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Hydroperoxide, decyl, also known as 1-decanol hydroperoxide or decyl hydroperoxide, is an organic compound with the chemical formula C10H21OOH. It is a colorless liquid with a molecular weight of 170.28 g/mol. Hydroperoxide, decyl is formed by the reaction of decanol with oxygen in the presence of a catalyst, such as a metal salt or an enzyme. Hydroperoxide, decyl, is an important intermediate in the synthesis of various chemicals, including surfactants, detergents, and plasticizers. It is also used as an oxidizing agent and a radical initiator in polymerization reactions. Due to its reactive nature, it is sensitive to heat, light, and impurities, and should be stored under controlled conditions to prevent decomposition.

4225-91-6

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4225-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4225-91-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,2 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4225-91:
(6*4)+(5*2)+(4*2)+(3*5)+(2*9)+(1*1)=76
76 % 10 = 6
So 4225-91-6 is a valid CAS Registry Number.

4225-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name n--decyl hydroperoxide

1.2 Other means of identification

Product number -
Other names decyl hydroperoxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:4225-91-6 SDS

4225-91-6Relevant academic research and scientific papers

Synthesis of alkyl hydroperoxides via alkylation of gem -dihydroperoxides

Kyasa, Shivakumar,Puffer, Benjamin W.,Dussault, Patrick H.

, p. 3452 - 3456 (2013/06/26)

2-Fold alkylation of 1,1-dihydroperoxides, followed by hydrolysis of the resulting bisperoxyacetals, provides a convenient method for synthesis of primary and secondary alkyl hydroperoxides.

Kinetic description of the oxidation of hydrocarbons inhibited by sufur-containing hydrogenated quinolines

Kasaikina, O. T.,Golovina, N. A.,Shikhaliev, Kh. S.,Shmyreva, Zh. V.

, p. 755 - 759 (2007/10/02)

The inhibiting effect of dithiolthione derivatives of hydrogenated quinolines (DTT) on the oxidation of various hydrocarbons (n-decane, n-decene, ethylbenzene, β-carotene) was investigated.The inhibiting effect of the DTTs is greater at high temperatures (>100 deg C) than that of the parent hydrogenated quinolines and weaker at moderate temperatures.The DTTs do not affect the decomposition of hydroperoxides.Probably, the introduction of a dithiothione cycle to a hydroquinoline molecule decreases its reactivity toward O2 and peroxide radicals, which favors the enhancement of the antioxidative activity of the DTTs at elevated temperatures. - Key words: hydrogenated quinolines, dithiothione derivatives; n-decane, n-decene, ethylbenzene, β-carotene, inhibited oxidation.

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