenol

F: 1-acetoxy-4-methoxy-2,3,5-trimethylbenzene

Conditions

Conditions	Yield
sulfuric acid at 50℃; for 0.5h; Mechanism; Thermodynamic data; effect of catalysts;	A 99.5% B 0.05% C 0.06% D 0.05% E 0.04% F 0.07%

...Expand

: 79-21-0
peracetic acid

: 108-94-1
cyclohexanone

: 502-44-3
hexahydro-2H-oxepin-2-one

Conditions

Conditions	Yield
at 60℃; under 150.015 Torr; for 4h; Pressure;	99.2%
With acetone
at 50℃; for 0.13h; Temperature;

: 79-21-0
peracetic acid

: 109323-90-2
(1'R,3S)-3-<1'-<(tert-butyldimethylsilyl)oxy>ethyl>azetidin-2-one

: 76899-07-5, 78963-47-0, 78963-48-1, 78963-60-7, 80951-41-3, 81275-02-7, 85647-75-2, 85954-95-6, 92217-74-8, 104527-11-9, 76855-69-1
(3R,4R)-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-acetoxyazetidin-2-one

Conditions

Conditions	Yield
With Ru-carbon; sodium acetate; acetic acid In ethyl acetate for 2.5h; Ambient temperature;	99%
With Ru-carbon; sodium acetate; acetic acid In ethyl acetate for 2.5h; Product distribution; Ambient temperature; other amides and lactams; other catalyst;	99%
With sodium acetate; acetic acid; cobalt(II) chloride In ethyl acetate at 0 - 40℃; for 3.5h; Reagent/catalyst; Temperature;	91%
With Ru/C; sodium acetate; acetic acid

: 79-21-0
peracetic acid

: 1255651-99-0
(2R,2'R)-dimethyl 2,2'-((2-iodo-1,3-phenylene)bis(oxy))dipropanoate

: 1255651-84-3
dimethyl-2,2'-((2-(diacetoxy-λ3-iodanyl)-1,3-phenylene)bis(oxy))(2R,2'R)-dipropionate

Conditions

Conditions	Yield
In acetic acid at 20℃;	99%

: 79-21-0
peracetic acid

: 625-38-7
but-3-enoic acid

: 19405-98-2, 128032-77-9, 138666-02-1
(S)-β-acetoxy-γ-butyrolactone

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid In acetic acid at 20℃; Cooling with ice;	99%

: 79-21-0
peracetic acid

: 1399008-27-5
N,N'-((2S,2'S)-((2-iodo-1,3-phenylene)bis(oxy))bis(propane-2,1-diyl))bis-(2,4,6-trimethylbenzamide)

: 1399009-21-2
C36H45IN2O8

Conditions

Conditions	Yield
With acetic acid at 25℃; for 9h;	99%
With acetic acid at 20℃;	94%

: 79-21-0
peracetic acid

: 608-28-6
2,6-dimethyliodobenzene

: 123084-61-7
(2,6-dimethylphenyl)-λ3-iodanediyl diacetate

Conditions

Conditions	Yield
In acetic acid at 20℃; for 20h;	99%
With acetic anhydride; acetic acid at -10 - 20℃;	69%

: 79-21-0
peracetic acid

: 27920-90-7
3-acetoxymethyl-7(R)-glutaroylaminoceph-3-em-4-carboxylic acid

: 61122-49-4
3-acetoxymethyl-7(R)-glutaroylaminoceph-3-em-4-carboxylic acid 1(S)-oxide

Conditions

Conditions	Yield
In isopropyl alcohol at 2 - 4℃; Industrial scale;	98%

: 79-21-0
peracetic acid

: 591-80-0
pent-4-enoic acid

: 5904-80-3, 79580-69-1, 112607-21-3, 112709-12-3
(5-oxotetrahydrofuran-2-yl)methyl acetate

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid In acetic acid at 20℃; Cooling with ice;	97%

: 79-21-0
peracetic acid

: 2-iodo-N-tosylbenzimidamide

: 3-(tosylimino)-2,3-dihydro-1H-1λ3-benzo[d][1,2]iodazol-1-yl acetate

Conditions

Conditions	Yield
In acetic acid at 0 - 30℃; for 2h; Inert atmosphere;	97%

: 79-21-0
peracetic acid

: 625-99-0
3-iodochlorobenzene

: 16308-17-1
(3-chlorophenyl)iodanediyl diacetate

Conditions

Conditions	Yield
at 4 - 30℃;	96%
at 30℃; for 12h;	92%

: 79-21-0
peracetic acid

: 97363-07-0, 101977-85-9, 101977-86-0, 106399-95-5, 106399-96-6, 106399-63-7
(2S,3S)-3-((R)-1-((tert-butyldimethylsilyl)oxy)ethyl)-1-(4-methoxyphenyl)-4-oxoazetidine-2-carboxylic acid

: 3-[(R)-1-tert-butyldimethylsiloxyethyl]-4-acetoxy-1-(4-methoxyphenyl)-2-azetidinone

Conditions

Conditions	Yield
With dicyclohexyl-carbodiimide In dichloromethane at 0 - 5℃; Temperature; Solvent;	96%

: 79-21-0
peracetic acid

: 24569-89-9
1,3-dehydroadamantane

: 1-Adamantyl peracetate

Conditions

Conditions	Yield
In diethyl ether for 0.5h; Ambient temperature;	95%

: 930-21-2
2-azetidinone

: 79-21-0
peracetic acid

: 28562-53-0
4-acetoxy azetidinone

Conditions

Conditions	Yield
With Ru-carbon; sodium acetate; acetic acid In ethyl acetate for 2.5h; Ambient temperature;	94%

: 79-21-0
peracetic acid

: 857502-04-6
ethyl 6-(4-iodophenoxy)hexanoate

: 857502-14-8
ethyl 6-(4-diacetoxyiodophenoxy)hexanoate

Conditions

Conditions	Yield
In dichloromethane at 0 - 20℃; for 2h;	94%
In dichloromethane	40%

: 79-21-0
peracetic acid

: 3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-azetidin-2-one

: 4-acetoxy-3-[(1R)-(tert-butyldimethylsilyloxy)-ethyl]-azetidin-2-one

Conditions

Conditions	Yield
With ruthenium trichloride In dichloromethane; acetic acid; acetonitrile at 0℃;	93.3%

: 79-21-0
peracetic acid

: 615-37-2
ortho-methylphenyl iodide

: 31599-59-4
2-(diacetoxyiodo)toluene

Conditions

Conditions	Yield
for 0.383333h;	93%
With acetic anhydride; acetic acid at -10 - 20℃;	65%

: 79-21-0
peracetic acid

: 625-95-6
3-Iodotoluene

: 19169-97-2
m-(diacetoxyiodo)toluene

Conditions

Conditions	Yield
In acetic acid at 20℃; for 20h;	93%
With acetic anhydride; acetic acid at -10 - 20℃;	83%
In acetic acid at 0 - 20℃;	46%
In diethyl ether; acetic acid for 2h; Ambient temperature; 1.) below 10 deg C, 1 h, 2.) r.t., 2 h;
With acetic acid

: 79-21-0
peracetic acid

: 64-19-7
acetic acid

: 109-75-1
but-3-enenitrile

: 98593-85-2
3,4-diacetoxybutyronitrile

Conditions

Conditions	Yield
C22H26ClN3O2Pd at 25℃; for 8h;	93%

...Expand

: 79-21-0
peracetic acid

: (2R,2’R)-2,2’-((2-iodo-1,3-phenylene)bis(oxy))bis(N,N-diisopropylpropanamide)

: 64-19-7
acetic acid

: (2,6-bis(((R)-1-(diisopropylamino)-1-oxopropan-2-yl)oxy)phenyl)-λ3-iodanediyl diacetate

Conditions

Conditions	Yield
In acetonitrile at 20℃; for 18h; Inert atmosphere;	93%

...Expand

: 79-21-0
peracetic acid

: 591-50-4
iodobenzene

: 3240-34-4
[bis(acetoxy)iodo]benzene

Conditions

Conditions	Yield
With acetic acid for 4h;	92%
With acetic acid at 23℃; for 7h;	92%
With sulfuric acid; dihydrogen peroxide; acetic acid In water 1.) 29-31 deg C, 65 min; 2.) 0 deg C, 75 min;	88.8%
With acetic acid at 20℃;

: 79-21-0
peracetic acid

: 4,5-diacetyl-2,7,9,9-tetramethylxanthen

: 64-19-7
acetic acid

: 858717-40-5
4,5-diacetoxy-2,7,9,9-tetramethylxanthen

Conditions

Conditions	Yield
at 35℃; for 19h; Baeyer-Villiger Oxidation;	92%

...Expand

: 79-21-0
peracetic acid

: 87281-08-1
(2R)-N,N-dibenzyl-2-chloropropan-1-amine

: 1126795-32-1
(2S)-2-[(dibenzylamino)oxy]propyl acetate

Conditions

Conditions	Yield
Stage #1: peracetic acid; (2R)-N,N-dibenzyl-2-chloropropan-1-amine In dichloromethane; acetic acid at 0℃; for 1.5h; Stage #2: With silver nitrate; triethylamine In dichloromethane; acetic acid at 0℃; for 3h; optical yield given as %ee;	92%

Peroxyacetic acid History

The United States Environmental Protection Agency first registered peracetic acid as an antimicrobial in 1985 for indoor use on hard surfaces.

Peroxyacetic acid Consensus Reports

EPA Extremely Hazardous Substances List. Community Right-To-Know List. Reported in EPA TSCA Inventory.

Peroxyacetic acid Standards and Recommendations

DFG MAK: Very strong skin effects; Confirmed Animal Carcinogen with Unknown Relevance to Humans
DOT Classification: 5.1; Label: Oxidizer, Corrosive (UN3149)

Peroxyacetic acid Specification

The Peroxyacetic acid, with the CAS registry number 79-21-0, is also known as Acetyl hydroperoxide. It belongs to the product category of Aliphatics. Its EINECS number is 201-186-8. This chemical's molecular formula is C₂H₄O₃ and molecular weight is 76.05. What's more, its systematic name is Ethaneperoxoic acid. Its classification codes are: (1)Agricultural Chemical; (2)Anti-Infective Agents; (3)Disinfectants; (4)Germicide, bactericide, disinfectant; (5)Noxae; (6)Oxidants; (7)Skin / Eye Irritant; (8)Tumor data. This chemical is a liquid that functions as a strong oxidizing agent. It has an acrid odor and is used as a disinfectant. It should be sealed and stored in a cool, ventilated and dry place. Moreover, it should be protected from oxides, heat and fire. The main use of peracetic acid is for the industrial synthesis of epoxides. Peracetic acid is an ideal antimicrobial agent due to its high oxidizing potential. It can be used over a wide temperature range (0–40 °C), over a wide pH range (3.0–7.5), in clean-in-place (CIP) processes, in hard water conditions, and is not affected by protein residues.

Physical properties of Peroxyacetic acid are: (1)ACD/LogP: -0.301; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -0.30; (4)ACD/LogD (pH 7.4): -0.38; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 16.30; (8)ACD/KOC (pH 7.4): 13.51; (9)#H bond acceptors: 3; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 46.53 Å²; (13)Index of Refraction: 1.384; (14)Molar Refractivity: 14.624 cm³; (15)Molar Volume: 62.537 cm³; (16)Polarizability: 5.798×10^-24cm³; (17)Surface Tension: 36.0019989013672 dyne/cm; (18)Density: 1.216 g/cm³; (19)Flash Point: 54.931 °C; (20)Enthalpy of Vaporization: 41.643 kJ/mol; (21)Boiling Point: 119.123 °C at 760 mmHg; (22)Vapour Pressure: 7.90700006484985 mmHg at 25°C.

Preparation: this chemical can be prepared by acetic acid butyl ester at the temperature of 29.9 °C. This reaction will need reagent H₂O₂ and solvent dioxane. This reaction will also need catalyst cation exchanger KU-2 x 8. The yield is about 65%.

Peroxyacetic acid can be prepared by acetic acid butyl ester at the temperature of 29.9 °C

Uses of Peroxyacetic acid: it can be used to produce 4-acetoxy-azetidin-2-one at the ambient temperature. It will need reagents 5% Ru-C, AcONa, AcOH and solvent ethyl acetate with the reaction time of 2.5 hours. The yield is about 94%.

Peroxyacetic acid can be used to produce 4-acetoxy-azetidin-2-one at the ambient temperature

When you are using this chemical, please be cautious about it as the following:
This chemical is harmful by inhalation, in contact with skin and if swallowed. It is flammable and may cause fire and severe burns. The substance is very toxic to aquatic organisms. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. When using it, you need wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, you must seek medical advice immediately (show the label where possible). This material and its container must be disposed of as hazardous waste. You should avoid releasing it to the environment just refering to special instructions/safety data sheet. You must keep the container tightly closed in a cool and well-ventilated place. You should not breathe gas/fumes/vapour/spray (appropriate wording to be specified by the manufacturer).

You can still convert the following datas into molecular structure:
(1)SMILES: CC(=O)OO
(2)Std. InChI: InChI=1S/C2H4O3/c1-2(3)5-4/h4H,1H3
(3)Std. InChIKey: KFSLWBXXFJQRDL-UHFFFAOYSA-N

The toxicity data is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Source
guinea pig	LD50	oral	10mg/kg (10mg/kg)	SPI Bulletin. Vol. 1/75-19B.
mouse	LD50	intravenous	17860ug/kg (17.86mg/kg)	Yaoxue Tongbao. Bulletin of Pharmacology. Vol. 23, Pg. 345, 1988.
mouse	LD50	oral	210mg/kg (210mg/kg)	Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 48(6), Pg. 28, 1983.
rabbit	LD50	skin	1410uL/kg (1.41mL/kg)	Union Carbide Data Sheet. Vol. 12/12/1968.
rat	LC50	inhalation	450mg/m³ (450mg/m³)	Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 48(6), Pg. 28, 1983.
rat	LD50	oral	1540uL/kg (1.54mL/kg)	Union Carbide Data Sheet. Vol. 12/12/1968.

Product Name

Peroxyacetic acid

Synthetic route

Peroxyacetic acid History

Peroxyacetic acid Consensus Reports

Peroxyacetic acid Standards and Recommendations

Peroxyacetic acid Specification

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