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☛ Official ☚ The Big & Dandy DMXE (3-me-2′-oxo-PCE, deoxymethoxetamine) Thread

ecstacylover

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Nov 26, 2014
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Hilbert space
Conceive the molecule and facilitate its creation = invent it
You can define it that way if you please. My point is that dreaming up molecules is easy, and I don't think any self-respecting person would want full credit for something where they didn't do the hard part.

Don't get me wrong, the guy is a saint either way. :)
 

Cosmic Charlie

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dEeP iN HyPerSPaCe
The guy we are talking about synthed 2C-EF himself before it wouldn't surprise me if he made the first batch of Methoxetamine as well. The guy we are speaking of is a one of a kind, I remember the day he posted the first trial with MXE I was so excited. I actually trialed it very early on when the first of it hit the states and spoke about it in the social back then. I'm gonna be getting my hands on a gram of DMXE soon god willing, can't wait honestly I hear this is the best of all the MXE analogs so far, regret not getting more honestly though but I had some other things I needed as well. Will report back in this thread after I sample it.
 

Asante

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May 4, 2012
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Holland
You can define it that way if you please. My point is that dreaming up molecules is easy, and I don't think any self-respecting person would want full credit for something where they didn't do the hard part.

Don't get me wrong, the guy is a saint either way. :)

The hard part was the conceiving and subsequent human testing. The synthesis is a minor part of the equasion. If the enormous number of failed RC's shows us anything, its that dreaming up a true blockbuster molecule is way harder than synthing.

A lab set out to have 5-APB synthed. The Chinese returned which proved to be 6-APB. They tested it and it was better than the intended molecule.
 
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MSK

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Apr 15, 2015
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Tried this at 20mg and 40mg orally and it really felt close to 3-MEO-PCE for me, nothing really special.

After years of dissociative abuse everyday, I stopped for 2 years and was excited to try this compound, but it was a deception (maybe I had very high expectations)

3-MeO-PCP, 2-OXO-PCE and DCK are still on my top three list.

I don't even think that MXE was the holy grail anymore, I think that nostalgia and a lack of tolerance and knowledge on other dissos apart from ketamine was what started all this "I wish MXE was back" thing, but we for sure have got a better disso menu to choose from now 😁
 

ecstacylover

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Nov 26, 2014
Messages
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Hilbert space
Tried this at 20mg and 40mg orally and it really felt close to 3-MEO-PCE for me, nothing really special.

3-MeO-PCP, 2-OXO-PCE and DCK are still on my top three list.

I don't even think that MXE was the holy grail anymore, I think that nostalgia and a lack of tolerance and knowledge on other dissos apart from ketamine was what started all this "I wish MXE was back" thing, but we for sure have got a better disso menu to choose from now 😁
I didn't think it was special either, sort of dysphoric actually. Although it was easy to hole on, which wasn't something I found with 3-MeO-PCE. Out of the newer crop the only ones I really found enjoyable were MXPr and MXiPr.

That's an interesting thought regarding MXE. For my part I'm inclined to think it was somewhat special. Back when I was using it heavily I was also using DCK, O-PCE, and 3-MeO-PCP from time to time, and didn't find any of them near as worthwhile. Although I did pay a hefty price for some "S-isomer" MXE a couple of summers ago and didn't really enjoy it at all. Perhaps it was actually S-isomer and that was responsible, although I'm inclined to doubt that.

In general ACH synthesis is somewhat involved and you can end up with overbromination, N-desalkyl, and O-desmethyl byproducts which are active in their own right. I think this has historically contributed to the batch variance with these substances, in addition to tolerance. I had this one batch of "MXE" from China that I was able to get a year or so after the ban. It reagent tested as MXE but I'm sure it was something else. Very short acting and euphoric, but less potent and the plugged onset was a little different than that of MXE.
 

Xorkoth

🎨 ARTministrator 🎨
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Feb 8, 2006
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55,262
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In the mountains
Tried this at 20mg and 40mg orally and it really felt close to 3-MEO-PCE for me, nothing really special.

After years of dissociative abuse everyday, I stopped for 2 years and was excited to try this compound, but it was a deception (maybe I had very high expectations)

3-MeO-PCP, 2-OXO-PCE and DCK are still on my top three list.

I don't even think that MXE was the holy grail anymore, I think that nostalgia and a lack of tolerance and knowledge on other dissos apart from ketamine was what started all this "I wish MXE was back" thing, but we for sure have got a better disso menu to choose from now 😁

I have had 2 doses of MXE left for ages, and a year and a half ago I took 30mg orally, thinking, you know, maybe it's just nostalgia. But no, it was pure magic, my vision became insanely sharp and I was able to read signs from farther away than my friend who has 20/20 vision (I am nearsighted but don't wear any corrective lenses). I had a deep experience that was very cathartic and experienced perfect peace and euphoria, and quit drinking for months afterwards.
 

MSK

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Joined
Apr 15, 2015
Messages
652
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Spain
In retrospect it could easily be that I perceive MXE like that because it was the first disso apart from ketamine I tried, and it felt awesome until I met 3-MeO-PCP and 2-OxO-PCE, that changed the game totally for me. Call me an extremist xDDD

I'm a huge dissohead, and probably permafucked with the tolerance, so 40mg probably were a low dose, I need to retry with a higher dose.

Tried MXiPr recently too, and felt very similar, the comparision with 3-MeO-PCE I did before was probably unfair and untrue, because neither MXiPr or DMXE are really similar to it.

It would be more fair to say it's something between the mania and stimulation of 3-MeO-PCP and the coldness and chilness from 2-OxO-PCE, more on the chill side. Both MXiPr or DMXE felt like they could be potential candidates for holing, with a huge dose or a little help from a psychedelic ;)

A pleasure to come back to Bluelight after so many years guys, I was lurking since a lot, following those new dissos, and with this one I couldn't resist to fall back again :)
 

electronDegenerate

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Joined
Dec 10, 2020
Messages
404
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Wildling Country
I don't even think that MXE was the holy grail anymore, I think that nostalgia and a lack of tolerance and knowledge on other dissos apart from ketamine was what started all this "I wish MXE was back" thing, but we for sure have got a better disso menu to choose from now
I mean, saying something is the holy grail is definitely subject to every one's personal preferences and opinions.
I guess I never really thought of MXE as the holy grail. But I can't deny the experiences I've had and I don't think I can
attribute their profound effects to my naivety.
I haven't tried all the available aryls yet but the few I have tried, including 3-MeO-PCP and DCK, have yet to impress me like that.
And I too have a tiny amount of MXE I can go to for nostalgia's sake.
It sometimes blows my mind how different people can react.
like
I find MXiPr a lot more holable than DMXE. You'd have to take a pretty large dose of it to have achieve that.
I could not hole with MXiPr, and while I haven't tested DMXE fully yet I can already tell its a stronger chemical for me.
I'm a little envious though that you can take it there.
Maybe I'm just a punk that wants his dissociation to be raw power and all encompassing magic.
But i'm seeing that people just react differently to things.
 

Img_9999

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Joined
Jun 17, 2015
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R'lyeh, Cono Sur
But i'm seeing that people just react differently to things.

This is true across all drug types, but I feel it's particularly true when talking about dissociatives. I think part of it is people take it for many very different reasons. Some people look for the hypomanic mood-lifting of low doses, others the feel good, opiate-like blanket warmth some of them have, while there's people that just like the wonky weirdness of the dissociative state, and also there's the ones that go for the mind-bending psychedelia of hole experiences. I guess that's part of why people have such differing opinions on these molecules. But also variances in neurochemistry I guess. And even intra-personal variability, at least for me dissos are usually pretty inconsistent, every experience feels a bit different even using the same compound, but that's part of why I find them fascinating.
 

Drogadicto

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Joined
Jan 29, 2016
Messages
1
Already did a total of 1.5 gram insufflation tests (around 20 dosages), not in a row but spaced in weeks or months, so is not apparently addictive or dangerous for me.

Doses around 50-80mg are fine for me, redosing after 2hr if I want to extend the experience..

I hope soon I can do an heroic dose of DMXE + LSD-25 (My best trip was 4 years ago with 80mg of MXE during a +800mics LSD-25 peak.

Anyway, pretty good disso, not so good as MXE, bust so far best analog I've tried since it dissapeared.

Only inconvenience,

- It burns a bit (insufflated) and causes me to "cry" and produce a lot of mocus.

- Little difficulties to pee on first times (like I was on opium or heroin), don't know how kind (or not) is on bladders and that, but I feel fine after my ~20 tests.

- Causes some kind of constipation for 1-2 days with my nasal cavities blocked for a while after a +100mg-150mg day of insufflations, this thing always happens to me with this RC.
 
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