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n-Tetratriacontane, also known as tetratriacontane or C34H70, is a hydrocarbon compound belonging to the alkane family. It is a white, waxy solid that is insoluble in water. Characterized by its high melting point and low volatility, n-tetratriacontane exhibits high stability across various temperatures, making it a versatile compound with a broad spectrum of industrial and commercial applications.

14167-59-0

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14167-59-0 Usage

Uses

Used in Lubricant Industry:
n-Tetratriacontane is used as a lubricant due to its high stability at different temperatures, making it an ideal high-temperature lubricant for industrial applications.
Used in Cosmetics Industry:
n-Tetratriacontane is used as a component in the manufacturing of cosmetics for its waxy texture and insolubility in water, contributing to the product's consistency and performance.
Used in Pesticide Industry:
n-Tetratriacontane is utilized in the production of pesticides, likely for its ability to provide a stable carrier or base for the active ingredients.
Used in Wax Manufacturing:
n-Tetratriacontane is a component in waxes and petrolatum, leveraging its waxy nature to enhance the properties of these products.
Used in Chemical Products:
n-Tetratriacontane is found in the manufacturing of various chemical products, capitalizing on its chemical stability and physical properties to improve the performance of these products.
Found in Natural Waxes:
n-Tetratriacontane is also present in natural waxes such as beeswax and the wax from the leaves of the carnauba palm, highlighting its occurrence in nature and potential use in natural product formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 14167-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,6 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14167-59:
(7*1)+(6*4)+(5*1)+(4*6)+(3*7)+(2*5)+(1*9)=100
100 % 10 = 0
So 14167-59-0 is a valid CAS Registry Number.
InChI:InChI=1/C34H70/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-34H2,1-2H3

14167-59-0 Well-known Company Product Price

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  • Sigma-Aldrich

  • (88152)  Tetratriacontane  analytical standard

  • 14167-59-0

  • 88152-250MG

  • 537.03CNY

  • Detail
  • Sigma-Aldrich

  • (88152)  Tetratriacontane  analytical standard

  • 14167-59-0

  • 88152-1G

  • 1,704.69CNY

  • Detail
  • Supelco

  • (442710)  Tetratriacontane  analytical standard

  • 14167-59-0

  • 000000000000442710

  • 1,269.45CNY

  • Detail
  • Aldrich

  • (287261)  Tetratriacontane  98%

  • 14167-59-0

  • 287261-1G

  • 795.60CNY

  • Detail

14167-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-TETRATRIACONTANE

1.2 Other means of identification

Product number -
Other names Tetratriacontane

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:14167-59-0 SDS

14167-59-0Downstream Products

14167-59-0Relevant academic research and scientific papers

WAX COMPOSITIONS COMPRISING LINEAR OLEFIN DIMERS OR HODROGENATED VARIANTS THEREOF AND METHODS FOR PRODUCTION THEREOF

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Paragraph 0142-0147; 150, (2021/09/17)

Wax compositions may be obtained by providing an olefinic feed comprising a first linear alpha olefin having m carbon atoms and a second linear alpha olefin having n carbon atoms, wherein m and n are independently selected integers each ranging from about 12 to about 100, and the olefinic feed optionally comprises one or more internal olefins and/or one or more branched olefins; contacting the olefinic feed with a metal carbene catalyst in a reactor; forming ethylene and a hydrocarbon substance comprising a linear olefin dimer comprising two carbon atoms less than a sum of m and n; removing the ethylene from the reactor while forming the linear olefin dimer; and isolating a wax composition comprising the linear olefin dimer, a hydrogenated reaction product thereof, or any combination thereof.

Efficient heterogeneous dual catalyst systems for alkane metathesis

Huang, Zheng,Rolfe, Eleanor,Carson, Emily C.,Brookhart, Maurice,Goldman, Alan S,El-Khalafy, Sahar H.,Roy MacArthur, Amy H.

experimental part, p. 125 - 135 (2010/06/20)

A fully heterogeneous and highly efficient dual catalyst system for alkane metathesis (AM) has been developed. The system is comprised of an alumina-supported iridium pincer catalyst for alkane dehydrogenation/olefin hydrogenation and a second heterogeneous olefin metathesis catalyst. The iridium catalysts bear basic functional groups on the aromatic backbone of the pincer ligand and are strongly adsorbed on Lewis acid sites on alumina. The heterogeneous systems exhibit higher lifetimes and productivities relative to the corresponding homogeneous systems as catalyst/catalyst interactions and bimolecular decomposition reactions are inhibited. Additionally, using a two-pot device, the supported Ir catalysts and metathesis catalysts can be physically separated and run at different temperatures. This system with isolated catalysts shows very high turnover numbers and is selective for the formation of high molecular weight alkanes.

Long chain (C22-C50) polyunsaturated hydrocarbons, derivatives, synthesis and uses thereof

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Page/Page column 18-19, (2009/09/08)

The present invention is directed to unsaturated or derivatized long chain (C22-C50) polyunsaturated hydrocarbons and a method of preparing the long chain hydrocarbons via electrocoupling of C12-C26 fatty acids. It has been found that soapstock is an inexpensive source of starting materials for the present method. The present invention is also directed to compositions comprising the long chain polyunsaturated hydrocarbons, which can be used as reactive diluents and modifiers in latex, epoxy, alkyd and polymer compositions. In another aspect, the present invention is directed to derivitization or ozonolysis of the long chain polyunsaturated hydrocarbons. The present method is also useful for preparing C12-26 alkyl esters and C12-26 carbon chain compounds containing a terminal olefin.

Electroorganic synthesis 65. Anodic homocoupling of carboxylic acids derived from fatty acids

Weiper-Idelmann, Andreas,Aus Dem Kahmen, Martin,Schaefer, Hans J.,Gockeln, Marianne

, p. 672 - 682 (2007/10/03)

Fatty acid derived carboxylic acids with double bonds, hydroxy-, amino-, keto-, ester- and epoxy groups are anodically coupled to dimers (Kolbe electrolysis) in 29 to 81% yield and up to a 2.5 mol scale. Problems due to the low conductivity of fatty acid salts were overcome by the use of a flow cell with a narrow electrode gap. Fatty acids with branched alkyl chains gave dimers with interesting emulsifying properties. Dimethyl hexadecanedioate, accessible from methyl azelate, could be cyclized and further converted into homomuscone and muscone in a few steps. A commercial mixture of dimeric fatty acids (C36-dicarboxylic acids) has been coupled to give C70-diesters. Acta Chemica Scandinavica 1998. Part 64: Nielsen, M. F., Batanero, B.,.

Synthesis of the Avocado Antifungal, (Z,Z)-2-Hydroxy-4-oxohenicosa-12,15-dien-1-yl Acetate

Bull, Steven D.,Carman, Raymond M.

, p. 1661 - 1672 (2007/10/02)

A synthesis of the avocado antifungal, (Z,Z)-2-hydroxy-4-oxohenicosa-12,15-dien-1-yl acetate (la), confirms the structure of the compound as isolated from both avocado fruit and leaves, and provides the absolute configuration of the natural lipid.

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