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inquiry1,ISO Certificate 2,Factory price 3,Free sample and Fast delivery Appearance:Colorless transparent liquid Storage:All products should be stored at a dry and ventilated location away from fire and other dangerous goods, and should avoid direct sunl
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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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inquiryHebei yanxi chemical co., LTD is a professional research, development and production Cyromazine、lead diacetate trihydrate /Lead acetate trihydrateC、 2-phenylacetamide 、 4-Aminophenyl-1-phenethylpiperidine 、Citric acid monohydrate 、 Citric acid/c
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inquirytert-Butyl hydroperoxide Basic information Product Name: tert-Butyl hydroperoxide Synonyms: Butylhydroperoxid;1,1-Dimethylethyl hydroperoxide;1,1-dimethylethyl-hydroperoxid;1,1-dimethyle
Product Name tert-Butyl hydroperoxide Synonyms tert-Butyl hydroperoxide;TBHP CAS: 75-91-2 MF: C4H10O2 MW: - EINECS:
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Appearance:white or yellowish white flaky crystal Storage:Keep the sun from direct sunlight ;prevention against high temperature Package:As customer request Application:Used for research and industrial manufacture. Transportatio
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:75-91-2
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inquiryProduct 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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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Jinlan Pharm-Drugs Technology Co.,Limited (with its export company Hangzhou Royall Import & Export Co.,Ltd.)is located in Hangzhou, Zhejiang Province. Neighboring Ningbo port, Shanghai port, Hangzhou Xiaoshan Int’l Airport and Shanghai Pudong Int’l A
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inquirySuperior quality, moderate price & quick delivery. Appearance:Colorless to light yellow transparent liquid Storage:Store in a cool, low-temperature, well-ventilated non-combustible warehouse Package:170kg/plastic pail (Grade one peroxid, can no
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
C-1513 TBHP,Tert Butyl Hydroperoxide Colour:60HazenMax. Fe:0.0003%Max.Appearance:Colorless to light yellow transparent liquid
1.High quality : the purity is 99% min . through multiple producing procedures. 2.Competitive price : low price because of our skilled production technolpgy ,save the production cost at most , and give big profit room to our customers406.Safe and fa
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Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
Tert-Butyl hydroperoxide,CAS 75-91-2 Application:Tert-Butyl hydroperoxide,CAS 75-91-2
1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highl
Tert-Butyl hydroperoxide,CAS 75-91-2Appearance:Clear liquid Storage:keep in dry place Package:Aluminum Foil Bag or as your requirement Application:75-91-2 Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airp
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inquiryA
1,1,1,3,3,3-hexafluoro-2-(2-iodo-5-methylphenyl)-propan-2-ol
B
tert.-butylhydroperoxide
Conditions | Yield |
---|---|
With 2,2,6,6-tetramethyl-piperidine-N-oxyl In cyclohexane at 81℃; for 30h; Decomposition; | A 100% B 30% |
9-tert-butyl-10-methyl-9,10-dihydroacridine
A
tert.-butylhydroperoxide
C
tert-butyl alcohol
Conditions | Yield |
---|---|
With 9,10-Dicyanoanthracene; oxygen; trifluoroacetic acid; scandium tris(trifluoromethanesulfonate) In [D3]acetonitrile at 24.85℃; for 1h; Irradiation; | A n/a B 100% C n/a |
Conditions | Yield |
---|---|
Stage #1: tert-butylamine With sodium hydrogen sulfate; 1,2-dibutoxyethane; lead(IV) tetraacetate; oxalic acid at 26℃; for 2.33333h; Stage #2: With cobalt(II) nitrate at 45℃; for 4h; Temperature; | 98.8% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; trifluoroacetic acid In water at 5 - 90℃; for 0.0583333h; Reagent/catalyst; Temperature; Flow reactor; | 94.3% |
With sulfuric acid; dihydrogen peroxide at 0 - 20℃; for 12h; | 59% |
With ferrocenedicarboxylate; water; oxygen; dinitrogen monoxide at 20℃; Rate constant; Irradiation; pH 8; pulse radiolysis; var. ferrocenes; |
cyclohexane
1-tert-butylperoxy-5-methyl-3,3-bistrifluoromethyl-1H-1,2-benziodoxole
A
1,1,1,3,3,3-hexafluoro-2-(2-iodo-5-methylphenyl)-propan-2-ol
B
tert.-butylhydroperoxide
C
1-iodocyclohexane
Conditions | Yield |
---|---|
at 81℃; for 30h; Decomposition; Further byproducts given; | A 3% B 1% C 94% D 94% |
methanol
t-butyl heptafluoroperoxybutyrate
A
tert.-butylhydroperoxide
B
methyl heptafluorobutyrate
C
2,2-dimethoxy-propane
Conditions | Yield |
---|---|
at 40℃; for 3h; Yield given. Yields of byproduct given; | |
In methanol at 10 - 40℃; for 3h; Rate constant; Kinetics; Thermodynamic data; ΔH(act.), ΔS(act.), various temperature; |
Isopropylbenzene
acetone di-tert-butylperoxyketal
A
tert.-butylhydroperoxide
B
tert-butyl peroxyacetate
C
dicumene
D
tert-butyl cumyl peroxide
E
acetone
F
tert-butyl alcohol
Conditions | Yield |
---|---|
at 120℃; for 2h; Product distribution; Kinetics; Mechanism; rate constants, ΔH(excit.), ΔS(excit.); | A 16 % Chromat. B 14 % Chromat. C 33 % Chromat. D 52 % Chromat. E 88 % Chromat. F 110 % Chromat. |
at 110℃; for 4h; Mechanism; |
tert-Butyl peroxybenzoate
aluminum ethoxide
A
tert.-butylhydroperoxide
B
ethanol
C
acetic acid
Conditions | Yield |
---|---|
With sulfuric acid Product distribution; Mechanism; multistep reaction; |
tert-Butyl peroxybenzoate
aluminum isopropoxide
A
tert.-butylhydroperoxide
B
isopropyl alcohol
Conditions | Yield |
---|---|
With sulfuric acid Product distribution; Mechanism; multistep reaction; |
tert-Butyl peroxybenzoate
aluminium propanolate
A
propan-1-ol
B
tert.-butylhydroperoxide
C
propionic acid
Conditions | Yield |
---|---|
With sulfuric acid Product distribution; Mechanism; multistep reaction; |
Conditions | Yield |
---|---|
With sodium hydroxide; cetyltrimethylammonium chloride at 25℃; Rate constant; basic hydrolysis with different cationic micelles with or without NaOH; |
2,3-Dimethyl-2-butene
azo-t-butane
A
2,3-dimethyl-2,3-epoxybutane
B
tert.-butylhydroperoxide
C
formaldehyd
D
acetone
E
tert-butyl alcohol
Conditions | Yield |
---|---|
With oxygen In gas at 69.9℃; under 200 Torr; for 1.33333h; Product distribution; Irradiation; different time, temperature and oxygen pressure; |
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) |
tert-butyl peroxyacetate
aluminum ethoxide
A
tert.-butylhydroperoxide
B
ethanol
C
acetic acid
Conditions | Yield |
---|---|
With sulfuric acid Product distribution; multistep reaction; |
tert-butyl peroxyacetate
aluminum isopropoxide
A
tert.-butylhydroperoxide
B
acetic acid
C
isopropyl alcohol
Conditions | Yield |
---|---|
With sulfuric acid Product distribution; Mechanism; multistep reaction; |
tert-butyl peroxyacetate
aluminium propanolate
A
propan-1-ol
B
tert.-butylhydroperoxide
C
propionic acid
Conditions | Yield |
---|---|
With sulfuric acid Product distribution; Mechanism; multistep reaction; |
Conditions | Yield |
---|---|
With sulfuric acid; water In 1,4-dioxane at 25℃; Kinetics; Mechanism; other aliphatic ketone di-tert-butylperoxyketals, induction and steric parameters of substituents at the carbonyl group of the ketones; | |
With sulfuric acid; water In 1,4-dioxane at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
In decane; toluene at 30℃; | 100% |
With [Cu(4-methyl-1,3-bis(2-pyridylimino)isoindole)(OAc)] In water | 86% |
With pyrazolate-based cobalt(II)-containing MFU-1 metal-organic framework at 70℃; for 2h; | 11.9% |
tert.-butylhydroperoxide
2,6-di-tert-butyl-4-methyl-phenol
2,6-di-tert-butyl-4-(tert-butylperoxy)-4-methylcyclohexa-2,5-dien-1-one
Conditions | Yield |
---|---|
With dirhodium(II) tetrakis(caprolactam) In water; 1,2-dichloro-ethane at 40℃; for 0.75h; chemoselective reaction; | 99% |
With tetra-(n-butyl)ammonium iodide In nonane; 1,2-dichloro-ethane at 20℃; for 24h; | 99% |
With cobalt naphthenate | |
(electrochemical oxidation); | |
With sodium chloride; sodium hydroxide; benzyl alcohol In water at 70℃; for 12h; Sealed tube; Green chemistry; |
tert.-butylhydroperoxide
phenyl isocyanate
phenyl-peroxycarbamic acid tert-butyl ester
Conditions | Yield |
---|---|
With copper acetylacetonate In tetrachloromethane at 20℃; for 1h; Product distribution; Mechanism; | 99% |
With copper acetylacetonate In benzene at 30℃; for 0.25h; | 29% |
With copper acetylacetonate In tetrachloromethane at 20℃; for 1h; Product distribution; Mechanism; other solvent (benzene), other temperature (30 deg C); | 6% |
With triethylamine In Petroleum ether |
tert.-butylhydroperoxide
3,5-di-tert-butyl-2-hydroxybenzonitrile
Conditions | Yield |
---|---|
With salcomine In dichloromethane for 0.333333h; Ambient temperature; | 99% |
Conditions | Yield |
---|---|
[Ti(NMe2){c-C6H11)7Si7O12}] at 79.85℃; Kinetics; Further Variations:; Catalysts; Epoxidation; | 99% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In decane; acetonitrile at -20 - 20℃; for 4h; | 99% |
tert.-butylhydroperoxide
{(C6H4(O)(CH2N(CH3)2))2Pd}
Conditions | Yield |
---|---|
bis(acetylacetonate)oxovanadium In chloroform-d1 react. with 2.0 equiv. Me3COOH and 2mol% VO(acac)2 at 20°C; | 99% |
In chloroform-d1; dichloromethane addn. of CH2Cl2 and the peroxide to the Pd-complex in CDCl3, react. for 5 d; | 60% |
bis(acetylacetonate)oxidovanadium(IV) In chloroform-d1; dichloromethane addn. of CH2Cl2 and the peroxide to the Pd-complex and catalyst in CDCl3, react. for 1.5 h; | >99 |
tert.-butylhydroperoxide
1-benzyl N-carbobenzoxy-L-glutamate
(2R)-benzyl 2-(benzyloxycarbonylamino)-5-(tert-butylperoxy)-5-oxopentanoate
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In decane; dichloromethane; acetonitrile at -20 - 20℃; for 4h; | 99% |
tert.-butylhydroperoxide
N-(4-chloro-6-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-1,3,5-triazin-2-yl)-N-(prop-2-ynyl)-methanesulfonamide
N-(4-(tert-butylperoxy)-6-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-1,3,5-triazin-2-yl)-N-(prop-2-ynyl)methanesulfonamide
Conditions | Yield |
---|---|
With potassium hydroxide In water; acetonitrile at 0 - 50℃; Inert atmosphere; | 99% |
styrene
tert.-butylhydroperoxide
pivalaldehyde
(1-(tert-butylperoxy)-3,3-dimethylbutyl)benzene
Conditions | Yield |
---|---|
With iron(II) chloride In decane; acetonitrile at 85℃; for 1h; Inert atmosphere; | 99% |
With iron(II) chloride In decane; ethyl acetate at 80℃; for 12h; Inert atmosphere; Sealed tube; Green chemistry; | 79% |
tert.-butylhydroperoxide
2-(4-chlorophenyl)-1,3-dioxolane
2-(tert-butylperoxy)-2-(4-chlorophenyl)-1,3-dioxolane
Conditions | Yield |
---|---|
With iron(III)-acetylacetonate In decane; acetonitrile at 20 - 80℃; for 3h; Molecular sieve; Inert atmosphere; | 99% |
tert.-butylhydroperoxide
tert-butyl (2-methoxyphenyl)methyl ether
tert-butyl (tert-butylperoxy)(2-methoxyphenyl)methyl ether
Conditions | Yield |
---|---|
With iron(III)-acetylacetonate In decane; acetonitrile at 20 - 80℃; for 3h; Molecular sieve; Inert atmosphere; | 99% |
tert.-butylhydroperoxide
benzyl methacrylate
pivalaldehyde
C19H30O4
Conditions | Yield |
---|---|
With iron(II) chloride In decane; acetonitrile at 85℃; for 1h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With copper quinolate In water; dimethyl sulfoxide at 120℃; for 24h; Solvent; | 99% |
With copper doped mesoporous polymelamine-formaldehyde In water; dimethyl sulfoxide at 100℃; for 16h; Catalytic behavior; | 97% |
Conditions | Yield |
---|---|
Stage #1: tert.-butylhydroperoxide; benzaldehyde In water; dimethyl sulfoxide Stage #2: In water; dimethyl sulfoxide at 100℃; for 20h; Sealed tube; | 99% |
With copper (II)-fluoride In water; dimethyl sulfoxide at 120℃; for 12h; Schlenk technique; Inert atmosphere; Green chemistry; | 65% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In dichloromethane at 20℃; for 0.5h; chemoselective reaction; | 99% |
With toluene-4-sulfonic acid In dichloromethane at 20℃; for 0.5h; | 99% |
tert.-butylhydroperoxide
2-(2-(5-methoxy-1H-indol-3-yl)ethyl)isoindoline-1,3-dione
isovaleraldehyde
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In dichloromethane at 20℃; for 0.5h; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 9h; | 99% |
tert.-butylhydroperoxide
tri(p-tolyl)antimony
2,4,6-tribromophenol
benzene
Conditions | Yield |
---|---|
Stage #1: tert.-butylhydroperoxide; tri(p-tolyl)antimony; 2,4,6-tribromophenol In diethyl ether at 20℃; for 24h; Stage #2: benzene In n-heptane | 99% |
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 24h; | 99% |
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 24h; | 99% |
Conditions | Yield |
---|---|
Stage #1: tert.-butylhydroperoxide; 2-chloro-benzaldehyde In water; dimethyl sulfoxide Stage #2: In water; dimethyl sulfoxide at 100℃; for 20h; Sealed tube; | 99% |
tert.-butylhydroperoxide
2-fluoro-6-(trifluoromethyl)benzoic acid
methyl 2-fluoro-6-(trifluoromethyl)benzoate
Conditions | Yield |
---|---|
Stage #1: tert.-butylhydroperoxide; 2-fluoro-6-(trifluoromethyl)benzoic acid In water; dimethyl sulfoxide Stage #2: In water; dimethyl sulfoxide at 100℃; for 20h; Sealed tube; | 99% |
tert.-butylhydroperoxide
2-ethylhexanoic acid chloride
tertiary butyl per-2-ethylhexanoate
Conditions | Yield |
---|---|
With potassium hydroxide In water at 27 - 35℃; | 98.5% |
With potassium hydroxide In water at 27 - 35℃; Product distribution / selectivity; Industry scale; | 98.5% |
In water at 40 - 45℃; Product distribution / selectivity; | 90% |
With 1-methyl-1H-imidazole at 25 - 35℃; Product distribution / selectivity; | 88% |
tert.-butylhydroperoxide
isononanoyl chloride
Conditions | Yield |
---|---|
With potassium hydroxide In water at 25℃; | 98.2% |
With potassium hydroxide In water at 25℃; Product distribution / selectivity; Industry scale; | 98.2% |
tert.-butylhydroperoxide
2-Iodobenzoyl chloride
tert-butyl 2-iodobenzoperoxoate
Conditions | Yield |
---|---|
With pyridine; dichloromethane In dichloromethane at -20℃; for 4.5h; Inert atmosphere; | 98% |
With pyridine In dichloromethane at -20 - 20℃; Oxidation; | 90% |
tert.-butylhydroperoxide
4-nitro-benzoyl chloride
tert-butyl 4-nitrobenzoperoxoate
Conditions | Yield |
---|---|
With pyridine In dichloromethane at -20 - 20℃; Oxidation; | 98% |
Stage #1: 4-nitro-benzoyl chloride With pyridine In dichloromethane at -20℃; for 0.166667h; Stage #2: tert.-butylhydroperoxide In dichloromethane at -20℃; for 4h; Further stages.; | 98% |
With pyridine In dichloromethane at -20℃; for 4h; Inert atmosphere; | 98% |
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