Revision as of 06:37, 23 January 2013 by 
JKim  (Talk)
Introduction
Macroscopic Entries
Microscopic Entries
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| Fragment of the corolla showing brown laticiferous vessels observed at 400x with Acidified Chloral Hydrate Glycerol Solution.cellular structures identified in this botanical specimen are fragment of the corolla showing brown laticiferous vessels and three pored pollen grain shown exuding contents when observed at 400x with Acidified Chloral Hydrate Glycerol Solution. Source: Elan M. Sudberg, Alkemist Laboratories [1] |  |  |  | 
HPTLC Entries
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Carthamus tinctorius HPTLC ID - Natural Product Reagent + PEG UV 365 nm Safflower (flower) (Carthamus tinctorius) Lane Assignments Lanes, from left to right (Track, Volume, Sample): 
1 μL Rutin, Caffeic Acid, Hyperoside, Chlorogenic Acid ~ 0.1% in Methanol3 μL Carthamus tinctorius-1 (flower)3 μL Carthamus tinctorius-2 (flower)3 μL Carthamus tinctorius-3 (flower)3 μL Carthamus tinctorius-3 (flower)3 μL Carthamus tinctorius-4 (flower)3 μL Carthamus tinctorius-5 (flower)1 μL Rutin, Caffeic Acid, Hyperoside, Chlorogenic Acid ~ 0.1% in Methanol 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 ethyl acetate: AcCOOH: HCOOH: H2O [10/1.1/1.1/2.4]  Sample Preparation Method 0.3 g + 3 ml CH3OH sonicated + heated @ 50° C ~ 1 hr  Detection Method Natural Product Reagent + PEG -> UV 365 nm  Reference see Adapted from Plant Drug Analysis, Wagner, H., 1996 Source: Elan M. Sudberg, Alkemist Laboratories [2]
 
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Other Points of Interest
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