14720-74-2

Basic information

• Product Name: 2,2,4-Trimethylheptane.
• Synonyms: 2,2,4-Trimethylheptane.
• CAS NO: 14720-74-2
• Molecular Formula: C₁₀H₂₂
• Molecular Weight: 142.28
• Mol File: 14720-74-2.mol
• Article Data: 3

Chemical Properties

• Melting Point: -53.99°C
• Boiling Point: 148.31°C
• Flash Point: 37.2°C
• Appearance: /
• Density: 0.7240
• Vapor Pressure: 5.17mmHg at 25°C
• Refractive Index: 1.4069
• CAS DataBase Reference: 2,2,4-Trimethylheptane.(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,4-Trimethylheptane.(14720-74-2)
• EPA Substance Registry System: 2,2,4-Trimethylheptane.(14720-74-2)

Safety Data

• Hazardous Substances Data: 14720-74-2(Hazardous Substances Data)

Usage

Uses

2,2,4-Trimethylheptane is used as a component of jet fuels.

InChI:InChI=1/C10H22/c1-6-7-9(2)8-10(3,4)5/h9H,6-8H2,1-5H3

Upstream product

• 57233-31-5 2,2,4-trimethyl-heptan-4-ol 
• 115-11-7 isobutene 
• 187737-37-7 propene 
• 75-28-5 Isobutane 
• 74-98-6 propane 
• 590-50-1 4,4-dimethyl-pentan-2-one 
• 106-98-9 1-butylene 
• 590-18-1 (Z)-2-Butene 
• 624-64-6 trans-2-Butene 
• 463-82-1 2,2-dimethylpropane 
• 96-37-7 methyl-cyclopentane 
• 106-97-8 n-butane 

Relevant articles and documents

GAS-TO-LIQUID REACTOR AND METHOD OF USING

A device and a process to propagate molecular growth of hydrocarbons, either straight or branched chain structures, that naturally occur in the gas phase to a molecular size sufficient to shift the natural occurring phase to a liquid or solid state is provided. According to one embodiment, the device includes a grounded reactor vessel having a gas inlet, a liquid outlet, and an electrode within the vessel; a power supply coupled to the electrode for creating an elecirostatic field within the vessel for converting the gas to a liquid and or solid state.

Mecanisme de l'alkylation de l'isobutane par le propene sur zeolithe. I. Etudes preliminaires de la selectivite de la reaction

Alkylation of isobutane by propylene has been studied at 70 and 80 deg C and 10 atm. of pressure over a cerium exchanged Y zeolite.Under these conditions large amounts of olefin are converted into adsorbed residues and C5-C9 isoalkanes (alkylate) are formed.Maximum alkylate yields are observed after 12 hours and become negligible after 24 hours.The main products result from alkylation, dimerization, self-alkylation and cracking reactions followed by hydride transfer.Catalyst poisonning is explained by the decrease of the zeolite cracking activity and dehydrogenation of the adsorbed species.