Abstract The present investigation was carried out to analyze the active constituents present in aerial parts (dry seeds) of Croton bonplandianum Baill (Euphorbiaceae) for by GC-MS analysis. The presence of phytochemical compounds was screened by qualitative method. Totally 4 bioactive Phytochemical compounds were identified in the n-hexane extract of Croton species, the components were identified by comparing their relation indices and mass spectra Fragmentation patterns with those stored on the MS-Computer library and also form the published literatures. The prevailing compounds were Squalene, (9Z,12Z)-octadeca-9,12-dienoic acid, methyl 12-oxo-octadec-9-enoate -, and 11,14,17-octadecatrienoate. The research reveals the potential of hexane …show more content…
bonplandianum is having wide range of phytochemical compounds. Plant and leaves contain alkaloids sparsiflorine, crotoflorine, crotsparine, crotsparinine, proaporphine, isoquinoline dienone, N-methylcrotsparine and N-methylcrotsparinine. Leaves and stem contains ß-sitosterol and taraxerol, vomifoliol, ursolic acid and tetrahydroglazievine. Leaves also contain rutin. Seeds contain phorbol diesters, phorbol trimesters, cocarcinogen; alkaloid, 3-OMe-4, 6-di-OH-morphinandien-7-one and norsinoacutine [10]. The roots in addition to ß-sitosterol contain phenolic quinonoid alkaloid norsinoacutine and 3-methoxy-4,6-dihydroxy morphinan-dien-7-one. An unusual finding of this species is the hyper accumulation of copper in it [10]. The seed of Croton bonplandianum contains diterpines, phorbol ester, including 12-orthotrideconeoly-phorbol-13-acetat (TPA) and myristoyl phorbol acetate (MPA). TPA is a carcinogen, affecting prostaglandin …show more content…
collection (in the month of May 2015) from surrounding areas of rural areas of Vijayawada, Krishna District. The plant material was authenticated at the Botanical Survey of India, Howrah, West Bengal, India. Figure 1: Croton bonplandianum- Fruits, Blooms, Leaves Preparation of plant extract Preparation of plant extract The dry material of C. bonplandianum passed through sieve (70). The coarse powdered drug (200grams) was extracted in Soxhlet apparatus for 48 h with n-hexane (60-75°C, 2L). n-Hexane extract obtained was concentrated under reduced pressure in rotatory evaporator below 60°C temperature to get semisolid sticky residue (15gm) Column chromatography n-Hexane extract of the plant material (5 g) was subjected to column chromatography using silica gel (80-120 #) as adsorbent and eluted with the mixture of n-hexane: ethyl acetate in gradient manner. n-hexane: ethyl acetate (90: 10) fraction yielded dark brown color liquid. GC-MS Analysis GC-MS analysis of the extract was performed using a Perkin-Elmer GC Clarus 500 system and Gas chromatograph interfaced to a Mass spectrometer (GC-MS) equipped with a
In this lab, the oxidation of a secondary alcohol was performed and analyzed. An environmentally friendly reagent, sodium hypochlorite, was used to oxidize the alcohol, and an IR spectrum was obtained in order to identify the starting compound and final product. The starting compound could have been one of four alcohols, cyclopentanol, cyclohexanol, 3-heptanol, or 2-heptanol. Since these were the only four initial compounds, the ketone obtained at the end of the experiment could only be one of four products, cyclopentanone, cyclohexanone, 3-heptanone, or 2-heptanone. In order to retrieve one of these ketones, first 1.75g of unknown D was obtained.
Method In this experiment, we tested our hypothesis through the use of chromatography paper. Chromatography paper have the ability to separate colored chemicals or substances. We also used 10 grams of grinded coleus leaves and grass leaves, 90% acetone, magnesium sulfate, pencil, ruler, forceps, 1 capillary, 1 jar with lid, and a timer to conduct this experiment. We began this experiment by grinding the 10 grams of coleus leaves and grass leaves in 10mL of 90% acetone.
If the plant was going to be turned into medicine for heart patients but could be poisonous and Mr.Longmire died from a heart attack the plant was the reason for his death. A couple of minutes before JBL Jr. died he was drinking bourbon in his room from a glass. The evidence the police uncovered found 2 percent of water, 42 percent of bourbon, and 56 percent of digoxin. Digoxin is a medicine used to treat heart patients but Desiree wasn’t done tweaking the medicine she was creating to make it safe to consume. Digoxin isn’t something you should have in your bourbon meaning JBL Jr. didn’t know that it was in there in the first place.
A mixture of 0.25 g of camphor (1.64 mmol), 1.5 mL of methanol, and 0.25 g of sodium borohydride (6.60 mmol, NaBH4) was boiled for 2 minutes. Moreover, the addition of 10 mL of ice deionized water resulted in a white solid after the organic solution was vacuum filtered. The organic solid was dissolved in 10 mL of dichloromethane (CH2Cl2) and small amounts of anhydrous sodium sulfate (NaSO4) to dry. The organic solution was decanted and evaporated for melting point (203.3-203.8 °C), NMR, and IR spectroscopy. Product formation and heats of formation (borneol = -1.203675E6 kJ/mol, isoborneol = -1.203687E6 kJ/mol) were analyzed.
In this lab, three unknown compounds were separated from a mixture and identified by melting point. Unknown mixture #124 has components of acid, base and neutral compound. The compounds were identified by melting point and matched up with the known melting points from a given list. In order to identify the compound it was important to separate by dissolving the mixture in an organic solvent which was not soluble in water, and then extracting the solution first with HCl, and then dilute sodium hydroxide solution. From the separation mixture, the aqueous layer were obtained and labeled as TT-1 (base), TT-2(acid) and TT-3 (neutral) in three different test tubes for later recovery.
With this, the reaction of 4-methylcyclohexanol with a strong acid (H3PO4) acting as a catalyst was successful, and the product 4-methylcyclohexene was obtained as
The main objective of this experiment was to isolate the compounds in a given mixture, which was composed of 50% fluorene, 42% o-toluic acid, and 10% 1, 4-dibrombenzene. Techniques of extraction and crystallization was used to perform the procedure. The two major compounds in the mixture (fluorene and o-toluic acid) was collected; these were separated by two major methods. The o-toluic acid was extracted first by using macroscale extraction and testing for acidity. By adding a strong acid to the aqueous layer, which contained o-toluic acid, the solution becomes acidic and also allows the solid in the layer to precipitate.
In this experiment, preparative gas chromatography was performed to isolate components present in a mixture before infrared spectroscopy was utilized to determine the separated parts. At the start of the lab, unknown # C-2 at 170C was provided for testing. When the GC was ran, the retention time for fraction 1 started with 2.12 minutes and ended with 2.96 minutes. The retention time for fraction 2 started at 4.56 minutes and ended at 5.96 minutes. After centrifugation, a small amount of the sample was pulled to the bottom of the conical vials to be used in the infrared spectroscopy.
Links between many dream related By Alex Kent theories and Inception In this essay I will be looking at whether Inception supports Freud’s Dream Theory or the Activation Synthesis Theory. I will be analysing multiple scenes that promote their corresponding theory. These can be the likes of external dream influences, Freud’s many theories or the Activation synthesis theory In my first analysis it is not of a scene but of a concept in the movie.
Serotonin is a monoamine neurotransmitter which is found in the blood, gastrointestinal tract, and in the nervous system in humans, animals and several plants. Its chemical formula is C10H12N2O. It is biosynthesized from tryptophan which is a chemical precursor of the serotonin. It was first reported lab synthesis by M.E. Speeter and his co-workers in 1951. This molecule initially started with 5-benzyloxyindole (C15H13NO).The majority of the serotonin in humans is found in the gut, where it regulates intestinal activity. It also regulates mood (As serotonin tension loosens, the person becomes less stressed and more relaxed.)
In the experiment, the primary initial chemical used was a 2.019 g mixture of benzocaine, and benzoic acid. Furthermore, the outcome of the experiment was 0.310 g of pure benzocaine, and 0.145 g of pure benzoic acid. Therefore, the percent recovery of the benzocaine and benzoic acid compounds was found to be 15.35%, and 7.18% respectively. In addition, later on in the process the melting points of the pure compounds were measured. The data of the benzocaine received from the lab was 93.2˚C, which is extremely close to the one reserved in literature (89˚C).
plant belongs to genus Hypercium specious. Scientific name is Hypericum perforatum. St. John’s wort was named so because it blooms around June 24th, the birthday of John the Baptist. Mostly found in Canada and U.S in the dry ground, woods, or meadows. Intended Uses: St. John’s wort mainly used for the treatment of minor to moderate
Belladonna prefers to thrive in areas that humans consider to be filthy, such as wasteland, garbage composts and old quarries. Belladonna has conceived a plant adaptation that is quite different from the sunny energy required for the growth of many flowers. In shaded environments the flowers can grow as a “tall man”, but in areas when sunlight is more generously supplied the plant has become “dwarfed” (British Homeopathic Association para 3-6). Once again adding to the strange characteristics of this plant; the taller it grows the more poisonous it becomes. This is because the more sunlight the flower receives the higher in alkaloid concentration it
3.2.4 The catalyst concentration on epoxidation of cyclooctene using the investigated VO-complexes The effect of the catalyst was discovered by insertion of different molar ratios of the complex catalysts (L1VO, L2VO, L3VO and L4VO) to cyclooctene in the oxidation process (0.02, 0.05 and 0.10 : 1, respectively) using aqueous H2O2 in acetonitrile at 90 °C for 2 h (the optimized reaction conditions). In another words, the effect of the amounts of the catalysts related to the amount of the substrate (cyclooctene) on the epoxidation processes with 0.02 : 1, 0.05 : 1 and 0.10 : 1 (cyclooctene : catalyst). The results are reported in Table 9. The catalytic potentials of L1VO, L2VO, L3VO and L4VO at catalytic amount of 0.02 mmol has been studied and reported in Tables 4-7.
pruriens seed extract and FeMPn were characterized with FTIR to determine the biomolecules contained in the extract that involved in the reaction to form FeMPn. The FTIR spectra of the extract and FeMPn are shown in Fig. 5. The FTIR spectrum of the extract showed a broad absorption band in an absorbance area of 3384.8 cm-1 that assigned to the overlapping of O-H stretching vibration of flavonoids, alkaloids, polyphenols, alcohols or water and N-H stretching vibration of amine compounds, due to the hydrogen bonding. The absorption band at 1627.8 cm-1 referred to C=C stretching vibration which is possible to be derived from aromatic ring in amino acid, while the absorption band in 1529.4 cm-1 referred to N-H bending vibration of amine which is possible to be derived from the L-dopa.