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3,4-Dimethylheptane, with the molecular formula C9H20, is a saturated hydrocarbon that belongs to the alkane family. It features a straight chain of seven carbon atoms with two methyl groups attached at the 3rd and 4th positions. This colorless liquid is known for its low reactivity, stability, and relatively non-toxic nature, making it suitable for various applications in the chemical industry.

922-28-1

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922-28-1 Usage

Uses

Used in Chemical Industry:
3,4-Dimethylheptane is used as a solvent for various chemical processes due to its ability to dissolve a wide range of substances. Its low reactivity and stability contribute to its effectiveness as a solvent, ensuring that it does not interfere with the reactions taking place.
Used in Fuel Industry:
As a component of the fuel mixture for internal combustion engines, 3,4-dimethylheptane enhances the performance and efficiency of the engine. Its high energy content and compatibility with other fuel components make it a valuable addition to the fuel blend.
Used in Chemical Analysis:
3,4-Dimethylheptane serves as a reference compound in chemical analysis due to its well-defined properties and predictable behavior. Its use as a standard allows for accurate comparisons and measurements in various analytical techniques.
Used in Gas Chromatography:
In the field of gas chromatography, 3,4-dimethylheptane is employed as a standard for calibrating instruments and ensuring the accuracy of results. Its distinct properties and consistent behavior make it an ideal reference compound for this analytical method.
Overall, 3,4-dimethylheptane's versatility, stability, and low toxicity make it a valuable compound in various industries, including the chemical, fuel, and analytical sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 922-28-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 922-28:
(5*9)+(4*2)+(3*2)+(2*2)+(1*8)=71
71 % 10 = 1
So 922-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H20/c1-5-7-9(4)8(3)6-2/h8-9H,5-7H2,1-4H3

922-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-Dimethylheptane

1.2 Other means of identification

Product number -
Other names Heptane, 3,4-dimethyl-

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:922-28-1 SDS

922-28-1Downstream Products

922-28-1Relevant academic research and scientific papers

GASOLINE PREPARED FROM BIOMASS-DERIVED LEVULINIC ACID

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Paragraph 0097, (2015/06/03)

The present invention provides methods for preparing a C6-C10 alkane, and mixture thereof. The methods include forming a reaction mixture containing an angelica lactone dimer, a catalyst, and a hydrogen source under conditions sufficient to reduce the angelica lactone dimer, thereby preparing the alkane. The methods can be used to prepare branched alkanes useful for fuels. Methods for preparing an angelica lactone, methods for preparing an angelica lactone dimer, and methods for reducing a lactone to an alkane are also described.

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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