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10508-09-5

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10508-09-5 Usage

Chemical Properties

Colorless to light yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 10508-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,0 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10508-09:
(7*1)+(6*0)+(5*5)+(4*0)+(3*8)+(2*0)+(1*9)=65
65 % 10 = 5
So 10508-09-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O2/c1-7-9(3,4)11-12-10(5,6)8-2/h7-8H2,1-6H3

10508-09-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-2-(2-methylbutan-2-ylperoxy)butane

1.2 Other means of identification

Product number -
Other names Di-tert-amyl peroxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Plasticizers
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10508-09-5 SDS

10508-09-5Synthetic route

tert-Amyl alcohol
75-85-4

tert-Amyl alcohol

di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

Conditions
ConditionsYield
Stage #1: tert-Amyl alcohol With sulfuric acid at 0℃; for 4h; Inert atmosphere;
Stage #2: With sulfuric acid; dihydrogen peroxide at 0℃; Inert atmosphere;
43%
With sulfuric acid; dihydrogen peroxide
tert-Amyl alcohol
75-85-4

tert-Amyl alcohol

tert-amyl hydroperoxide
3425-61-4

tert-amyl hydroperoxide

di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

Conditions
ConditionsYield
With sulfuric acid
methylbutane
78-78-4

methylbutane

di-tert-butyl peroxide
110-05-4

di-tert-butyl peroxide

di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

Conditions
ConditionsYield
at 150℃; under 20594.2 Torr; Leiten von Luft;und Behandeln des Reaktionsprodukts mit tert-Pentylalkohol und 60prozentig.wss.Schwefelsaeure;
methylbutane
78-78-4

methylbutane

di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

Conditions
ConditionsYield
With hydrogen bromide; oxygen at 165℃;
i-Amyl alcohol
123-51-3

i-Amyl alcohol

di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

Conditions
ConditionsYield
(i) Al2O3, (heating), (ii) aq. H2SO4, (iii) aq. H2O2; Multistep reaction;
2-bromo-2-methylbutane
507-36-8

2-bromo-2-methylbutane

di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

Conditions
ConditionsYield
With dihydrogen peroxide; silver trifluoroacetate
tert-pentylsulfuric acid

tert-pentylsulfuric acid

di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

Conditions
ConditionsYield
With sulfuric acid; dihydrogen peroxide at 5℃;
methylbutane
78-78-4

methylbutane

hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

A

tert-Amyl alcohol
75-85-4

tert-Amyl alcohol

B

tert-amyl hydroperoxide
3425-61-4

tert-amyl hydroperoxide

C

di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

Conditions
ConditionsYield
at 165℃; Bei der Oxydation;
tert-Amyl alcohol
75-85-4

tert-Amyl alcohol

A

tert-amyl hydroperoxide
3425-61-4

tert-amyl hydroperoxide

B

di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

C

tert-amyl hydrogen peroxysulfate
1642887-92-0

tert-amyl hydrogen peroxysulfate

D

acetone
67-64-1

acetone

Conditions
ConditionsYield
With sulfuric acid; dihydrogen peroxide In water at 24.84℃; for 2h; pH=1; Kinetics;
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

S,S-diphenylsulphoximine
22731-83-5

S,S-diphenylsulphoximine

N-ethyl diphenyl sulfoximine
62129-79-7

N-ethyl diphenyl sulfoximine

Conditions
ConditionsYield
With copper diacetate In dimethyl sulfoxide at 110℃; for 16h; Inert atmosphere; Schlenk technique;81%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

phenyl(4-phenylphenyl)sulfoximine

phenyl(4-phenylphenyl)sulfoximine

N-ethyl 4-phenyldiphenyl sulfoximine

N-ethyl 4-phenyldiphenyl sulfoximine

Conditions
ConditionsYield
With copper diacetate In dimethyl sulfoxide at 110℃; for 16h; Inert atmosphere; Schlenk technique;81%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

N-phenyl-N-tosylmethacrylamide
1356668-56-8

N-phenyl-N-tosylmethacrylamide

2-methyl-N-phenyl-2-(p-tolyl)pentanamide

2-methyl-N-phenyl-2-(p-tolyl)pentanamide

Conditions
ConditionsYield
With iron(III) sulfate In fluorobenzene at 115℃; for 8h; Inert atmosphere; Sealed tube;79%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

1-isocyano-3,5-dimethylbenzene
20600-56-0

1-isocyano-3,5-dimethylbenzene

C11H15NO

C11H15NO

Conditions
ConditionsYield
With ferrocene In 1,2-dichloro-ethane at 85℃; for 12h; Sealed tube;77%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

S-methyl-S-(p-tolyl)sulfoximine
20414-85-1, 22132-97-4, 52720-03-3, 121123-21-5

S-methyl-S-(p-tolyl)sulfoximine

N-methyl methylphenyl sulfoximine

N-methyl methylphenyl sulfoximine

Conditions
ConditionsYield
With copper diacetate In dimethyl sulfoxide at 110℃; for 16h; Inert atmosphere; Schlenk technique;75%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

N-(4-methoxyphenylsulfonyl)-N-phenylmethacrylamide

N-(4-methoxyphenylsulfonyl)-N-phenylmethacrylamide

2-(4-methoxyphenyl)-2-methyl-N-phenylpentanamide

2-(4-methoxyphenyl)-2-methyl-N-phenylpentanamide

Conditions
ConditionsYield
With iron(III) sulfate In fluorobenzene at 115℃; for 8h; Inert atmosphere; Sealed tube;75%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

N-(p-tolyl)-N-tosylmethacrylamide

N-(p-tolyl)-N-tosylmethacrylamide

2-methyl-N,2-di-p-tolylpentanamide

2-methyl-N,2-di-p-tolylpentanamide

Conditions
ConditionsYield
With iron(III) sulfate In fluorobenzene at 115℃; for 8h; Inert atmosphere; Sealed tube;74%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

bis(4-chlorophenyl)(imino)-λ6-sulfanone

bis(4-chlorophenyl)(imino)-λ6-sulfanone

N-ethyl 4,4'-dichlorodiphenyl sulfoximine

N-ethyl 4,4'-dichlorodiphenyl sulfoximine

Conditions
ConditionsYield
With copper diacetate In dimethyl sulfoxide at 110℃; for 16h; Inert atmosphere; Schlenk technique;73%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

N-(4-chlorophenylsulfonyl)-N-phenylmethacrylamide

N-(4-chlorophenylsulfonyl)-N-phenylmethacrylamide

2-(4-chlorophenyl)-2-methyl-N-phenylpentanamide

2-(4-chlorophenyl)-2-methyl-N-phenylpentanamide

Conditions
ConditionsYield
With iron(III) sulfate In fluorobenzene at 115℃; for 8h; Inert atmosphere; Sealed tube;71%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

C17H14F3NO3S

C17H14F3NO3S

2-methyl-N-phenyl-2-(4-(trifluoromethyl)phenyl)pentanamide

2-methyl-N-phenyl-2-(4-(trifluoromethyl)phenyl)pentanamide

Conditions
ConditionsYield
With iron(III) sulfate In fluorobenzene at 115℃; for 8h; Inert atmosphere; Sealed tube;71%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

1-isocyano-3,5-dimethylbenzene
20600-56-0

1-isocyano-3,5-dimethylbenzene

C23H30N2O3

C23H30N2O3

Conditions
ConditionsYield
With copper(I) bromide In 1,2-dichloro-ethane at 85℃; for 8h; Sealed tube;71%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

N-phenyl-N-((2-(phenylethynyl)phenyl)sulfonyl)methacrylamide

N-phenyl-N-((2-(phenylethynyl)phenyl)sulfonyl)methacrylamide

5-((ethylsulfonyl)methyl)-5-methyl-12-phenylindolo[2,1-a]isoquinolin-6(5H)-one

5-((ethylsulfonyl)methyl)-5-methyl-12-phenylindolo[2,1-a]isoquinolin-6(5H)-one

Conditions
ConditionsYield
With iron(II) chloride at 120℃; for 12h; Sealed tube; Inert atmosphere;70%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

N-(4-chlorophenyl)-N-tosylmethacrylamide

N-(4-chlorophenyl)-N-tosylmethacrylamide

N-(4-chlorophenyl)-2-methyl-2-(p-tolyl)pentanamide

N-(4-chlorophenyl)-2-methyl-2-(p-tolyl)pentanamide

Conditions
ConditionsYield
With iron(III) sulfate In fluorobenzene at 115℃; for 8h; Inert atmosphere; Sealed tube;69%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

4-methylphenyl isocyanide
7175-47-5

4-methylphenyl isocyanide

N-p-tolylpropionamide
2759-55-9

N-p-tolylpropionamide

Conditions
ConditionsYield
With ferrocene In 1,2-dichloro-ethane at 85℃; for 12h; Sealed tube;64%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

1-(2-(4-fluorophenyl)-1H-benzo[d]imidazol-1-yl)-2-methylprop-2-en-1-one

1-(2-(4-fluorophenyl)-1H-benzo[d]imidazol-1-yl)-2-methylprop-2-en-1-one

3-fluoro-5-methyl-5-propylbenzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-one

3-fluoro-5-methyl-5-propylbenzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-one

Conditions
ConditionsYield
In fluorobenzene at 120℃; for 12h; Sealed tube;61%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

4-methyl-4'-phenyldiphenyl sulfoxide imine

4-methyl-4'-phenyldiphenyl sulfoxide imine

N-ethyl 4-phenyl-4'-methylphenyl sulfoximine

N-ethyl 4-phenyl-4'-methylphenyl sulfoximine

Conditions
ConditionsYield
With copper diacetate In dimethyl sulfoxide at 110℃; for 16h; Inert atmosphere; Schlenk technique;60%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

2-isocyanobiphenyl
3128-77-6

2-isocyanobiphenyl

6-ethylphenanthridine
13362-58-8

6-ethylphenanthridine

Conditions
ConditionsYield
With iron(II) chloride; DavePhos In fluorobenzene at 130℃; for 6h; Sealed tube; Inert atmosphere; regioselective reaction;59%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

iminodi-p-tolyl-λ6-sulfanone

iminodi-p-tolyl-λ6-sulfanone

N-ethyl 4,4'-dimethyldiphenyl sulfoximine

N-ethyl 4,4'-dimethyldiphenyl sulfoximine

Conditions
ConditionsYield
With copper diacetate In dimethyl sulfoxide at 110℃; for 16h; Inert atmosphere; Schlenk technique;58%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

4-methylphenyl isocyanide
7175-47-5

4-methylphenyl isocyanide

C21H26N2O3

C21H26N2O3

Conditions
ConditionsYield
With copper(I) bromide In 1,2-dichloro-ethane at 85℃; for 8h; Sealed tube;57%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

2-methyl-1-(2-phenyl-1H-benzo[d]imidazol-1-yl)prop-2-en-1-one

2-methyl-1-(2-phenyl-1H-benzo[d]imidazol-1-yl)prop-2-en-1-one

5-methyl-5-propylbenzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-one

5-methyl-5-propylbenzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-one

Conditions
ConditionsYield
In fluorobenzene at 120℃; for 12h; Sealed tube;55%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

N-methacryloyl-2-p-ethylphenylbenzimidazole

N-methacryloyl-2-p-ethylphenylbenzimidazole

3-ethyl-5-methyl-5-propylbenzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-one

3-ethyl-5-methyl-5-propylbenzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-one

Conditions
ConditionsYield
In fluorobenzene at 120℃; for 12h; Sealed tube;48%
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

ethyl radical
2025-56-1

ethyl radical

Conditions
ConditionsYield
bei der thermischen Zersetzung;
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

A

ethane
74-84-0

ethane

B

propane
74-98-6

propane

C

acetone
67-64-1

acetone

D

n-butane
106-97-8

n-butane

Conditions
ConditionsYield
at 250℃;
at 250℃; wietere Produkten: Aethylen; Methan;
di-tert-amyl peroxide
10508-09-5

di-tert-amyl peroxide

tert-butylisonitrile
119072-55-8, 7188-38-7

tert-butylisonitrile

C10H20NO
69563-12-8

C10H20NO

Conditions
ConditionsYield
With cyclopropane Irradiation;

10508-09-5Relevant articles and documents

Kochi

, p. 483,497 (1962)

Organic hydroperoxide formation in the acid-catalyzed heterogeneous oxidation of aliphatic alcohols with hydrogen peroxide

Liu, Qifan,Wang, Weigang,Liu, Ze,Wang, Tianhe,Wu, Lingyan,Ge, Maofa

, p. 19716 - 19724 (2014/05/20)

Organic hydroperoxides (ROOH) are reactive species which play significant roles in atmospheric processes, such as acid precipitation, hydroxyl radical cycling and secondary organic aerosol formation. Despite their observation in the atmosphere, our understanding of their formation mechanism is still incomplete. In the present work, ROOH formation was found in the acid-catalyzed heterogeneous oxidation of aliphatic alcohols with hydrogen peroxide. The kinetics and mechanism of acid-catalyzed heterogeneous oxidation of three aliphatic alcohols (2-methyl-2-butanol, 3-buten-2-ol and 2-butanol) with hydrogen peroxide were investigated. Based on the experimental results, tertiary or allyl alcohols may contribute to ROOH formation through this route while secondary alcohols may not. The kinetic experiments were conducted in a rotated wetted-wall reactor coupled to a mass spectrometer at room temperature (298 K) with 40-70 wt% H2SO4 solution. The reactive uptake coefficients were acquired for the first time. The generation and degradation mechanisms of ROOH in acidic media were proposed according to the product information. Once formed, ROOH are found to undergo two degradation pathways: the acid-catalyzed rearrangement reaction and the organic hydrogen peroxysulfate formation pathway. The newly found acid-catalyzed process may occur under certain conditions and influence particle growth in the atmosphere.

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