It ’s believe that last week the Syrian government bump off 100 of its own civilian with chemical weapons . We do n’t know which weapon they used , but we do get it on it’sone of a handful of chemicals called heart factor .

Nerve agents were invented accidentally by a Nazi - era scientist trying to make a more effective pesticide . That ’s why these molecules are so alike in their structure to the most unwashed course of instruction of insecticides , chemical substance called organophosphate because they control carbon - ground ( “ constitutive ” ) radical coupled to a phosphoric speck . And the way a nerve agent kills you is very like to the way an organophosphate pesticide pour down an insect .

It looks like last week ’s massacre could contribute to state of war ( the White House is talking about a projectile strike ) . With that in head , here ’s a feel at the science of what chance .

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This postoriginally appear on Puff the Mutant Dragon , and has been republish with permission .

How do we know the Syrian govt used nerve agents?

The symptom are evident . For example , the pupil of victims ’ eyes had constrict to the size of it of pinpoint . That ’s exactly what happened to the German scientist who forge GA , the first nerve agentive role . The pinpoint pupils is a hallmark of nerve agentive role poisoning . There is no other chemical weapon that would cause these sort of symptoms .

What did they use?

All the nerve agents cause standardised symptoms , so there ’s no means to know for sure without a sampling for testing .

From leave to rightfield : Sarin , soman , VX and GA . The orange atom is a phosphorus ; that ’s why these are all “ organophosphates ” . Carbon is black , N is blue , atomic number 8 is crimson , S is yellow and fluorine is immature . The phosphorus mote is the part of the molecule that reacts with acetylcholinesterase .

Reuters says the weapon was probably sarin because the Syrian govt apparently has stockpiles of that especial chemical . Sarin is a chemical substance with an ugly account , BTW ; it seems that back in the 1950s the British government activity illicitly try out sarin on some unsuspecting British soldier who were evidence they were participating in a trial run for a new cold medicine . One of these soldiers died in the physical process . The Guardian has the tale onthat at this tie .

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These four chemicals are more thought-provoking to make than something , like , say , crystal deoxyephedrine . They ’re not something you could cook in your backyard . But any halfway decent synthetic organic chemist could make them . So middling much any government that wants them badly enough can get them … which is why they ’re a problem .

What happens to you when you’re poisoned by a nerve agent?

Your brain loses the ability to control your muscles , include the muscle in your contraceptive diaphragm that enable you to take a breather , so you go into fit ( your muscle contracting uncontrollably ) , drool , lose control of your vesica , your dresser tighten up up , you block up breathing and eventually drop dead from respiratory failure . It ’s not an easy way to die . Whoever decided to fuel this at civilian is one sick puppy , no two ways about it .

How do nerve agents work?

Your brain charge signals to your muscles through nerve called motor neurons . At the stage where the motor neuron meet the muscle , the nerve cell pumps out a chemical substance telephone acetylcholine that tells the muscle to contract bridge . Acetylcholine gets broken down by an enzyme called acetylcholinesterase ( I ’ll call it A - prime for shortsighted ) . It ’s an esterase because it breaks an ester bond in acetylcholine ; an ester is two oxygens bonded to a carbon copy in the middle of a carbon chain . Ester bonds run to break down very slowly in weewee , but an enzyme like A - prime accelerates this chemical reaction so it take place rapidly .

This is acetylcholine . It actuate your muscle to contract . Acetylcholinesterase ( A - heyday ) breaks it up rapidly so that your muscle do n’t stay put narrow once the signal from your brain telling them to compact is over .

An organophosphate like sarin slides into a time slot on the A - premier protein like a central fitting into a ignition lock – because its shape enables it to slide right in there . Once it ’s in the slot , it reacts with an amino group dot call serine in the A - blossom particle , and now it ’s mystify onto A - bloom for commodity . A molecule of A - prime that has an organophosphate stuck to it can no longer separate down acetylcholine , so acetylcholine hangs around and your muscular tissue call back your brain is recite them to stick permanently cut because the acetylcholine does n’t go away – it ’s still there . So your brawniness contract and stick around contracted – and at that point you may no longer take a breather . That ’s why the pupils of your eyes flinch to pinpoints ( because the dance band of muscle called the iris has contracted and ca n’t relax ) .

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The chemical reaction between GB and A - prime is very immobile and very irreversible . That ’s why sarin ( and other nerve broker ) are deadly even at very low doses – because even at low assiduousness nerve agent react with A - bloom very cursorily . And you may absorb nerve agents through your skin . These compound are actually liquids at elbow room temperature , BTW ; a lot of people call them “ cheek flatulence ” , and true , they are moderately volatile , meaning they can evaporate fairly easily . But if you spray them you dust a mist of bantam droplets called an aerosol bomb , just like the spray from a can of air freshener , and people can breathe in these diminutive droplets very easily .

Is there an antidote?

Yes . There ’s a chemical substance called 2 - PAM which look like this :

On one goal of 2 - PAM is what ’s hollo an oxime mathematical group , a nitrogen double - bonded to carbon with an Ohio on it . This group is very polar ( i.e. electrons are n’t shared as ) and the OH is electron - rich , so it can react with the Lucifer from sarin that ’s mystify to the serine in A - flower . When it does that , A - prime is exempt up again to get back to doing its chore .

This does n’t always run because an organophosphate that ’s already react with A - prime can actually undergo a subsequent reaction called “ aging ” * * which ensures it can not be remove by 2 - PAM . This “ aging ” reaction is slow for most nerve agentive role , however .

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Typically doctors co - administer 2 - PAM together with atropine , a chemical from the Jimson mourning band plant that blocks acetylcholine from binding to a specific eccentric of receptor on muscle cells , so it helps you recover from nerve agent poisoning .

Depending on the federal agent and how much you inhaled , injecting you with some 2 - PAM and atropine can preserve your life-time – IF the doctor can get to you cursorily enough . I have a feeling the Syrian regular army was n’t on the button make agency for the ambulance though .

How were these invented?

By fortuity . A German pharmacist was trying to come up with a powerful new pesticide . He did n’t know any of this hooey about acetylcholinesterase ; he just knew that some morning star compounds with atomic number 6 - based groups coupled to them seemed to do a corking job killing bug . He did n’t really know why , but he knew he was onto something . So he kept on tweaking these chemical compound , making little changes , add together new and different chemical substance group then quiz them to see whether they were even just at killing insect , and one sidereal day he came up with something that smell mistily like apples . He take a whiff and nearly kill himself .

Rumors about this young compound got round to the German political science . A chemical that ’s lethal in diminutive doses and it smells like yield ? You better trust Hitler was concerned . Thatcrazy illegitimate was always looking for new ways to kill masses .

Why don’t pesticides like malathion kill humans too if their structure is so similar to the nerve agents?

Take a look at malathion below :

you’re able to see it looks like one of the nerve agent but it ’s different enough you’re able to state them aside , right ? And these differences mean that the organophosphate pesticide are typically more toxic to insects than they are to man , because the structural differenecs change the elbow room the chemical is absorbed and metabolized and so forth . Malathion , for exercise , has sanely low toxicity to humans because your body give way it down and excretes it fairly quickly * . Like most organophosphate pesticide , it also breaks down fairly apace in the environment .

And yet , many of the organophosphate pesticides are still highly toxic to humans . Parathion , for example , is so toxic you could call it a weak boldness agent . Farm worker are the masses most at risk , and chemicals like parathion have in fact caused legion accidental deaths among farm prole , specially in break nations . Many of the most toxic chemicals used in Department of Agriculture are organophosphate pesticides .

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It ’s noteworthy how much history organophosphate pesticides and chemical weapons plowshare in common . VX , for lesson , is based on a nerve agent called VG , which was in the beginning made and sell as a pesticide until somebody in the end noticed it was crazily toxic to world .

Hmm. I don’t really like the sound of these organophosphate insecticides. Aren’t there alternative chemicals that kill insects?

option include the carbamate pesticides , the organochlorine pesticide and the pyrethroids .

The carbamates work by criticise out louse acetylcholinesterase . The way they disable acetylcholinesterase is a little different from the way an organophosphate work . Nonetheless , some of them are also very dangerous to human or creature wellness – carborufan get to mind . Most of the carbamates tend to break away down cursorily in the environment .

The organochlorine pesticide are hydrocarbon with atomic number 17 atoms attach . DDT is the most infamous . Most of the organochlorine pesticide tend to break down slowly in the environment . Since they ’re so fat - soluble your organic structure and those of other fauna can only get rid of them slow , which is why they incline to accumulate going up the intellectual nourishment strand . The EPA has banned or trammel most of these because of their environmental impact .

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The pyrethroids are compound base on an insect - killing chemical found in the chrysanthemum flush . They work in a completely different way from the organphosphate / carbamate phratry ; their targets are ion channel in nerve cells . Your liver can go against most of these down very rapidly , and they tend to be much less toxic to razz and mammals than most organophosphate pesticides so they ’ve been becoming more and more popular , especially for indoor uses . Most of them tend to let on down rapidly in the surroundings . That does n’t imply they ’re totally benignant , however . They kill beneficial insects like bee , and they ’re highly toxic to fish .

There are other insecticides out there , but these are the fully grown class .

Well…ok. I can see not all pesticides are created equal. But it sounds like even the most benign of them come with drawbacks. Isn’t there another way to kill insects besides using these compounds?

beaming you asked . There is , although a lot of people do n’t wish it . I ’ll retrovert to that in a future Emily Post . For now permit ’s get back to Syria .

Yes…about Syria. What should we do about it?

Sure , I have my opinions about what we should and should not do just like anyone else . But this is n’t a political blog , and my two cents about government is n’t worth all that much either way . So I ’ll forget that part up for debate .

  • The important point here is that malathion is really a “ prodrug ” if you will ; inside the the human liver or an insect , cytochrome P450 enzyme change it to malaoxon , i.e. that double - bond S is replaced by an oxygen , and malaoxon is the chemical compound that actually binds and inactivates acetylcholinesterase . In humans and other mammals , carboxylesterase enzymes typically split up malathion down apace which limits the amount of malaoxon that gets bring forth . Some insects seem to have evolved resistance to malathion through genetic mutation that result in eminent layer of carboxylesterase enzyme so they can tolerate much in high spirits degree of the pesticide .

    • The real chemical reaction is hydrolysis of one of the ester bonds to the phosphorus atom attach to serine .

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Puff the Mutant Dragonis an analytical pill pusher in the biotech industriousness with a background in biochemistry who maintainsa little blogto assay and go around the joy of scientific discipline , and scrap misunderstanding . you could read more of Puff ’s work over athis / her web log .

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