Leaf |
Hydrodistillation |
Using a Clevenger-type apparatus. |
GCxGC–TOFMS |
4-Hydroxy-4-methyl-2-pentanone, nopinone, p-mentha-1,5-dien-8-ol, verbenone, methyl eugenol, spathulenol, mustakone |
Silva et al. [18] |
Hydrodistillation |
Ground cinnamon and submitted to hydrodistillation using a Clevenger-type apparatus. |
GC–MS GC–FID |
α-thujene, camphene, sabinene, p-cymene, trans-linalool oxide (furanoid), linalool, borneol, α-terpineol, (E)-cinnamaldehyde, eugenol, (E)-caryophyllene, (E)-cinnamyl acetate, α-humulene, ar-curcumene, γ-gurjunene, caryolan-8-ol, camphor, limonen |
Farias et al. [19]; Pragadheesh et al. [20] |
Hydrodistillation, supercritical extraction techniques |
Small pieces of samples were immersed in distilled water. |
GC–MS |
Linalool, eugenol |
Farias et al. [19]; Jayaprakasha & Jagan Mohan Rao [21] |
Maceration extraction |
Crushed cinnamon samples were placed in ethanol. |
GC–MS |
Eugenol, trans-caryophyllene, 1,4,8-cycloundecatriene, glycerol triacetate, 4,6-dimethyldodecane, benzyl benzoate, trans-2-tridecenal, tetradecanamide, oleic acid amide |
Khasanah et al. [10] |
Fruit |
Hydrodistillation |
Ground cinnamon and submitted to hydrodistillation using a Clevenger-type apparatus. |
GC GC–MS |
Linalool |
Kaul et al. [22] |
Bark |
Hydrodistillation |
Small pieces of cinnamon bark were immersed in distilled water and extracted using a Clevenger-type apparatus. |
GC–FID |
Linalool, eugenol, α-pinene, sabinene, α-terpinene, limonene, 1,8-cineole, α-terpinene, terpinolene, terpinen-4-ol, terpineol, methyl eugenol, α-selinene |
Abdelwahab et al. [23] |
|
Hydrodistillation |
Small pieces of cinnamon bark were immersed in distilled water. |
GC–MS |
Cinnamaldehyde, trans-cinnamyl acetate, coumarin acid, 9-octadecenoic acid, 1,4-benzenedicarboxylic acid, α-pinene, 1,8-cineole, benzaldehyde, γ-terpinene, linalool, camphenilol, borneol, cyclohexane, α-terpinene, eugenol, hydrocinnamic acid, δ-cadinene, propenoic acid, caryophyllene oxide, naphthalenol, hexadecanoic acid, phthalic acid |
Kallel et al. [24] |
|
Hydrodistillation |
Small pieces of samples were immersed in distilled water. |
GC–MS |
α-pinene, camphene, β-pinene, p-cymene, limonene, 1,8-cineole, linalool, borneol, 4-terpineol, β-terpineol, bornyl acetate, α-copaene, β-elemene, zingiberene, trans-β-caryophyllene, α-humulene, γ-muurolene, α-guaiene, α-muurolene, δ-cadinene, cadina-1,4-diene, α-calacorene, α-cubebene, δ-cadinol, benzaldehyde, benzylacetaldehyde, cinnamaldehyde, cinnamyl acetate, coumarin |
Muhammad et al. [25] |
|
Distillation |
Dry ground samples of cinnamon were mixed with distilled water in bottom flask. |
GC–MS |
Eucalyptol, benzene propanol, trans-cinnamaldehyde, cinnamyl acetate, α-muurolene, coumarin (2H-1-benzopyran-2-one), linalool, eugenol, caryophyllene, eugenyl acetate, benzyl benzoate |
Gotmare & Tambe [26] |
|
Steam distillation method |
Cinnamon sticks were mashed in smaller pieces and placed in the distillation flask. |
HPLC |
Cinnamaldehyde |
Wong et al. [27] |
|
Supercritical CO2 extraction |
Crushed cinnamon was placed in an apparatus. |
GC |
Cinnamaldehyde, eugenol |
Masghati & Ghoreishi [28] |
|
Subcritical extraction |
Ground samples of cinnamon were extracted in n-butanol and ethanol. |
GC–MS (n-butanol extract) HPLC–MS (ethanol extract) |
N-butanol extract—styrene, benzaldehyde, camphene, β-pinene, linalool, (Z)-cinnamaldehyde, (E)-cinnamaldehyde (main) α-copaene, eugenol, coumarin, methyl cinnamate ethanol extract—procyanidin trimer, catechin, coumarin, (E)-cinnamaldehyde, (Z)-cinnamaledehyde, cinnamyl alcohol |
Liang et al. [29] |
|
Subcritical extraction |
Pulverized cinnamon was mixed with distilled water. |
HPLC |
Coumarin, cinnamic acid, cinnamaldehyde, cinnamyl alcohol |
Cha et al. [12] |
|
Soxhlet extraction |
Cinnamon sticks were mashed into smaller pieces and placed inside a thimble made from thick filter paper. |
HPLC |
Cinnamaldehyde |
Wong et al. [27] |
|
Water extraction |
Crushed samples of cinnamon were dissolved into distilled water after lyophilization. |
GC–MS |
Cinnamaldehyde, 1,8-cineol, α-terpinolene, borneol, γ-terpinene, benzaldehyde, carvacrol, δ-3-carene |
Jin & Cho [30] |
|
Water extraction |
Cinnamon dust was immerged in distilled water and heated. |
UPLC–MS/MS |
Quinic acid, shikimic acid, L-tyrosine, nicotinamide, adenosine, gallic acid, methyl-4-hydroxy-3-methoxycinnamate, protocatechuic acid, protocatechualdehyde, perillene, (+)-catechin hydrate, melittoside, abscisic acid, camphor, coumarin, azelaic acid, isopropyl-4-hydroxybenzoate, 6-gingerol, citric acid, protocatechuic acid, ferulaldehyde, (+)-magnoflorine, curdione, rosavin, abscisic acid, arglabin, L(−)-carnitine |
Tang et al. [16] |
|
Sonohydrodistillation |
Extraction of essential oil from powdered cinnamon was performed in a sonohydrodistillation unit consisting of a two-neck round-bottom flask. |
GC–MS |
Cinnamaldehyde |
Modi et al. [31] |
|
Ethanol extraction |
Plant cinnamon barks were powdered and mixed with ethanol. |
LC–MS/MS |
Caffeic acid, ferulic acid, pyrogallol, p-hydroxybenzoic acid, vanillin, p-coumaric acid, gallic acid, ascorbic acid |
Gulcin et al. [32] |
|
Maceration extraction |
Liquid extracts were dried and diluted in ethanol 95%. |
RP–HPLC, Folin–Ciocalteu colorimetric method |
Cinnamaldehyde, phenols |
Othman et al. [13] |
|
Solvent extraction |
Cinnamon powder was subjected to different solvents (methanol, ethanol, acetone, water). |
UPLC–HRMS |
Protocatechuic acid, 3,4-dihydroxybenzaldehyde (protocatechualdehyde), catechin, epicatechin, procyanidin B2, cinnamic acid, quercitrin (quercetin-3-rhamnoside), coumarin, syringic acid, rutin |
Muhammad et al. [33] |
|
Pulsed electric field extraction |
Ground samples of cinnamon were diluted in ethanol. The mixture was introduced between electrodes. |
Folin–Ciocalteu method |
Phenols |
Pashazadeh et al. [34] |
|
- |
Cinnamon powder was applied to the capillary by dipping it in the powder. The capillary was then placed in the helium stream. |
DART–MS |
Coumarin, cinnamaldehyde, trans-cinnamaldehyde, trans-cinnamic acid, eugenol, benzaldehyde, estragole, linalool, cinnamyl alcohol |
Pavlovich et al. [35] |