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589-43-5

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589-43-5 Usage

Description

2,4-Dimethylhexane is an organic compound belonging to the alkane family, characterized by its molecular structure with two methyl groups attached to the 2nd and 4th carbon atoms in a hexane chain. It is known for its ability to be enantioseparated through gas chromatography on various modified cyclodextrins, which is a technique used to distinguish between enantiomers of chiral compounds.

Uses

Used in Chemical Industry:
2,4-Dimethylhexane is used as a reference compound for gas chromatography, particularly in the enantioseparation of chiral compounds. Its distinct properties make it suitable for analyzing and distinguishing between different enantiomers, which is crucial in various chemical and pharmaceutical applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,4-dimethylhexane serves as a valuable tool for the development and optimization of chiral drugs. The ability to separate enantiomers is essential for understanding the different biological activities and potential side effects of each enantiomer, leading to the creation of safer and more effective medications.
Used in Research and Development:
2,4-Dimethylhexane is utilized in research and development for the study of chiral compounds and their interactions with modified cyclodextrins. This helps scientists gain insights into the structural and functional aspects of chiral molecules, which can be applied to the design of new drugs, materials, and other chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 589-43-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 589-43:
(5*5)+(4*8)+(3*9)+(2*4)+(1*3)=95
95 % 10 = 5
So 589-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H18/c1-5-8(4)6-7(2)3/h7-8H,5-6H2,1-4H3

589-43-5 Well-known Company Product Price

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  • Aldrich

  • (110574)  2,4-Dimethylhexane  99%

  • 589-43-5

  • 110574-10G

  • 1,670.76CNY

  • Detail

589-43-5SDS

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 2,4-Dimethylhexane

1.2 Other means of identification

Product number -
Other names Hexane, 2,4-dimethyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:589-43-5 SDS

589-43-5Relevant articles and documents

Impact of cationic surfactant chain length during SAPO-11 molecular sieve synthesis on structure, acidity, and n-octane isomerization to di-methyl hexanes

Guo, Lin,Bao, Xiaojun,Fan, Yu,Shi, Gang,Liu, Haiyan,Bai, Danjiang

, p. 161 - 170 (2012)

The structure, acidity, and n-octane di-branched isomerization of SAPO-11 synthesized with surfactants of different chain lengths in water-propanol system were investigated. The results showed that with the increasing chain length of surfactants, the crys

The effect of metal (Nb, Ru, Pd, Pt) supported on SBA-16 on the hydrodeoxygenation reaction of phenol

Feliczak-Guzik, Agnieszka,Szczyglewska, Paulina,Nowak, Izabela

, p. 61 - 67 (2018/07/21)

Ordered silica materials of SBA-16 type were synthesized, characterized as to their physicochemical properties and used as supports of the active phases which were niobium, ruthenium, palladium or platinum ions. Physicochemical properties of the systems o

IONIC LIQUID ALKYLATION OF 1-BUTENE TO PRODUCE 2,5-DIMETHYLHEXANE

-

Page/Page column 17, (2015/09/23)

A process for producing dimethylhexanes (DMH) is provided. The DMH can be used to produce p-xylene. The process involves the alkylation of isobutane and 1-butene using an ionic liquid to produce naphtha that is rich in DMH. The DMH is then converted in high selectivity to xylene, including p-xylene, by dehydrocyclization.

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