Botanical Information Curcuma aromatica Salisb.
| Synonyms | Curcuma wenyujin Y.H.Chen & C.Ling |
| Common name (en) | Wild turmeric |
| Common name (ja) | キョウオウ |
| Common name (ko) | 쿠르쿠마 아로마티카 |
| Common name (ru) | Куркума ароматная |
| Common name (th) | ว่านนางคำ |
| Common name (vi) | Nghệ rừng |
| Common name (zh) | 郁金 |
Related herbal drug(s)
Curcuma amada Roxb.
Curcuma longa L.
Curcuma zanthorrhiza Roxb.
Curcuma zedoaria Roscoe
| Sample preparation | Mix 0.2 g of powdered sample with 3 mL of methanol, sonicate for 10 min, the centrifuge and use the supernatant as test solution |
| Mobile phase | Toluene, acetic acid 4:1 (v/v) |
| Derivatization | Derivatize with anisaldehyde reagent, and heat the plate at 100°C for 3 min |
| System Suitability Test (SST) | Under development |
| Specific marker(s) | Under UV 366 nm, after derivatization
|
| HPTLC Chromatograms |
|
| HPTLC Chromatograms |
|
| ATLAS documents |
ATLAS Method document of Curcuma aromatica Image comparison of Curcuma aromatica Image comparison of Curcuma aromatica and related herbal drugs Selection of the ATLAS method of Curcuma aromatica visionCATS data (CAMAG software) |
| Sample preparation | Weigh 10.0 g of the powdered sample and place it in a 100-mL conical flask, then add 50 mL of ethanol (95%). Sonicate (400 W) the mixture for 30 min. Filter and transfer the filtrate to a 150-mL round-bottomed flask. Evaporate the solvent to dryness at reduced pressure in a rotary evaporator. Dissolve the residue in 1 mL of ethanol (95%). Filter the solution |
| Mobile phase | Petroleum ether (60-80°C) , ethyl acetate 18:2 (v/v) |
| Derivatization | No derivatization |
| HPTLC Chromatograms |
|
| Sample preparation | Mix 0.2 g of powdered sample with 3 mL of methanol, sonicate for 10 min, the centrifuge and use the supernatant as test solution |
| Mobile phase | Toluene, acetic acid 4:1 (v/v) |
| Derivatization | Derivatize with anisaldehyde sulfuric acid reagent, then heat the plate at 100°C for 3 min |
| HPTLC Chromatograms |
|
| Sample preparation | Macerate 2.0 g of the coarsely powdered substance under examination with 10 mL of methanol for 24 hours, cool and filter |
| Mobile phase | Chloroform, ethanol, acetic acid 94:5:1 (v/v/v) |
| Derivatization | Heat the plate at 105°C for 5 min |
| HPTLC Chromatograms |
|
| Sample preparation | Weigh 1 g of powder, add 50 mL of petroleum ether, sonicate for 1 hour, filter, concentrate the filtrate to make 2 mL and use as the test solution |
| Mobile phase | Petroleum ether, ethyl acetate 9:1 (v/v) |
| Derivatization | Spray with vanillin-sulfuric acid reagent and heat the plate at 105°C |
| Sample preparation | To 0.5 g of powder add 10 mL of petroleum ether in a stoppered centrifuge tube, ultrasonicate for 20 min, filter, evaporate the filtrate to dryness and dissolve the residue to 1 mL of dehydrated ethanol as the test solution |
| Mobile phase | Petroleum ether (60-80ºC), acetone, ethyl acetate 94:5:1 (v/v/v). |
| Derivatization | Spray with 1% solution of vanillin in sulfuric acid and heat at 105 °C until the spot become visible |
| HPTLC Chromatograms |
|
| Sample preparation | Macerate 1 g of powdered drug with 10 mL of hexane overnight. Filter it and remove the solvent under reduced pressure. Dissolve the residue in 5 mL of hexane and use this solution |
| Mobile phase | Toluene, ethyl acetate 93:7 (v/v) |
| Derivatization | Derivatize with anisaldehyde sulfuric acid reagent, then heat the plate at 105°C for 5 min |
| HPTLC Chromatograms |
|