Ventrusii
Bluelighter
The one thing I am absolutely clueless on concerning any psychoactive is anything dealing with modification/preparation concerning chemistry. If anyone knows a site where I could learn this stuff (like, literally anywhere. Coursera I already know about.), that would be GREATLY appreciated. I haven't even knowledge of how to identify a basic substance compared to an acidic one.
I was looking into how to convert cyclohexane (a hydrogen-saturated carbon ring) to benzene (a carbon ring with three double-bonds, none bordering one another) , in hopes of applying this process to propylhexedrine. Doing so would create something amazing, just look up propylhexedrine's structure to see and replace the cyclohexane ring with a benzene ring to see what I'm talking about.
I found a website that has the only information I could find ANYWHERE on the clearnet and even in the parts of the deep web I've explored.
http://chem-guide.blogspot.com/2010/04/cracking-and-reforming.html
If this link shouldn't be here, please message me before this thread is (re)moved so I can add the adequate pictures and explanations for what it contains.
It shows that if you heat cyclohexane rings (in this case with a methyl group attached to it, like propylhexedrine would have) to 670 kelvin (746.33 Farenheit / 396.85 Celsius) with a platinum catalyst in the absence? of three dihydrogen (H2)(The stable form of hydrogen, hydrogen sharing an electron with another hydrogen & vice versa), it would create benzene with four extra dihydrogen.
Would applying this to the full propylhexedrine molecule provide for the same results, or would there be variables that would interfere with such process, such as the molecule vaporizing or decomposing before it reacts, or even a different reaction occurring completely due to the extra parts that are in propylhexedrine that are not there in plain cyclohexane with a methyl group?
Any help would be GREATLY appreciated on this topic. If you don't want to post it on the thread, please DM me. The only reason I don't rush right into this is because I think if I do something stupid it would kill me like I hear so many people who do things like that have happen to them.
~V
I was looking into how to convert cyclohexane (a hydrogen-saturated carbon ring) to benzene (a carbon ring with three double-bonds, none bordering one another) , in hopes of applying this process to propylhexedrine. Doing so would create something amazing, just look up propylhexedrine's structure to see and replace the cyclohexane ring with a benzene ring to see what I'm talking about.
I found a website that has the only information I could find ANYWHERE on the clearnet and even in the parts of the deep web I've explored.
http://chem-guide.blogspot.com/2010/04/cracking-and-reforming.html
If this link shouldn't be here, please message me before this thread is (re)moved so I can add the adequate pictures and explanations for what it contains.
It shows that if you heat cyclohexane rings (in this case with a methyl group attached to it, like propylhexedrine would have) to 670 kelvin (746.33 Farenheit / 396.85 Celsius) with a platinum catalyst in the absence? of three dihydrogen (H2)(The stable form of hydrogen, hydrogen sharing an electron with another hydrogen & vice versa), it would create benzene with four extra dihydrogen.
Would applying this to the full propylhexedrine molecule provide for the same results, or would there be variables that would interfere with such process, such as the molecule vaporizing or decomposing before it reacts, or even a different reaction occurring completely due to the extra parts that are in propylhexedrine that are not there in plain cyclohexane with a methyl group?
Any help would be GREATLY appreciated on this topic. If you don't want to post it on the thread, please DM me. The only reason I don't rush right into this is because I think if I do something stupid it would kill me like I hear so many people who do things like that have happen to them.
~V
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