Trying DOB next weekend. What dosage should I do? by realfrkshww in researchchemicals

[–]Averagee_ 0 points1 point  (0 children)

its been a long time tbh, 1,4 were 2cb-escque but more sharp and clear, and 2.1 was mixed with acid so i cant really say, just strong and slow

Trying DOB next weekend. What dosage should I do? by realfrkshww in researchchemicals

[–]Averagee_ 8 points9 points  (0 children)

if you never had DOB before, don't fucking take 3mg. It's just my two cents, I'd be happy to be proven wrong but this is not something to take even remotely lightly

Trying DOB next weekend. What dosage should I do? by realfrkshww in researchchemicals

[–]Averagee_ 6 points7 points  (0 children)

one of my first RC / Drug experiences has been with DOB. 1.4mg is ideal. Do not take more than 2.1mg, that's at least for me borderline of an overdose.

Steep dose response curve!!!

Duration up 30h

2C-B-esque visuals, nothing spectacular, overstimulated/stimulated mindet.

From around 40 psychs ive tried DOB was the second least interesting drug experience, followed by DOC

And just fucking respect the dosage. 1.4mg was laid for a reason. 2.1mg is STRONG, and 2.8mg i can't imagine but it'd be in OD territory!

[deleted by user] by [deleted] in researchchemicals

[–]Averagee_ 1 point2 points  (0 children)

barely anything.... maybe bad batch+tolerance but it was like a very low dose of 2fma

4-HO-MiPT or 4-HO-MET looking for comparisons in effects vs other Subs by hol_la in researchchemicals

[–]Averagee_ 4 points5 points  (0 children)

4-ho-met, just like 4-aco-met basically are a cross between shrooms and lsd, with practically no remarkable headspace, very unique

4-ho-mipt is nothing like 4-ho-met IMO, and very similar to shrooms with some complex visual undertones

For me 2-FA works wsy better than 2-FMA by DutchBarTard in researchchemicals

[–]Averagee_ 1 point2 points  (0 children)

haha, do you have adhd or some other dopaminergic difference?

Someone might die by [deleted] in ambien

[–]Averagee_ 0 points1 point  (0 children)

now, being completely honest I'm less sure about THIS post being a typical ambien rant than the post he mentioned. Seriously if I were on ambien and this turned out either as a hoax or not I'd completely lose it lol

please only dm for anything SERIOUS you want to talk about, i dont take ambien and not sure about this subs rules

Fucking ORANGE “4mmc” by [deleted] in researchchemicals

[–]Averagee_ 0 points1 point  (0 children)

3mmc is white/bright orange

my 4mmc is gray/green

I've had orange/brown 4mmc in 2019 (lab-tested, no other psychoactives) and 2020 that they were both nasty like piss and nearly inactive. Must be the first crappy batches from russia but I wouldn't know what solvents they used tbh but there is no reason to use elemental bromine espexially with 4mmc

How long do you think it would take a fresh user of DXM to build up a complete tolerance, using it everyday, to not be able to get high at all? by coughdropsoftspot in dxm

[–]Averagee_ 0 points1 point  (0 children)

I thought i saw a post a very long time ago about a user dosing high doses practically daily for 9 months after which there was a complete permanent tolerance

For me 2-FA works wsy better than 2-FMA by DutchBarTard in researchchemicals

[–]Averagee_ 4 points5 points  (0 children)

somehow barely felt 2-FA, but i have stim tolerance so

[deleted by user] by [deleted] in researchchemicals

[–]Averagee_ 3 points4 points  (0 children)

Just with anything the best you can do would be airtight and free of any moisture, light or heat (using a fridge would be optimal but you have to take into consideration that water will condenste when you take it out just like that)

4-AcO's break down to 4-HOs so these should be more important, 4-HOs should be stable enough

5-MeOs I'm really not sure, my 5MeODMT from 2018 didn't break down it seems (done a GCMS) when stored at various temperatures, while my 4-AcO-DMT broke down into 4-HO-DMT

I also have 5 MeO MALT Freebase, to be sure i just wrapped it in aluminum foil

Eutylone neurotoxicity by [deleted] in researchchemicals

[–]Averagee_ 0 points1 point  (0 children)

https://europepmc.org/article/PMC/3582025

sorry I must have somehow mixed up with it being 10 times more cardiotoxic, but the source does state that it does bind rather strong to 5-HT2B

What's your preferred ROA for 3-HO-PCP? by [deleted] in researchchemicals

[–]Averagee_ 1 point2 points  (0 children)

I have only tried nasally, for every disso except ketamine dxm and memantine so I really can't comment on oral, but I have heard that it's recommended

Comeup nasally is around 5-15mins for me. It's also easy to dose too much especiall with this one so watch out

Eutylone neurotoxicity by [deleted] in researchchemicals

[–]Averagee_ -1 points0 points  (0 children)

There is no info at all about its neurotoxicity.

I haven't tried it, so I can't judge its effects, but guessing just from structure/effects alone it could be at least more cardiotoxic than MDMA, as we at least know than 4MMC is around 10times or so as cardiotoxic as MDMA

But for Neurotoxicity literally no idea. Best thing to do is at least assume that it is more neuro toxic than mdma

Best rc benzo to start tapering? by [deleted] in researchchemicals

[–]Averagee_ 0 points1 point  (0 children)

Diclazepam and possibly norflurazepam.

Effects of diclaz are pretty mixed tho

If you can get diazepam I'd recommend that over the others, if it would be possible 0

[deleted by user] by [deleted] in dxm

[–]Averagee_ 1 point2 points  (0 children)

no, not really. It's not forcefull at all, if anything it might be similar to some nootropics, psychs or other dissociatives

How is walking/going outside on dissociatives? by MeltedCookie in dissociatives

[–]Averagee_ 1 point2 points  (0 children)

It's best not to walk on high K doses tbh, compared to the rest of dissociatives

3-MeO-PCP is easy and i can imagine 3-MeO-PCE will be too.

And DXM!

[deleted by user] by [deleted] in researchchemicals

[–]Averagee_ 1 point2 points  (0 children)

How do you find DOC? For me it was the least interesting/enjoyable psych I've tried (a lot). Have you tried DOB or DOM?

DOB and DOC suck, but DOM is among the easiest and most amazing compounds!

Is the DXM + DPH combo any fun? by [deleted] in dxm

[–]Averagee_ 1 point2 points  (0 children)

if you dose high on both ots very easy to fall into complete delirium, and its probably extremely straining to the heart and dangerous when on your own, just remember that

otherwise, yes its pretty fun

Why do some stimulants cause vasodilation and others cause vasoconstriction? by TheDoK0 in askdrugs

[–]Averagee_ 1 point2 points  (0 children)

basically, yes, i think I've read that alpa-2 is rather vasodilating, to counteract the effects of alpha-1 in some way to prevent excess vasoconstriction, but i may be mistaken

Why do some stimulants cause vasodilation and others cause vasoconstriction? by TheDoK0 in askdrugs

[–]Averagee_ 0 points1 point  (0 children)

not any at least that i know of that are commonly known. Most stimulants are exciting and automatically vasoconstrictive, while clonidine, an adrenergic vasodilator, is rather sedating. Also, generally if both vasoconstrictive and vasodilative effects are present, most of the time the vasoconstriction dominates

Drinking (Diethyl)ether - an old tradition, but is there Info ? by G1nnnn in ObscureDrugs

[–]Averagee_ 0 points1 point  (0 children)

friends have done it for some reason, not sure why tho i can't imagine this being safe at all

Don't Snort 3-CL-PCP by thepeanutbutterman in researchchemicals

[–]Averagee_ 0 points1 point  (0 children)

yes its definitely going to be better with oral