• Psychedelic Drugs Welcome Guest
    View threads about
    Posting RulesBluelight Rules
    PD's Best Threads Index
    Social ThreadSupport Bluelight
    Psychedelic Beginner's FAQ

The Big & Dandy 25I-NBOMe Thread

Status
Not open for further replies.
No, not at all. We know the NBOMe series quickly produce a high tolerance which lasts for a good 2 weeks.

I still can't for the life of me find sensibly priced HPBCD, there is one place in america which does the endotoxin controlled stuff, but shipping is $100!
I'm investigating getting some from china now, a kilo is around $100!
 
No, not at all. We know the NBOMe series quickly produce a high tolerance which lasts for a good 2 weeks.

I still can't for the life of me find sensibly priced HPBCD, there is one place in america which does the endotoxin controlled stuff, but shipping is $100!
I'm investigating getting some from china now, a kilo is around $100!

I don't think we "know" this at all, as the reports I've read in this thread and at other forums seem to be all over the map. I think what we "know" is that the nbomes are likely to produce a variable and unpredictable tolerance in users.
 
Today I tried a 500ug dose of 25I-NBOMe using liquid dosing onto a strip of paper which was then dried and applied to my upper gums for a half hour. I didn't try any of this complexing stuff; instead I tried to dissolve it in distilled water, but it wouldn't dissolve, so I guessed that I have freebase (despite it being sold as HCl) and added some vinegar to convert it to the acetate salt. I noticed as I was preparing the dose that I started to get a headache and also feel a little "floaty" at the same time. I don't know if that was placebo or if I accidentally inhaled a few specks of powder as I was measuring it out...?

About an hour after I took the paper out of my mouth the floaty feeling got a little stronger, and I started to feel very relaxed and open. But I didn't get any visuals or have anything progress beyond a +1. It felt somewhat like low-dose DOC, but without as much of the amphetamine pushiness. I even kept yawning the whole time. About four hours after dosing, I started to notice little aches in my joints and hands, and the headache which was in the background became more persistent. I also felt a heaviness in my gut and a vague sense of unease that developed over a couple of hours. I took some ibuprofen for the achiness and half a Unisom for the anxiety, and it seems to be helping a little. It's been ten hours since dosing now, and I'm still at a mild +1, and back to the more positive mood I started out with.

I'm not sure if I'm going to try this substance again. The body load wasn't that bad really, but there wasn't much else going on besides a mood uplift and a slightly psychedelicized mental space. I'm kind of worried the aching and body tension will get worse if I try higher doses.
 
No, not at all. We know the NBOMe series quickly produce a high tolerance which lasts for a good 2 weeks.

I still can't for the life of me find sensibly priced HPBCD, there is one place in america which does the endotoxin controlled stuff, but shipping is $100!
I'm investigating getting some from china now, a kilo is around $100!
i dunno i took about 1mg today and i tripped major balls so i guess its different for everyong
 
About an hour after I took the paper out of my mouth the floaty feeling got a little stronger, and I started to feel very relaxed and open. But I didn't get any visuals or have anything progress beyond a +1. It felt somewhat like low-dose DOC, but without as much of the amphetamine pushiness. I even kept yawning the whole time.

We don't understand yawning very well, but certainly for me, serotonegeric drugs will bring on yawning.

Interesting to know sheekle - how many days after the first dose was that?
 
We don't understand yawning very well, but certainly for me, serotonegeric drugs will bring on yawning.

Interesting to know sheekle - how many days after the first dose was that?

8 days


i took 2 and then about an hour and a half later if i remember correctly I took a third but with the immediate tolerance idk if the third one worked so yeah like 1-1.5mg
 
shut up.. I can do more 25i than you and your whole family put together. Also the redose period is definitly more than 2 days. I tried after 2 days, nada. So i'm going to try again in about 3 days.. and i don't do the sissy hbcpd complex like you people ahahaha.

lol dexermeth i know you man ur on topix.. hahah

but i'm certain it's not 2 weeks. maybe 1 week tops

i say 4-5 days but not tested yet , def more than 2, probibly 3 days.. also upping the dose doesn't seem to make any difference believe me.

Please don't quadruple post.. Also "dick-sizing" with doses etc is not cool. ~Jesusgreen

Wow, it bothers me that people this ignorant end up getting access to these compounds. Go back to Mephedrone and stop wasting our time with your posts. "Sissy complexing"... seriously, how old are you?
 
In re: tolerance. I'm going to have to say it seems you can get pretty close to baseline after about 72hrs. However during some other tests it's quite obvious tolerance spikes hard during the first 24-48hrs. (IE: ts1 - 25i hcl @ 1mg, nice good +3, but in an effort to keep it going, redosed another 700mcg about 6hours in.. This had little to no effect)

Also - I acquired my 25i in freebase form, and converted it to HCL form. No testing was done with the freebase.

However I'm seeing little to no benefit from HCL to complexed HCL =/ A couple pm's are out trying to confirm results, and or see if I messed up during complex.
 
Pleasingly, 25I-NBOMe does not seem to suppress appetite in any significant way. On an LSD comedown I can barely stomach the sight of food, but I was able to put away two hearty platefuls of whole grain pasta while still significantly intoxicated on 25I.
 
I got a nasal spray to dose my 25i. I mixed 50mg in 10ml of water, and had measured each spray at 0.1ml, so each spray should be 0.5mg. I tried dosing the first time with 2 sprays, and I got a ++ experience. I was expecting more. Are my calculations off, or should I try upping my dose?

so how did you manage to measure out the individual sprays? im just curious.....
also, it might be that not the entire dose went in your nose where it should have... did you have a drip? did you also remember to shake the bottle well before using?
whats the stability/shelf life of this compund in this solution?
 
I have some 25I-NBOMe on blotters. I thought that it would not degrade as I heard that its lifespan was 2 - 3x as long as us humans so I wasn't worried. Then I realised that it is probably much different and should be stored differently then the powder form. I dont know what the NBOMe was disolved in but it said they were ion exchance blotters, whatever that means. Anyway, I gave 1 3/4 to a friend who took them when he went to see netsky, he was also taking speed and mdma that night I think. He told me he didn't feel anything from them but 1. He might just be trying to rip me off 2. The other drugs effected his trip 3. It has degraded. He said the only effects that were felt was a potentation of the speed.

As I was under the impression they would not degrade, I kept the blotters in the baggie that they were shipped in, sealed. In another fitted plastic open envelope inside another package coated in bubble wrap. The package was mostly kept out of sunlight but might have been lying out for a few hours once or twice. I have had the blotters for around 1 - 2 months.

So, have they degraded? That is a shame if they have as I only got a chance to take this once and still have 5 tabs left. Any help on the situation is apreciated

EDIT: I know this was pretty stupid as most people store tabs in tin foil or something just as good, I just wasn't thinking as I haven't been using as many psych's or drugs in general so they have not been on my mind as much.
 
I'm fairly certain that the paper isn't any fancy modified cellulose but just plain paper, and that the substance in/on blotters is about as stable as in powder form (it could have higher surface area though). I don't believe it's option 3.

Does your friend know how to use these blotters? Dosing NBOMe substances as blotters is reportedly very inconsistent. Allegedly they don't work if the substance ends up in the stomach for metabolic and/or kinetic and/or other reasons. Perhaps only a fraction of the dose made it to the brain and he didn't notice the weaker effects in that mix.

Have you tested these blotters for activity yourself? That could be option 4.
 
I'm fairly certain that the paper isn't any fancy modified cellulose but just plain paper, and that the substance in/on blotters is about as stable as in powder form (it could have higher surface area though). I don't believe it's option 3.

Does your friend know how to use these blotters? Dosing NBOMe substances as blotters is reportedly very inconsistent. Allegedly they don't work if the substance ends up in the stomach for metabolic and/or kinetic and/or other reasons. Perhaps only a fraction of the dose made it to the brain and he didn't notice the weaker effects in that mix.

Have you tested these blotters for activity yourself? That could be option 4.

Yes I tested them myself and recieved a reasonably strong trip from 1mg although a little underwhelming. He said he held them subbucally without swallowing for 20 - 30mins, he then swallowed the tab + his saliva.
When I dosed I ended up swallowing multiple times as I had weird cottonmouth and held them in the same manor moving it around my mouth for about 40 - 50mins, it definatley worked for me although I think it would have been more ffective if I kept it in the same place and didn't swallow.

I have no idea what he did wrong as he is experienced with various psychedelics and is no idiot, probably just trying to scam me out of some DOI tabs he promised me. Thanks for the input, my main concern was that it had degraded and I could no longer trip. There was a yellow blotch on the blotter that seems more prominent and bright then it is now (hard to see with the naked eye) although that might just be my memory playing tricks on me. Thanks again for your reply
 
i tried 25i nbome my first time this week at 6 mg dose 3 500 mcg complexed blotters and 5 1mg blotters non complexed and i had DMT closed eye visual complex patterns and had intense 3d visuals of fractal type patterns coming out into the air. was totally sober minded through the whole thing no mind fuck at all totally a great time will definately try it again. visuals were nice color morphing was alot like doi and tracers like 2ce but the visuals at high doses have the complexity of DMT fractals in mid air it but you can make the patterns how you want and light adds patterns dramatically on this substance.
 
My question is...

but my question was supposed to be: How similar is the 25I experience to the LSD experience?
 
Last edited by a moderator:
I notice from other trip reports that people seem to enjoy 500mcg to 1mg doses of 25i. It appears thats because they want a full blown psychadelic experience. But what if someone wanted to retain decent motor control and be able to "put aside the trip" to do something while tripping- like make tea on the stove or pack a bowl or find your way in and out of a concert arena without getting lost and be able to find the bathroom when you are there and just be able to deal with people if need be? The purpose of this experiment was to find a low dose quantity that would produce an enjoyable psychadelic experience without losing mental ability and physical dexterity. Not everyone is a hard head and this subject certainly takes no pride in bragging about taking stupidly huge dosages.

Subject: very healthy male, 117 lbs., accustomed to very sedentary lifestyle, 40y/o, last trip was 2 months earlier on insulfated 25i.

Using a cheap mg scale with known linearity of +- 4mg, 16 to 25 mg freebase 25i-NBOMe was weighed out and dissolved in 20 ml dehydrated etoh. The etoh was dehydrated in advance using 3A molecular sieves. The actual amount of 25i weighed out was probably closer to 16 mg. The goal was to produce 1mg/ml solution. Then, 200 mg HPBCD was weighed out and added to the solution. Both components easily dissolved. A solution of 0.7mg/ml (25i:etoh) was probably acheived instead.

0.25 mL solution was drawn out with 1mL syringe marked with .01mL increments. The solution was then slowly applied to a suspended blotter over the course of maybe 10 minutes and allowed to dry. The goal was to produce a 160 to 250 mcg dose of 25i complexed with HPBCD on blotter but an amount closer to 160mcg was probably acheived. The blotter was a 1 x 3/4 inch piece of coffee filter.

The blotter was cut in half lengthwise and both halves placed between upper lip and gums and held for 30 minutes. 30 minutes was probably unnecessary but the blotter stayed in place very easily. No taste or numbing was sensed. Just felt like having a piece of paper in the mouth.

2 hrs later mild OEVs began to be noticeable. Euphoria and increased energy was noticed. OEVs werent much more than waves of visual distortion and very mild tracers. There was very little loss of motor control.

3 hrs after dosing, Oolong tea was made; dinner was cooked and consumed. Some time was then spent on the computer reading and responding to online forums. Enjoyed listening to Sunday Baroque.

6 hrs after dosing, CEVs became evident. And it was like exactly 6 hrs to the minute like a switch was flipped. It was noticed that suddenly something was different. The CEVs werent immediately apparent when closing the eyes but with calming the mental activity and focusing the attention on the CEVs, after maybe 2 minutes, they exploded like kaleidoscopic fireworks. Really freakin beautiful. So it would take a bit of meditation to make the CEVs happen but they did! Problem was maintaining the focus on the CEVs, for as soon as the mind wandered onto some other subject, the CEVs dissappeared. This could be good practice for learning meditation. Also, at this stage, a lot of the earlier stimulation had worn off. So, it was easier to sit/lie down and try to experience the CEVs. This stage continued for another 4-5 hrs until sleep was attained.

8 hrs after dosing, synthabinoids JWH-081 and JWH-250 were smoked at a rate of about 0.5mg or less every 30 minutes or so until subject finally went to sleep. The synthabinoids seemed to enhance the over all experience with particular regard to the OEVs and CEVs.
The following day was great. No residual body load or back of the head headache or brain drain feelings. Normal energy and activity levels were felt.
Total experience from time of dosage was 11 hrs.

Summary/conclusions: I think many people like higher doses because they want their face rubbed in the psychadelic experience. But for a more controlable experience, lower doses can be just as enjoyable. The dose produced as described above may really have been a bit low but is definitely above threshold. The accuracy of the amount measured was limited by the linearity of the scale used. This subject suspects threshold may be around 100mcg but doesnt remember what others have to say in that regard. A similar amount of bodily control could probably be retained with a dose between 250 to 350 mcg. The OEVs may be a bit more developed at that dosage range. CEVs would be easier to enjoy. At that range, the first 6 hrs may also not be too physically stimulating. Dosing in this range may also be more amenable to being in a social environment in comparison to a high dose. Still, driving would not be recommended but the subject should retain good fine motor control and a sitter should not have to worry much about the subject. Late in the trip, the two above mentioned synthabinoids seemed to compliment the 25i very well. Overall message, try lower doses if you want to run around, be with people, and have manual dexterity with out being a tripped out spaz.

Oh yeah, people who make blotters with freebase and dont complex it and find that it doesnt do anything didnt actually absorb any of it- you wasted your material. The reason behind complexing with HPBCD is to make this stuff absorbable since it is not water soluble. Please do your homework. I believe that complexing with HPBCD is the easiest, least problematic and most effective way to handle this stuff. 25i complexed in this manner should also increase its stability since the HPBCD surrounds the 25i molecule which would theoretically reduce its exposure to oxygen, humidity, light, blah blah blah, although probably no legitimate studies have been done to determine if this is so. Thank tregar for your contribution on this subject.
 
Status
Not open for further replies.
Top