Chamaemelum nobile (flower)
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=Macroscopic Characteristics= | =Macroscopic Characteristics= | ||
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{{Macroscopy | source=United States Dispensatory (1918) | {{Macroscopy | source=United States Dispensatory (1918) | ||
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By cultivation the yellow disk florets are often converted into the white ray florets. Thus altered, the flowers are said to be double, while those which remain unchanged are called | By cultivation the yellow disk florets are often converted into the white ray florets. Thus altered, the flowers are said to be double, while those which remain unchanged are called | ||
single; but, as the conversion may be more or less complete, it generally happens that with each of the varieties there are intermingled some flowers of the other kind, or in different stages of the change. The double flowers are generally preferred; though, as the sensible properties are found in the greatest -degree in the disk florets, the single flower heads are the more powerful. [...] If not well and quickly dried, the flowers lose their beautiful white color, and are less efficient. The flowers which are largest, most double, and whitest should be preferred. They are thus described: "Flower-heads hemispherical, from about twelve to twenty millimetres in diameter, white or pale buff in color. Involucre composed of several rows of oblong bracts with membranous margins; receptable solid, conical, and densely covered with concave, blunt, narrow, scaly bracts; florets mostly ligulate and white, the ligula possessing four veins and terminating in three teeth." Br}} | single; but, as the conversion may be more or less complete, it generally happens that with each of the varieties there are intermingled some flowers of the other kind, or in different stages of the change. The double flowers are generally preferred; though, as the sensible properties are found in the greatest -degree in the disk florets, the single flower heads are the more powerful. [...] If not well and quickly dried, the flowers lose their beautiful white color, and are less efficient. The flowers which are largest, most double, and whitest should be preferred. They are thus described: "Flower-heads hemispherical, from about twelve to twenty millimetres in diameter, white or pale buff in color. Involucre composed of several rows of oblong bracts with membranous margins; receptable solid, conical, and densely covered with concave, blunt, narrow, scaly bracts; florets mostly ligulate and white, the ligula possessing four veins and terminating in three teeth." Br}} | ||
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=Microscopic Characteristics= | =Microscopic Characteristics= | ||
{{Media2 |cat=Microscopy | source=Elan M. Sudberg, Alkemist Laboratories | {{Media2 |cat=Microscopy | source=Elan M. Sudberg, Alkemist Laboratories |
Latest revision as of 21:57, 5 May 2015
Contents |
Nomenclature
Chamaemelum nobile (L.) All. Asteraceae
Syn. Anthemis nobilis L.
Standardized common name (English): Roman chamomile
Botanical Voucher Specimen
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Organoleptic Characteristics
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Macroscopic Characteristics
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Microscopic Characteristics
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High Performance Thin Layer Chromatographic Identification
Roman chamomile (flower) (Chamaemelum nobile) Lane Assignments Lanes, from left to right (Track, Volume, Sample):
Reference Sample(s) Reference: Dissolve 1.5 mg of apigenin in 5 mL of methanol. Dissolve 1 mg of parthenolide in 5 mL of methanol. Stationary Phase Stationary phase, i.e. Silica gel 60, F254 Mobile Phase Ethyl acetate, cyclohexane 1:1 (v/v) Sample Preparation Method Sample:Mix 1 g of powdered sample with 10 mL of methanol and sonicate for 10 minutes, then centrifuge or filter the solutions and use the supernatants / filtrates as test solutions. Dissolve 10 µL of the essential oil in 1 mL of toluene. Derivatization reagent: Anisaldehyde reagent; Preparation: 170 mL of ice-cooled methanol are mixed with 20 mL of acetic acid, 10 mL of sulfuric acid and 1 mL of anisaldehyde; Use: Dip (time 0, speed 5), heat at 100°C for 4 min. Detection Method Saturated chamber; developing distance 70 mm from lower edge; relative humidity 33% Other Notes Images presented in this entry are examples and are not intended to be used as basis for setting specifications for quality control purposes. System suitability test (UV 366 nm): Apigenin: blue zone at Rf ~ 0.20; Parthenolide: pink zone at Rf ~ 0.48 Identification: Compare result with reference images. The fingerprint of the test solution is similar to that of the corresponding botanical reference sample. Additional weak zones may be present. Under UV 366 nm the chromatogram of the test solution shows a strongly tailing blue zone at the position of reference substance apigenin at Rf ~ 0.20. There is a characteristic greenish zone (red zone under white light) at Rf ~ 0.30 and an intense orange zone (violet zone under white light) at Rf ~ 0.7 (yellow arrows). Test for adulteration: Under UV 366 nm there are no intense red zones (violet zone under white light) between Rf ~ 0.20 and 0.30. No blue zone is seen at the position of parthenolide (orange arrows; Feverfew flower from Mexico). Under UV 366 nm no pink zone (violet zone under white light) at Rf ~ 0.48 corresponding to reference substance parthenolide is seen and there are no brown zones at the position of apigenin at Rf ~ 0.20 (green arrows, Feverfew flower). Under UV 366 nm no blue zone is seen at the position of parthenolide (blue arrow; Chamomile flower). Chamomile flower oil does not show any zones below Rf ~ 0.60. Source: HPTLC Association [7] |
Supplementary Information
Sources
- ↑ Royal Botanic Gardens, Kew. http://specimens.kew.org/herbarium/K000410976
- ↑ United States Dispensatory (1918)
- ↑ United States Dispensatory (1918)
- ↑ PlantaPhile http://plantaphile.com/
- ↑ Elan M. Sudberg, Alkemist Laboratories http://www.Alkemist.com
- ↑ Elan M. Sudberg, Alkemist Laboratories http://www.Alkemist.com
- ↑ HPTLC Association http://www.hptlc-association.org/