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Author: Subject: 2,6-dinitro 4-acetaminophenol + Potassium Chlorate
Energetics-testin
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cool.gif posted on 26-1-2024 at 04:22
2,6-dinitro 4-acetaminophenol + Potassium Chlorate


After a year of procrastination,im coming back with a new energetic mixture containing DNAc and potassium chlorate in a 60:40 ratio.

Properties:burns very quick(flashpowder like).
Detonates from heat, if its well confined.
Detonates confined and unconfined when hit with a hammer.
A bam test will be done to determine its sensitivity.
Friction insensitive (suprising for a chlorate mixture)

*More info will be posted once enough research is done*

Questions and help is always appreciated.

[Edited on 26-1-2024 by Energetics-testin]
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Sir_Gawain
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[*] posted on 26-1-2024 at 09:44


What’s your source of nitroacetaminophenol? Nitrating paracetamol? Is the DNAc itself a high explosive? If not, I see great potential in this as a binary NPED that can be prepared onsite.



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[*] posted on 26-1-2024 at 10:36


Yes, I nitrate purified acetaminophen extracted from tylenols.

I dont believe that pure dinitroacetaminophen is explosive at all, it is barely able to burn.

It doesn't detonate when hit with strong hammer blows and doesn't detonate when confined and heated.


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[*] posted on 26-1-2024 at 11:31


Energetics-testin.......If this chlorate mixture can initiate ETN, it will be an interesting alternative in the ignition....:cool:
However, there are many binary compounds with KCLO3 that behave as described but do not have initiation properties.




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[*] posted on 26-1-2024 at 12:01


As always, thanks for the information doctor, I will definitely do some tests to see if it is able to detonate ETN.

I will however do more sensitivity tests before to be sure that it is safe to work with.

Let's hope for the best :cool:
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[*] posted on 27-1-2024 at 05:41


How did you nitrate the acetaminophen? I’d assume the acetyl group is hydrolyzed by conc acid (HNO3 or H2SO4) at high temps required for the addition of the second nitro group, and in that case, you might’ve formed 2(3),5(6)-dinitro-4-aminophenol.

I’d argue the p-aminophenol analogue is better than the acetyl counterpart simply due to OB and the stabilization that the unprotected amine imparts. Also, if the 4-aminophenol is actually formed, nitration at the 3 or 5 position followed by nitrosation could form the benzotriazole which is an even better base EM to nitrate.
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[*] posted on 27-1-2024 at 10:23


I followed the paper posted by nitro-genes and roscobodine on how to make p-ddnp,during the synthese (second step) we have to nitrate paracetamol,they talk a bit about why the nitro groups chooses these position instead of the other way.explosions and fire also talks a bit about the nitration and tells us why the nitro groups are choosing these placements.

Oh,seems quite intresting,i'm gonna look into that.

Nitrogenes & rosco's writeup on p-DDNP and isopicramic acid.
https://www.sciencemadness.org/whisper/files.php?pid=419166&...


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[*] posted on 27-1-2024 at 19:45


I completely forgot about DDNP, my apologies. It does look like the nitro groups are unable to be directed towards the 3 and/or 5 position, so cyclization to the benzotriazole could be practically impossible.

The isopicramate/chlorate mix could might have promise though, good luck with it and be safe
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[*] posted on 29-1-2024 at 11:37


No worries.
I will definitely try to experiment with isopicramate,thanks!
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[*] posted on 29-1-2024 at 12:12


Would this work with sodium picramate or picramic acid (2-amino-4,6-dinitrophenol) made from picric acid? I made some with the intention of making DDNP, then discovered NHN.



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[*] posted on 30-1-2024 at 01:34


I will test it if you dont first,I have some old picric acid lying in a cabinet somewhere, I just need to turn it into sodium picramate.
I will however have to check the compatibility of chlorates with picramates and isopicramates before proceeding.

:cool:
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[*] posted on 8-2-2024 at 11:03


Unfortunately, the DNAc mixture cannot be used to initiate ETN.

The isopicramic acid/KClO3 mixture looks way more promising than the DNAc/KClO3 mixture.

To be tested.
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[*] posted on 8-2-2024 at 11:51


Energetics-testin...For example KClO3 + potassium ascorbate looks a like primer according properties on air. Unfortunatley, in solid cavity are his
properties weak. Preparation is same as for TEJO game.
https://www.youtube.com/watch?v=BZqG3RGFQVc




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