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

General Description

1,3-Dimethylcyclopentane is a chemical compound classified as a cycloalkane, with the molecular formula C7H14. It is a colorless liquid with a faint odor, and is insoluble in water but soluble in organic solvents. 1,3-Dimethylcyclopentane is commonly used as a solvent in various industrial processes, and can also be used as a precursor in the synthesis of other organic compounds. It is flammable and should be handled with care, as it can pose a fire hazard. Additionally, it is important to note that 1,3-Dimethylcyclopentane may cause irritation to the skin and eyes upon contact, and should be handled in a well-ventilated area.

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

Upstream product

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• 82166-21-0 methyl cyclohexane 
• 108-88-3 toluene 
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• 64-19-7 acetic acid 
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• 5989-27-5 D-limonene 
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• 58728-82-8 4-bromo-octa-1,7-diene 
• 4041-09-2 2,5-dimethylcyclopentanone 

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.