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771-29-9

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771-29-9 Usage

Chemical Properties

Hydroperoxide is formed by the oxidation of tetralin, a DuPont product, and used as a turpentine replacement. The technical grade hydroperoxide is a liquid and will have a residual odor of benzene/menthol. No rapid reaction occurs with air or water. Most alkyl monohydroperoxides are liquid, the explosivity of the lower members (e.g., methyl hydroperoxide or possibly due to traces of the dialkyl peroxides) decreasing with increasing chain length and branching. Tetralin hydroperoxide explodes on superheating the liquid. Its interaction with strong reducing agents, like lithium tetrahydroaluminate, is vigorously exothermic (13d).

Uses

Tetralin hydroperoxide has been prepared by the oxidation of tetralin in the presence of cobalt naphthenate, manganese stearate, and ceric stearate or naphthenate. Tetralin hydroperoxide, produced by the oxidation of tetralin, may be separated from reaction products by formation of its sodium salt. The kinetics of the liquid-phase oxidation of tetralin have been studied . Chen and Lin used tetralin hydroperoxide as an intermediate in the hydroxylation of tetralin to tetralol in rat liver homogenate.

General Description

Hydroperoxide formed by the oxidation of tetralin, a DuPont product, used as a turpentine replacement. The technical grade hydroperoxide is a liquid and will have a residual odor of benzene/menthol.

Reactivity Profile

Most alkyl monohydroperoxides are liquid, the explosivity of the lower members (e.g., methyl hydroperoxide, or possibly due to traces of the dialkyl peroxides) decreasing with increasing chain length and branching [Bretherick 2nd ed. 1979 p. 10]. 1,2,3,4-tetrahydro-1-naphthyl hydroperoxide explodes on superheating the liquid [Hock et al. Ber. 1933. pp. 66, 61]. It's interaction with strong reducing agents, like lithium tetrahydroaluminate, is vigorously exothermic.

Purification Methods

Crystallise the tetralin hydroperoxide from hexane, toluene at -30o (m 54.0-54.5o). The oxygen content should be ~9.70%. [Knight & Swern Org Synth Coll Vol 1V 895 1963.]

Check Digit Verification of cas no

The CAS Registry Mumber 771-29-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 771-29:
(5*7)+(4*7)+(3*1)+(2*2)+(1*9)=79
79 % 10 = 9
So 771-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H12.H2O2/c1-2-6-10-8-4-3-7-9(10)5-1;1-2/h1-2,5-6H,3-4,7-8H2;1-2H

771-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrahydro-1-naphthyl hydroperoxide

1.2 Other means of identification

Product number -
Other names 1,2,3,4-TETRAHYDRO-1-NAPHTHALENYL 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:771-29-9 SDS

771-29-9Relevant articles and documents

Hiatt et al.

, p. 1428 (1968)

Benzylic Hydroperoxidation via Visible-Light-Induced Csp3-H Activation

Inoa, Joan,Patel, Mansi,Dominici, Grecia,Eldabagh, Reem,Patel, Anjali,Lee, John,Xing, Yalan

, p. 6181 - 6187 (2020/05/22)

A highly efficient benzylic hydroperoxidation has been realized through a visible-light-induced Csp3-H activation. We believe that this reaction undergoes a direct HAT mechanism catalyzed by eosin Y. This approach features the use of a metal-free catalyst (eosin Y), an energy-economical light source (blue LED), and a sustainable oxidant (molecular oxygen). Primary, secondary, and tertiary hydroperoxides as well as silyl, benzyl, and acyl peroxides were successfully prepared with good yields and excellent functional group compatibility.

Fabrication of CuCr2O4 spinel nanoparticles: A potential catalyst for the selective oxidation of cycloalkanes via activation of Csp3-H bond

Acharyya, Shankha S.,Ghosh, Shilpi,Adak, Shubhadeep,Tripathi, Deependra,Bal, Rajaram

supporting information, p. 145 - 150 (2015/01/09)

We report here preparation of CuCr2O4 spinel nanoparticle catalyst, mediated by cationic surfactant CTAB in hydrothermal route. XRD revealed the formation of CuCr2O4 spinel phase and TEM showed the particle size of 30-60 nm. The catalyst was speculated to be highly active for selective oxidation of cyclohexane to cyclohexanone with H2O2. A cyclohexane conversion of 70% with 85% cyclohexanone selectivity was achieved over this catalyst at 50 °C temperature. Moreover, the catalyst did not show any significant activity loss even after 8 reuses and proved its efficacy in the oxidation of other cycloalkanes also.

Superhydrophobic materials as efficient catalysts for hydrocarbon selective oxidation

Chen, Chen,Xu, Jie,Zhang, Qiaohong,Ma, Yinf,Zhou, Lipeng,Wang, Min

supporting information; scheme or table, p. 1336 - 1338 (2011/03/22)

A new type of superhydrophobic material, FP-Co-SiO2 was prepared with organic groups immobilized on the surface of the SiO2-based nanocomposite. This material showed much higher catalytic activity for selective oxidation of hydrocarbons than an equivalent hydrophilic catalyst.

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