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2,6,10-trimethyltridecane is an organic compound with the molecular formula C16H34. It is a branched-chain alkane, characterized by the presence of three methyl groups attached to the main carbon chain at the 2nd, 6th, and 10th carbon atoms. This structure results in a highly symmetrical and compact molecule, which contributes to its unique physical and chemical properties. The compound is a colorless liquid with a low melting point and boiling point, and it is insoluble in water but soluble in organic solvents. 2,6,10-trimethyltridecane is primarily used as a solvent, a component in fuels, and as a precursor in the synthesis of other organic compounds. Its stability and low reactivity make it a valuable substance in various industrial applications.

3891-99-4

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3891-99-4 Usage

Appearance

Colorless and odorless liquid

Usage

Lubricant and additive in industrial products (plastics, rubber, coatings)

Thermal stability

Excellent

Oxidation resistance

Excellent

Suitable for

High-temperature applications

Base stock

Synthetic lubricants

Volatility

Low

Flash point

High

Preferred in

Automotive and aerospace industries

Environmentally friendly

Non-toxic and environmentally friendly

Popular in

Consumer and personal care products

Check Digit Verification of cas no

The CAS Registry Mumber 3891-99-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,9 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3891-99:
(6*3)+(5*8)+(4*9)+(3*1)+(2*9)+(1*9)=124
124 % 10 = 4
So 3891-99-4 is a valid CAS Registry Number.

3891-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6,10-trimethyltridecane

1.2 Other means of identification

Product number -
Other names Tridecane,2,6,10-trimethyl

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:3891-99-4 SDS

3891-99-4Downstream Products

3891-99-4Relevant academic research and scientific papers

The formation features of C10–C20 regular petroleum isoprenanes

Gordadze,Giruts,Poshibaeva,Koshelev

, p. 672 - 676 (2016/10/04)

To model the formation processes of C10–C20 petroleum isoprenanes, thermolysis of regular and irregular C20–C40 isoprenanes (phytane, crocetane, squalane, and lycopane) and the suggested precursors of regular pe

Catalytic Production of Branched Small Alkanes from Biohydrocarbons

Oya, Shin-Ichi,Kanno, Daisuke,Watanabe, Hideo,Tamura, Masazumi,Nakagawa, Yoshinao,Tomishige, Keiichi

, p. 2472 - 2475 (2015/08/24)

Squalane, C30 algae-derived branched hydrocarbon, was successfully converted to smaller hydrocarbons without skeletal isomerization and aromatization over ruthenium on ceria (Ru/CeO2). The internal CH2-CH2 bonds located between branches are preferably dissociated to give branched alkanes with very simple distribution as compared with conventional methods using metal-acid bifunctional catalysts.

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