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62016-28-8

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62016-28-8 Usage

General Description

2,2,6-Trimethyloctane is a colorless liquid chemical compound with a molecular formula of C11H24. It is a branched alkane and belongs to the class of organic compounds known as monoterpenoids. It is commonly used as a solvent in various industrial processes and as a blending agent in the production of gasoline. 2,2,6-Trimethyloctane has a strong odor and is flammable, and therefore must be handled and stored with care. It is also considered to be environmentally friendly and is used in certain eco-friendly products. Overall, 2,2,6-Trimethyloctane is a versatile chemical widely used in the manufacturing and industrial sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 62016-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,1 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62016-28:
(7*6)+(6*2)+(5*0)+(4*1)+(3*6)+(2*2)+(1*8)=88
88 % 10 = 8
So 62016-28-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H24/c1-6-10(2)8-7-9-11(3,4)5/h10H,6-9H2,1-5H3

62016-28-8Downstream Products

62016-28-8Relevant articles and documents

Paraffin alkylation

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Page/Page column 7, (2008/06/13)

A liquid acid process is disclosed in which a hydrocarbon component containing an olefin, an olefin precursor or mixture and an isoalkane and a liquid acid catalyst is fed to a downflow reaction zone containing a disperser, under conditions to induce pulse flow at or near the outlet to react the isoalkane and olefin to produce a reaction product and feeding the reaction product to a vaporization zone containing a disperser under conditions to induce pulse flow at or near the outlet of the vaporization zone. A pressure drop across the disperser in the vaporization zone causes partial vaporization of the hydrocarbon which quench es the heat reaction and cooling the unvaporized portion of said reaction product, which is recovered and allowed to separate into an acid phase and hydrocarbon phase containing the alkylate. The acid catalyst and hydrocarbons may be fractally fed to the reaction zone.

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