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3-Methyltridecane, an alkane hydrocarbon with the molecular formula C14H30, is a colorless, odorless liquid at room temperature. It features a chain of 14 carbon atoms with methyl groups attached to the third, seventh, and eleventh carbon atoms. 3-METHYLTRIDECANE is insoluble in water and is known for its pleasant, long-lasting scent.

6418-41-3

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6418-41-3 Usage

Uses

Used in Fragrance Industry:
3-Methyltridecane is used as a fragrance ingredient for its pleasant and enduring scent, enhancing the appeal of perfumes and other personal care products.
Used in Lubricant Production:
This chemical compound serves as a component in the production of lubricants, contributing to their performance and efficiency in various mechanical applications.
Used as an Industrial Solvent:
3-Methyltridecane is utilized as a solvent in a range of industrial processes, facilitating the dissolution of other substances and aiding in various manufacturing tasks.

Check Digit Verification of cas no

The CAS Registry Mumber 6418-41-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6418-41:
(6*6)+(5*4)+(4*1)+(3*8)+(2*4)+(1*1)=93
93 % 10 = 3
So 6418-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H30/c1-4-6-7-8-9-10-11-12-13-14(3)5-2/h14H,4-13H2,1-3H3

6418-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyltridecane

1.2 Other means of identification

Product number -
Other names 3-Methyl-tridecan

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:6418-41-3 SDS

6418-41-3Downstream Products

6418-41-3Relevant academic research and scientific papers

Cobalt-catalyzed cross-coupling reaction between functionalized primary and secondary alkyl halides and aliphatic Grignard reagents

Cahiez, Gerard,Chaboche, Christophe,Duplais, Christophe,Giulliani, Arianna,Moyeux, Alban

supporting information; experimental part, p. 1484 - 1488 (2009/07/01)

The coupling of primary and secondary unactivated alkyl bromides with alkyl-Grignard reagents was performed in good yields under mild conditions by using a new catalytic system: consisting of cobalt chloride and tetramethylethylenediamine (CoCl2·2 LiI, 4TMEDA). The reaction is very chemoselective since ketone, ester and nitrile functions are tolerated.

Process for hydrogenation of carboxylic acids and derivatives to hydrocarbons

-

Page/Page column 7-8, (2008/06/13)

A process for hydrogenating a carboxylic acid and/or derivative thereof having a carboxylate group represented by the general formula R1COO-, which process comprises feeding hydrogen and the carboxylic acid and/or derivative thereof to a reactor and maintaining conditions within the reactor such that hydrogen reacts with the carboxylic acid and/or derivative thereof to produce a product stream comprising carbon dioxide, carbon monoxide, methane and hydrocarbons represented by general formulae R1H and R1CH3, characterised in that the molar ratio of R1H : R1CH3 is above a pre-determined value and/or the mole ratio of the sum of carbon dioxide, carbon monoxide and methane to carboxylate groups is above a pre-determined value.

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