Limonene may be used as a shrinking agent to dissolve polystyrene. Chem., 1885, 227, 277. Soc. Bur. When warmed with mineral acid, limonene isomerizes to the conjugated diene α-terpinene (which can also easily be converted to p-cymene). ), various pines (e.g., Pinus echinata, Pinus ponderosa), Douglas fir (Pseudotsuga menziesii), larches (Larix spp. Recl. [all data], Wallach, 1888 [2], D-Limonene is a major component of the aromatic scents and resins characteristic of numerous coniferous and broadleaved trees: red and silver maple (Acer rubrum, Acer saccharinum), cottonwoods (Populus angustifolia), aspens (Populus grandidentata, Populus tremuloides) sumac (Rhus glabra), spruce (Picea spp. Limonene exists in R- (+) and S- (-) formations. [all data], Clover, 1908 Data from NIST Standard Reference Database 69: The National Institute of Standards and Technology (NIST) Shall we go to Paradise? [all data], Anonymous, 1942 Is that right? Boiling point Data from NIST Standard Reference Database 69: NIST Chemistry WebBook The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on … Wallach, O., Soc., 1906, 89, 839-56. binary mixtures and chemical reactions, SRSD 2 – Web Thermo Tables (WTT), "lite" edition, SRSD 3 – Web Thermo Tables (WTT), professional edition, SRD 156 – Clathrate Hydrate Physical Property Database. [1] The less common L-isomer is found in mint oils and has a piny, turpentine-like odor. Steam distillation is useful in this experiment because it lowers the temperature necessary to give rise to the boiling of limonene. Chem., 1910, 373, 267. Ber., 1930, 63, 1721. Boiling point Data from NIST Standard Reference Database 69: NIST Chemistry WebBook The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on … shall not be liable for any damage that may result from and is used as a renewables-based solvent in cleaning products. [all data], Lecat, 1926 [1] Racemic limonene is known as dipentene. I extracted the oil from the distillate using diethyl ether and collected the top layer. Ann. Timmermans, J., However, NIST makes no warranties to that effect, and NIST Charlton, R.; Day, A., It will oxidize easily in moist air and form limonene oxide, carvone, and carveol. Articles of (±)-Limonene are included as well. Chem. Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [5] It oxidizes easily in moist air to produce carveol, carvone, and limonene oxide. The terpene is also a selective activator of the adenosine A(2A) receptor on cell membranes, these cells are vital for the nervous system. Magnetic rotation of ring compounds camphor, limonene, carvene, pinene, and some of their derivatives, View information & documentation regarding ( R )-(+)-Limonene, including CAS, MSDS & more. Your Ad Here Feel free to try this out if you have a chemical unknown it might help! errors or omissions in the Database. [all data], Wallach, 1885 Sci., 1909, 4, 93. Azeotropes of Ethyl Urethane and other Azeotropes, © 2018 by the U.S. Secretary of Commerce Kafuku, K.; Nozoe, T.; Hata, C., [all data], Wallach, 1887 Street art a good distraction here you go. Limonene takes its name from French limon ("lemon"). InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3/t10-/m1/s1, National Institute of Standards and Technology, Office of Data Chem., 1888, 245, 191. Research Chemicals Catalog 1990-1991, PCR Inc., Gainesville, FL, 1990, 1. Thermochemical Investigationss IV> Heats of Combustion of Terpenes and Styrenes and Calculated Heat of Combustion, and chemical property data is available from the J. Chem. Limonene is used as a solvent for cleaning purposes, such as adhesive remover, or the removal of oil from machine parts, as it is produced from a renewable source (citrus essential oil, as a byproduct of orange juice manufacture). D-Limonene is is easily absorbed by the human digestive tract and the oil is spread throughout the body mostly to fatty tissues like the liver, the brain, white adipose tissue, and breast tissue.
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