14167-59-0

Basic information

• Product Name: n-Tetratriacontane
• Synonyms: NSC 2998;n-Tetratriacontane
• CAS NO: 14167-59-0
• Molecular Formula: C₃₄H₇₀
• Molecular Weight: 0
• EINECS: 238-013-0
• Mol File: 14167-59-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 482.4°Cat760mmHg
• Flash Point: 345.3°C
• Appearance: /
• Density: 0.812g/cm³
• Vapor Pressure: 5.36E-09mmHg at 25°C
• Refractive Index: 1.453
• CAS DataBase Reference: n-Tetratriacontane(CAS DataBase Reference)
• NIST Chemistry Reference: n-Tetratriacontane(14167-59-0)
• EPA Substance Registry System: n-Tetratriacontane(14167-59-0)

Safety Data

• Hazardous Substances Data: 14167-59-0(Hazardous Substances Data)

Usage

General Description

n-Tetratriacontane, also known as tetratriacontane or C34H70, is a hydrocarbon compound in the alkane family. It is a white, waxy solid that is insoluble in water and is primarily used as a lubricant and a component in waxes and petrolatum. It is also used in the manufacturing of cosmetics, pesticides, and other chemical products. Due to its high melting point and low volatility, n-tetratriacontane is highly stable at various temperatures and is often used as a high-temperature lubricant in industrial applications. It is also found in natural waxes, such as beeswax and the wax from the leaves of the carnauba palm. Overall, n-tetratriacontane is a versatile compound that has a wide range of industrial and commercial applications.

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

Upstream product

• 62154-85-2 1-iodo-tetratriacontane 
• 26825-83-2 1-iodoheptadecane 
• 593-29-3 potassium stearate 
• 64-19-7 acetic acid 
• 57-11-4 stearic acid 
• 106593-78-6 4-ethyl-4-methyl-octanoic acid 
• 3508-00-7 1-bromoheptadecane 
• 106976-78-7 2-<2,3-(isopropylidenedioxy)propyl>-1,3-dithiane 
• 64-17-5 ethanol 
• 60-33-3 linoleic acid 
• 124-18-5 decane 
• 57-09-0 17-tetratriacontene 

Downstream Products

• 124-38-9 carbon dioxide 

Relevant articles and documents

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Efficient heterogeneous dual catalyst systems for alkane metathesis

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.

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

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.,.