You get it from different sources. Breakdown of onions and as someone else mentioned, carrots. Balsamic vinegar has some. There’s other sources as well, I’m just blanking on them.
But agreed, I rarely add actual plain sugar to my pasta sauces.
You get it from different sources. Breakdown of onions and as someone else mentioned, carrots. Balsamic vinegar has some. There’s other sources as well, I’m just blanking on them.
But agreed, I rarely add actual plain sugar to my pasta sauces.
Lots of people who like $$$ in TO, I’d expect. We need more turnout from everyone else.
Anti-Bredt double bonds have been a thing for a long time. Taxol (Paclitaxol) comes to mind.
Sorry if this is touched on in the article. I’m going to read it now.
Watching it now on Tubi (free), but even the thumbnail is a moderate spoiler. Would rather not have seen it before watching. It should be blurred or something.
Yeah. I just wasn’t sure at what point things are considered to be bilateral or otherwise.
I thought it may have been during the development process, but can’t remember.
I just posted because I posted a similar image where it reads fine left-to-right, and it fits in the other instance, not this one. I guess this one is for when it reads weirdly left-to-right.
I just posted the link someone posted on my post the other day for the same reason. Thanks though. I do not know how to format things here very well.
White chocolate Reese’s peanut butter cups.
Quoth the raven, nevermore.
https://sh.itjust.works/c/nosafetysmokingfirst
This reads fine left-to-right.
Space colonies. That way they can be dropped to earth to start colony independence wars.
TL;DR for the moment. I’ll try to read it later. Hopefully it’s worth it.
Manger les milliardaires!
Another commenter pointed out the jist and carcinogenic nature of them. There’s been many recalls in actually OTC and prescribed drugs due to them.
But it’s mainly due to the “dimethlyamine” portion of DMT. It’s a tertiary amine, but those can form nitrosamines in some conditions. It’s mainly the synthesis of it that may make it more at risk. There’s potential with a secondary amine in the presence of oxidizing agents. But I guess somewhat low looking at the potential synthetic routes.
Although with the amount people do and (probably the lack of frequency) it’s probably fine.
Even better if it’s extracted from a plant (but can still pose a nitrosamine risk depending on solvents used to extract the DMT).
My earlier deleted comment was due to me not clicking reply on your post… Just on the of one. Sorry.
deleted by creator
Direct action?
UWU.