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2,4-DIMETHYLHEPTANE, also known as isoheptane, is a hydrocarbon compound with the molecular formula C9H20. It is a colorless liquid characterized by a strong odor. 2,4-DIMETHYLHEPTANE is recognized for its use as a solvent in various industrial applications and as a fuel additive, while also being noted for its flammability and relatively low toxicity.

2213-23-2

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2213-23-2 Usage

Uses

Used in Chemical Industry:
2,4-DIMETHYLHEPTANE is used as a solvent for the production of paints, varnishes, and adhesives, due to its ability to dissolve a wide range of substances and enhance the manufacturing process.
Used in Automotive Industry:
2,4-DIMETHYLHEPTANE is used as a fuel additive to improve the octane rating of gasoline, which helps in reducing engine knocking and improving the overall performance of the fuel.
Used in Safety Measures:
Given its highly flammable nature, 2,4-DIMETHYLHEPTANE requires careful handling and storage to prevent accidents and ensure the safety of workers and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 2213-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2213-23:
(6*2)+(5*2)+(4*1)+(3*3)+(2*2)+(1*3)=42
42 % 10 = 2
So 2213-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H20/c1-5-6-9(4)7-8(2)3/h8-9H,5-7H2,1-4H3

2213-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-DIMETHYLHEPTANE

1.2 Other means of identification

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

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:2213-23-2 SDS

2213-23-2Downstream Products

2213-23-2Relevant academic research and scientific papers

GAS-TO-LIQUID REACTOR AND METHOD OF USING

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Paragraph 0143, (2019/08/15)

A device and a process to propagate molecular growth of hydrocarbons, either straight or branched chain structures, that naturally occur in the gas phase to a molecular size sufficient to shift the natural occurring phase to a liquid or solid state is provided. According to one embodiment, the device includes a grounded reactor vessel having a gas inlet, a liquid outlet, and an electrode within the vessel; a power supply coupled to the electrode for creating an elecirostatic field within the vessel for converting the gas to a liquid and or solid state.

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.

Alkene oligomerization process

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Page 4-5, (2008/06/13)

A process for oligomerising alkenes having from 3 to 6 carbon atoms which comprises contacting a feedstock comprising a) one or several alkenes having x carbon atoms, and, b) optionally, one or several alkenes having y carbon atoms, x and y being different, with a catalyst containing a zeolite of the MFS structure type, under conditions to obtain selectively oligomeric product containing predominant amounts of certain oligomers. The process is carried out at a temperature comprised between 125 and 175° C. when the feedstock contains only alkenes with 3 carbon atoms and between 140 and 240° C., preferably between 140 and 200° C. when the feedstock contains comprises at least one alkene with 4 or more carbon atoms.

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