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inquiryWe are manufacturer of this product. If you are looking for the material's manufacturer or supplier in China, Ality Group is your best choice. Specifications of our Di-tert-butyl peroxide CAS 110-05-4: Items
High quality,low price Di-tert-butyl peroxide Basic information Product Name: Di-tert-butyl peroxide Synonyms: T-BUTYL PEROXIDE;TERT-BUTYL PEROXIDE;(tert-C4H9O)2;(tributyl)peroxide;2-(
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inquiryChemical Name: Di-Tert Butyl Peroxide Alias: DTBP CAS No.: 110-05-4 Molecular formula: C8H18O2 Molecular weight: 146.2 Brief Introduction: SF-A is a light yellow transparent liquid, is a dialkyl organic peroxides. Mainly used as a cross-l
Company profile Shandong Hanjiang Chemical Co., Ltd. is located in Qilu Petrochemical Industrial Park, Zibo City, Shandong Province. The best-selling products include DMF, dichloromethane, acetonitrile, glacial acetic acid, cyclohexanone, cyclohexan
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inquiryProduct Detail Minimum Order Qty. 10 Gram
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inquiryDi-tert-butyl peroxide CAS: 110-05-4 Specification items specification results appearance clear liquid clear liquid hema content (%, min) 98 98.2 color (apha, max) 30 16 residual
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inquirySuperior quality, moderate price & quick delivery. Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical Intermediat
Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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inquiryGood price, high purity, mature production technology, accept custom synthesis per customer's requirements Package:As per Customer‘ requirements Application:Pharmaceutical intermediate
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Di-tert-butyl peroxide,CAS 110-05-4 Application:Di-tert-butyl peroxide,CAS 110-05-4
Di-tert-butyl peroxide CAS NO.110-05-4Appearance:colourless liquid Storage:Dry and ventilated Package:Standard or as customer's require Application:intermediates Transportation:Delivery by EMS, DHL, FEDEX, UPS, TNT
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inquiryDi-tert-butyl peroxide,CAS 110-05-4Appearance:Clear liquid Storage:keep in dry place Package:Aluminum Foil Bag or as your requirement Application:110-05-4 Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airp
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inquiryConditions | Yield |
---|---|
Stage #1: tert-butylamine With potassium sulfate; aluminum isopropoxide at 10℃; for 2h; Stage #2: With nickel(II) fluoride for 4h; Temperature; Concentration; | 98.2% |
Conditions | Yield |
---|---|
With sulfuric acid; dihydrogen peroxide at 35 - 45℃; for 2h; | 96% |
With dihydrogen peroxide In Petroleum ether at 70 - 80℃; for 4h; Reagent/catalyst; Temperature; | 95.3% |
With sulfuric acid; dihydrogen peroxide at 29 - 39℃; for 2h; Cooling; | |
With dihydrogen peroxide at 60℃; Temperature; Large scale; |
tert.-butylhydroperoxide
Martins sulfurane
A
di-tert-butyl peroxide
B
diphenyl sulfide
C
1,1'-sulfinylbisbenzene
D
diphenyl sulphone
E
1,1,1,3,3,3-hexafluoro-2-phenylisopropyl alcohol
F
isobutene
Conditions | Yield |
---|---|
With 2,2-diphenyl-1-picrylhydrazine In chloroform-d1 at -78℃; Product distribution; chemiluminescence, other peroxides; | A n/a B 2% C 94% D 2% E n/a F n/a |
tert.-butylhydroperoxide
tert-Butyl 2,2,2-trichloroacetimidate
di-tert-butyl peroxide
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In pentane 1.) -5 deg C, 15 min, 2.) up to r.t.; | 63% |
tert.-butylhydroperoxide
tert-butyl hydrogen sulfate
di-tert-butyl peroxide
Conditions | Yield |
---|---|
With sulfuric acid |
tert-butyl hydrogen sulfate
A
tert.-butylhydroperoxide
B
di-tert-butyl peroxide
Conditions | Yield |
---|---|
With dihydrogen peroxide at 0℃; | |
With dihydrogen peroxide In water at 25℃; for 7.91667h; Temperature; | A 65.94 %Chromat. B 23.92 %Chromat. |
tert-butyl hydrogen sulfate
di-tert-butyl peroxide
Conditions | Yield |
---|---|
With sulfuric acid; dihydrogen peroxide |
Conditions | Yield |
---|---|
With hydrogen bromide; oxygen at 158℃; | |
With hydrogen bromide; oxygen at 158℃; |
Conditions | Yield |
---|---|
With dihydrogen peroxide; acid | |
With sulfuric acid; water; dihydrogen peroxide |
tert.-butylhydroperoxide
A
methanol
B
di-tert-butyl peroxide
C
acetone
D
isobutene
Conditions | Yield |
---|---|
With antimonypentachloride In acetonitrile at 52℃; Product distribution; Thermodynamic data; other time, other reagents, activation energy of total decomposition and of homolysis; |
tert.-butylhydroperoxide
A
methane
B
di-tert-butyl peroxide
C
acetone
D
isobutene
Conditions | Yield |
---|---|
With perchloric acid; cyclohexanone In acetonitrile at 302℃; Rate constant; Mechanism; kinetic curves of decomposition; in presence of methyl ethyl ketone instead of cyclohexanone; |
tert.-butylhydroperoxide
A
2,2'-oxybis(2-methyl-propane)
B
di-tert-butyl peroxide
C
acetone
D
isobutene
E
tert-butyl alcohol
Conditions | Yield |
---|---|
With vanadia; silica gel In benzene at 60℃; for 2h; Rate constant; Mechanism; other metal catalysts; |
tert.-butylhydroperoxide
A
di-tert-butyl peroxide
B
acetone
C
tert-butyl alcohol
Conditions | Yield |
---|---|
With dicobalt octacarbonyl In benzene at 6 - 8℃; for 0.5h; Product distribution; various amounts of Co2(CO)8, Fe(CO)5; various amounts of educt; | A 1 % Chromat. B 2 % Chromat. C 88 % Chromat. |
With 3,5-di-tert-butyl-1,2-benzoquinone In toluene at 70℃; Reduction; addition; |
Conditions | Yield |
---|---|
cobalt(II) phthalocyanine In various solvent(s) at 40℃; Rate constant; Product distribution; use of iron phthalocyanine, 20 deg C, effects of added various solvents; | |
With water; oxygen In chlorobenzene at 70℃; for 2h; Product distribution; Further Variations:; Reagents; Decomposition; |
tert-butylperoxytrimethylsilane
A
tert.-butylhydroperoxide
B
tertiary butyl chloride
C
di-tert-butyl peroxide
D
Hexamethyldisiloxane
E
isobutene
F
tert-butyl alcohol
Conditions | Yield |
---|---|
With phosphorus trichloride In nonane Kinetics; Mechanism; other solvent : butyl methacrylate; | A 0.56 (unit not given) B 0.04 (unit not given) C 0.11 (unit not given) D 0.46 (unit not given) E 0.09 (unit not given) F 0.04 (unit not given) |
di-t-butyldiazene
A
methanol
B
tert.-butylhydroperoxide
C
di-tert-butyl peroxide
D
acetone
E
tert-butyl alcohol
Conditions | Yield |
---|---|
With oxygen at 59.9℃; Quantum yield; Mechanism; Irradiation; Other temperatures (298, 373 K), the effect of added t-butyl hydroperoxide.; |
tert-butylperoxyl
A
methanol
B
formaldehyd
C
methyl tert-butyl peroxide
D
di-tert-butyl peroxide
E
acetone
F
tert-butyl alcohol
Conditions | Yield |
---|---|
In water at 19.9℃; Rate constant; Product distribution; Mechanism; | A 0.01 mmol B 0.37 mmol C 0.08 mmol D 0.08 mmol E 0.98 mmol F 0.56 mmol |
di-tert-butoxydiazene
di-tert-butyl peroxide
Conditions | Yield |
---|---|
In tert-butyl alcohol at 70℃; var solv.: c-C6D12 at 62.2 degC; cage effect determined; |
di-tert-butyl hyponitrite
A
di-tert-butyl peroxide
B
acetone
C
tert-butyl alcohol
Conditions | Yield |
---|---|
With oxygen; sodium chloride; egg lecithin at 30℃; under 760 Torr; for 600h; Product distribution; other solvent, reagent, concentrations; |
tert-Butyl-(tert-butylphenoxy)peracetat
A
formaldehyd
B
di-tert-butyl peroxide
C
tert-butyl alcohol
Conditions | Yield |
---|---|
In various solvent(s) at 40 - 60℃; Rate constant; Thermodynamic data; E(activ.) and preexponential factor; |
2-tert-butylperoxy-2-methyl-propyl
A
2-methyl-1,2-epoxypropane
B
di-tert-butyl peroxide
Conditions | Yield |
---|---|
With tri-n-butyl-tin hydride In benzene at 24.9℃; Rate constant; Irradiation; |
2,6-Di-tert-butyl-(N-tert-butylnitrono)phenoxyl
A
di-tert-butyl peroxide
B
acetone
C
tert-butyl alcohol
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide In benzene for 4h; Product distribution; Ambient temperature; other solvents: chlorbenzene, freone-1,1,3; other temperatures: 70 deg C for 30 min; |
tert.-butylhydroperoxide
A
methanol
B
di-tert-butyl peroxide
C
acetone
D
isobutene
E
tert-butyl alcohol
Conditions | Yield |
---|---|
With aluminium trichloride In ethyl acetate at 69.9℃; Product distribution; Kinetics; Thermodynamic data; variation of temperature, further chlorides of elements of group III or IV; |
Di-t-butyl ketone
A
tetramethyl-2,2,3,3 butane
B
Isobutane
C
di-tert-butyl peroxide
D
isobutene
E
tert-butyl alcohol
Conditions | Yield |
---|---|
With oxygen In decane at 323℃; Product distribution; Mechanism; Kinetics; Irradiation; other temperatures: 348, 373, 398 K; |
azo-t-butane
A
tetramethyl-2,2,3,3 butane
B
Isobutane
C
di-tert-butyl peroxide
D
isobutene
E
tert-butyl alcohol
Conditions | Yield |
---|---|
With oxygen In decane at 323℃; Product distribution; Mechanism; Kinetics; Irradiation; other temperatures: 298, 348 K; |
Conditions | Yield |
---|---|
With [5,10,15,20-tetrakis(heptafluoropropyl)porphinato]iron(II)-(3-fluoropyridine)2; oxygen In benzene at 80℃; under 6464.3 Torr; for 91h; Product distribution; Mechanism; other reagent: (5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato)iron(II) bis(3-fluoropyridine) complex; | A 7.8 % Turnov. B 8.1 % Turnov. C 84 % Turnov. |
With oxygen; [5,10,15,20-tetrakis(pentafluorophenyl)porphinato]iron(II)-(3-fluoropyridine)2 In benzene at 80℃; under 6464.3 Torr; for 20h; other catalyst: (5,10,15,20-tetrakis(heptafluoropropyl)porphyrinato)iron(II) bis(3-fluoropyridine) complex; | A 10.3 % Turnov. B 3.6 % Turnov. C 86 % Turnov. |
di-tert-butylhydroperoxide
A
di-tert-butyl peroxide
B
acetone
C
tert-butyl alcohol
Conditions | Yield |
---|---|
In dichloromethane at -20.5 - 17℃; Kinetics; Mechanism; Rate constant; |
tert-butoxy radical
A
methyl radical
B
di-tert-butyl peroxide
C
acetone
Conditions | Yield |
---|---|
In tetrachloromethane at 295℃; Rate constant; other solvents, other temperature; |
sulfuric acid
dihydrogen peroxide
tert-butyl alcohol
A
tert.-butylhydroperoxide
B
di-tert-butyl peroxide
Conditions | Yield |
---|---|
With pyridine In fluorobenzene at 10℃; Kinetics; Temperature; Concentration; | 100% |
Conditions | Yield |
---|---|
Stage #1: di-tert-butyl peroxide; copper hydroxide In water at 60℃; for 0.5h; Inert atmosphere; Stage #2: In water for 5h; Sonication; Inert atmosphere; | 100% |
di-tert-butyl peroxide
4,4-dimethyl-cyclohexanol
ethyl acrylate
8,8-dimethyl-1-oxa-spiro[4.5]decan-2-one
Conditions | Yield |
---|---|
Stage #1: di-tert-butyl peroxide; 4,4-dimethyl-cyclohexanol; ethyl acrylate at 50 - 160℃; for 4.16667h; Stage #2: With sodium hydroxide; water In tert-butyl methyl ether at 40℃; Stage #3: With sulfuric acid In tert-butyl methyl ether; water pH=1; | 96.3% |
titanium(IV) isopropylate
di-tert-butyl peroxide
DIPT
water
phytol
Conditions | Yield |
---|---|
silica gel In diethyl ether; dichloromethane | 95% |
Conditions | Yield |
---|---|
With copper(l) chloride In chlorobenzene at 130℃; for 12h; Schlenk technique; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With copper(I) bromide In hexane at 50℃; for 5h; Inert atmosphere; | 95% |
tetrahydrofuran
di-tert-butyl peroxide
p-ethoxycarbonylphenyl isocyanate
Conditions | Yield |
---|---|
With copper(l) chloride at 130℃; for 12h; Inert atmosphere; Schlenk technique; Glovebox; | 95% |
Conditions | Yield |
---|---|
With palladium diacetate; trifluoroacetic acid In cyclohexane at 100℃; for 0.5h; | 94% |
tetrahydrofuran
di-tert-butyl peroxide
p-trifluoromethyl-phenylisocyanate
Conditions | Yield |
---|---|
With copper(l) chloride at 130℃; for 12h; Inert atmosphere; Schlenk technique; Glovebox; | 94% |
Conditions | Yield |
---|---|
With copper(I) bromide In hexane at 50℃; for 5h; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
In water at 100℃; for 12h; Sealed tube; | 93% |
With water at 110℃; for 12h; Temperature; Sealed tube; Green chemistry; | 93% |
di-tert-butyl peroxide
[(C5HiPr4)Sm(μ-I)(THF)2]2
(C5HiPr4)SmIOtBu(THF)
Conditions | Yield |
---|---|
In toluene Sm-complex and ligand were loaded in flask, toluene was condensed at -20°C, stirred for 10 min at room temp.; toluene was removed; | 92% |
Conditions | Yield |
---|---|
With copper(I) bromide In hexane at 50℃; for 5h; Inert atmosphere; | 92% |
di-tert-butyl peroxide
sodium 4-methoxybenzenesulfinate
p-anisyl methyl sulfone
Conditions | Yield |
---|---|
In water at 80℃; for 12h; Sealed tube; | 92% |
With water at 110℃; for 12h; Sealed tube; Green chemistry; | 92% |
di-tert-butyl peroxide
sodium 4-bromobenzenesulfinate
4-bromoohenyl methyl sulfone
Conditions | Yield |
---|---|
With water at 110℃; for 12h; Sealed tube; Green chemistry; | 92% |
di-tert-butyl peroxide
1-iodo-4-(methylsulfonyl)benzene
Conditions | Yield |
---|---|
With water at 110℃; for 12h; Sealed tube; Green chemistry; | 92% |
Conditions | Yield |
---|---|
With copper(l) chloride at 130℃; for 12h; Inert atmosphere; Schlenk technique; Glovebox; | 92% |
tert.-butylhydroperoxide
di-tert-butyl peroxide
β-naphthaldehyde
tert-butyl naphthalene-2-carboperoxoate
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In water for 2h; Irradiation; Green chemistry; | 92% |
Conditions | Yield |
---|---|
With copper(I) bromide In hexane at 50℃; for 5h; Inert atmosphere; | 91% |
tert.-butylhydroperoxide
di-tert-butyl peroxide
3,4,5-trimethoxy-benzaldehyde
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In water for 2h; Irradiation; Green chemistry; | 91% |
tert.-butylhydroperoxide
di-tert-butyl peroxide
6-methoxynaphthalene-2-carbaldehyde
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In water for 2h; Irradiation; Green chemistry; | 91% |
di-tert-butyl peroxide
4-methyl-benzaldehyde
tert-butyl 4-methylbenzoate
Conditions | Yield |
---|---|
With copper(I) bromide In hexane at 50℃; for 5h; Inert atmosphere; | 90% |
di-tert-butyl peroxide
N-phenyl-N-tosylmethacrylamide
Conditions | Yield |
---|---|
With iron(III) sulfate In fluorobenzene at 115℃; for 8h; Reagent/catalyst; Solvent; Temperature; Inert atmosphere; Sealed tube; | 90% |
di-tert-butyl peroxide
sodium p-chlorobenzenesulphinate
4-chlorophenyl methyl sulfone
Conditions | Yield |
---|---|
In water at 100℃; for 12h; Sealed tube; | 90% |
With water at 110℃; for 12h; Sealed tube; Green chemistry; | 90% |
di-tert-butyl peroxide
sodium 3-methylbenzenesulfinate
methyl 3-methylphenyl sulfone
Conditions | Yield |
---|---|
With water at 110℃; for 12h; Sealed tube; Green chemistry; | 90% |
Conditions | Yield |
---|---|
With copper(l) chloride at 130℃; for 12h; Inert atmosphere; Schlenk technique; Glovebox; | 90% |
Conditions | Yield |
---|---|
With copper(l) chloride at 130℃; for 12h; Catalytic behavior; Reagent/catalyst; Temperature; Inert atmosphere; Schlenk technique; Glovebox; | 90% |
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