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No more tomfoolery this time

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Winds of Change

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Interesting stuff, Firefly.  Thanks.

deez

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Nada, a down-on-his-luck construction worker, discovers a pair of special sunglasses. Wearing them, he is able to see the world as it really is: people being bombarded by media and government with messages like "Stay Asleep", "No Imagination", "Submit to Authority". Even scarier is that he is able to see that some usually normal-looking people are in fact ugly aliens in charge of the massive campaign to keep humans subdued.

DimensionsOfYou

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RARE. I have had pranaview as a saved search on eBay since the glasses were first discussed here ca. 2016-2017. This is the  first time in all those years an auction has been listed with them. These are the one invented by the australian fellah who's been MIA since ca. 2011-12 AFAIK.

So if you have the means and want to see some reptays this is your chance.

SomethingCreative

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Interesting. A recipe to create the dycyanin dye needed to create the aura goggles from Tylenol. Any organic chemists here?

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This guy did some work on creating a pair and provides some instruction.

Nrgiseternal

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Interesting. A recipe to create the dycyanin dye needed to create the aura goggles from Tylenol. Any organic chemists here?

You are not allowed to view links. Register or Login

This guy did some work on creating a pair and provides some instruction.

Does he address how he got dycy?

DimensionsOfYou

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RARE. I have had pranaview as a saved search on eBay since the glasses were first discussed here ca. 2016-2017. This is the  first time in all those years an auction has been listed with them. These are the one invented by the australian fellah who's been MIA since ca. 2011-12 AFAIK.

So if you have the means and want to see some reptays this is your chance.
Damn, they're already sold. Was it any of you guys?

SomethingCreative

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Interesting. A recipe to create the dycyanin dye needed to create the aura goggles from Tylenol. Any organic chemists here?

You are not allowed to view links. Register or Login

This guy did some work on creating a pair and provides some instruction.

Does he address how he got dycy?

the direct dicyanin A precursor (2,4-dimethyl-6-ethoxyquinoline) from paracetamol. So the product that is 1 step away from dicyanin A.
I'm quite experienced in the lab, but I don't want to break laws let alone be "suicided" or experience a freak accident.
Anyway, pic related outlines the process. Paracetamol is extracted from OTC pain killer tablets. This is ethylated under gentle conditions using ethyl iodide, as to only attack the ring oxygen and avoid attack on the nitrogen. The resulting product is hydrolysed to obtain 4-ethoxyaniline.
Ethyl iodide is made from ethyl bromide by Finkelstein swap with sodium iodide. Ethyl bromide is distilled from an ethanol/sulfuric acid/sodium bromide mixture.
Acetaldehyde is made either using the classic route from ethanol with sodium dichromate. But since dichromate is a listed carcinogen banned in some countries, alternative processes can be considered. Paraldehyde is obtained by polymerisation of acetaldehyde.
The acidic aldol condensation product from acetaldehyde and acetone is added to the previously prepared 4-ethoxyaniline under conditions that will close the ring, forming 2,4-dimethyl-6-ethoxyquinoline which is the direct precursor to dicyanin A.
The final step to dicyanin A involves adding some of the previously prepared ethyl iodide set aside for this purpose and silver nitrate.

Nrgiseternal

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Interesting. A recipe to create the dycyanin dye needed to create the aura goggles from Tylenol. Any organic chemists here?

You are not allowed to view links. Register or Login

This guy did some work on creating a pair and provides some instruction.

Does he address how he got dycy?

the direct dicyanin A precursor (2,4-dimethyl-6-ethoxyquinoline) from paracetamol. So the product that is 1 step away from dicyanin A.
I'm quite experienced in the lab, but I don't want to break laws let alone be "suicided" or experience a freak accident.
Anyway, pic related outlines the process. Paracetamol is extracted from OTC pain killer tablets. This is ethylated under gentle conditions using ethyl iodide, as to only attack the ring oxygen and avoid attack on the nitrogen. The resulting product is hydrolysed to obtain 4-ethoxyaniline.
Ethyl iodide is made from ethyl bromide by Finkelstein swap with sodium iodide. Ethyl bromide is distilled from an ethanol/sulfuric acid/sodium bromide mixture.
Acetaldehyde is made either using the classic route from ethanol with sodium dichromate. But since dichromate is a listed carcinogen banned in some countries, alternative processes can be considered. Paraldehyde is obtained by polymerisation of acetaldehyde.
The acidic aldol condensation product from acetaldehyde and acetone is added to the previously prepared 4-ethoxyaniline under conditions that will close the ring, forming 2,4-dimethyl-6-ethoxyquinoline which is the direct precursor to dicyanin A.
The final step to dicyanin A involves adding some of the previously prepared ethyl iodide set aside for this purpose and silver nitrate.

So why did he stay 1 step away

SomethingCreative

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Interesting. A recipe to create the dycyanin dye needed to create the aura goggles from Tylenol. Any organic chemists here?

You are not allowed to view links. Register or Login

This guy did some work on creating a pair and provides some instruction.

Does he address how he got dycy?

the direct dicyanin A precursor (2,4-dimethyl-6-ethoxyquinoline) from paracetamol. So the product that is 1 step away from dicyanin A.
I'm quite experienced in the lab, but I don't want to break laws let alone be "suicided" or experience a freak accident.
Anyway, pic related outlines the process. Paracetamol is extracted from OTC pain killer tablets. This is ethylated under gentle conditions using ethyl iodide, as to only attack the ring oxygen and avoid attack on the nitrogen. The resulting product is hydrolysed to obtain 4-ethoxyaniline.
Ethyl iodide is made from ethyl bromide by Finkelstein swap with sodium iodide. Ethyl bromide is distilled from an ethanol/sulfuric acid/sodium bromide mixture.
Acetaldehyde is made either using the classic route from ethanol with sodium dichromate. But since dichromate is a listed carcinogen banned in some countries, alternative processes can be considered. Paraldehyde is obtained by polymerisation of acetaldehyde.
The acidic aldol condensation product from acetaldehyde and acetone is added to the previously prepared 4-ethoxyaniline under conditions that will close the ring, forming 2,4-dimethyl-6-ethoxyquinoline which is the direct precursor to dicyanin A.
The final step to dicyanin A involves adding some of the previously prepared ethyl iodide set aside for this purpose and silver nitrate.

So why did he stay 1 step away

He seems concerned for his safety since some other researchers in the past have seemingly disappeared.

Nrgiseternal

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Interesting. A recipe to create the dycyanin dye needed to create the aura goggles from Tylenol. Any organic chemists here?

You are not allowed to view links. Register or Login

This guy did some work on creating a pair and provides some instruction.

Does he address how he got dycy?

the direct dicyanin A precursor (2,4-dimethyl-6-ethoxyquinoline) from paracetamol. So the product that is 1 step away from dicyanin A.
I'm quite experienced in the lab, but I don't want to break laws let alone be "suicided" or experience a freak accident.
Anyway, pic related outlines the process. Paracetamol is extracted from OTC pain killer tablets. This is ethylated under gentle conditions using ethyl iodide, as to only attack the ring oxygen and avoid attack on the nitrogen. The resulting product is hydrolysed to obtain 4-ethoxyaniline.
Ethyl iodide is made from ethyl bromide by Finkelstein swap with sodium iodide. Ethyl bromide is distilled from an ethanol/sulfuric acid/sodium bromide mixture.
Acetaldehyde is made either using the classic route from ethanol with sodium dichromate. But since dichromate is a listed carcinogen banned in some countries, alternative processes can be considered. Paraldehyde is obtained by polymerisation of acetaldehyde.
The acidic aldol condensation product from acetaldehyde and acetone is added to the previously prepared 4-ethoxyaniline under conditions that will close the ring, forming 2,4-dimethyl-6-ethoxyquinoline which is the direct precursor to dicyanin A.
The final step to dicyanin A involves adding some of the previously prepared ethyl iodide set aside for this purpose and silver nitrate.

So why did he stay 1 step away

He seems concerned for his safety since some other researchers in the past have seemingly disappeared.

You do see why that is specious don't you?

SomethingCreative

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Interesting. A recipe to create the dycyanin dye needed to create the aura goggles from Tylenol. Any organic chemists here?

You are not allowed to view links. Register or Login

This guy did some work on creating a pair and provides some instruction.

Does he address how he got dycy?

the direct dicyanin A precursor (2,4-dimethyl-6-ethoxyquinoline) from paracetamol. So the product that is 1 step away from dicyanin A.
I'm quite experienced in the lab, but I don't want to break laws let alone be "suicided" or experience a freak accident.
Anyway, pic related outlines the process. Paracetamol is extracted from OTC pain killer tablets. This is ethylated under gentle conditions using ethyl iodide, as to only attack the ring oxygen and avoid attack on the nitrogen. The resulting product is hydrolysed to obtain 4-ethoxyaniline.
Ethyl iodide is made from ethyl bromide by Finkelstein swap with sodium iodide. Ethyl bromide is distilled from an ethanol/sulfuric acid/sodium bromide mixture.
Acetaldehyde is made either using the classic route from ethanol with sodium dichromate. But since dichromate is a listed carcinogen banned in some countries, alternative processes can be considered. Paraldehyde is obtained by polymerisation of acetaldehyde.
The acidic aldol condensation product from acetaldehyde and acetone is added to the previously prepared 4-ethoxyaniline under conditions that will close the ring, forming 2,4-dimethyl-6-ethoxyquinoline which is the direct precursor to dicyanin A.
The final step to dicyanin A involves adding some of the previously prepared ethyl iodide set aside for this purpose and silver nitrate.

So why did he stay 1 step away

He seems concerned for his safety since some other researchers in the past have seemingly disappeared.

You do see why that is specious don't you?

Yeah I mean he just compiled some research that was already out there. Hes either a bit too paranoid, trying to mislead us, or perhaps he thinks that each individual should research this final step on their own.

I’ll have to do some digging into the actual chemistry. Might take a bit, but it will be worthwhile.
Last Edit: April 18, 2021, 01:44:38 AM by SomethingCreative

SomethingCreative

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Interesting. A recipe to create the dycyanin dye needed to create the aura goggles from Tylenol. Any organic chemists here?

You are not allowed to view links. Register or Login

This guy did some work on creating a pair and provides some instruction.

Does he address how he got dycy?

the direct dicyanin A precursor (2,4-dimethyl-6-ethoxyquinoline) from paracetamol. So the product that is 1 step away from dicyanin A.
I'm quite experienced in the lab, but I don't want to break laws let alone be "suicided" or experience a freak accident.
Anyway, pic related outlines the process. Paracetamol is extracted from OTC pain killer tablets. This is ethylated under gentle conditions using ethyl iodide, as to only attack the ring oxygen and avoid attack on the nitrogen. The resulting product is hydrolysed to obtain 4-ethoxyaniline.
Ethyl iodide is made from ethyl bromide by Finkelstein swap with sodium iodide. Ethyl bromide is distilled from an ethanol/sulfuric acid/sodium bromide mixture.
Acetaldehyde is made either using the classic route from ethanol with sodium dichromate. But since dichromate is a listed carcinogen banned in some countries, alternative processes can be considered. Paraldehyde is obtained by polymerisation of acetaldehyde.
The acidic aldol condensation product from acetaldehyde and acetone is added to the previously prepared 4-ethoxyaniline under conditions that will close the ring, forming 2,4-dimethyl-6-ethoxyquinoline which is the direct precursor to dicyanin A.
The final step to dicyanin A involves adding some of the previously prepared ethyl iodide set aside for this purpose and silver nitrate.

So why did he stay 1 step away

He seems concerned for his safety since some other researchers in the past have seemingly disappeared.

You do see why that is specious don't you?

Also I purchase both available sets of these vintage cobalt lenses. You are not allowed to view links. Register or Login

Would these work you think? I plan to try regardless

AllKeyMe

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I find that seeing auras is not that hard, takes only a second or two and I can see an outline while looking at my hands. If i look a bit longer I start seeing color. If i look around and try to see auras, especially at night when the light is very dim, I can see all sorts of things.
Would it be any different with the dicyanin glasses? I assume the glasses would only make it easier to see
Last Edit: April 18, 2021, 05:43:31 AM by AllKeyMe

stgermaine

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Nrg, as many have taken the (((jab))) now, how do their auras and subtle bodies look like?

Nrgiseternal

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Nrg, as many have taken the (((jab))) now, how do their auras and subtle bodies look like?

I've not been in a position to view people who get the jab in a while. I will let you know when I see one

 

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