Rosmarinus officinalis (leaf)

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AHPA recognizes other valuable resources exist regarding the identity of Rosmarinus officinalis.

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

Contents

Nomenclature

Rosmarinus officinalis L.   Lamiaceae  
Standardized common name (English): rosemary

Botanical Voucher Specimen

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Rosmarinus officinalis Tropicos 100002347 (S).jpg
Source: MOBOT, Tropicos.org[1]

Organoleptic Characteristics

[Rosmarinus officinalis'] leaves ... have a strong balsamic odor, which is possessed, but in a less degree, by all parts of the plant. Their taste is bitter and camphorous.

The tops lose a portion of their sensible properties by drying, and become inodorous by age.
Source: United States Dispensatory (1918) [2]

Macroscopic Characteristics

Rosemary is a small evergreen shrub, with an erect stem, divided into many long, slender, ash-colored branches. The leaves are numerous, sessile, opposite, about 2.5 cm. long, rigid, linear, entire, obtuse at the summit, folded backward at the edges, of a firm consistence, smooth and green on the upper surface, whitish, woolly, and glandular beneath. The flowers are axillary, pale blue or white.

Source: United States Dispensatory (1918) [3]

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PlantaPhile - 1997.jpg
Source: PlantaPhile[4]

PlantaPhile - 2567.jpg
Source: PlantaPhile[5]

Microscopic Characteristics

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Rosemary Alkemist Laboratories.jpg
Branched covering trichomes from the lower surface of the leaf observed at 400x with Acidified Chloral Hydrate Glycerol Solution.
Source: Elan M. Sudberg, Alkemist Laboratories[6]

Rosemary-1 Alkemist Laboratories.jpg
Large glandular scales observed at 400x with Acidified Chloral Hydrate Glycerol Solution.
Source: Elan M. Sudberg, Alkemist Laboratories[7]


High Performance Thin Layer Chromatographic Identification

AP-LOGO-Laboratories Crop - Copy.jpg
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Rosmarinus officinalis HPTLC ID - Natural Product Reagent + PEG UV 365 nm

Rosemary (leaf) (Rosmarinus officinalis)

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

  1. 3 μL Rosmarinic Acid ~0.1% in CH3OH
  2. 3 μL Rosmarinus officinalis-1 (leaf)
  3. 3 μL Rosmarinus officinalis-2 (leaf)
  4. 3 μL Rosmarinus officinalis-3 (leaf)
  5. 3 μL Rosmarinus officinalis-3 (leaf)
  6. 3 μL Rosmarinus officinalis-4 (leaf)
  7. 3 μL Rosmarinus officinalis-5 Vouchered Specimen (herb)
  8. 1 μL Caffeic acid, Chlorogenic Acid, Hyperoside, Rutin ~0.1% in CH3OH

Reference materials used here have been authenticated by macroscopic, microscopic &/or TLC studies according to the reference source cited below held at Alkemists Laboratories, Costa Mesa, CA. 

Stationary Phase Silica gel 60, F254, 10 x 10 cm HPTLC plates 

Mobile Phase toluene: ethyl formate: HCOOH [5/4/1] 

Sample Preparation Method 0.3g+3mL 80% CH3OH sonicate/heat @ 50°C ~ 1/2 hr 

Detection Method Natural Product Reagent + PEG -> UV 365 nm 

Reference see British Pharmacopoeia, 2003


Source: Elan M. Sudberg, Alkemist Laboratories [8]

HPTLC-assoc-Logo-farbig-Text-schwarz-300x47.png
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Rosemary (leaf) HPTLC ID - NP and PEG reagent, UV 366 nm

Rosemary (leaf) (Rosmarinus officinalis)

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

  1. 4 µL Rosemary leaf
  2. 8 µL Rosemary leaf
  3. 16 µL Rosemary leaf
  4. 1 µL Rosemary leaf 1 (Ph. Eur extract.)
  5. 2 µL Rosemary leaf 1 (Ph. Eur extract.)
  6. 4 µL Rosemary leaf 1 (Ph. Eur extract.)
  7. 2 µL Rosmarinic acid
  8. 2 µL Caffeic acid
  9. 8 µL Oregano leaf (old sample)
  10. 8 µL Rosemary leaf 2
  11. 8 µL Rosemary leaf 3
  12. 8 µL Thyme leaf
  13. 8 µL Holy basil leaf
  14. 8 µL Sweet basil leaf
  15. 8 µL Marjoram leaf 

Reference Sample(s) Reference: Dissolve 5 mg of rosmarinic acid in 10 mL of methanol. Dissolve 6 mg of caffeic acid in 10 mL of methanol. 

Stationary Phase Stationary phase, i.e. Silica gel 60, F254 

Mobile Phase Ethyl acetate, formic acid, water 15:1:1 (v/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.

Derivatization reagent: 1.) NP reagent Preparation: 1 g of natural products reagent in 200 mL of ethyl acetate 2.) PEG reagent Preparation: 10 g of polyethylene glycol 400 in 200 mL of dichloromethane Use: Heat plate 3 min at 100°C, then dip (time 0, speed 5) in NP reagent, dry and dip (time 0, speed 5) in PEG reagent 

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: Rosmarinic acid: light blue fluorescent zone at Rf ~ 0.73. Caffeic acid: light blue fluorescent zone at Rf ~ 0.76.

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. The chromatogram of the test solution shows a red zone right below the solvent front. At the position of reference substance rosmarinic acid an intense light blue zone is seen. A green zone is detected at Rf ~ 0.50 (blue arrow). Below this zone there is a pattern of characteristically colored zones of low intensity (pink arrow). An intense orange zone is detected at Rf ~ 0.21 (yellow arrow).

Test for other species: There are no two orange zones at Rf ~ 0.27 and 0.20 (red arrows, Oregano leaf or Thyme leaf). No light blue zone is seen at Rf ~ 0.32 (white arrow, Holy basil leaf). No orange zone is seen at Rf ~ 0.27 and no zone is seen at Rf ~ 0.63 (green arrows, Sweet basil leaf).


Source: HPTLC Association [9]


Supplementary Information

Sources

  1. MOBOT, Tropicos.org http://www.tropicos.org/Image/100002347
  2. United States Dispensatory (1918)
  3. United States Dispensatory (1918)
  4. PlantaPhile http://plantaphile.com/
  5. PlantaPhile http://plantaphile.com/
  6. Elan M. Sudberg, Alkemist Laboratories http://www.alkemist.com
  7. Elan M. Sudberg, Alkemist Laboratories http://www.alkemist.com
  8. Elan M. Sudberg, Alkemist Laboratories http://www.alkemist.com
  9. HPTLC Association http://www.hptlc-association.org/
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