Pure and Organic CBD & and Hemp Products

Effective medicine provided by mother nature

  • Powerful relaxant

  • Strong painkiller

  • Stress reduction
  • Energy booster

Why CBD?

More and more renowned scientists worldwide publish their researches on the favorable impact of CBD on the human body. Not only does this natural compound deal with physical symptoms, but also it helps with emotional disorders. Distinctly positive results with no side effects make CBD products nothing but a phenomenal success.

This organic product helps cope with:

  • Tight muscles
  • Joint pain
  • Stress and anxiety
  • Depression
  • Sleep disorder

Range of Products

We have created a range of products so you can pick the most convenient ones depending on your needs and likes.

CBD Capsules Morning/Day/Night:

CBD Capsules

These capsules increase the energy level as you fight stress and sleep disorder. Only 1-2 capsules every day with your supplements will help you address fatigue and anxiety and improve your overall state of health.

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CBD Tincture

CBD Tincture

No more muscle tension, joints inflammation and backache with this easy-to-use dropper. Combined with coconut oil, CBD Tincture purifies the body and relieves pain. And the bottle is of such a convenient size that you can always take it with you.

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Pure CBD Freeze

Pure CBD Freeze

Even the most excruciating pain can be dealt with the help of this effective natural CBD-freeze. Once applied on the skin, this product will localize the pain without ever getting into the bloodstream.

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Pure CBD Lotion

Pure CBD Lotion

This lotion offers you multiple advantages. First, it moisturizes the skin to make elastic. And second, it takes care of the inflammation and pain. Coconut oil and Shia butter is extremely beneficial for the health and beauty of your skin.

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6. How was the CBD extracted?

Methods Pioneering New Ethanol Extraction:



  • Methods Pioneering New Ethanol Extraction:
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  • Ethanol, Butane, or Supercritical CO2: Which is Best for Cannabis Extraction?
  • including Maytag Appliances, Wells Fargo Financial, and DuPont Pioneer. Ethanol is a relatively common solvent for performing cannabis extractions. like shatter and require more post-processing than other methods. . of a rotary evaporator or to Capna's newest engineering marvel, the Faling Film. Learn how ethanol is becoming a solvent of choice when manufacturing high- quality cannabis Ethanol Extraction: Pioneering New Methods. Finding a safe & efficient method to extract CBD at an industrial scale is key in this its own way forward, pioneering new techniques for ethanol extraction.

    Methods Pioneering New Ethanol Extraction:

    Two layers form which are then well-mixed. The acid compound reacts with the base to form a salt which is then dissolved in the aqueous solution. The organic layer — which contains the impurities - is discarded. You then acidify and extract into a new layer of organic solvent. The procedure can be repeated several times although you lose quite a lot of product. Solid-phase extraction method Solid-phase extraction SPE is an extraction method that uses a solid phase and a liquid phase to isolate the impurity of interest from a solution.

    It is usually used to clean up a sample before using a chromatographic or other analytical method to quantitate the amount of analyte s in the sample. SPE uses the affinity of solutes dissolved or suspended in a liquid which act as a mobile phase for a solid through which the sample is passed which act as the stationary phase to separate a mixture into desired and undesired components. The result is that either the desired analytes of interest or undesired impurities in the sample are retained on the stationary phase.

    When the sample passes through the stationary phase, the analytes in the sample will interact and retain on the sorbent but the solvent, salts and other impurities pass through the cartridge. After the sample is loaded, the cartridge is washed with buffer or solvent to remove further impurities.

    Then, the analyte is eluted with a non-polar solvent or a buffer of the appropriate pH. Liquid-liquid extraction method In this type of extraction, two immiscible liquids are selected. Usually, one phase is aqueous hydrophilic and the other is a hydrophobic organic solvent. In that the solute is distributed between two immiscible solvents.

    The extraction is based on Distribution Coefficient or Partition Co-efficient Kd , which is the ratio of concentration of solute in two different solvents. ASE operates at temperatures above the normal boiling point of most solvents, using pressure to keep the solvents in liquid form during the extraction process. Typically, ASE methods are completed in 15—25 min, while consuming only 15—50 mL of solvent. This means that a solvent has to be found in which the compound or the impurity is soluble under either hot or cold conditions.

    In either case, a saturated solution of compound A is prepared. Compound A then will recrystallize or precipitate from the solution. The impurity will stay in solution when the impurity is more soluble than compound A or will not dissolve when less soluble than A. In this case, the solid to be purified is placed in the solvent, the solvent is heated and the compound will dissolve. If necessary, the solution can be filtered while hot to remove an insoluble impurity. Then the solution is cooled.

    The compound will form crystals and precipitate from the solution if a saturated solution has been prepared. The crystals will be rather pure. It is essential that the solvent and the compound do not react with each other. Frequently, a compound has to be purified and a solvent has to be chosen for the recrystallization for purification. The rule of thumb for choosing a solvent is like dissolves like. This means that compounds with similar functional groups are usually mutually soluble in each other.

    Sucrose that is a polyhydroxy compound is soluble in water. Alcohols and carboxylic acids, which also contain the -OH group, are soluble in water, which contains the -OH group. Benzene is not water-soluble but will dissolve other hydrocarbons like hexane. Grease is soluble in gasoline because both are hydrocarbons. It is desirable to have a compound dissolve upon heating and then precipitate when cool. If precipitation does not occur after a compound has been dissolved, there are two techniques that may be used to attempt precipitation: This method is called "seeding".

    The filtration has to be done with the hot solution and has to be rapid. If the hot solution filters too slowly, precipitation will occur in the stem of the funnel and plug it so badly that the solution will not flow from the funnel. This type of precipitation can be avoided by placing the funnel under hot water jacket during its use.

    The inconvenience of this method is the use of another piece of hot equipment. A short-stemmed funnel is definitely better than a long-stemmed one for filtration. Stir the mixture with a glass rod or spatula to determine whether the solid is soluble in water at room temperature.

    If the solid is not completely soluble at room temperature, warm the test tube in the hot-water or steam bath and stir or swirl its contents to determine whether the solid is soluble in hot water. After completing these additional tests, record which of the three solvents you consider best suited for recrystallization of each of the solutes.

    For unknown compounds, a systematic approach is important for determining their solubility, and the following protocol accomplishes this. The following solvents may be tried: Place about 20 mg a spatula-tip full of the finely crushed unknown in each test tube and add about 0. Stir each mixture and determine the solubility of the unknown in each solvent at room temperature. Use the definitions of soluble, slightly soluble, or insoluble given earlier.

    Stir or swirl the contents of the tube and note whether the unknown is soluble in hot solvent. If the solid is soluble in the hot solvent but only slightly soluble or insoluble at room temperature, allow the hot solution to cool to room temperature slowly. If crystals form in the cool solution, compare their quantity, size, color, and form with the original solid material and with those obtained from other solvents.

    Even though nice crystals may form in the first solvent you try, another one might prove better if it provides either better recovery or higher-quality crystals.

    To assist in determining the best solvent to use in recrystallizing an unknown, you should construct a table containing the solubility data you gather by the systematic approach described above. Before trying any combinations of solvent pairs take about 0. If they are not, that particular combination cannot be used.

    These may often be induced to crystallize by scratching the oil against the side of the flask with a glass rod at the interface of the oil and the solution. If this fails, several small seed crystals of the original solid may be added to the oil, and the mixture allowed to stand for a period of time.

    Failure of these alternatives may necessitate separation of the oil from the solution and crystallization of it from another solvent. Using a pencil draw a very light line across the sheet short dimension about 1 cm from one end. Then make 4 small light marks at even intervals along the line for spotting the samples.

    Draw another light line about 1 cm from another end of the plate for the solvent front. Chromatography separates components of a mixture based upon the principle that how well they are adsorbed on the stationary phase, versus how well they dissolve in the mobile phase. The components with greater affinity for the mobile phase will move faster than those components with greater affinity for the stationary phase, causing the components to separate.

    There are many chromatographic methods characterized by the nature of the stationary and mobile phases. Among these methods, column chromatography, thin-layer chromatography and paper chromatography are more common ones. Place a piece of filter paper around the inside surface of the container and extend into the solvent.

    If a more intense spot is desired, let the spot dry and re-spot in the same location. Then gently close the chamber. Push a small piece of cotton wool with a copper wire to loosely pack at the neck of a Pasteur pipette. Add a small amount of fine sand to make a small layer before adding the adsorbent.

    Do not look directly at the UV lamp. Calculate the retention factor Rf for each compound. Swirl or stir gently with a glass rod to obtain the slurry of alumina. Tap the side of the column gently to produce even packing of the adsorbent in the column.

    Add 1 drop of the mixture of impure compound to the top of alumina. Allow the mixture to adsorb into the top of the alumina. Add a few drops of ethanol and allow ethanol to drain to the top of adsorbent. Switch to the second eluting solvent, water and fill up the column with water. Collect the second band into another container Flash chromatography Flash Chromatography is a rapid form of preparative column chromatography based on an optimized prepacked column through which is pumped solvent at a high flow rate.

    It is a simple and economical approach to Preparative LC. It is "an air pressure driven hybrid of medium and short column chromatography optimized for rapid separation. Still at Columbia University.

    Flash chromatography utilizes a plastic column filled with some form of solid support, usually silica gel, with the sample to be separated placed on top of this support. The rest of the column is filled with an isocratic or gradient solvent which, with the help of pressure, enables the sample to run through the column and become separated.

    Flash chromatography used air pressure initially, but today pumps are used to speed up the separation. This technique is considered a low to medium pressure technique and may be scaled up for separations from a few mg to many tens or hundreds of gams. Gas chromatography GC Gas chromatography is an analytical technique for separating compounds based primarily on their volatilities. Gas chromatography provides both qualitative and quantitative information for individual compounds present in a sample.

    Compounds move through a GC column as gases with their linear velocity and flow rates, because the compounds are normally gases or they can be heated and vaporized into a gaseous state. The compounds partition between a stationary phase, which can be either solid or liquid and a mobile phase gas. The differential partitioning into the stationary phase allows the compounds to be separated in time and space. NP-HPLC uses a polar stationary phase and a non-polar, non-aqueous mobile phase, which effectively separates the analytes that are readily soluble in non-polar solvents.

    The with and is retained by the polar stationary phase. Adsorption strengths increase with increased analyte polarity and the interaction between the polar analyte and the polar stationary phase relative to the mobile phase increases the elution time. The interaction strength depends not only on the functional groups in the analyte molecule, but also on steric factors. With these stationary phases, retention time is longer for molecules which are less polar, while polar molecules elute more readily.

    The retention time can be increased by adding more water to the mobile phase; thereby making the affinity of the hydrophobic analyte for the hydrophobic stationary phase stronger. Similarly, the decreasing of retention time by adding more organic solvent to the eluent can be done. The compounds under the influence of mobile phase driven by capillary action travel over the surface of stationary phase.

    During this movement the compounds with higher affinity to stationary phase travel slowly while the others travel faster. Thus separation of components in the mixture is achieved. Once separation occurs individual components are visualized as spots at respective level of travel on the plate.

    Their nature or characters are identified by means of suitable detection techniques. Capillary Electrophoresis CE Capillary Electrophoresis CE is a separation technique based on the differential transportation velocities of charged species in an electric field through a conductive medium.

    The basic instrumental set-up consists of a high voltage power supply 0 to 30 kV , a fused silica SiO2 capillary, two buffer reservoirs ,two electrodes and an column detector. A pure supercritical fluid SCF is any compound at a temperature and pressure above the critical values above critical point.

    Above the critical temperature of a compound the pure, gaseous component cannot be liquefied regardless of the pressure applied. The critical pressure is the vapor pressure of the gas at the critical temperature. In the supercritical environment only one phase exists. The fluid, as it is termed, is neither a gas nor a liquid and is best described as intermediate to the two extremes.

    This phase retains solvent power approximating liquids as well as the transport properties common to gases. One of the primary drivers for the growth of this technique has been the evolution of packing materials used to effect the separation. The underlying principles of this evolution are governed by the van Deemter equation, which is an empirical formula that describes the relationship between linear velocity flow rate and plate height HETP or column efficiency.

    Since particle size is one of the variables, a van Deemter curve can be used to investigate chromatographic performance. According to the van Deemter equation, as the particle size decreases to less than 2. By using smaller particles, speed and peak capacity number of peaks resolved per unit time in gradient separations can be extended to new limits, termed Ultra Performance Liquid Chromatography, or UPLC.

    They shows a stability indicating assay of five related substances accomplished in under one minute, proving that the resolving power of UPLC is not compromised even at high speed.

    The current USP lists multiple HPLC methods for the analysis of these same compounds with run times approaching 20 min, with broad, tailed peaks. Fast Performance Liquid Chromatography Liquid chromatography is a term which refers to all chromatographic methods in which the mobile phase is liquid. The stationary phase may be a liquid or a solid. Fast performance liquid chromatography FPLC is a type of liquid chromatography where the solvent velocity is controlled by pumps.

    The pumps control the constant flow rate of the solvents. It uses innumerable data and information from a wide variety of expert sources and market studies, and distills these inputs and data into intelligence and a roadmap that you can use. It will provide entrepreneurs with an idea of how to derive more benefits from their algal energy ventures. The report provides detailed case studies, success stories and factoids of companies that have been involved in the algae products venture.

    There is no other comprehensive report available for castor oil anywhere in the world. This is the first of its kind, and currently, the only one. Animal and Fish Feed. Oil extraction from algae is a hotly debated topic currently because this process is one of the more costly processes which can determine the sustainability of algae-based biodiesel.

    In terms of the concept, the idea is quite simple: Harvest the algae from its growth medium using an appropriate separation process , and extract the oil out of it.

    Extraction can be broadly categorized into two methods: The mechanical methods are further classified into: The chemical methods are further classified into: Many manufacturers of algae oil use a combination of mechanical pressing and chemical solvents in extracting oil. Apart from these, there are some other methods which are not well-known. This includes the following: Enzymatic extraction - Enzymatic extraction uses enzymes to degrade the cell walls with water acting as the solvent, this makes fractionation of the oil much easier.

    The costs of this extraction process are estimated to be much greater than hexane extraction. Osmotic shock - Osmotic Shock is a sudden reduction in osmotic pressure, this can cause cells in a solution to rupture.

    Osmotic shock is sometimes used to release cellular components, such as oil. The Single Step Process harvests, concentrates and extracts oil from algae, and separates oil, water and biomass in one step. The process does not use chemicals or heavy machinery and no initial dewatering is required, and separates the oil, water and biomass in less than an hour.

    CTI has developed a technology that is able to extract oil from algae on a continuous basis utilizing cavitation based extraction. The company plans to license the technology to algal fuel developers. The balance of the algal oil, which contains free fatty acids FFA and triglycerides, will be converted to biodiesel using Catilin's commercially available T catalyst.

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    An example of a warm ethanol extraction processes is the Soxhlet technique. This technique essentially boils ethanol in a flask or pot, then. Which extraction method is best for your cannabis company: CO2? Hydrocarbon ? Ethanol? The answer simply comes down to what your. CANNABIS COMPANY PIONEERING ETHANOL EXTRACTION method, and in they engineered their own proprietary Ethanol extraction system. This year, Capna Systems will debut two new extraction machines.

    Ethanol, Butane, or Supercritical CO2: Which is Best for Cannabis Extraction?



    An example of a warm ethanol extraction processes is the Soxhlet technique. This technique essentially boils ethanol in a flask or pot, then.


    Which extraction method is best for your cannabis company: CO2? Hydrocarbon ? Ethanol? The answer simply comes down to what your.


    CANNABIS COMPANY PIONEERING ETHANOL EXTRACTION method, and in they engineered their own proprietary Ethanol extraction system. This year, Capna Systems will debut two new extraction machines.


    Leaves of a new variety of Stevia rebaudiana with a high content of chromatography techniques and membrane separation methods. 28 In brief, the treatment of stevia leaves with ethanol before the extraction of steviol glycosides Indeed, this pioneering study revealed that ASF can be used to.


    Classical solvent extraction, ultrasonication, maceration, and shaking methods were compared. Phenolic compounds were identified based on.


    and (iii) exploration of new alternatives to conventional solvents during the Extraction techniques for plant‐derived polyphenols A domestic application of conventional solvent extraction (CSE) is quite The application of hot water in the PHWE technique dates back to the s with the pioneering.

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