CAS No.7722-84-1,Hydrogen peroxide Suppliers,MSDS download

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Synthetic route

: 931-88-4, 22770-27-0, 3958-30-3
1,2-cyclooctene

A: 638-54-0
1,8-octanedial

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With oxygen; ozone In acetic acid at 16℃;	A n/a B 100%
With oxygen; ozone; Fe-(ll)-Kat In acetic acid at 16℃;	A n/a B 74%
With oxygen; ozone; Mn-(ll)-Kat In acetic acid at 16℃;	A n/a B 71%

: 80937-33-3
oxygen

: 65-85-0
benzoic acid

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With (CH3(CH2)3)4NClO4; 1-methylimidazole In dichloromethane Electrolysis; electrolysis (10-30 min) of O2 in CH2Cl2-0.1 M Bu4NClO4 soln. in presence of 0.1 M benzoic acid and 1-methylimidazole, working electrode: polymer-coated (poly-(Ru(vbpy)3)(2+)) glassy-carbon, reference electrode: Ag/Ag(1+), potential -1.3 and -1.1 V; extn. with distd. H2O, colorimetric analysis;	100%
With (CH3(CH2)3)4NClO4 In dichloromethane Electrolysis; electrolysis (10-30 min) of O2 in CH2Cl2-0.1 M Bu4NClO4 soln. in presence of 0.1 M benzoic acid, working electrode: polymer-coated (poly-(Ru(vbpy)3)(2+)) glassy-carbon, reference electrode: Ag/Ag(1+), potential -1.3 V; extn. with distd. H2O, colorimetric analysis;	99%
With (CH3(CH2)3)4NClO4; 1-methylimidazole In dichloromethane Electrolysis; electrolysis (10-30 min) of O2 in CH2Cl2-0.1 M Bu4NClO4 soln. in presence of 0.1 M benzoic acid and 1-methylimidazole, working electrode: polymer-coated (poly-(Ru(vbpy)3)(2+)) glassy-carbon, reference electrode: Ag/Ag(1+), potential -1.0 V; extn. with distd. H2O, colorimetric analysis;	97%

: 80937-33-3
oxygen

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With perchloric acid In water at 20℃; Reagent/catalyst; Electrochemical reaction;	100%
With N21,N22-dimethyl-2,3,7,8,12,13,17,18-octaphenyl-5,10,15,20-tetrakis(4-trifluoromethylphenyl)porphyrin; trifluoroacetic acid In water; acetonitrile at 20℃; for 0.5h; Catalytic behavior; Solvent; Reagent/catalyst; Concentration;	100%
With diphenyl hydrazine In ethanol 0°C;;	97%

: tetra-n-butylammonium hydroxide

: 10507-76-3
tris(benzene-1,2-dithiolate)molybdenum(VI)

A: tris(benzene-1,2-dithiolato)molybdenum(IV)(2-)

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In tetrahydrofuran Kinetics; not isolated, detected by UV;	A 100% B n/a

...Expand

: tetra-n-butylammonium hydroxide

: 10507-76-3
tris(benzene-1,2-dithiolate)molybdenum(VI)

A: tris(benzene-1,2-dithiolato)molybdenum(V)(1-)

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In tetrahydrofuran Kinetics; not isolated, detected by UV;	A 100% B n/a

...Expand

: 7601-90-3
perchloric acid

: 80937-33-3
oxygen

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With C57H42CoFe3N4 at 20℃; Catalytic behavior; Reagent/catalyst; Electrochemical reaction;	100%
With catalyst: Ba/carbon In perchloric acid aq. HClO4; Electrochem. Process; electroreduced on Ba/carbon in 0.1 M HClO4 (1 bar, 21+/-0.5°C, 1.2 V vs. RHE);
With catalyst: Ce/carbon In perchloric acid aq. HClO4; Electrochem. Process; electroreduced on Ce/carbon in 0.1 M HClO4 (1 bar, 21+/-0.5°C, 1.2 V vs. RHE);

: 18406-93-4
1,4-bis(trimethylsilyl)-2-methyl-1,4-cyclohexadiene

: 80937-33-3
oxygen

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In acetonitrile at 20℃; under 760.051 Torr; for 16h; Solvent;	98%

: dipotassium peroxodisulfate

: 7664-93-9
sulfuric acid

: 7732-18-5
water

A: 7646-93-7
potassium hydrogensulfate

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In sulfuric acid hydrolysis by heating; simultaneous distn. (by H2O vapor);; distn.; 40-60% aq. soln. of H2O2;;	A n/a B 95%
In sulfuric acid aq. H2SO4; hydrolysis by heating; simultaneous distn. (by H2O vapor);; distn.; 40-60% aq. soln. of H2O2;;	A n/a B 95%
In sulfuric acid hydrolysis by heating; simultaneous distn. (by H2O vapor);; distn.;;	A n/a B 92%

...Expand

: (bis(2-pyridylmethyl)(2-quinolylmethyl)amine)(triphenylphosphino)copper(I) hexafluorophosphate * 0.25 diethylether

A: (μ-1,2-peroxo)bis(bis(2-pyridylmethyl)(2-quinolylmethyl)amine)copper(II) bis(hexafluorophosphate)

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With HBF4Et2O In further solvent(s) HBF4Et2O is added to a soln. of copper dioxygen compound in propionitrile at -80°C, mixt. is stirred for 15 min;; ether is added, ppt. is allowed to settle, supernatant is transferred toa soln. of KI in distd. H2O and EtCOOH, ppt. is washed (ether) and supernatant is transferred again, mixt. containing KI is stirred for 15 min at room temp. and titrated (Na2S2O3);	A 94% B n/a

Yield

With HBF4*Et2O In further solvent(s) HBF4*Et2O is added to a soln. of copper dioxygen compound in propionitrile at -80°C, mixt. is stirred for 15 min;; ether is added, ppt. is allowed to settle, supernatant is transferred toa soln. of KI in distd. H2O and EtCOOH, ppt. is washed (ether) and supernatant is transferred again, mixt. containing KI is stirred for 15 min at room temp. and titrated (Na2S2O3);

A 94%
B n/a

: 80937-33-3
oxygen

: potassium hydroxide

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With N-doped carbon nanoflowers Reagent/catalyst; Electrochemical reaction;	94%
In water Electrochemical reaction;	41.5%
With nitrogen doped porous carbon nanoparticle derived from zeolitic imidazolate framework Reagent/catalyst; Electrochemical reaction;	14%

: 1333-74-0
hydrogen

: 80937-33-3
oxygen

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In sulfuric acid Electrolysis; oxyhydrogen gas-cel; electrolyt: 0.5 n H2SO4; electrode spaces separated by a clay-diaphragma; electrodes: platinated Pt calcinated for 2 1/2 h at 1200-1400°C; 1 mA current strength; reaction time: 45 min; ice cooling;;	93.5%
In sulfuric acid aq. H2SO4; Electrolysis; oxyhydrogen gas-cel; electrolyt: 0.5 n H2SO4; electrode spaces separated by a clay-diaphragma; electrodes: platinated Pt calcinated for 2 1/2 h at 1200-1400°C; 1 mA current strength; reaction time: 45 min; ice cooling;;	93.5%
In sulfuric acid Electrolysis; oxyhydrogen gas-cel; electrolyt: 0.5 n H2SO4; electrode spaces separated by a clay-diaphragma; electrodes: platinated Pt calcinated for 2 1/2 h at 1200-1400°C; 2 mA current strength; reaction time: 45 min; ice cooling;;	86.3%

: 50981-12-9, 10193-30-3
sulfuric acid monohydrate

: ammonium sulfate-hydrogen peroxide(1/1)

A: 7722-86-3
caro's acid

B: 7722-84-1
dihydrogen peroxide

C: 13445-49-3
Marshall's acid

Conditions

Conditions	Yield
without water, -10°C;	A 93.5% B 1.4% C 5.1%
without water, -10°C;	A 93.5% B 1.4% C 5.1%

...Expand

: 7647-14-5
sodium chloride

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In water Electrolysis; spark electrolysis of a 0.1n NaCl solution below 10°C, 40 mA under O2;;	90%
In water Electrolysis; spark electrolysis of a 0.1n NaCl solution below 10°C, 40 mA under O2;;	90%
In water Electrolysis; spark electrolysis of a 0.1n NaCl solution below 10°C, 40 mA under H2;;	80%
In water Electrolysis; spark electrolysis of a 0.1n NaCl solution below 10°C, 40 mA under H2;;	80%

: (bis(2-quinolylmethyl)(2-pyridylmethyl)amine)(triphenylphosphino)copper(I) hexafluorophosphate * 0.25 diethylether

A: 155311-10-7
(bis(2-quinolylmethyl)(2-pyridylmethyl)amine)(triphenylphosphino)copper(I) perchlorate

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With HBF4Et2O In further solvent(s) HBF4Et2O is added to a soln. of copper dioxygen compound in propionitrile at -80°C, mixt. is stirred for 15 min; ether is added, ppt. is allowed to settle, supernatant is transferred toa soln. of KI in distd. H2O and EtCOOH, ppt. is washed (ether) and supernatant is transferred again, mixt. containing KI is stirred for 15 min at room temp. and titrated (Na2S2O3);	A 89% B n/a

Yield

With HBF4*Et2O In further solvent(s) HBF4*Et2O is added to a soln. of copper dioxygen compound in propionitrile at -80°C, mixt. is stirred for 15 min; ether is added, ppt. is allowed to settle, supernatant is transferred toa soln. of KI in distd. H2O and EtCOOH, ppt. is washed (ether) and supernatant is transferred again, mixt. containing KI is stirred for 15 min at room temp. and titrated (Na2S2O3);

A 89%
B n/a

: hexafluorophosphoric acid

: {Cu2(XYL-O)(O2)}(1+)

A: C36H40Cu2N6O3(2+)

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In diethyl ether; dichloromethane to a soln. of Cu-complex in CH2Cl2 at -80°C under Ar (generated in situ from (((C5H4NCH2CH2)2NCH2)2(C6H3O)Cu2)PF6 and O2) was added 10 equiv. HPF6/Et2O (purple soln. instantly turned blue), mixt. stirred 15 min; addn. Et2O, pptn., washed (ether);	A n/a B 88%

...Expand

: {{(((2-pyridyl)CH2CH2)2NCH2)2C6H3O}(peroxo)dicopper(II)}(1+)

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With HBF4 or HPF6 React. with excess HBF4 or HPF6.;	88%

: 7647-01-0
hydrogenchloride

: 187034-69-1
[RhCl(O2)(2,6-(C(Me)=NiPr)2C5H3N)]

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In water detd. by iodometry;	88%

: 7647-01-0
hydrogenchloride

: 943218-68-6
[(6-t-butyl-phenyl-2-pyridylmethyl)bis(2-pyridylmethyl)amine)Cu(I)]B(C6F5)4

: 80937-33-3
oxygen

A: [(6-t-butyl-phenyl-2-pyridylmethyl)bis(2-pyridylmethyl)amine)Cu(II)Cl]2(B(C6F5)4)2

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In diethyl ether under Ar; O2 bubbled through soln. of Cu complex in Et2O at -80°Cfor 10 s; excess O2 removed; HCl in Et2O added at -80°C; stirred for 30 min; warmed to room temp.; distd. H2O added; stirred at room temp. for 1 h; Et2O layer washed with pentane; ppt. recrystd. from THF-pentane; vac. dried; elem. anal.;	A 85% B 80%

...Expand

: ((tris{(2-pyridyl)methyl}amine)Cu(II))2O2(PF6)2

A: tris{(2-pyridyl)methyl}amineCu(II)(CH3CN)(PF6)2

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With 2HPF6*Et2O -80°C;;	A 77% B 81%

: 7732-18-5
water

A: 7722-84-1
dihydrogen peroxide

B: 80937-33-3
oxygen

Conditions

Conditions	Yield
With sodium persulfate; tris(bipyridine)ruthenium(II) dichloride hexahydrate In aq. buffer for 2h; pH=10; pH-value; Irradiation; Inert atmosphere; Darkness;	A 8.8% B 80%
With anthracene; cerium(IV) In sulfuric acid Electrochem. Process; the discharge of electrochemically generated holes at an anthracene/water interface at 400 μA cm**-2 in 0.28 M Ce(4+) in 12 M H2SO4;
With air; carbon nanodots-Co3O4-Fe2O3 photoanode pH=13.6; Irradiation; Electrochemical reaction;
With tetrakis(N-methy.4-pyridyl) porphyrin copper tetrakis(trifluoromethanesulfonate) In aq. phosphate buffer pH=7; Electrolysis;

: Pb(OH)3(1-)*Na(1+)=NaPb(OH)3

A: sodium hexahydroxoplumbate(IV)

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With oxygen In sodium hydroxide Irradiation (UV/VIS); photolysis (254 nm) of an oxygen-satd. soln. of Pb compd. in aq. NaOH at room temp. (continuous stream of O2); not isolated; UV spect.;	A 80% B >1

: {Cu2(((C5H4NCH2CH2)2N)2CH2C6H3O)(O2)}(1+)*PF6(1-)={Cu2(((C5H4NCH2CH2)2N)2CH2C6H3O)(O2)}PF6

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With H(1+) In not given protonation;;	80%

: 1020-31-1
3,5-Di-tert-butylcatechol

A: 3383-21-9
3,5-di-tert-butyl-o-benzoquinone

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With [(6-chloro-N2,N2,N4,N4-tetrakis(pyridin-2-ylmethyl)-1,3,5-triazine-2,4-diamine)Cu(II)(-OH)2Cu(II)].(ClO4)2; oxygen In methanol at 25℃; pH=6; Kinetics; Mechanism; pH-value;	A n/a B 78%
With [CoII(3,5-ditert-butylsemiquinonate)(hydrotris(3,5-dimethylpyrazolyl)borate)]; oxygen In toluene at 39.84℃; under 760.051 Torr; for 24h; pH=4.4; Inert atmosphere;
With [Cu{(5-pyrazinyl)tetrazolate}(1,10-phenanthroline)2](NO3)0.5(N3)0.5·2(H2O); oxygen In methanol at 25℃; for 0.75h; Catalytic behavior; Kinetics; Mechanism;

: 7732-18-5
water

: 80937-33-3
oxygen

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With [Cu(N,N-bis(2-pyridylmethyl)amine)](BF4)2 at 24.84℃; pH=6.7; Catalytic behavior; Reagent/catalyst; Electrolysis;	77%
With [Cu(N,N-bis(2-pyridylmethyl)amine)](BF4)2 at 24.84℃; for 0.0194444h; pH=6.7; Catalytic behavior; Reagent/catalyst; Electrolysis;	67%
With NiFe-layered double hydroxide derived mixed metal oxide(at)carbon nitride for 1.5h; pH=3; Kinetics; Reagent/catalyst; Irradiation;	63%

: 1579297-38-3
(2,6-bis(4,4-dimethyloxazolinyl)-3,5-dimethylphenyl)Ir(acetate)(OOH)

A: 1423875-77-7
(2,6-bis(4,4-dimethyloxazolinyl)-3,5-dimethylphenyl)Ir(acetate)(H)

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With sulfuric acid; oxygen at 20℃; under 2280.15 Torr; Inert atmosphere;	A n/a B 77%

: {((C3H2NNCH3(CH3))3Cu)2O2}(2+)

: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With HPF6*Et2O In dichloromethane react. with an excess of acid; further unidentified Cu(II) products; detn. by iodometric titration;	75%

: 91-01-0
1,1-Diphenylmethanol

A: 119-61-9
benzophenone

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With N-hydroxyphthalimide; oxygen In ethyl acetate at 75℃; under 7600.51 Torr; for 12h; Temperature; Solvent; Reagent/catalyst; Pressure; Autoclave; Industrial scale;	A 75% B 57%

: 358625-60-2
[(bathocuproine)Pd(O2)]

: 64-19-7
acetic acid

: 152506-88-2
(2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline)palladium(II) acetate

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In dichloromethane-d2 mixing palladium complex with acetic acid in CD2Cl2 in NMR tube for 5 min; detected by NMR;	A n/a B 73%

...Expand

: 358625-60-2
[(bathocuproine)Pd(O2)]

: 7664-93-9
sulfuric acid

A: 358625-80-6
(C6H5)2(CH3)2C6H2(C3HN)2*Pd(2+)*SO4(2-)=(C6H5)2(CH3)2C6H2(C3HN)2PdSO4

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
In not given	A n/a B 73%

...Expand

: Co(II) tetra(4-NN'N''-trimethylanilinium)porphyrin chloride

: 80937-33-3
oxygen

A: Co(III) tetra(4-NN'N''-trimethylanilinium)porphyrin chloride

B: 7722-84-1
dihydrogen peroxide

Conditions

Conditions	Yield
With hydrogen cation In water Kinetics; Electrochem. Process; overvoltage of O2 reduction and H2O2 yield (catalytic effect) dependingon pH of soln. (1 - 8); cyclic voltammetry; voltammetry on glassy carbon rotating ring - disc electrode;	A n/a B 70%

...Expand

: 7722-84-1
dihydrogen peroxide

: 13598-52-2
peroxomonophosphoric acid

Conditions

Conditions	Yield
In tetrachloromethane; water byproducts: H3PO4; to suspn. of P2O5 in CCl4 added aq. H2O2 (70 wt %) dropwise (mole ratio >0.9) at 2°C under stirring, monitoring of temp., stirred for 2 h; aq. phase sepd., CCl4 layer extd. (deionized H2O), combined aq. solns.;	100%
In tetrachloromethane; water byproducts: H3PO4; to suspn. of P2O5 in CCl4 added aq. H2O2 (90 wt %) dropwise (mole ratio >0.9) at 2°C under stirring, monitoring of temp., stirred for 2 h; aq. phase sepd., CCl4 layer extd. (deionized H2O), combined aq. solns.;	99%
In tetrachloromethane; water at 0℃; for 3h;

: 7722-84-1
dihydrogen peroxide

: 108061-34-3
(S)-methyl 2-benzyloxy-4-methylpentanoate

: 108061-23-0
(S)-4-methyl-2-(phenylmethoxy)valeric acid

Conditions

Conditions	Yield
With hydrogenchloride In methanol; water	100%
With hydrogenchloride In methanol; water	100%

: 7722-84-1
dihydrogen peroxide

: 3352-57-6
hydroxyl

Conditions

Conditions	Yield
With nitrogen In gas Kinetics; very rapid react. of metastable excited state N2 in Ar with H2O2 in discharge-flow apparatus, total gas pressure: 1-5 Torr; not isolated, detected by fluorescence spect.;	100%
In gas Irradiation (UV/VIS); OH produced by pulsed photolysis of H2O2 at 248 nm (KrF excimer laser);
iron(III) In water Kinetics; catalitic decompn. of H2O2 was studied; catalyst: Fe(3+)-ion; spectrophotometry;

: 198962-37-7
(ethene)[N,N,N-tris(2-pyridylmethyl-κN)amine-κN]rhodium(I) hexafluorophosphate

: 7722-84-1
dihydrogen peroxide

: Rh(N(CH2C5H4N)3)(C2H4O)(1+)*PF6(1-)*1.5H2O=[Rh(N(CH2C5H4N)3)(C2H4O)]PF6*1.5H2O

Conditions

Conditions	Yield
In methanol N2-atmosphere; addn. of 35% aq. H2O2 to Rh-complex, stirring at -10°C for 1 h; pptn. on Et2O addn., collection (filtration), washing (Et2O), drying (vac.); elem. anal.;	100%

: 198962-21-9
Rh(C6H12(NCH3)3)(C8H12)(1+)*PF6(1-)=[Rh(C6H12(NCH3)3)(C8H12)]PF6

: 7722-84-1
dihydrogen peroxide

: 198962-27-5
Rh(C6H12(NCH3)3)(C8H12O)(1+)*PF6(1-)=[Rh(C6H12(NCH3)3)(C8H12O)]PF6

Conditions

Conditions	Yield
In methanol N2-atmosphere; addn. of 35% aq. H2O2 to Rh-complex, stirring at room temp. for 1 h; pptn. on Et2O addn., collection (filtration), washing (Et2O), drying (vac.); elem. anal.;	100%

: C22H17BF2N2S

: 7722-84-1
dihydrogen peroxide

: C22H17BF2N2OS

Conditions

Conditions	Yield
With acetic acid In chloroform at 20℃; for 12h; Inert atmosphere; Cooling with ice;	100%

: 61825-94-3
(1R,2R)-[cyclohexane-N,N'-diamine](ethanedioato-O,O')platinum(II)

: 7732-18-5
water

: 7722-84-1
dihydrogen peroxide

: (SP-4-2)-(trans-R,R-cyclohexane-1,2-diamine)dihydroxo(oxalato) platinum(IV)

Conditions

Conditions	Yield
at 20℃; for 24h; Darkness;	100%
at 20℃; under 760.051 Torr; Darkness;

...Expand

: borax

: 7722-84-1
dihydrogen peroxide

: 1310-73-2
sodium hydroxide

: sodium perborate hexahydrate

Conditions

Conditions	Yield
In water a soln.of H2O2 in anthraquinone (from the prepn. of H2O2 by the anthraquinone-method) is stirred with an aq. soln. of borax-NaOH at 30°C,to the formed aq. phase NaOH is added;; isoln. from the aq. phase and mother liqour;;	99.8%
In water a soln.of H2O2 in anthraquinone (from the prepn. of H2O2 by the anthraquinone-method) is stirred with an aq. soln. of borax-NaOH at 30°C,to the formed aq. phase NaOH is added;; isoln. from the aq. phase and mother liqour;;	99.8%
With florisil In water 15 kg MgSiO3 and 107 kg of H2O2 (in form of 20, 30 or 40weight% H2O2-soln.) are added to 1263 l of a soln. (15°C) containing 139 kg NaOH and 665 kg borax; further addition of H2O2 (equal amount) at 20°C and slow cooling down to 0°C;; separation and drying of the pptd. salt;;

...Expand

: borax

: 7732-18-5
water

: 7722-84-1
dihydrogen peroxide

: 1310-73-2
sodium hydroxide

: sodium monoborate peroxohydrate trihydrate

Conditions

Conditions	Yield
In water stirring H2O2 (from anthraquinone process) in anthraquinone with aq. borax-NaOH-soln. at 30°C, addn. of NaOH to the aq. layer containing Na-perborate, borax and H2O2, pptn.;;	99.8%
In water stirring H2O2 (from anthraquinone process) in anthraquinone with aq. borax-NaOH-soln. at 30°C, addn. of NaOH to the aq. layer containing Na-perborate, borax and H2O2, pptn.;;	99.8%
In water formation of a NaBO2-soln. from borax and NaOH, treatment with H2O2-vapor at 30-35°C, apparatus described;;

...Expand

: oxalato((S,S,S)-spiro[4,4]nonane-1,6-diamine)platinum(II)

: 7722-84-1
dihydrogen peroxide

: (dihydroxy)malonato((S,S,S)-spiro[4,4]nonane-1,6-diamine)platinum(IV)

Conditions

Conditions	Yield
In water at 70℃; for 2h;	99.6%

: rhenium

: 1643-19-2
tetrabutylammomium bromide

: 7722-84-1
dihydrogen peroxide

: tetrabutylammonium perrhenate

Conditions

Conditions	Yield
With aq. NH3 In water add. of 30 % aq. H2O2 and aq. NH3 to Re powder, stirring (room temp., 1 h), addn. of further H2O2 until a clear sol. is obtained, then boiling to destroy excess H2O2, addn. of aq. NBu4Br; filtration, recrystn. (MeOH); elem. anal.;	99%

...Expand

: 7722-84-1
dihydrogen peroxide

: 7721-01-9
tantalum pentachloride

: potassium hydroxide

: 3K(1+)*[Ta(O2)4](3-)=K3[Ta(O2)4]

Conditions

Conditions	Yield
In methanol TaCl5 and H2O2 stirred in ice-water bath, KOH added, MeOH added, cooled to 5-8°C, MeOH added; filtered, washed with MeOH, dried in air for 45 min to 1 h;	99%

...Expand

: 88635-40-9
[(η6-p-cymene)RuCl2(η1-bis(diphenylphosphino)methane)]

: 7722-84-1
dihydrogen peroxide

: 240803-86-5
[(η(6)-cymene)RuCl2(η(1)-Ph2PCH2P(O)Ph2)]

Conditions

Conditions	Yield
In tetrahydrofuran Ru complex treated with H2O2 in THF;	99%

: cis-dichloro[η(2)-cis,cis-1,3,5-tris(diphenylphosphino)-1,3,5-tris-(methoxymethyl)cyclohexane]platinum(II)

: 7722-84-1
dihydrogen peroxide

: cis-dichloro[η(2)-cis,cis-1,3-bis(diphenylphosphino)-5-(diphenylphosphinyl)-1,3,5-tris-(methoxymethyl)cyclohexane]platinum(II)

Conditions

Conditions	Yield
In dichloromethane Ar-atmosphere; slight excess of aq. H2O2, stirring (room temp., 2 h); concn., pptn. on pentane addn., collection (filtration), washing (pentane), drying (reduced pressure); elem. anal.;	99%

: ammonium hexafluorophosphate

: iron(II) chloride tetrahydrate

: 7722-84-1
dihydrogen peroxide

: 4'-diphenylphosphino-2,2':6',2''-terpyridine

: Fe(C27H20N3OP)2(2+)*2PF6(1-)*3H2O = [Fe(C27H20N3OP)2](PF6)2*3H2O

Conditions

Conditions	Yield
In ethanol; water (N2); refluxing the Fe salt and ligand in EtOH for 2 h, stirring (room temp., 60 h), addn. of aq. H2O2 (1 h), addn. of aq. NH4PF6; filtration (Celite), washing (H2O), dissoln. (MeCN), removal of solvent (vac.); elem. anal.;	99%

...Expand

: (Co(PyAS)2)Cl*2MeOH

: 7722-84-1
dihydrogen peroxide

: (Co(PyASO2)(PyPepSO2))

Conditions

Conditions	Yield
In methanol; water 30 % H2O2 was added slowly to soln. (Co(PyAS)2)Cl in MeOH and stired in air for 2 days; solid was collected and dried under vac.;	99%

: 211688-02-7
1,1'-diphenylphosphinooctamethylferrocene

: 7722-84-1
dihydrogen peroxide

: 211688-09-4
Fe(1,2-bis(diphenylphosphinoxide)-3,4,5-trimethylcyclopentadienyl)2

Conditions

Conditions	Yield
In dichloromethane Ar-atmosphere; addn. of 15 drops of 30% H2O2 to Fe-complex soln., stirring for 30 min; washing (H2O), drying of org. layer (MgSO4), solvent removal, recrystn. (CH2Cl2/pentane); elem. anal.;	99%

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CAS No.:7722-84-1
Name:Hydrogen peroxide
Article Data:1328
Molecular Structure:
Formula:H₂O₂
Molecular Weight:34.0147
Synonyms:Wasserstoffperoxid;Perone 30;HOOH;T-Stuff;Hybrite;Inhibine;Perossido di idrogeno;Dentasept;Hydrogen dioxide solution;UN 2014 (20%-52%);Oxydol;Hydrogen peroxide solutions;Oxyfull;Hydrogen peroxide, solution;Oxydol (JP14);Lensan A;Metrokur;Kastone;Hydrogen peroxide (> 52% conc.);dihydrogen peroxide;Albone 70CG;Peroxaan;Peroxide;Hydrogen peroxide, solution, 3%;Hipox;Elawox;Hydrogen peroxide solutions (over 60% but not over 70%);Superoxol;Peroxyde dhydrogene;Hydrogen peroxide solution (DOT);Hydrogen peroxide, 8% to 20%;Oxysept I;Dihydrogen dioxide;Oxigenal;Hydrogen dioxide;bis(hydridooxygen)(O--O);Albone 35CG;PEO;Asepticper;Hioxyl;Peroxan;Hydrogen peroxide solution;Hydrogen peroxide, solution, 35%;Perone 50;Mirasept;Albone 50CG;Perone;Xtra White;Hydrogen peroxide (USP);Albone 70;Albone 35;Crestal Whitestrips;Hydrogen oxide;Hydrogen peroxide, 3%;Albone 50;Hydrogen peroxide, 30%;UN 2984 (8%-20%);Hydrogen peroxide, aqueous solutions with not <8% but <20% hydrogen peroxide (stabilized as necessary) [UN2984] [Oxidizer];Hydrogen peroxide, 90%;Hydrogen peroxide, 20% to 60%;Lensept;Wasserstoffperoxid 30%;Perhydrol;Perone 35;Odosat D;Peroxclean;Hydrogen peroxide solutions (over 8% but not over 60%);Anti-Keim 50;Hydrogen peroxide (8CI);Adeka Super EL;Albone;Hydrogen peroxide (conc > 52%);EPA Pesticide Chemical Code 000595;Pegasyl;Crystacide;Albone DS;Oxysept;Interox;Select Bleach;Waterstofperoxyde;UN 2015 (>52%);Baquashock;
EINECS:231-765-0
Density:1.444 g/cm³
Melting Point:-11 °C
Boiling Point:150.2 °C at 760 mmHg
Flash Point:107 °C
Solubility:miscible in water
Appearance:colourless liquid
Hazard Symbols:Xn,C,O
Risk Codes22-41-37/38-34-20/22-8
Safety: 26-39-45-36/37/39-28A-17
Transport Information:UN 2015/2014/2984
PSA:40.46000
LogP:0.01740

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