ethane
A
peracetic acid
B
methyl hydroperoxide
C
ethyl hydroperoxide
D
hydroxymethylhydroperoxide
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% |
propane
A
peracetic acid
B
methyl hydroperoxide
C
ethyl hydroperoxide
D
hydroxymethylhydroperoxide
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% |
Conditions | Yield |
---|---|
With dihydrogen peroxide | |
With dihydrogen peroxide | |
With potassium hydroxide; dihydrogen peroxide man saeuert 10-stdg. Schuetteln mit Schwefelsaeure an und destilliert das zwischen 90grad und 100grad uebergegangene Destillat wird mit Kalilauge versetzt und im Vakuum konzentriert darauf saeuert man abermals an und destilliert ueber; | |
With potassium hydroxide; dihydrogen peroxide In water Heating; |
Conditions | Yield |
---|---|
With dihydrogen peroxide |
Conditions | Yield |
---|---|
With oxygen at 25℃; Irradiation.mit UV-Licht <253.7 nm; Quecksilber-Sensibilisierung>; | |
With AuPd; dihydrogen peroxide In water at 21℃; under 750.075 Torr; for 1h; |
Conditions | Yield |
---|---|
With diethyl ether; oxygen at -75℃; |
Conditions | Yield |
---|---|
With hydrogen; fluorine at -63.1 - 89.9℃; Rate constant; Irradiation; investigated by flash photolysis-time-resolved UV spectroscopy; |
ethane
A
methanol
B
formaldehyd
C
formic acid
D
ethene
E
ethyl hydroperoxide
F
acetaldehyde
Conditions | Yield |
---|---|
With nitrogen; oxygen; chlorine at 298℃; under 700 Torr; for 4h; Product distribution; Irradiation; |
azoethane
A
ethanol
B
ethyl hydroperoxide
C
diethyl peroxide
D
carbon dioxide
E
carbon monoxide
F
acetaldehyde
Conditions | Yield |
---|---|
With nitrogen; oxygen at 298℃; under 700 Torr; for 0.416667h; Product distribution; Irradiation; |
Conditions | Yield |
---|---|
With dihydrogen peroxide |
Conditions | Yield |
---|---|
With hydroperoxyl at -63.1 - 89.9℃; Rate constant; Mechanism; Irradiation; investigated by flash photolysis-time-resolved UV spectroscopy; | |
With HO2 at 24.84℃; under 75 Torr; Kinetics; Further Variations:; Pressures; Temperatures; |
ethylperoxy radical
A
ethanol
B
ethyl hydroperoxide
C
acetaldehyde
Conditions | Yield |
---|---|
With oxygen In gaseous matrix Kinetics; Mechanism; Irradiation; in nitrogen-atmosphere; variation of oxygen pressure; |
Conditions | Yield |
---|---|
With oxygen In gaseous matrix Product distribution; Mechanism; Kinetics; Irradiation; in nitrogen-atmosphere; variation of oxygen pressure; |
ethane
A
ethanol
B
ethene
C
ethyl hydroperoxide
D
acetaldehyde
Conditions | Yield |
---|---|
With oxygen; chlorine at 255.9℃; under 1000 Torr; Product distribution; Kinetics; Mechanism; Irradiation; ΔH(excit.), variation of pressure; |
ethyl radical
A
ethanol
B
ethene
C
ethyl hydroperoxide
D
acetaldehyde
Conditions | Yield |
---|---|
With oxygen at 255.9℃; under 1000 Torr; Product distribution; Kinetics; Mechanism; ΔH(excit.), variation of pressure; |
ethane
A
ethanol
B
ethyl hydroperoxide
C
acetaldehyde
D
acetic acid
Conditions | Yield |
---|---|
With 2-pyrazylcarboxylic acid; air; dihydrogen peroxide; [n-Bu4N]VO3 In acetonitrile at 40 - 75℃; Product distribution; Mechanism; | |
With dihydrogen peroxide; chromic acid In acetonitrile at 60℃; under 22501.8 Torr; for 1h; Product distribution; | |
With 2-pyrazylcarboxylic acid; C30H34N4O10V2; dihydrogen peroxide In water; acetonitrile at 50℃; under 7600.51 Torr; for 6h; Catalytic behavior; Kinetics; Time; Autoclave; Overall yield = 10 %; |
Conditions | Yield |
---|---|
With air; tris(μ-oxo)di[(1,4,7-trimethyl-1,4,7-triazanonane)manganese(IV)] hexafluorophosphate; dihydrogen peroxide; acetic acid In acetonitrile at 0℃; under 750.06 Torr; for 21h; Product distribution; Mechanism; | |
With dihydrogen peroxide; iron(III) perchlorate In acetonitrile at 25℃; under 20252 Torr; for 3h; Product distribution; Further Variations:; Catalysts; |
Conditions | Yield |
---|---|
at 40 - 200℃; Kinetics; |
1-(ethylperoxy)ethanol
water
A
ethyl hydroperoxide
B
acetaldehyde
Conditions | Yield |
---|---|
With HO2 In gas at -25.1℃; under 760 Torr; Kinetics; up to 480 K; |
diperoxyterephthalic acid diethyl ester
water
A
ethyl hydroperoxide
B
terephthalic acid
diperoxyterephthalic acid diethyl ester
A
ethyl hydroperoxide
B
terephthalic acid
Ethyl peroxybenzoate
ethyl hydroperoxide
Conditions | Yield |
---|---|
With bis(tri-n-butyltin)oxide In diethyl ether at -10℃; for 12h; |
Conditions | Yield |
---|---|
With 2-pyrazylcarboxylic acid; dihydrogen peroxide; [Fe2(HPTB)(μ-OH)(NO3)2](NO3)2*CH3OH*2H2O In acetonitrile at 25℃; under 22501.8 Torr; for 6h; Product distribution; | |
With AuPd; dihydrogen peroxide In water at 21℃; under 750.075 Torr; for 1h; Time; | |
With oxygen at 35℃; for 2h; Temperature; Irradiation; Autoclave; |
Conditions | Yield |
---|---|
With oxygen; chlorine In methanol Product distribution; Further Variations:; Solvents; |
(tetraphenylporphyrin)(germanium(IV))(ethylhydroperoxide)2
A
dihydroxo(meso-tetraphenylporphyrinato)germanium(IV)
B
ethyl hydroperoxide
Conditions | Yield |
---|---|
With water In benzene water is added to benzene soln. of TPPGe(OOCH2CH3)2; detected by NMR spectroscopy; |
(tetraphenylporphyrin)(germanium(IV))(OOCH2CH3)(CH2CH3)
A
(tetraphenylporphyrin)(germanium(IV))(Cl)(CH2CH3)
B
ethyl hydroperoxide
Conditions | Yield |
---|---|
With hydrogen chloride treatment of TPPGe(OOCH2CH3)(CH2CH3) with hydrogen chloride; (1)H-NMR; |
dihydroxo(meso-tetraphenylporphyrinato)germanium(IV)
ethyl hydroperoxide
(tetraphenylporphyrin)(germanium(IV))(ethylhydroperoxide)2
Conditions | Yield |
---|---|
In diethyl ether; dichloromethane soln. of ethyl hydroperoxide in ether is added to TPPGe(OH)2 dissolved in dichloromethane in a darkened room, stirring for 5 min; solvent is removed (vac.); (1)H-NMR; | 92% |
Conditions | Yield |
---|---|
With Petroleum ether |
formaldehyd
diethyl ether
ethyl hydroperoxide
ethylperoxy-methanol
Conditions | Yield |
---|---|
reagiert analog mit Acetaldehyd und Propionaldehyd; |
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With cis-nitrous acid |
Conditions | Yield |
---|---|
at 170 - 200℃; bei langsamer Zersetztung; |
ethyl hydroperoxide
2-ethoxy-1-methyl-6,8-dinitro-1,2-dihydro-quinoline
ethyl-(1-methyl-6,8-dinitro-1,2-dihydro-[2]quinolyl)-peroxide
Conditions | Yield |
---|---|
With acetic acid; benzene |
Conditions | Yield |
---|---|
With sodium hydroxide at 50 - 60℃; |
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With diethyl ether |
ethyl hydroperoxide
propionic acid
methylammonium carbonate
Conditions | Yield |
---|---|
in Gegenwart von Mohrschem Salz; |
formaldehyd
ethyl hydroperoxide
dimethyl amine
ethylperoxymethyl-dimethyl-amine
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
With potassium hydroxide anfangs unter Kuehlung, dann bei 70grad; | |
With potassium hydroxide |
Conditions | Yield |
---|---|
With diethyl ether |
ethyl hydroperoxide
isopentyl nitrite
A
ethyl nitrate
B
i-Amyl alcohol
ethyl hydroperoxide
isopentyl nitrite
A
ethyl nitrate
B
pentan-1-ol
Conditions | Yield |
---|---|
With catalase In water at 25℃; Kinetics; Mechanism; |
Conditions | Yield |
---|---|
(TMP)Fe(III)OH In (2)H8-toluene for 12h; Mechanism; | A 11 % Spectr. B 72 % Spectr. |
Molecular Structure of Ethyl hydroperoxide (CAS NO.3031-74-1):
IUPAC: Hydroperoxyethane
Molecular Formula:C2H6O2
Molecular Weight:62.0678
Density:0.948 g/cm3
Flash Point:11.3oC
Boiling Point:95oC at 760 mmHg
SMILES:O(O)CC
InChI:InChI=1/C2H6O2/c1-2-4-3/h3H,2H2,1H3
InChIKey:ILHIHKRJJMKBEE-UHFFFAOYAS
Index of Refraction:1.364
Molar Volume:65.4 cm3
Surface Tension:26.2 dyne/cm
Molar Refractivity:14.59 cm3
Enthalpy of Vaporization:39.01 kJ/mol
Vapour Pressure:27.4 mmHg at 25oC
Explodes violently when superheated. The barium salt is heat- and impact-sensitive. Explosive reaction with hydroiodic acid or finely divided silver. When heated to decomposition it emits acrid smoke and irritating fumes. See also PEROXIDES, INORGANIC; PEROXIDES, ORGANIC.
DOT Classification: Forbidden
Ethyl hydroperoxide with cas registry number of 3031-74-1 is also known as Hydroperoxide, ethyl ; Ethyl hydrogen peroxide . It is stable under normal temperatures and pressures but it also should be stored in a tightly closed container when not in use and stored in a cool, dry place. Ethyl hydroperoxide with cas registry number of 3031-74-1 is used as a pharmaceutical intermediate. It can be used to produce singlet molecular oxygen by decomposition.
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