Home Location and Hours Products and Services Current Sales Articles and News Artist Directory
Easel Weasels
Home
Location and Hours
Get Directions
Art Classes
Online Library
Articles and News
Art and Craft Ideas
Art Encyclopedia
Community
Artist Directory
Community Sites
Bookmark Us!
 
 
Affiliates
Affiliate Sites
Local Businesses

Easel Weasels708-361-5881

Turpentine

Turpentine

From Wikipedia, the free encyclopedia.

Turpentine
Chemical name Turpentine
Chemical formula C10H16 (approximate)
Molecular mass 136 g/mol (approximate)
CAS number [8006-64-2]
Density [0.85-0.87] g/cm3 (approximate)
Melting point < −50 °C (approximate)
Boiling point 150-170 °C (approximate)
SMILES  
Disclaimer and references

Turpentine is a fluid obtained by the complex distillation of resin obtained from trees, mainly various species of pine (Pinus). It is composed of terpenes, mainly the monoterpenes alpha-pinene and beta-pinene. Alternative names are wood turpentine, spirit of turpentine, oil of turpentine and gum turpentine. It is also known colloquially as just turps, although this more often refers to turpentine substitute (or mineral turpentine). Boiling in large tubs takes place at 155 degrees Celsius to obtain turpentine oil.

Medicinal uses

Turpentine has been used medically since ancient times.

  • Applied externally to the affected areas, turpentine is a highly effective treatment for lice.
  • Turpentine can be mixed with animal fat as a primitive chest rub for nasal and throat complaints. Some modern chest rubs still contain some turpentine (e.g., Vicks).

Industrial uses

The two primary uses of turpentine in industry are as a solvent and as a source of materials for organic synthesis.

As a solvent, turpentine is used for thinning oil-based paints, producing varnishes, and as a raw material for the chemical industry. Its industrial use as a solvent in first-world nations have largely been replaced by the much cheaper turpentine substitutes distilled from crude oil.

Turpentine is also used as a source of raw materials in the synthesis of fragrant chemical compounds. Commercially used camphor, linalool, alpha-terpineol, and geraniol are all usually produced from alpha-pinene and beta-pinene, which are two of the chief chemical components of turpentine. These pinenes are separated and purified by distillation. The mixture of diterpenes and triterpenes that is left as residue after terpentine distillation is sold as rosin.

Turpentine is also added to many cleaning and sanitary products due to its antiseptic properties and its "clean scent".

Hazards

Turpentine is an organic solvent, and thus poses many of the same hazards as do other such substances. It can burn the skin and eyes, damage the lungs and respiratory system, as well as the central nervous system when inhaled, and cause kidney failure when ingested, among other things. It is highly flammable.

 
Related Items