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Don't know vendors, but this compound is easy to make. I'm wondering why there is suddenly no new analogues, maybe it's politics or blanket bans.

In theory you can make it from benzonitrile and butylmagnesium bromide. It's a well-known method to make ketones.

For small batches you can use hexamine (HMTA), look for sciencemadness or rhodium threads about methylamine from this.

Thanks

Don't do that. Your life costs much more than 17g of coke.

Which route they're using?

Have you tried all of it? What about duration of every compound?

Please note that diazoalkanes is extremely dangerous. "In one instance a laboratory worker consumed a hamburger near a fumehood where he was generating a large quantity of diazomethane, and died four days later from fulminating pneumonia." From wikipedia. This chemical is only for very skilled...

Benzoyl indole will get you weak cannabinoid. https://en.wikipedia.org/wiki/JWH-167 This phenylacetylindole 45% potency of thc, benzoyl will be weaker. https://en.wikipedia.org/wiki/RCS-4 This 25% potency of THC. Benzoyl probably will be about 30-40% of thc...

Nobody knows, i guess 10-50% potency of parent compound. Try to find original paper on 5Cl derivates, maybe phenyl ethyl derivate was tested.

Don't mess with carf, its extremely dangerous. You can make fent safely, but not carf, it requires serious safety measures, tons of money and equipment. Nitrile and carboxamide should be much more dangerous than NPP or ANPP.

https://en.wikipedia.org/wiki/Perrottetinene Phenyl ethyl side chain is known, but it probably will be weaker.

It must be unpleasant shit, with long duration. And action starts 20-30 minutes after consumption, as it in wiki article. This is sucks. Its a "heavy" and lipophilic molecule, like in antidepressants, methadone, etc. Not good for ***** and bumps. Its hard to quickly metabolize this, you need...

How its possible? Draw formula please. Looks fake.

Can you crush it? Dissolve to complete liquid or colloid solution. Then use ammonia to make free base (NaOH may react with filler, but try it too). Then extract it with dichloromethane, use stir it hard to make emulsion, if its colloid. Then let it separate and take dcm solution. You can use...

Can i get access?

Any info?

KI3 occurs in equilibrium with I2 and KI, its better to oxidize all iodine to improve yields by one third in theory, if you talking about to pour tincture in water. Look for videos on youtube.

It meets, as core structure (3-(1-naphtoyl)indole). 3 position - nitrogen, 5-fluoropentyl is alkyl group attached to nitrogen. Maybe aryl sulfone not meets, i've heard about new class with this group.

How china labs making it so cheap? Is it made in tube furnace (like p2p from phenylacetic and acetic acids)? Friedel Crafts is very expensive for large batches.