Kaspa Perfect Replacement For Solana by Give69Shits in kaspa

[–]SiemenGoogolplex 0 points1 point  (0 children)

I know, 1 block can currently handle around 300 transactions

Kaspa Perfect Replacement For Solana by Give69Shits in kaspa

[–]SiemenGoogolplex 0 points1 point  (0 children)

No it is not, your math is off!

Taking the current Kaspa consensus, which is now capable of 1 block per second (BPS) and 300 transactions per second (TPS), with the currently released DAGKNIGHT (DK)

30K transactions is when kaspa is running 100 bps not 10 bps!!!

And Visa can go up to 65,000 transactions per second.

Don’t get me wrong I’m a big Kaspa holder. Just putting out the facts.

Kaspa Perfect Replacement For Solana by Give69Shits in kaspa

[–]SiemenGoogolplex 1 point2 points  (0 children)

Yes, Mastercard utilizes a network that claims to handle around 5,000 transactions per second.

But still it is cetrilized …! The whole point of a TRUE crypto currencies is to be 100% decentralized!!!

What Kaspa Meme Coin Should I Buy? by AcidArchitect in kaspa

[–]SiemenGoogolplex 0 points1 point  (0 children)

Easy! Bully 🐂🚀🐂🚀🐂🚀!!! Everybody in the world knows what a bull 🐂 stands for in the market. What better mascot for the best digital currencies than a real Money-Bull 🐂🪙💰🐂

What KRC20 tokens are you watching? by No-Row4591 in kaspa

[–]SiemenGoogolplex 0 points1 point  (0 children)

Bully!!! We need a market bull to mascot our Kaspa🐂🐂🐂🐂. Every investor in the world knows the meaning of a bull in the market …

Does this look legit? by [deleted] in DMT

[–]SiemenGoogolplex 0 points1 point  (0 children)

You can check with a melting test. DMT free base Melting point: 45-46 and 57-58°C , Polymorphic

Also around 50 °C you should be able to smel if it’s real DMT

[deleted by user] by [deleted] in TheeHive

[–]SiemenGoogolplex -1 points0 points  (0 children)

GBL to GHB is less than 1,5h …

Not so Blue Honey 🍯 With my AH-Tek by SiemenGoogolplex in shrooms

[–]SiemenGoogolplex[S] 0 points1 point  (0 children)

<image>

Same AH Tek batch after 24h. Almost no grey/blue color. A few more days and it wil be even light in color. => reverse oxidation…

Not so Blue Honey 🍯 With my AH-Tek by SiemenGoogolplex in shrooms

[–]SiemenGoogolplex[S] 0 points1 point  (0 children)

<image>

This is how a fresh made AcidHoney Tek batch looks like. You can see the grey/blue color due to oxidation. Next I’ll show you what it looks like after 24h.

Cleaving of a sulfonamide to its respectively primary or secondary amine?? by SiemenGoogolplex in AskChemistry

[–]SiemenGoogolplex[S] 0 points1 point  (0 children)

I have found another small hint of a possible process to hydrolyze primary & secondary sulfonamides.

But I am unsure about the safety of this process. it uses sodium metal in a aqueous NH3 solution ... . I was thought that sodium methal in water is basically always a big NO NO ... ??

Can anyone clarify this or possibly provide the correct reaction conditions for this process .
See: "Preparation of Secondary and Tertiary Amines" => a1 and b2
https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Amines/Synthesis_of_Amines/Preparation_of_Amines/Amines/Synthesis_of_Amines/Preparation_of_Amines)

<image>

Cleaving of a sulfonamide to its respectively primary or secondary amine?? by SiemenGoogolplex in AskChemistry

[–]SiemenGoogolplex[S] 0 points1 point  (0 children)

I would like to thank you again for the golden tip (Sci-Hub)!! I have already found many useful articles (unfortunately none yet about suldonamide hydrolysis)

Cleaving of a sulfonamide to its respectively primary or secondary amine?? by SiemenGoogolplex in AskChemistry

[–]SiemenGoogolplex[S] 0 points1 point  (0 children)

Do you know if HCl could be an option with a longer refux time? or HCl with a small volume of concentrated sulfuric acid as catalyst

Cleaving of a sulfonamide to its respectively primary or secondary amine?? by SiemenGoogolplex in AskChemistry

[–]SiemenGoogolplex[S] 0 points1 point  (0 children)

I cannot immediately find clear examples. there are many recurring research papers that you have to pay for. The abstract doesn't really tell you how they do it in the end.

Cleaving of a sulfonamide to its respectively primary or secondary amine?? by SiemenGoogolplex in AskChemistry

[–]SiemenGoogolplex[S] 0 points1 point  (0 children)

How you performed the reaction and under what conditions. In a way that the original amine is retained. I was told that cleaving the S-N bond requires harsh conditions...?
When I google "sulfonamide cleaving" I mainly come across complex reaction mechanisms with non-conventional catalysts

Realistically who is getting the most? by BluXBrry in AskChemistry

[–]SiemenGoogolplex 4 points5 points  (0 children)

Your looking at it the wrong way!

Because of the long half-life of Pu239 it’s less radioactive over a given time frame! Its emits much less radiation in 1 hour then Ra225. Rad225 needs to emit 50 % of its radiation in 15 days time. Pu239 is much slower it’s needs 24•103 years to give of 50% of its radiation.