Kanabidiolio (CBD) izomerizacija į psichoaktyvius kanabinoidus

MuricanSpirit

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Taigi dabar sumaišiau 20 g maistinės sodos (prieš tai vis tiek susipainiojau, tad kodėl gi ne tęsti). Maišiau su maišykle apie 1 val. Nebuvo pakankamai etanolio, kad atsiskirtų, todėl įpyliau (prieš maišant) 40 ml etanolio.

J0vNamVctE


Švirkštu pašalinau viršutinį sluoksnį - juokinga, bet galiausiai jo buvo 50 ml, taigi apie 13 ml vis dar įstrigo sodoje - ir įmečiau į virimo puodą (žemiausia kaitinimo temperatūra 56°).


SoG74csAHi


Netrukus tą šūdą surūkysiu. Jis vis dar kvepia, bet daug geriau nei anksčiau.
 

mycelium

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Just so you know, after the reaction, it is distilled again or maybe twice, in order to clean it up and remove reaction byproducts
 

WillD

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Paprastai gryni CBD milteliai pasiduoda izomerizacijai, nežinau, kaip grynas procesas vyksta su aliejumi
 

mycelium

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I think anyone who is making it for sales should use isolate, and DISTILL END PRODUCT AT LEAST ONE TIME
 

PossumKid

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Ar galite jų paklausti, kokio grynumo tai yra?
Paprastai, jei tai izoliatas, turėtų būti gerai, bet tai, kad taip pat parašyta "plataus spektro", mane šiek tiek klaidina.
 

mycelium

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Broad spectrum means all cannabinoids, not isolated like CBD isolate
 

Kvadprime

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I love vape with TGK ... I think I can do:

1. Start reaction in ethanol with acetic acid for 12-24h.
2. After - we evaporate all the ethanol and acetic acid
3. Pour the resin with a mixture of glycerol and propylene glycol, dissolving gravs completely
4. Pour into a comfortable jar and smoke

The issue of health safety - alcohol and acetic acid should clearly not be synthetic - only food (We make THC from the CBD using trembling and sugar, aahahhaha)

Experienced isomerization specialists - what do you think? Is it worth a try?
 

WillD

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You do not have to evaporate it. You can dilute with water and separate the oil if you use ethanol.
 
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Kvadprime

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Ok! I try to do it, thx!!

But 5g cbd in my town i cant get with good price for first try

I try with 1g cbd in 10ml ethanol with ~1ml AcOH

Thx!!!!!!!
 

WillD

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The reaction time can be a little longer than we wrote before. You need to examine to choose the best time if you do not have the opportunity to make an analyst.
 

Rafa

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what substitutes can i use for Et2O?
 

WillD

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We need more details to a specific task.
 

Rabidreject

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Yeah, I’m probably going to end up just running it a few diff ways, I said HCl purely because I have some lol
I saw someone synthesise some p-tsa the other day and it was far less violent than I’d expected so I’ll probably whip some of that up and also give the citric acid method a go also.
 

Rabidreject

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In terms of vacuum distilling out the product for purification, I assume I’ll be able to vacuum distil to separate the d9 and d8 right? If I use a collumn?
 

mycelium

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@Rabidreject No sir, they come out at same temp.
It's damn near impossible, even with chromatography and lots of solvent, and this is from the professionals over at future
 
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