Tanacetum parthenium (flower)

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AHPA recognizes other valuable resources exist regarding the identity of Tanacetum parthenium.

To submit a suggestion or contribution, please contact Merle Zimmermann.

Contents

Nomenclature

Tanacetum parthenium (L.) Sch. Bip.   Asteraceae  
Syn. Chrysanthemum parthenium (L.) Bernh.  
Standardized common name (English): feverfew

Botanical Voucher Specimen

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Tanacetum parthenium Tropicos 100018502.jpg
Source: MOBOT, Tropicos.org[1]

Tanacetum parthenium MA31406JD A0606.jpg
Source: Botanical Voucher Specimen Library, Alkemists Laboratories[2]

Organoleptic Characteristics

[Tanacetum parthenium] has an odor and taste analogous to those of chamomile.

Source: United States Dispensatory (1918) [3]

Macroscopic Characteristics

A tall, perennial, branching herbaceous plant, with bipinnately divided leaves, the divisions being ovate, and compound flowers in a corymb.

[The flowers may be distinguished from] those of the true chamomile plant, Anthemis nobilis, which they closely resemble, especially when double ... by their peculiar odor, their small receptacle, which is, moreover, rounded and flattened above, instead of being conical and somewhat pointed as in the Anthemis, and by the tubular five-toothed central florets, which in the chamomile are small, few, and scarcely visible, but in the two former species are large, very numerous, and very long.

Source: United States Dispensatory (1918) [4]

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PlantaPhile - 350.jpg
Source: PlantaPhile[5]

PlantaPhile - 3056.jpg
Source: PlantaPhile[6]

Microscopic Characteristics

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Tanacetum - Alkemist Laboratories.jpg
Long slender terminal cell of a multicellular trichome observed at 400x with Acidified Chloral Hydrate Glycerol Solution.
Source: Elan M. Sudberg, Alkemist Laboratories[7]

Tanacetum-1 - Alkemist Laboratories.jpg
Uniseriate covering trichome with numerous isodiametric basal cells and an elongated tapering end observed at 400x with Acidified Chloral Hydrate Glycerol Solution.
Source: Elan M. Sudberg, Alkemist Laboratories[8]

Tanacetum-2 - Alkemist Laboratories.jpg
Epidermis of leaf showing wavy anticlinal wall & short biseriate glandular trichomes observed at 400x with Acidified Chloral Hydrate Glycerol Solution.
Source: Elan M. Sudberg, Alkemist Laboratories[9]

High Performance Thin Layer Chromatographic Identification

HPTLC-assoc-Logo-farbig-Text-schwarz-300x47.png
(thumbnail)
Feverfew (flower) HPTLC ID - Anisaldehyde reagent, UV 366 nm

Feverfew (flower) (Tanacetum parthenium)

Lane Assignments Lanes, from left to right (Track, Volume, Sample):

  1. 1 µL Feverfew flower from Mexico
  2. 2 µL Feverfew flower from Mexico
  3. 4 µL Feverfew flower from Mexico
  4. 3 µL Feverfew flower
  5. 3.5 µL Feverfew flower
  6. 4 µL Feverfew flower
  7. 2 µL Parthenolide
  8. 2 µL Apigenin
  9. 1 µL Roman Chamomile flower
  10. 2 µL Roman Chamomile flower
  11. 4 µL Roman Chamomile flower
  12. 1 µL Chamomile flower
  13. 2 µL Chamomile flower
  14. 4 µL Chamomile flower
  15. 1 µL Chamomile flower oil 

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 prominent pink zone (violet zone under white light) at Rf ~ 0.48 corresponding to reference substance parthenolide. Above it there is a greenish zone (grey zone under white light) and a weak brownish zone (violet zone under white light). At the position of reference substance apigenin (Rf ~ 0.20) there are two brown zones (grey zone under white light) (green 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 blue zone at the position of apigenin (Rf ~ 0.20) is seen (yellow arrow; Roman Chamomile 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 [10]

Supplementary Information

Sources

  1. MOBOT, Tropicos.org http://www.tropicos.org/Image/100018502
  2. Botanical Voucher Specimen Library, Alkemists Laboratories http://www.alkemist.com
  3. United States Dispensatory (1918)
  4. United States Dispensatory (1918)
  5. PlantaPhile http://plantaphile.com/
  6. PlantaPhile http://plantaphile.com/
  7. Elan M. Sudberg, Alkemist Laboratories http://www.alkemist.com
  8. Elan M. Sudberg, Alkemist Laboratories http://www.alkemist.com
  9. Elan M. Sudberg, Alkemist Laboratories http://www.alkemist.com
  10. HPTLC Association http://www.hptlc-association.org/
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