Metatags:
(+)-limonene
(-)-limonene
(4S)-1-methyl-4-isopropenylcyclohex-1-ene
(D)-limonene
1-methyl-4-(1-methylethenyl)cyclohexene
4-mentha-1,8-diene
AISA 5203-L (+)limonene
d-limonene
dipentene
limonene
limonene, (+-)-isomer
limonene, (R)-isomer
limonene, (S)-isomer
D-Limonene
(+)-Limonene
(+)-carvene
(R)-(+)-Limonene
(+)-(4R)-Limonene
5989-27-5
(+)-p-Mentha-1,8-diene
(4R)-Limonene
Citrene
(+)-Dipentene
(+)-R-Limonene
D-(+)-Limonene
(R)-p-Mentha-1,8-diene
(R)-4-Isopropenyl-1-methyl-1-cyclohexene
D-LİMONEN, Likit formlu, renksiz bir hidrokarbondur. Güçlü turunç kokusu, genel şekliyle D-isomeri olarak geçer. Limon / portakal kabuğu yağı olarak su buharı distilasyonuyla elde edilir. Limonen güçlü antiseptik yeteneği ile temizlik malzemelerinde ve pestisitlerde kullanılır. Ayrıca pek çok leke çıkarıcıda çözücü özelliği bulunmaktadır.
Limonene is a colorless liquid hydrocarbon classified as a cyclic terpene. The more common d-isomer possesses a strong smell of oranges. It is used in chemical synthesis as a precursor to carvone and as a renewables-based solvent in cleaning products.
Limonene takes its name from the lemon, as the rind of the lemon, like other citrus fruits, contains considerable amounts of this compound, which contributes to their odor. Limonene is a chiral molecule, and biological sources produce one enantiomer: the principal industrial source, citrus fruit, contains d-limonene ((+)-limonene), which is the (R)-enantiomer. Racemic limonene is known as dipentene. d-Limonene is obtained commercially from citrus fruits through two primary methods: centrifugal separation or steam distillation.
