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592-13-2

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592-13-2 Usage

General Description

2,5-Dimethylhexane is a chemical compound classified as an alkane and falls under the category of organic compounds. It is an isomer of octane, meaning it has the same chemical formula but a different structure. It is characterized by its structural composition of two methyl groups on the third carbon atom in a hexane chain. This organic compound appears as a colorless liquid and is primarily used in the field of chemistry for research and experimental purposes. Though it is relatively less reactive like other alkanes, it can react with strong oxidizing agents and can be a potential fire hazard under certain conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 592-13-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 592-13:
(5*5)+(4*9)+(3*2)+(2*1)+(1*3)=72
72 % 10 = 2
So 592-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H18/c1-7(2)5-6-8(3)4/h7-8H,5-6H2,1-4H3

592-13-2 Well-known Company Product Price

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  • Alfa Aesar

  • (A15221)  2,5-Dimethylhexane, 99%   

  • 592-13-2

  • 5g

  • 928.0CNY

  • Detail
  • Alfa Aesar

  • (A15221)  2,5-Dimethylhexane, 99%   

  • 592-13-2

  • 25g

  • 4639.0CNY

  • Detail
  • Aldrich

  • (110582)  2,5-Dimethylhexane  99%

  • 592-13-2

  • 110582-5G

  • 528.84CNY

  • Detail

592-13-2SDS

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 2,5-DIMETHYLHEXANE

1.2 Other means of identification

Product number -
Other names 2,5-Dimethyl-hexan

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:592-13-2 SDS

592-13-2Relevant articles and documents

-

Young,Fortey

, p. 1126 (1900)

-

Selective hydrogenation of terminal alkynes over palladium nanoparticles within the pores of amino-modified porous aromatic frameworks

Karakhanov, Edward,Maximov, Anton,Terenina, Maria,Vinokurov, Vladimir,Kulikov, Leonid,Makeeva, Daria,Glotov, Aleksandr

, p. 176 - 184 (2019/05/24)

Palladium catalysts, based on porous aromatic frameworks, synthesized via Suzuki cross-coupling reaction and further modified with amino groups, were prepared and tested in hydrogenation of several unsaturated compounds. Catalysts obtained were characterized by several techniques including IR spectroscopy, solid-state NMR spectroscopy, low-temperature nitrogen adsorption, transmission electron microscopy, atomic emission spectroscopy and X-ray photoelectron spectroscopy. It was shown that the amino-groups within the structure of aromatic frameworks interact with palladium nanoparticles and enhance their selectivity towards hydrogenation of terminal alkynes.

Dendrimer-Encapsulated Pd Nanoparticles, Immobilized in Silica Pores, as Catalysts for Selective Hydrogenation of Unsaturated Compounds

Karakanov, Edward A.,Zolotukhina, Anna V.,Ivanov, Andrey O.,Maximov, Anton L.

, p. 358 - 381 (2019/04/04)

Heterogeneous Pd-containing nanocatalysts, based on poly (propylene imine) dendrimers immobilized in silica pores and networks, obtained by co-hydrolysis in situ, have been synthesized and examined in the hydrogenation of various unsaturated compounds. The catalyst activity and selectivity were found to strongly depend on the carrier structure as well as on the substrate electron and geometric features. Thus, mesoporous catalyst, synthesized in presence of both polymeric template and tetraethoxysilane, revealed the maximum activity in the hydrogenation of various styrenes, including bulky and rigid stilbene and its isomers, reaching TOF values of about 230000 h?1. Other mesoporous catalyst, synthesized in the presence of polymeric template, but without addition of Si(OEt)4, provided the trans-cyclooctene formation with the selectivity of 90–95 %, appearing as similar to homogeneous dendrimer-based catalysts. Microporous catalyst, obtained only on the presence of Si(OEt)4, while dendrimer molecules acting as both anchored ligands and template, demonstrated the maximum activity in the hydrogenation of terminal linear alkynes and conjugated dienes, reaching TOF values up to 400000 h?1. Herein the total selectivity on alkene in the case of terminal alkynes and conjugated dienes reached 95–99 % even at hydrogen pressure of 30 atm. The catalysts synthesized can be easily isolated from reaction products and recycled without significant loss of activity.

Unsaturated-compound hydrogenation nanocatalysts based on palladium and platinum particles immobilized in pores of mesoporous aromatic frameworks

Kulikov,Terenina,Kryazheva, I. Yu.,Karakhanov

, p. 222 - 229 (2017/04/07)

Heterogeneous catalysts for the hydrogenation of unsaturated hydrocarbons have been synthesized on the basis of palladium and platinum nanoparticles immobilized in pores of mesoporous aromatic frameworks, which represent a new class of carbon supports with a diamond-like ordered structure. The resulting materials have been characterized by transmission electron microscopy, IR spectroscopy, and NMR spectroscopy. It has been shown that the catalyst activity in the hydrogenation reaction depends on the substrate molecule size and adsorbability on the surface of nanoparticles. Catalytic activity has been studied in the hydrogenation of a number of unsaturated compounds at temperatures of 60 and 80°C and pressures of 1.0 and 3.0 MPa.

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