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  • Trip Reports Moderator: Xorkoth

(25C-NBOMe/500 µg) First time: Van-Goghian masterpiece

Dondante

Bluelighter
Joined
Dec 6, 2005
Messages
1,641
I planned for a springtime trip with a good friend, M. I’d taken 1 tab of LSD about 10 days earlier in Canyonlands National Park, Utah. Otherwise, I hadn’t used a serotonergic psychedelic in about 3 months. I’d also recently experimented with methoxetamine, a couple weeks before, having had an extraordinarily enveloping experience with 20 mg insufflated at a showing of Black Swan. No residual tolerance was present.

T+0:00; 6:30 p.m.

I nasally administer 500 µg 2C-C-NBOMe in 10 µL water (required gentle heating to remain in solution) with a 2.0-20.0 µL pipet. The volume of liquid was too small to feel the drop. Initial uncertainty as to whether or not the volume was dispensed disappeared as I sensed a very minor burn.

T+0:02

Abrupt departure from baseline. I can almost feel the molecules diffusing through my CNS.

T+0:05

I feel slightly off kilter and for a few moments I’m alarmed by the rapidity of the onset, but my facial muscles are slowly overtaken by an irresistible grin as I realize that I am okay. I remain lucid, but am propelled into a state of powerful psychedelia. The unremarkable room I'm in is suddenly transfigured into a Van-Goghian masterpiece. Looking out the window, the world has come alive, flowing in wavy brushstrokes. Visual trails leave clearly discernable ribbons of color in the air. I am completely enraptured by the stunning visual effects. My entire sensory experience takes on full salience. Every sight, sound, and smell enters my conscious awareness with unfiltered vitality.

The thought occurs to me that this compound could somehow be of immense value in the field of human perception research.

T+0:10

My friend, M, decides to first make all necessary preparations for our outdoor adventure before taking 375 µg (7.5 µL) of the same compound.

We both agree that the substance felt very clean from the start. There is no nausea (a rapid come-up from insufflated 2C-T-2 once resulted in unrelenting vomiting and sickness for myself). There is not even a hint of gastrointestinal distress. There is surprisingly little anxiety, except for minor concerns regarding the fact that we are venturing into a public area in such a state. Fortunately, we didn’t end up having to interact with anyone, except briefly with a territorial dog after dark. Could we gather ourselves? I think so, at least for a very quick interaction. Mild muscle tension and a fine tremor are apparent. Mydriasis is prominent. No bruxism. We both noted some minor changes in mucous production, but nothing like the flowing snot that can accompany certain tryptamines at high doses. Appetite is suppressed. No significant vasoconstriction or thermoregulatory problems are noted. My heart rate seemed slightly elevated, but I never measured vital signs.

T+0:20

Transition #1: leaving the house. There are minor difficulties that delay our departure. My friend becomes ensnared in a thought loop on his front door step after dropping his water bottle. Is it damaged, dripping perhaps? Damaged? … yes. Dripping? … maybe. Dropped? Dripping? Somehow, confusion ensues. What were we doing again? Ah, yes…

We finally leave his house and set out for an open field with a grand view of rolling hills, immersing ourselves in the intoxicating beauty of early spring. The sky is brilliantly blue and the sun hangs low on the horizon, bathing our surroundings in a rich warm glow.

It’s about a 15-20 minute walk. We bring frisbees, as we think this will make us appear less suspicious...we’re embarking on a free-range disc golf adventure.

T+0:40

We find a perfect spot near the top of the hill beneath a lone tree casting its great form out into the resplendent skies overhead. I am finally able to lay down and stretch out on Mother Earth as I had desired since the chemical had taken hold. A standing cloud shape shifts on the horizon, dripping impossibly deep aurelian hues as the sun’s last rays are scattered above.

Thought patterns are significantly altered, but yield to creative analytical tangents. Words are elusive at times and conversation is anything but linear, but we talk. My memory is a porous sieve. I have some difficulty differentiating real memories from my imagination. Short term memory is significantly impaired; neural circuitry is overwhelmed by the flood of sense information. I frequently lose thoughts before I am able to articulate them.

T+2:00

Before long, stars begin to emerge like jewels out of the deep violet. We stay as long as we can bear the dropping temperatures.

Proto-language systems inform my thinking at times. Thoughts often present themselves without definite form, comprehended but in a pre-linguistic fashion. Attaching symbols (words) to these thoughts for the purpose of communication occasionally proves impossible. Are there genuine insights? I think so, except that the constant struggle to maintain verbal communication makes it difficult to dwell on these deeper reflections. A solo trip would certainly be very different. At other times, explicit articulation of an idea is unnecessary to convey the intended message. In a few instances, we seem to understand each other’s thoughts to an eerie degree.

T+3:30

A little after 9:00 p.m. we start the journey beck to M’s house. His roommates are watching the final four, so we decide that we need to find a new environment – a warm, safe place. What’s going on in my head at the moment is much too interesting for me to shift my attention to the television. Not long after the four hour mark, the effects had subsided significantly, and I felt comfortable making the short drive home. Psychomotor skills were fully intact. After some debating as to our next move, we drive back to my house together. The night ends with copious pot smoking (we both rarely smoke, but his friend had recently left him with some high quality herb). We talk my wife into joining us. Giggling ensues. Finally, we are able to add music to our experience, and it is fantastic.

T+6:30

I get in bed around 1:00 p.m. and drift to sleep around an hour later. I woke up feeling a bit fuzzy headed from the pot, but otherwise in good spirits.

In summary, 2C-C-NBOMe is a spectacular compound, a highly refined psychedelic molecule with all the positives and few of the negatives of the vast repertoire of serotonergic psychedelics. I may prefer it to any phenethylamine or even LSD. The unique attributes of tryptamines, and a particularly influential peak experience, prevent me from declaring a further relative value judgment.

I suspect that the lack of 5-HT1A agonism keeps the trip more lucid, soaring above the grungy feel that can contaminate high dose tryptamines, which M eloquently refers to as “the sticky ickies.” Although I’m not certain, I think he’s referring to the more grotesque hallucinations that can occur with tryptamines – viscera, flesh, weirdness – and also to the carnal feeling that you’re crawling out of the muck toward the end of a tryptamine experience. I only include this because I think it’s an interesting concept, though it doesn’t apply to the majority of my tryptamine experiences. There is little to no adrenergic component, though there is some cardiovascular response likely directly resulting from 5-HT2A/2C activation. 2C-C-NBOMe also lacks the overpowering eroticism of 4-HO-DIPT, 5-MeO-DMT, and 5-MeO-DIPT (I’m curious about the mechanism for this unique effect). That said, I still think this compound could lend itself to a sexual experience in the proper setting. Lastly I had the impression that the increased preference for 5-HT2A over 5-HT2C, even if mild, is responsible for decreased anxiety.

<3
 
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Great report. Thanks for sharing your experience with us!! So much information coming out about this one I think I'm sold :)
 
Thanks!

I feel like I should add that although I consider 25C-NBOMe to be a particularly benign compound, it's critical to get the dosing correct. Accidentally doubling or tripling the dose could be disastrous. I measured 7 mg out on a 0.001 g scale, and dissolved it into a known quantity of H2O (140 µL), giving me a concentration of 500 µg/10 µL, easy to dispense with an accurate pipet. For pretty much all of us, liquid dosing is the only way to achieve the precision necessary for compounds active in the microgram range.
 
Nice report & thank you, my interest in this stuff is growing as all the reports I've read seem positive.
 
Great report, Dondante -- clear and pleasant to read, with a nice mix of practical info and interesting theory, as usual.
The thought occurred to me that this compound could somehow be of immense value in the field of human perception research.
Heh, I had a similar thought after noticing some of the unique properties of 25C visuals my first time using. Have I ever tried the idea that follows? Of course not.
I really like this drug. It makes me wonder how much I could take without losing it. It's that clear headed. The visuals are pretty spectacular: for instance, when I washed my face with my gf's red towel and took the towel away from my face I saw a bunch of "psystrings" of the same color as the towel. I noticed a few other psystrings of different colors hooked into the red string, and, not by coincidence I think, they were the same hue of green as the decorative circles on her shower curtain just adjacent the towel.

What's interesting is how salient the visuals are and how much they incorporate features of the environment into their production in ways that appear to be somewhat systematic. That's what's unique abut the visuals of this drug. They are very clearly "there" and are three dimensional, but despite their salience cognitively I remain near normal. It would be interesting to set up a poster, with various colors and patterns next to a blank white wall, to see if by staring at the colors and patterns on the poster I could reproduce them on the white wall next to the poster, by "dipping" my visual memory in "red," for example, then seeing if red string patterns emerge on the wall projection. Perhaps I could deduce some inference rules of psychedelic projection from such a contrivance. There did seem to be an associative intelligence behind the features visuals had assigned to them (for example, the red towel string visuals occurring immediately after using a frayed red towel to dry my face). It could be a way to peak behind the scenes of perception and literally see how our minds use specific environmental cues to project specific and predictable hallucinatory projections. Playing such a "game" could be a first step to helping us to start to learn the mental and perceptual rules for how to consciously manipulate the production of visuals.
 
Great report. No need for emulsifiers to get 25C-NBOMe into solution, just gentle heating? Any concerns about loss of potency over time in solution?
 
Great report. No need for emulsifiers to get 25C-NBOMe into solution, just gentle heating? Any concerns about loss of potency over time in solution?

I'm not sure about stability in solution, but I think it would keep well at -20°C. I'm hoping the dry salt is stable at room temperature. If it is anything like its PEA counterpart, it'll be stable enough to last a long time.
 
i'm going to keep on the lookout for 2C-C-NBOMe. I really dig the designer drugs. There's more specific trip serotonin receptors turned on it seems.
 
wow, awesome report mate.

This is now on my to do list for the next few weeks. sounds really great.

I especially like that you said it had not body load. i wish it weren't so darn expensive :(
 
Where do you find LSD that cheap??? LSD's like 20 pounds per milligram.
 
Where do you find LSD that cheap??? LSD's like 20 pounds per milligram.

i never compared it to LSD price wise.

I was comparing it to what I have available at the moment which are 2c-x chemicals, at much cheaper prices. ~£30 a gram (very high quality)

I have only ever tried lsd once and it was given to me by a mate at SGP. Other than that I have no links to it and none of my London mates are really into it tbh.
 
Orally active 25c-neome

Is this compound orally active, as in sublingually, or do you have to inject it nasally?
 
^Sublingual seems to be somewhat less effective than nasal or IM. Orally (i.e. swallowed), it is inactive.
 
Anyone have an opinion on the likely efficacy of rectal admin?
 
^It's been reported as active in the big and dandy thread (by Nuke, I think). I assume it's on par with insufflation.
 
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