2453-00-1

Basic information

• Product Name: 1,3-DIMETHYLCYCLOPENTANE
• Synonyms: 1,3-DIMETHYLCYCLOPENTANE;Cyclopentane,1,3-dimethyl-
• CAS NO: 2453-00-1
• Molecular Formula: C₇H₁₄
• Molecular Weight: 98.19
• EINECS: 219-521-1
• Mol File: 2453-00-1.mol
• Article Data: 11

Chemical Properties

• Melting Point: -138.55°C
• Boiling Point: 91.18°C
• Flash Point: °C
• Appearance: /
• Density: 0.7361 (estimate)
• Vapor Pressure: 48.2mmHg at 25°C
• Refractive Index: 1.4140
• CAS DataBase Reference: 1,3-DIMETHYLCYCLOPENTANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-DIMETHYLCYCLOPENTANE(2453-00-1)
• EPA Substance Registry System: 1,3-DIMETHYLCYCLOPENTANE(2453-00-1)

Safety Data

• Hazardous Substances Data: 2453-00-1(Hazardous Substances Data)

Usage

Description

1,3-Dimethylcyclopentane, a cycloalkane with the molecular formula C7H14, is a colorless liquid characterized by a faint odor. It is insoluble in water but readily soluble in organic solvents. 1,3-DIMETHYLCYCLOPENTANE is known for its flammable nature, necessitating careful handling to avoid fire hazards.

Uses

Used in Chemical Synthesis:
1,3-Dimethylcyclopentane is utilized as a precursor in the synthesis of other organic compounds, contributing to the creation of a variety of chemical products.
Used in Industrial Processes:
As a solvent, 1,3-Dimethylcyclopentane is employed in various industrial applications, facilitating processes that require the dissolution of specific substances in a liquid medium.
Used in Fuel Industry:
Due to its flammable properties, 1,3-Dimethylcyclopentane can be used in the fuel industry, potentially contributing to the formulation of fuels or fuel additives.
Used in Research and Development:
In the scientific community, 1,3-Dimethylcyclopentane serves as a valuable compound for research and development purposes, aiding in the study of cycloalkane properties and their applications in different fields.

InChI:InChI=1/C7H14/c1-6-3-4-7(2)5-6/h6-7H,3-5H2,1-2H3

Upstream product

• 108-88-3 toluene 
• 7446-70-0 aluminium trichloride 
• 82166-21-0 methyl cyclohexane 
• 589-34-4 3-methyl-hexane 
• 592-42-7 1,5-Hexadien 
• 4056-78-4 cyclopentane-1,3-dicarboxylic acid 
• 58728-81-7 octa-1,7-dien-4-ol 
• 108-39-4 3-methyl-phenol 
• 52244-30-1 2,6-Dimethoxy-3-methylphenol 
• 5989-27-5 D-limonene 
• 58728-82-8 4-bromo-octa-1,7-diene 
• 4041-09-2 2,5-dimethylcyclopentanone 
• 19550-48-2 1,4-dimethylcyclopentene 
• 64-19-7 acetic acid 

Relevant articles and documents

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PROCESS FOR SELECTIVE RING OPENING OF CYCLIC HYDROCARBONS

PURPOSE: A process for ring opening is provided to obtain improved conversion ratio and selectivity in comparison with the case of using hydrogen as a reducing agent. CONSTITUTION: A cyclic hydrocarbon and a reducing agent are provided as supplying materials. The supplying materials are transferred into a reactor (5) and reacted under the presence of a catalyst. A product is separated from the effusion of reaction zone. The catalyst is a heterogeneous catalyst having both acid site and metallic component. The product is obtained by evaporating and heating a mixture containing 100 parts by weight of porous molecular sieve and 0.01-20 parts by weight of water soluble metallic salt. The cyclic hydrocarbon is a naphthene group cyclic hydrocarbon which is pentagonal or hexagonal compound, or an alkyl derivative thereof selected from cyclopentane and cyclohexane. The alkyl derivative is methyl, ethyl, profile, butyl, isopropyl or an isobutyl derivative.

A new approach for bio-jet fuel generation from palm oil and limonene in the absence of hydrogen

The traditional methodology includes a carbon-chain shortening strategy to produce bio-jet fuel from lipids via a two-stage process with hydrogen. Here, we propose a new solution using a carbon-chain filling strategy to convert C10 terpene and lipids to jet fuel ranged hydrocarbons with aromatic hydrocarbon ingredients in the absence of hydrogen.