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Technology Process of PETROLEUM ETHER

PETROLEUM ETHER

Base Information
  • Chemical Name:PETROLEUM ETHER
  • CAS No.:8032-32-4
  • Molecular Formula:C7H7BrMg
  • Molecular Weight:195.33948
  • Hs Code.:27101299
PETROLEUM ETHER

Synonyms:BP 2;BP 2(solvent);Benzine (light petroleum distillate);Benzoline;Canadol;Naphtha, ligroine;Painters' naphtha;Refined solvent naphtha;Skellysolve F;Skellysolve G;V.M. and P. naphtha;P. naphtha;Varnishmakers' and painters' naphtha;Varnish makers' naphtha;Varnish makers' naphtha and painters' naphtha;Petroleum ether 90-120℃;Ligroin;

Suppliers and Price of PETROLEUM ETHER
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Petroleum ether
  • 250ml
  • $ 75.00
  • Sigma-Aldrich
  • Petroleum ether ACS reagent
  • 4x4l
  • $ 734.00
  • Sigma-Aldrich
  • Petroleum Ether BP 65-100°C Reagent
  • 20 L
  • $ 622.52
  • Sigma-Aldrich
  • Petroleum ether anhydrous
  • 2l
  • $ 136.00
  • Sigma-Aldrich
  • Petroleum ether spectrophotometric grade
  • 2l
  • $ 136.00
  • Sigma-Aldrich
  • Gasoline, premium unleaded
  • 3
  • $ 176.00
  • Sigma-Aldrich
  • Ligroine Practical
  • 20 L
  • $ 447.00
  • Sigma-Aldrich
  • Petroleum ether
  • 5
  • $ 432.00
  • Sigma-Aldrich
  • Gasoline, premium unleaded
  • 5
  • $ 432.00
  • Sigma-Aldrich
  • Petroleum ether ACSreagent
  • 18 L
  • $ 361.00
Total 20 raw suppliers
Chemical Property of PETROLEUM ETHER
Chemical Property:
  • Appearance/Colour:Clear liquid 
  • Vapor Pressure:25.8 psi ( 55 °C) 
  • Melting Point:-40oC 
  • Refractive Index:n20/D 1.428  
  • Boiling Point:35-60oC 
  • Flash Point:-30oC 
  • PSA：0.00000 
  • Density:0.64 
  • LogP:0.00000 
  • Storage Temp.:Store at room temperature. 
  • Water Solubility.:Insoluble in water. 
Purity/Quality:

99% *data from raw suppliers

Petroleum ether *data from reagent suppliers

Safty Information:
  • Pictogram(s): R11:Highly flammable.; 
  • Hazard Codes:Xn,T,F,N,F+ 
  • Statements: 12-65-45-67-51/53-38-11-22-50/53-10-39/23/24/25-23/24/25-46-66-52/53 
  • Safety Statements: 62-45-53-61-16-60-23-36/37-24 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Description Petroleum ether, a petroleum distillation fraction, is a mixture of low molecular weight aliphatic hydrocarbons (mostly pentanes and hexanes) with a low boiling range, typically around 30-60oC. Its name is derived from its origin and its ease of evaporation.The majority components include paraffins, olefins, naphthenes, aromatics, and about 10%–40% ethyl alcohol。 Petroleum ether is commonly used as a nonpolar solvent for oils, fats, and waxes. Petroleum ether is used in pharmaceutical industries as a solvent to isolate compounds, e.g. petroleum ether can extract stigmasterol and beta-sitosterol from the aerial parts of Ageratum conyzoides and compounds with immunomodulatory activity from Anacyclus pyrethrum. It is also used as a detergent, a fuel, insecticide, in paints and varnishes, and in photography.
  • uses Petroleum ether is generally a mixture of low boiling aliphatic hydrocarbons mainly hexane and pentane. It is generally used as a laboratory solvent and also as an extraction solvent.Petroleum ether has been used for the analysis of total dietary fiber content by employing a total dietary fibre assay kit. It may be used in the absorption chromatographic purification of organic compounds.
  • Uses Petroleum ether 35/60 is used as a mobile phase in High Performance Liquid Chromatography and Liquid Chromatography coupled with Mass Spectrometry. Thinners in paints and varnish.
Refernces

Aminomethylation and hydroxymethylation of purine-6(1H)-thione and 6-alkylthiopurines.

10.1021/jm00313a025

The research focuses on the chemical synthesis and analysis of various purine derivatives, specifically 6-(alkylthio)-9-(hydroxymethyl)-SH-purines. The study investigates the hydroxymethylation of purine-6(1H)-thione and its derivatives, revealing that substitution occurs at the 9 position of the purine ring. Key chemicals involved include ethyl acetate, ligroin, benzene, ethyl alcohol, and petroleum ether, used as solvents in the synthesis and analysis processes. The researchers also utilized aqueous formaldehyde and sodium carbonate for hydroxymethylation reactions. Additionally, the study examines the infrared and ultraviolet spectra of these compounds, as well as their stability and reactivity with isocyanates. One of the synthesized compounds was screened for antitumor activity, showing promising results in certain leukemia models. The research provides valuable insights into the structure and potential applications of these purine derivatives.

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