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man you are such a pussy haha go back to your press and shut up
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Im at all the east coast meetups. Feel free to tell me that in person.
Love how this thread keeps going, maybe one day that guy will tell his magic formula of getting rid of the bubbles with nothing or whatever he is saying.
Since this was started back up.
Heres a question for the sciency homies who test alot.
A company I work with a bit on the east coast got some decarbed “rosin” in. At least thats what they were told and believed.
They trust the source and saw the material before it was put in oven.
Came in, in liquid decarbed looking state.
It stayed this way for multiple weeks, 50% of that time was in a feeezer tho.
When asked from the person who did original decarb if he did anything to remediate the bubbles he seemed to not really know what the person who asked that meant.
Rosin was heated to 150 and spun out until clear again with a bho oven for heating and hot plate and mag stir, each jar was ~460g in a quart mason/ball jar.
It was then heated again to fill carts after being left out for another 5 days, and accidently left in oven over the weekend.(I was only there for the 1st heating to remove bubbles, this was company employee, i was brought it cause when they heated to fill first time the bubbles made the carts overfill and leak/clog)
When it was left it oven,(heated to 155-175 per employee, then oven turned off after 1 hr as its on a timer) and then room temp in a 65 degree room for 3 days until discovered on Monday.
That jar, and one other, out of ~10, had recrystalized like when you dont take the rosin far enough for carts and make jam.
And it gets even more confusing.
The company had it tested, it came back at ~79%THCA 9%D9 3%CBG and 9% terps, so basically 100% major cannabinoids + terps, no room for fats or waxes like rosin should have.
None of that makes sense to me.
How can something be in a decarbed looking state for multiple weeks at room temp, heated multiple times, then crash out?
Normally Im used to about a 72 hr window I keep the solution at 100 for to make sure its not going to crash back out. I know it could possibly go later than that, but how could this be in a translucent decarbed looking state for that long then change?
And even more confusing is how could that solution test at ~80%THCA, wouldnt it have to have been originally decarbed to a greated % to achieve the disty type look?
I hope the testing lab gave them the wrong report and accidentally tested something else, but if anyone has an ideas on explanations I would love to hear them.
They do have cameras and there isnt other concentrates in the whole building so unless an employee snuck in something to swap and managed to get it done without cameras seeing, whatever came in, in those jars, is what was in them when it crashed back out.
It tested clean and high % which is good for the packaging so they didnt seem to care much but I want to figure out what happened.
sounds like you’re dissolving the THCa in solution/melting, not decarbing
you can test for decarb with bromocresol green or run TLC plates
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sounds like you’re dissolving the THCa in solution/melting, not decarbing
I would say that sounds like a correct answer from my experience. Additionally decarb takes more heat for longer than most think, especially the rsoin jar tek boyz. No surprise that there is a ton of thca in the dacarbed rosin.
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It’s like drowning a man. You don’t stop until the bubbles do.
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Sounds like bubble mites
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Gor reference, i didnt do the initial cook down and am very familiar with how far to heat and what to watch for, but this still doesnt explain how it stayed at a decarbed/disty looking state for weeks.
And how you could achieve that state while only converting around 10% of the THCA to D9
I have. Spoken with some other labs who test alot more and the numbers I get from other labs when their solution has crashed back out is always under 40% THCA
Has anyone ever had this happen with something of these test numbers?
Has anyone ever had something prepped for carts stay in a stable state at room temp for multiple weeks before crashing back out?
For the ones saying Im melting the THCA, not decarbing, as stated, i didnt cook it down, it was sent to the company allegedly prepped for carts.
But, can a THCA solution like rosin or live resin be converted to a “liquid” form at 80% THCA? Wouldnt that immediately crash back out?
Dude you’ve been putting on a clinic with all the info you drop every time with the ego you have, why not tell us.
Let’s use occam’s razor here.
Which is more likely. An incomplete decarb? Or someone solid-snaking into the lab just to throw THCA in the mix?
Also - If there’s NO THCA left there’s NO CRASHING that can be done.
For someone that comes on here like you, the basics really fuckin` flew over your head.
Oh fuck looks like we’ve even got footage from the cameras!
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“If theres no THCA left theres nothing to decarb”
What is this useless statement? 80% THCA 9%D9
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Didnt answer literally anything and there are impossible test results so figured one of you know it all BHO bois could answer but so far literally nothing other than
DiDnT dEcArB RiTe
Yea dummies.
Something not being right is obvious.
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No one on getting it to a distillate looking state but at 80% THCA which by my understanding is impossible.
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No one on being stable for weeks then crashing.
Looking for anyone who has had something similar happen that isnt gonna tell me the basics of decarbing as stated.
I was brought in because when the company went to originally fill, they experienced bubbles forming in the solution and it was causing leaking/clogging.
I only removed the bubbles so they could fill. Then it crashed back out a week later when they went to fill.
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If crashing occured because it was heated to ~150, this was done twice previously and it didnt crash then, so why would it wait weeks and to be heated 3 times to crash.
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0% room left for fats or waxes if going by testing so this doesnt appear to be rosin.
Telling me its an incomplete decarb doesnt account for those first 3 things above^ and also #4 being its probably a hydrocarbon extract not rosin.
Looking for answers as to those 3 things that dont make sense.
Im just a rosin presser lol, you guy all talked alot of shit, lets hear an answer that doesnt sound like you dont know anything so you just say bad decarb.
The test method extracts the oil from the sample, if it was with methanol then it wouldn’t pick up fats and would inflate the potency numbers if not accounted for
It’s incomplete decarb, buy a tlc kit if you want to check yourself and don’t want to shell out for real testing
That’s from THCa decarbing in the filler
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@ThePhilosopherStoned indirectly told us what he is doing to remove CO2. Reread the thread.
spin it in a speedmixer for 7 minutes and fill
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Why does it really matter why? You just need to complete the decarb, flatten, and fill. No bubbles, no crash out, easy peasy.
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Who the fuck is Tony v?
You’ve had multiple people from Months back telling you that you have not fully decarboxylated the “thca” oil. Meaning you still have thca present. Quit being so dense and realize you’ve been doing this wrong and inadequately since you made this post. You’ve had many people point you in a proper direction. Yet still can’t grasp the straws you’ve been given on a silver platter.
Also why the fuck does your decarb take so long? Oh it’s cause your equipment is inefficient and inaccurate. Maybe change your paces before trying to report “science” at folks that actually do months worth of r&d to perfect the craft we utilize.
Fucking simp.
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Fuck you you dumb shit.
First thing first.
Decarbed oil has bubbles, no one is debating that.
The incomplete decarb is a separate issue that was just discussed. You have the reading comprehension of a toddler. And IT WASNT DONE BY ME.
some dipshit in cali sent it that way.
Love how no one can answer with relating to the 1. 2. 3. Points made above.
Just some dumbass BHO people trying to flex while saying literally nothing.
And the fucking name calling, any of you pussies feel free to come say that shit in person.
Youre literally quoting shit years old BTW
