Turpentine in the context of "Camphene"

A solvent (from the Latin solvō, "loosen, untie, solve") is a substance that dissolves a solute, resulting in a solution. A solvent is usually a liquid but can also be a solid, a gas, or a supercritical fluid. Water is a solvent for polar molecules, and the most common solvent used by living things; all the ions and proteins in a cell are dissolved in water within the cell.

Major uses of solvents are in paints, paint removers, inks, and dry cleaning. Specific uses for organic solvents are in dry cleaning (e.g. tetrachloroethylene); as paint thinners (toluene, turpentine); as nail polish removers and solvents of glue (acetone, methyl acetate, ethyl acetate); in spot removers (hexane, petrol ether); in detergents (citrus terpenes); and in perfumes (ethanol). Solvents find various applications in chemical, pharmaceutical, oil, and gas industries, including in chemical syntheses and purification processes

Larches are deciduous conifers in the genus Larix, of the family Pinaceae. Growing to as much as 60 m (195 ft) tall, they are native to the cooler regions of the Northern Hemisphere. They grow in lowland forests in the far north, and high in mountains further south. Larches are among the dominant plants in the boreal forests of Siberia and Canada, making them the most abundant genus of trees on earth. Larch wood is tough and relatively durable. The wood is used in boatbuilding, cladding, decking, garden furniture, fencing, and construction. Products extracted from larch include arabinogalactan, rosin, turpentine, and an essential oil.

Limonene (/ˈlɪmənˌiːn/) is a colorless liquid aliphatic hydrocarbon classified as a cyclic monoterpene, and is the major component in the essential oil of citrus fruit peels. The (+)-isomer, occurring more commonly in nature as the fragrance of oranges, is a flavoring agent in food manufacturing. It is also used in chemical synthesis as a precursor to carvone and as a renewables-based solvent in cleaning products. The less common (−)-isomer has a piny, turpentine-like odor, and is found in the edible parts of such plants as caraway, dill, and bergamot orange plants.

Terpenes (/ˈtɜːrpiːnz/ TUR-peenz) are a large and diverse class of natural products with the general formula (C₅H₈)_n, where n ≥ 2. They serve as crucial biosynthetic building blocks in many organisms, particularly plants. Comprising more than 30,000 compounds, these unsaturated hydrocarbons are produced predominantly by plants, particularly conifers. In plants, terpenes and terpenoids are important mediators of ecological interactions, while some insects use some terpenes as a form of defense. Other functions of terpenoids include cell growth modulation and plant elongation, light harvesting and photoprotection, and membrane permeability and fluidity control.

Terpenes are classified by the number of carbons: monoterpenes (C₁₀), sesquiterpenes (C₁₅), diterpenes (C₂₀), as examples. The terpene alpha-pinene is a major component of turpentine, a common solvent.

Singlet oxygen, systematically named dioxygen(singlet) and dioxidene, is a gaseous inorganic chemical with two oxygen atoms in a quantum state where all electrons are spin-paired, known as a singlet state. It is the lowest excited state of the diatomic oxygen molecule, which in general has the chemical structure O=O and chemical formula O
₂. Singlet oxygen can be written more specifically as
[O
₂] or
O
₂. The more prevalent ground state of O
₂ is known as triplet oxygen. At room temperature, singlet oxygen will slowly decay into triplet oxygen, releasing the energy of excitation.

Singlet oxygen is a gas with physical properties differing only subtly from the ground state. In terms of its chemical reactivity, however, singlet oxygen is far more reactive toward organic compounds. It is responsible for the photodegradation of many materials but can be put to constructive use in preparative organic chemistry and photodynamic therapy. Trace amounts of singlet oxygen are found in the upper atmosphere and in polluted urban atmospheres where it contributes to the formation of lung-damaging nitrogen dioxide. It often appears and coexists confounded in environments that also generate ozone, such as pine forests with photodegradation of turpentine.