raptor Posted October 23, 2006 Posted October 23, 2006 I was wondering if anyone knew if it was possible to remove glycine from glyphosate (herbicide), leaving methylphosphonic acid?
YT2095 Posted October 23, 2006 Posted October 23, 2006 you REALLY don`t want to messing about with organo-phosphates! trust me!!!
woelen Posted October 23, 2006 Posted October 23, 2006 Glyphosate is not that dangerous. It can be purchased OTC at concentrations of up to 30% or so, in so-called Round-up replenisher. Round-up is a weed-killer, used a lot over here. In general, however, I must say that playing around with organo-phosphorous compounds is not the smartest thing to do, when you don't know exactly what you are doing.
YT2095 Posted October 23, 2006 Posted October 23, 2006 Glyphosate itself is reasonably harmless, I have several litres of it myself as Agricultural concentrations (it`s like Honey when that strong), enough to do several hectares of land. but since you`re thinking about adulterating an OTC product such as this, and asking such questions, I have to think to myself that this is NOT a wise move on your part!
raptor Posted October 27, 2006 Author Posted October 27, 2006 I really wasn't planning on trying it as I agree that this isn't the kind of thing you should be playing around with, but I was curious as to whether such a procedure would be possible.
raptor Posted November 5, 2006 Author Posted November 5, 2006 What I was wondering was if there is a way to separate an amine like this, similar to hydrolysis of an ester.
Gilded Posted November 5, 2006 Posted November 5, 2006 If you don't mind me asking, what's so bad about organic phosphates then? Except that ATP is a necessity for a mischievous thing called life (with a few exceptions probably).
raptor Posted November 6, 2006 Author Posted November 6, 2006 Those are the most toxic eg. sarin, tabun, VX etc. while a lot of similar compounds are powerful insecticides eg. parathion. Most of these seem to be esters of methylphosphonic acid or similar, though most of the insecticides have the double bonded oxygen replaced with a sulfur.
orgopete Posted November 11, 2006 Posted November 11, 2006 Why make what you can buy from Aldrich? If you could hydrolyze (like water), then the leaving NH2 group would have to be replace with an OH. That compound is really easy to make. Toxicity is toxicity. DNA is an organophosphate. Somehow, I'm not worried. The insecticides you mention are cholinesterase inhibitors. Beware of cholinesterase inhibitors.
chiwi Posted January 18, 2015 Posted January 18, 2015 (edited) Here we are, applying glyphosate like water, over the earth, and I had no idea! does anyone know what happens when animals ingest this? nerve gases? for real? wow, I have so much to learn. As a child, I sat on the trailer, behind the tractor, driving through fields of young almond trees, spraying malathion, as the wind blew the malathion into our faces, for hours, ( that is what is wrong with me, haha). I really like this forum, have been enjoying reading everyone's posts, even though i have to go to google, and look everything up afterwards, ha! Edited January 18, 2015 by chiwi
chiwi Posted January 20, 2015 Posted January 20, 2015 ok, does any scientist on this forum know what happens when you apply glyphosate to a plant, and then the plant is fed to cattle, and then we eat the cattle, as beef? Is it just like eating salt? I have always wondered about that. but do not know the chemical reactions, does anyone know? Is the glyphosate broken down into harmless products? or? Chiwi
BabcockHall Posted January 20, 2015 Posted January 20, 2015 An environmental chemist told me some years ago that glyphosate broke down relatively quickly in the environment. Given that glyphosphate is a phosphonate, I always found that a little surprising.
Strange Posted January 20, 2015 Posted January 20, 2015 Searching for "glyphosate degradation" or "glyphosate metabolism" should produce lots of results. One of the main products is aminomethylphosphonic acid, which seems pretty harmless. http://en.wikipedia.org/wiki/Aminomethylphosphonic_acid
Altered State Posted January 24, 2015 Posted January 24, 2015 An environmental chemist told me some years ago that glyphosate broke down relatively quickly in the environment. Given that glyphosphate is a phosphonate, I always found that a little surprising. It does it like that: http://upload.wikimedia.org/wikipedia/commons/thumb/5/53/Glyphosate_degradation.svg/820px-Glyphosate_degradation.svg.png
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