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Where's the 25B-NBOMe?

Calm down. Yes in a scientific community this is not acceptable, without a citation a claim is unfounded but Erny is clearly giving us a choice: take some free hints that are derived from some research or forget about it.
Considering I love new info on these compounds I too would kill for some articles and info on novel research but I can also show respect for people who are not in a position to share everything they know with the public. Step back or get your post u/a'd. We are not in an intellectual battle here.
 
Reformer, that is amusing what you wrote here. How does this relate to the matter, especially safety? Who's safety is threatened by what I've wrote? And what do you need a citation for? Are you going to cite me? That's right, we're not in a scientific community of any kind, we're on a drug discussion board.
 
Someone I know has expressed great interest in 25B especially, even in the context of the other NBOMe's. Why, because of 2C-B? Considering we have to be careful about comparisons that seems like a short-sighted reason at best. Maybe there have only been few reports on it at all, but it does sound like it's not worth the (potential) side-effects. Though that does not seem to be an isolated case if I understand Erny's anecdotes correctly. I for one am not looking for a DOB-like compound body-load wise and that is what it sounds like to me. Not sure how they compare but I'd rather shelf this one.

It's strange though, I do feel interested to try my 2C-N when the time is right and that too promises to be a tough one.

Erny would you say you find this experience worth the trouble? For example with DOB, I felt like: I wouldn't take it back, but I have no desire to pursue it any further either. Did you regret taking this? I don't need any big warnings and this is not a "should I do this or not" type question that we don't allow. Anyway everyone's info on this is welcome, there does not seem to be a whole lot of it.
 
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You may find it strange, but I find it to be worthwhile even with DOB itself. Although I did not touched it for several years already, I've explored it excessively in the past. DOB has a bad reputation, and for a reason, it's physiological side effects are comparatively strong. Strong side effects may hamper any chances to enjoy the experience and direct our mind into what may be called "a physiological bad trip" instead. That happens often with DOB.

I can tolerate it's side effects well, probably even too well. If we abstract from this reputation of physiological disaster, DOB is a magnificent grotesque representation of reality, the one that only bromine offers. It is also one of the most insane psychedelics I know, related both to the thinking itself and the possibility to have a maddening experience, i. e. to flip out. The latter often happens with people on DOB too.

All above is also true for 2C-B-NBOMe. Sans it has no certain reputation, though is the one that is probably the most explored here at our place. Most people who try it do like it, but the number of those who don't is still high enough to have it in mind.
 
Jesus, people should be happy that he took the time out to pass on some knowledge to you guys even if it is partial.
At the moment the only kind of information we will get on this chem will be partial.

Sad to hear that you don't think this one will live up to 2C-B's reputation, Solipsis.
Do you have much experience with other DOx? I have not tried DOB but I have tried DOC and DOI, the first I find to be a wonderful psychedelic and the latter is nothing short of horrible in my experiences. How does DOM compare? Just trying to gauge some relative effects to see how bad you think the bodyload will be.
Same questions to you Erny.
 
DOI may seem scary but it has it's own delight. Though the one that is enough to see just once. DOM differs from all halogens, DOI, DOB and DOC much. DOC is more grounded, and actually resembles DOB if without physiology and it's paralogical thinking. DOM is a clear spiritual psychedelic, and a very serious one, though tend to give somewhat idealistic view of things. 2C-D-NBOMe is that same spiritual sans the stern seriousness of DOM. I find these 4-methyl substituted PEAs to be among the mildest for the body. The only issue here may be the nausea, but not vasoconstriction.
 
Has anyone ever experimented with adding things on the second ring?

Yes. There are some that work. We don't like discussing novel structures here because then people want to sell them.

Which is a shame because the few reports on 25b-NBOMe seem to indicate empathogenic characteristics much like 2c-b

All of the NBOMe's [so far] display entactogenic effects; it's silly to expect 25B to be much better than the others based on structural analogy with some other molecule. None of them are very similar to their 2C analogs.

If you drop a single methyl group from the diethylamide on LSD, potency drops 20-fold. The apparent similarity of the chemical pictures used for didactic purposes has no relevance to activity.
 
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From the article by Ralf Heim about the pharmacology, here, it appears that 25B may be about 1/3 the potency of 25I. Page 160, table 3-11 shows that 25B (compound 231) has a potency relative to 5-HT of 384x and 25I (236) has 1240x the potency, making 25I more than 3x the potency of 25B. Oddly, they don't have 25C. It's also odd that 25B would be 1/3 potency while it is known that 25C is at least as potent as 25I. Also, the hydroxy versions are slightly more potent than the methoxy versions.

Something I was thinking about is that since the NBOMe's are made from the PEA and o-anisaldehyde, what if you made them using vanillin instead? Vanillin is o-anisaldehde with a hydroxy on the para carbon in addition to the methoxy on the ortho carbon. What effect would the hydroxy have on it I wonder. Versions with a methylenedioxy bridging the para and ortho carbons are around, so I assume they are active. Therefore, the vanillin version should also be active, though probably less potent.
 
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DOI may seem scary but it has it's own delight. Though the one that is enough to see just once. DOM differs from all halogens, DOI, DOB and DOC much. DOC is more grounded, and actually resembles DOB if without physiology and it's paralogical thinking. DOM is a clear spiritual psychedelic, and a very serious one, though tend to give somewhat idealistic view of things. 2C-D-NBOMe is that same spiritual sans the stern seriousness of DOM. I find these 4-methyl substituted PEAs to be among the mildest for the body. The only issue here may be the nausea, but not vasoconstriction.

Thanks mate.
Sounds like I might like 25B and DOB, they will go down on my list to try.

I don't think DOI is overly scary, just ridden with horrible physical side effects for me. A 16 hour trip filled with nausea, pins and needles from vasoconstriction, elevated body temp, HR and blood pressure, mixed with over-stimulation and intense psychedelia leaves me with the feeling of being poisoned through out the trip.
 
Something I was thinking about is that since the NBOMe's are made from the PEA and o-anisaldehyde said:
No, vanillin is 3-methoxy-4-hydroxybenzaldehyde. You may be thinking of ortho-vanillin, which is 2-hydroxy-3-methoxybenzaldehyde.
 
Oh yeah, I see what you mean. The methoxy has to be on the very next carbon from the aldehyde group. Thanks for pointing that out.

Now, I'm wondering why the NBOMe's are so much more expensive than the 2C-X's when the only difference is one extra step, and not even a complicated one. That's a very simple reaction and anisaldehyde isn't that expensive. I think they are just jacking the price up because people are willing to pay it, for now. I'll just make my own, for crying out loud. 2C-I is cheap and readily available. Of course, we can't discuss actual recipes on this forum, so I won't. Let's just say, if you can't do that reaction you probably can't bake a cake either.
 
Yes. There are some that work. We don't like discussing novel structures here because then people want to sell them.

All of the NBOMe's [so far] display entactogenic effects; it's silly to expect 25B to be much better than the others based on structural analogy with some other molecule. None of them are very similar to their 2C analogs.

If you drop a single methyl group from the diethylamide on LSD, potency drops 20-fold. The apparent similarity of the chemical pictures used for didactic purposes has no relevance to activity.

Hah a couple things:

Better close down the 'dimemebfe' threads and a good portion of the posts in ADD because novel or at least mostly unknown chemicals are discussed, right?

Second, I mention entactogenic effects because I have spoken with someone lucky enough to try 25B-NBOMe and they specifically mentioned that they felt it to be less similar to the other 2c-x n-benzyl compounds and specifically that it was entactogenic. I made no assumptions or claims about 25B-NBOMe being 'better' as you mention. Nor did I claim that the NBOMe series closely parallels the 2c-x series.

And third this is nothing personal but I believe you have jumped on me about posting threads asking about unusual compounds before. Apologies if it was someone else and I'm mistaken, but the same argument was given before: structural similarity doesn't correlate with activity.

And the problem is that structure DOES partially correlate with binding affinity at the various types of 5-HT receptors! If looking at a molecule and saying 'Gee, all these compounds have substituents at the 4 position and are active so perhaps the 4 position is important for binding affinity' is wrong then Shulgin must have been such a fool to investigate how structure and activity correlate in the phenethylamine and amphetamine families, right?

I realize that's a gross oversimplification because other factors influence the PEA structure-activity relationship (look at the tweetios) but it should serve to get my point across.

Not to mention the same thing taking place with tryptamines as well albeit with a different relationship between structure and activity.

Please do not take this as a flame but really I would hope that people around here would be a bit less likely to make assumptions about the motivations and education behind my or anyone else's posts. How would you or anyone know whether or not I have any knowledge of chemistry?

It would take a very dull mind to have some knowledge about why psychedelics work and NOT ponder what might come of related compounds.

Back on topic:
I have enjoyed DOB myself. And DOI as well. I think that DOB specifically is interesting at lower doses. It produces a somewhat unique state of mind. I wouldn't take it again but I wouldn't take back having taken it before. Besides, I have put far worse into my body daily for years as a massive cocaine addict first and then a heroin junkie. I have a hunger for new, interesting psychedelic states and from the experiences of people that have indeed taken 25B-NBOMe I find myself interested.
 
N-Benzyloxy 2C-B was the 2nd Bomamine I tried, and honestly it is one of the lesser interesting substituents. But really, in my experiences thus far the differences between Bomamines is rather small, nothing like the differences between their 2C brethren. The 25B feels like what it is, a strong and selective 5HT2a agonist, but lacked the particular nuances that make its close relatives so fascinating (25C and 25I in particular).

It is slightly less potent than 25C, and substantially stronger than 25I. I usually dose around 500-700 mcg via intramuscular injection, and this takes me to a strong plus 3, roughly equivalent to 400-500 mcg of 25C by the same ROA.

The halides are all very close in effects though, and the alkyls all share some similarities. And they ALL share the effects of being selective 5HT2a agonists, which kind of overshadows the differences. Worthwhile absolutely but it's not like you are missing a big piece of the puzzle if you've tried other NBOM 2C's.

Cheers
 
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