QWET Extraction With Ethanol

Quick Wash Ethanol, also know as QWET is one of the techniques commonly employed to extract oil from cannabis.

Here is skunk pharm’s QWET formula to produce an absolute using a 3 minute quick wash.

As most of our extracted oil goes into oral meds, we also decarboxylate ours. This process is based on the 252F curve shown in the attached graph.

The first question is why use a quick wash technique to extract the resins, instead of long soaks to extract as much resin as possible, or just boiling the material in alcohol to get the greatest amount of extracted material?

The answer to that is that because alcohol is a polar solvent that is soluble in water, the latter two techniques also extract the water solubles like chlorophyll and plant alkaloids, as well as the plant waxes and vegetable oil.

Even quick wash does to a lesser degree, but the added steps that we include here minimize pickup even further and we take additional steps to remove the impurities that we do pick up.

The first wash will usually extract 75 to 80%, leaving the balance for the second. The second extraction will be more sedative and less heady. If you use a hand microscope, you can easily see when the trichome heads are gone and the stalks look like wet fur.

You can also use the material for other extraction methods after it has dried. I have subsequently used BHO after the first QWET wash that yielded 16% oil by weight, and got 5% more pristine oil, or about 21.6% total.

A cured material QWET absolute is one of the most aromatic and tasty of the extraction methods and consistently gets high raves from the volunteer test panels, as well as the patients and students. Both from an efficacy, as well as a flavor standpoint.

The first step in the process is to get as much water as possible out of the material.

A fresh material QWET is possible, but this procedure is specifically for material that has been cured to about 15% water content, which is typical of cured material. 15% is a lot of water and the alcohol already has 5% in it, so unless we reduce the water content even further, we will be extracting a lot of water solubles.

We dry our cured material even further by spreading it on a cookie sheet and baking it in a 200F oven until just frangible when rolled between the finger and thumb.

If the material is prime bud, we break it up loosely by hand and extract from trim as is.

We never, ever, use a blender or coffee grinder to reduce material, because it produces a lot of ultra fine powder that makes it through conventional filters.

Next, while it is still warm, we seal the material in a jar, which we place in the freezer to tie up any remaining water as ice. We also put the 190 proof grain alcohol in the freezer.

When they have both stabilized at about 0F, pour the alcohol into the jar of plant material, so that it is at least an inch above the material, and shake it gently a few times to make sure everything is wet. Place back in the freezer.

Remove and gently shake twice more until the material has soaked for 3 minutes, and then dump it through a wire strainer to drain quickly.   We set the strainer atop a fine mesh stainless French Chinoise strainer, or a stainless coffee filter can be used.  Don’t press on the material to extract more, but just let it drain.
Set the material aside to dry for a second extraction. We usually keep the two extractions separate, as they will have different properties, as does the third extraction using water.

After refreezing, the second extraction is done like the first, but when it is drained this time, the material is returned to the jar, which is then refilled with water and set aside.

Filter the extracted liquid.

We use either a #1 lab filter with a vacuum assist, or a simple coffee filter to further filter the solution, depending on the quantity we are processing.

Place that filtered liquid in a suitable container and set that container in an oil bath heated to 250F. We use bain marie and other stainless ware from a restaurant supply or a still, so as to recover the alcohol.

Make sure that the container is sitting on something that suspends it up off the bottom of the oil pot. I throw four jar lids in the bottom of my electric fondue pot and use it for that purpose.

Never trust the numbers on the dial and use a good thermometer to set temperatures. We use either a mercury lab thermometer, or a digital one. Good temperature control is key to the process.

That means the device that you use to control the oil temperature must have a narrow dead band, so that the temperature control is stable.

We paid about $60 for a Quisinart fondue pot that was designed to heat sensitive sauces like chocolate and has excellent control throughout its temperature range. We also have a couple of Revels, that are slightly larger and work well, plus cost only about $30, though they have a slightly larger dead band.

Some fry cookers have sensitive enough controls, but many deep fryers designed to primarily run at 375F, lack control sensitivity and have large dead bands at 250F.

Either boil or distill off the alcohol until the liquid is reduced to a pool of oil, with no large solvent bubbles.

We suck it out of the container using a 60ml syringe, and then filter it to 0.2 microns using a PTFE syringe filter, but a coffee filter or a #1 lab filter may be used..

Place in a suitable container for return to the oil bath and this time cook it until there are not only no large alcohol bubbles, but the production of small CO2 bubbles along the edge dramatically slows down, even when stirred with a bamboo skewer.

Since you have much less material, a smaller one may be used. At this point we put them in small stainless cups with their tare engraved on their sides or a Pyrex beaker. The smaller container reduces the surface area that will be coated with oil when we cook it down the last time and knowing the cups tare weight allows me to take it directly from the oil bath and place it on a scale after simply wiping the exterior.

Since we know the tare, we then know the extracted weight, and exactly how much other ingredients to add. Once adding those ingredients, we place the cup back in the oil bath, where we stir it until well mixed and then decant into its final container.

Since the added ingredients include things that lower the cannabis oils viscosity, very little is left as a film in that container.
If we plan to use the oil as is, without adding any other ingredients, we extract it from the container using the syringe, or a pipette, so as to not leave a streak of material in the vessel. After we have extracted all that I can using a syringe or pipette, we wash the container and pipette out with hot alcohol, and save the wash for the next run.  Nothing is wasted or left behind.

In that vein, as a final step, and for a different product, we strain the water from the plant material, the same way we did the alcohol and cook it off exactly the same way.  When the water is cooked off, we redissolve the remaining oleoresin in hot alcohol, and place it in the freezer for a couple of days, before filtering it.  This time there will also be red waxy globs of insoluble material collected in the bottom of the jar.

Cook off the alcohol, and it produces an oil that is more sedative that either of the first two extractions.

Attached thumbnail(s)

6-30-13

For all of ya’ll living where 190 proof isn’t readily available, here are a couple sites that will ship most anywhere,

East coasters check out, http://www.winechateau.com/

West coasters, try http://organicalcohol.com/store/

214 responses to this post.

  1. Posted by Shawn on September 20, 2014 at 5:21 PM

    After a QWET extraction does the absolute oil need to be decarboxylated if it will be added to oil vaporizer e-cig type of device? 

    Reply

  2. Posted by JuneBuechting on September 9, 2014 at 11:10 AM

    Thank you for your information on the 3rd water extraction. I’m not sure I will do this again, as it is time consuming for very little end medicine.

    I boiled off the water, added the ethanol, froze for 2 days and strained. I didn’t observe the “red waxy blobs” that I expected. just some sludgy green stuff.

    I then processed using an Air Still.

    I evap’d using a coffee warmer.

    My resulting extract has 2 parts to it.

    1-this lovely bright green oil that is around the edges of my dish
    2- a thick (like honey) clear amber “oil” substance that has a bitter scent (and taste) to it.

    so far, I don’t know how to separate the 2

    my question is: Is this amber stuff medicine or is it some other by product that I don’t want? (I guess I could be the quinea pig and try some in a capsule….)

    Reply

  3. Posted by Blujay on August 13, 2014 at 8:08 PM

    Glad to see others care about GMO. Good luck and have fun!

    Reply

  4. Posted by AlcoholExtractor on August 13, 2014 at 5:32 PM

    Hello! First off, thank you so much for maintaining such a wealth of information. So, I have my hands on some medical/lab grade ethyl alcohol. It is 200 proof, should work just as well as the 190, right?

    Reply

    • Posted by Blujay on August 13, 2014 at 7:11 PM

      Its the same thing; alcohol is hygroscopic which means as soon as you open the sealed bottle it absorbs H2O from the atmosphere making it 190-195 or so proof. Almost no point to buy anything other than 190 proof unless u want organic.

      Reply

  5. Posted by Jeff on July 23, 2014 at 2:33 AM

    Could you please tell us the exact model # for the fondue pot you use? I found two different Cuisinart models (CFO-3SS & CFO-1000) both priced at $59.99 that fit the “about $60″ price you mentioned. I’m not sure if they have similar dead bands so I’d like to play it safe and get the model you have.
    Thanks!

    Reply

  6. Posted by Charles on July 14, 2014 at 7:12 AM

    Any videos on this?

    Reply

  7. Posted by otherone420 on July 9, 2014 at 2:49 PM

    How about using anhydrous alcohol for the extraction? Do you think there may be any health hazards associated with the end product?

    Reply

  8. Posted by Eli Elixer on March 5, 2014 at 8:24 AM

    Well, I just want to say thank you for your wealth of information. I did my first go at making an absolute by winterizing and filtering 12 g’s of some bho wax I got and then decarbing and then adding to coconut oil. The absolute came out great. Mythically good. Completely golden orange red hard shatter at room temp and when heated between fingers can be stretched paper thin and becomes golden see through. I washed the razors and pyrex pan and got another half g of oil out of it, but it is much darker red? does a secondary extraction cause this? I did make a few mistakes, but still rather enjoy my end result. The first mistake I made was underestimating the shatter consistency of the absolute. Completely shattered and a bunch landed under the fridge. So, after decanting into the liquid coconut oil I used, I simply re-filtered the liquid. Worked like a charm. The other mistake I made was I used a water bath as opposed to oil bath, heating the material to only 212 for the decarb. Do you think that the 250 bath would have been very noticiably better? My oil worked wonderfully and is fully heady, which is good, as I have a lot of oil that is made from very dry kief that is very sedative. I’ve spent the last year making 150 ml mct oil that was slow cooked with kief for five hours at whatever temp my slowcooker is on low, probably around 200. I also noticed the possibility for the pyrex to tip into the boiling oil, but luckily this didn’t happen. For future projects, any recommendations to better stabilize this part? Also, I ended up mixing 60 ml coconut oil into the 7 g’s decarbed absolute and baked at 220 for 2 hours (per badkittysmiles guide), winterizing for 18 hours halfway through. I went ahead and tried roughly .2-.4 ml subliminally, and felt the intensive head effects within 1 minute. Much much much much stronger sublingual effects than any other method I’ve done. Do you think it’s possible that thc lends itelf better to sublingual administration than the CBN’s? Have you experimented with making sublinguals at these lower temperatures?

    Reply

  9. Posted by chunker on February 24, 2014 at 12:25 PM

    Can you please describe the taste difference of oil passed through a .2 mu syringe filter vs just passing through coffee filter. I noticed my QWET leaves a little bit more residue on my nail than bho, but still dabs very well. It comes out golden colored when looked at in a small layer under a light, but looks black and non-translucent when in a large quantity. Do you think the syringe will take away the minimal residue and make it more translucent? someone on the comments mentioned that the syringe removed alot of the ABV taste, would it also remove good flavors from oil made from fresh material? for example maybe the oil that only goes through the coffee filters has more flavor, but also more harshness because of more junk, whereas the syringe filtered oil may be less harsh and also less flavorfull.

    Reply

  10. Posted by BrianTC on February 22, 2014 at 11:04 AM

    Greetings Skunk Pharm folk! First, as always, a HUGE thank you is due. You guys rock.

    Second — I’m wondering what method/tools you use or suggest to determine water content of starting materials, for this and all extractions. Reviews I’ve read on many of the readily available hygrometers

    (ex: http://www.amazon.com/dp/B00A9W41GI/ref=wl_it_dp_o_pd_nS_ttl?_encoding=UTF8&colid=3ADS0L6RJ0S9F&coliid=I3NCP8CN7XRUSS)

    say that the readings vary dramatically from unit-to-unit placed in the exact same environment. Lab technique would suggest weighing before and after a complete dry, then calculate, but that not only wastes bud, but takes a long time and is not feasible when using material stored in multiple jars, etc. Any suggestions would be greatly appreciated.

    Reply

  11. Posted by davewessell on February 17, 2014 at 9:07 AM

    hey guys… just had a few things to figure out that stumped me a month ago. i have some erl which apparently was contaminiated by being left unsealed in a freezer. it has absorbed the smell of what could be described as leftover mongolian bbq. so, i was just looking everywhere for the best method of removing this smell. yet to find a fitting solution for what i am faced with.

    second- for the qwet method i stumble upon a method by using what i had- i winterized some erl with 196 eth (10 parts ethanol to 1 erl) and hot bath at 120f…. found that a simple plastic trashbag over the top of the pot kept evaporating water out of the erl dish. this method seems to get the initial bulk of etanol out quickly (2 hours or so it was thick). i then proceeded to do a 3 hour finish at -29hg in a 3 gallon chamber. i would then open all valves to replenish the air and start over for another 2 hour -29hg vac. this seemed to work really well considering how janky of a lab guy i am. i am just wondering if anyone has any comments to offer. the product came out quite nice, but there was the smallest hint of ethanol left behind. taste was fine overall.

    thank you all for the info that is all over this site. this place is a wonderland. i am not a retailer of any sort. i only try to help my friends and family be safer and happier, who which are even more ignorant than me… only because i read the threads here!

    Reply

  12. Posted by Matt b on February 16, 2014 at 9:22 PM

    Would putting it in the oven at 250 finishhe dedecarb rocess.? If so, how long do I keep it in there?

    Reply

  13. Posted by Matt b on February 16, 2014 at 9:17 PM

    I burn off the ethanol in rice cooker at 180°F. According to the graph im not fully decarbing

    Reply

  14. Posted by Sand Blaster on February 16, 2014 at 12:32 PM

    Hello, thanks for all the great guides! I was wondering if you could describe from your experience the visual and taste differences between the same QWET filtered through just coffee filters or through .2um syringe filters. Will the syringe filtered extract be more translucent? I make about 450 grams of trim into QWET oil for meds, mostly smoked, yielding between 20 and 40 grams per run. I notice that my oil does leave a little bit more residue compared to BHO and QWISO I have made in the distant past. It tastes great, but gets harsher with bigger hits, more harsh than the same size bho dab would be, leaving me mostly taking small/moderate sized dabs (which is fine). The color is usually yellowish and translucent until gathered into a large amount, making it look black, with minimal light penetration coming through the 1 oz oily gloop. Do you think syringe filters will give me a nicer effect (in terms of color and ability to take large hits) compared to the unbleached coffee filters I currently use?

    Reply

  15. Posted by Daniel Moore on February 10, 2014 at 9:11 PM

    Have you tried using nitrous oxide in a whipping siphon to aid the QWET? Nitrous oxide is nonpolar and it dissolves readily into lipids/fats/oils, it also dissolves right into cold ethanol. If using a 1 litre siphon bottle you can extract using two nitrous whippers and 750 ml of everclear. Mix into the siphon, charge with two nitrous whippers and shake for one minute and let sit for the next. Quickly discharge the siphon upright and release the gas, cavitation from the gas escaping causes agitation to the glands at a microscopic level, also it aids in extracting the non polar essentials as well. let me know what the pharm thinks,

    Reply

  16. Posted by Cannaseurs on January 19, 2014 at 8:03 PM

    Maybe it was butane

    Reply

  17. Posted by Cannaseurs on January 19, 2014 at 8:01 PM

    I was asking about mixing keif with ethyl alcohol and then filtering the wax out. Since non polar solvents don’t dissolve wax you should be able to winterize it before evaporating the alcohol. Use a Büchner funnel. Then steam or a vacuum.

    Reply

  18. Posted by Geoff Muller on January 18, 2014 at 10:18 AM

    Ran QWET for the first time yesterday and I really like the results. As has been said over and over, this site is a treasure.

    I have one process question: after the first ethanol wash, your instructions say to “Set the material aside to dry for a second extraction.” It seemed to me that there would be moisture left behind from the first wash after remaining alcohol evaporated, so I repeated the beginning step of drying the herb in the oven.

    Was this a good practice or am I adding an unnecessary (or detrimental) step?

    Reply

  19. Posted by chris brown on January 14, 2014 at 9:24 PM

    is it really necessary to decarboxylate since the heat from boiling off alcohol in a distiller, I think would do the trick?

    Reply

  20. […] of bud the preferred way to make a alcohol tincture is to do the cold method aka QWET extraction http://skunkpharmresearch.com/qwet-extraction/ this will give you a tasty potent tincture Reply With […]

    Reply

  21. Posted by Cannaseurs on December 31, 2013 at 5:42 PM

    What if instead of running butane through trim or bud in my shatter tube, you can fill a cup with kief, add butane to it. Then stir it up good letting it all dissolve while adding more butane. Once it is fully melted you add grain alcohol and let it react for an hour. Then you put it into the freezer. You take it out, stir it a lot, pour it through a filter, then pour it into a pyrex over Steam a little at a time until it is shatter. Scrape it while hot. Add it to a parchment.

    Reply

  22. Posted by Cannaseurs on December 31, 2013 at 4:43 PM

    Why can’t you dry deive keif and add alcohol to it and stir. Then boil some of the alcohol off, winterize it and evaporate the alcohol?

    Reply

  23. Posted by Georg Williams on December 20, 2013 at 4:08 PM

    Love this website … just what I was looking for.
    Thanks so much for sharing your professial knowledge.
    I have a question concerning the QWET method:
    Towards the end of the tutorial, after the oil has finished boiling, you mention adding further ingredients without getting precise. I assume something to make the cannabis oil more suitable for oral usage. What ingredients would or could that be?
    Ethanol and / or Glycerin to make a tincture?
    Coconut oil or Ghee?
    Which ingredients work / mix best with the cannabis oil?

    Reply

  24. Posted by Dylan on December 17, 2013 at 4:12 AM

    So much great info that it is overwhelming!

    I want to make QWET extraction for vaping. I have a filter flask and a hand vac pump. I also have a ceramic Buchner filter (and filter papers) and the ability to cork the flask after filtering.

    My intention is to mix PG and VG Before cold boiling off the ethanol and collect the ethanol (I have 95% drinking alcohol available but it is very exp) using an ice bath heat exchanger into a gas trap connected to the vacuum.

    My thinking is that leaving it in liquid form will make removing it from the flask easier and result in a ready to use mixture for vaporising.

    Would you kindly be able to break down the steps I should take into the most basic instruction points? I will refer back to your detailed post to clarify each point if need be.

    Many thanks! Your efforts are appreciated all across the globe.

    Reply

  25. Hi all,

    I hope all is well with you! A quick question to make sure I have my thinking straight (in this instant). I am extracting high quality kif with 190 proof ethanol, at about 75f. The kif has no visible green. Once I’ve extracted the oil, I plan on filtering the extract and then freezing it at 0f for 2 days … (as if I was winterizing BHO) ….. and then filtering the 0f extract again to remove any waxes/alkyls that may coagulate over the 2 days.

    Would you say that this step will remove some dissolved waxes etc? Is it worth the extra 2 days, and extra loss in the extra steps? (is enough wax removed to make it worth the effort?)

    Thanks in advance

    Steve

    ps My wife is up to 6 drops a day of HAO, and it seems we are passing the ‘tipping’ point. After the initial slight diminution of her BP, things stayed fairly steady at the slight improvement. She has been at 6 drops for 5 days now and there is every indication that her bp is now dropping again … she is now between 3 and 4 BP medications now per day, whereas previous to this she was at 4 and sometimes 5 BP caps per day. I am having trouble getting CBD material to work with, unfortunately, with a result that she gets pretty wasted once in a while.
    She is also halfway dosing up at this point, and it certainly looks like she will be able to reduce if not eliminate her BP med, eventually …. however, we monitor her bp 4 times a day, and will continue that regimen for a long time … no reason to risk a bp flare-up undetected … which could lead to a stroke

    Reply

  26. Posted by William on October 17, 2013 at 11:57 AM

    Thank you very much for making such excellent information so widely and freely available, your site is an amazing resource.

    I was making quite large (60 gram) batches of oil using the ‘Rick Simpson method’ of evaporating the Ethanol in a rice cooker before moving to a coffee warmer for the final stage. I have noticed a huge increase in the quality of the oil since I adopted your QWET method and used the fondue pot to decarboxylate.

    My question involves the third wash, which I thought was an exciting concept but I seem to be messing it up somehow because I keep ending up with a hard resin that sticks so solidly to the pot that both resin and pot end up in the bin!

    If I could throw a couple of questions at you hopefully I can find out where I have been going wrong..

    1. When you cook off the water, should the oil in the fondue pot be at 250F?

    2. I am assuming I could be going too far in cooking off the water and the oleoresin may become too solid to even dissolve with hot Ethanol?

    3.Is it important for the Ethanol to be preheated before it is added to the oleoresin? I tried it once without preheating and after thinking this was a misstep tried adding heated Ethanol but it didn’t seem to dissolve the material which had by then become quite solid.

    4. You mention that the third wash is more sedative than the first two: would you a hazard a guess as to its potency compared to the first two? (or maybe it has been tested..) which would lead to the follow up question:

    5. What do you think would be the best use of material from the third wash: a sedative night time med..or maybe topicals..?

    Many thanks in advance for your time and patience!

    Reply

    • The oil can start at 250F, because the boiling water won’t exceed 212F at sea level, but that would bee to hot for a finish if the plant waxes are still present.

      Heating the alcohol just makes it easier to dissolve the oleoresin. The last wash will have some things in the water, that aren’t soluble in alcohol and which you don’t want. If they won’t dissolve in warm ethanol, they aren’t cannabinoids or terpenes.

      Not much head and lots of sedation. Haven’t tested the difference.

      Evening meds or a topical.

      Reply

      • Posted by William on October 20, 2013 at 8:07 PM

        Thank you for your help! I’ll make some adjustments..

        On another topic..whenever you have the time.. I tried to filter the oil once the solvent bubbles had disappeared using a 0.45 syringe filter, but the oil would not
        pass through…prior to this I had used a coffee filter and a vacuum filter with a Whatman # 11..

        I was wondering if I needed to filter more carefully prior to this point or might it help to use the syringe filter when the oil contains more Ethanol and is less viscous?

        Thank you!

        Reply

  27. Posted by Frank on October 8, 2013 at 12:16 PM

    Thanks for this great info! I recently made some Green Dragon tincture from directions stating to water bath decarbbed medicine in ever clear for 30min. I still can’t wrap my head around the discrepancy between your instructions with the 3 minute soak and the 30min water bath. The tincture did work for me, but severely cramped my stomach, which is how i indirectly found this site googling chlorophyll poisoning.

    I had one question:
    After the oil is obtained and alcohol is still present, can coconut oil be used to extract the cannabinoids from the alcohol?

    Thanks again for your amazing patience with newbs! Much respect!

    Reply

  28. Hello …. I would like to try a QWET on some freshly harvested material. I would assume you at least trim off any fan leaves, and probably at least a rough trim on the flowers…. but beyond that, I would like to know how to proceed, to produce a QWET ‘concrete’. Thank you in advance!!!
    Steve

    Reply

    • QWET Concretes have a soapy taste, so try a small batch first, before committing your whole crop. We get the best concretes using frozen fresh cut material, and a non polar solvent.

      To do a QWET on fresh material, I would remove the buds and sugar trim from the lumber and fan leaves, and loosely cut the material into ~1/4/1/2″ chunks, minimizing broken cell boundaries where the alcohol can directly access the chlorophyll, and freeze it and the 190 proof down to 0F, before combining them for a soak.

      I start with a three minute ethanol soak, and watch it like a hawk beyond that point, occasionally gently shaking it to refresh the grain boundaries.

      If you watch closely, and even draw a sample if necessary, you can see any undesirable color shift toward the green and immediately decant the liquid into a strainer to rapidly drain, and then through a paper filter to remove the balance of the solids.

      If you thin film vacuum cold boil away the ethanol, you can retain the most monoterpenes and carboxylic acids. You can also evaporate it off the other conventional ways using evaporation an heat.

      Reply

      • Thank you …. I would have guessed a different method ….. trim the flowers from fan and stems …. cut into 1/4-1/2 inch chunks …. so far the same, but I, was thinking to remove a substantial amount of water in the oven at 200f, perhaps removing the fresh flowers and pan from the oven every 20 min or so to reheat the oven, without burning the flowers.

        My Skywalker OG, loses 80% of its weight during normal drying, wouldn’t cooking off some of this water gently, allow the QWET to capture less of the undesirable water solubles.

        Would this cook off too many possibly desirable terpenes, or …. ?

        Reply

        • Let’s make sure we’re saying the same thing. You asked about a QWET concrete, which I interpreted as from fresh material.

          I consider the oil from dried material an oleoresin, and is how we do ours.

          We cut the plant, remove the fan leaves, and hang it upside down until the small twigs snap, which is about 25% water content. We cut the buds into 1/4 to 1/2″ chunks and freeze them along with the alcohol for the extraction.

          We use oven drying only for oil to be decarboxylated, where we will lose the monoterpenes anyway. Oven drying also drives off monoterpenes, which is why the house reeks when you do it.

          Reply

          • Posted by FeelingFactory on October 21, 2013 at 1:37 PM

            Hi GW,

            Thank you for your continual spread of information and seemingly endless support!

            To clarify, does the oven drying step take place exclusively with cured material, or should it be also used when working with fresh trim to reduce water content? I realized the post mentions “A cured material QWET absolute is one of the most aromatic and tasty of the extraction methods…”, but then the comments reveal oven drying step removes aromatic monoterpenes during decarbing. Is oven drying therefore reserved exclusively for decarbing the material for edibles & topicals, or does the final product still possess the aromatic & tasty qualities mentioned in the above post?

            I hope to be processing fresh trim soon, and I am still determining whether or not to heat the fresh trim first to remove water before the 3-min, 0-degree QWET for a higher purity. I have a food dehydrator that could be set lower than an oven to remove water but minimize decarbing & possible loss of aromatic compounds while drying, if this would help. Thank you in advance for any clarification!

          • I only use the drying oven on material that will made into decarboxylated oral oil. For vaporizing material, I freeze the material at 5 to 7 days drying and about 25% moisture content.

            The monoterpenes will leave with the water if you make it bone dry.

  29. […] technique cheers Graywolf you and your crew, thank you.rnrnQWET quick wash Ethanol extraction. QWET Extraction With Ethanol | Skunk Pharm Research LLCrnrn The only difference I didn't decarboxylate my trim by putting it in the oven, it was just […]

    Reply

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