#azide chemistry

[teet-swea]

HI FELLOW CHEMISTRY NERD HERE PLEASE RAMBLE ABOUT AZIDES I LOVE AZIDES

Ok! So I haven’t actually done much with asides since organic chemistry two years ago, BUT while I was refreshing my memory on their properties I found the loveliest of papers…

and I think that sums up azide chemistry very nicely.

Fav paragraph has to go to:

In the first case, the combination of sodium azide and acid affords hydrazoic acid. Hydrazoic acid is both acutely toxic (mouse LD50 = 22 mg/kg) (3) and a powerful explosive; in its neat form, hydrazoic acid is more explosive than TNT and orders of magnitude less stable. (4) The first scientists to isolate hydrazoic acid (Curtius and Radenhausen, in 1891) (5) found that “the blast of 50 mg was sufficient to disintegrate the apparatus to dust” and when a subsequent 700 mg batch “exploded spontaneously”, it seriously injured the coauthor (Radenhausen) and the shock wave from the explosion shattered every glass vessel nearby. There is no safe quantity when dealing with neat hydrazoic acid.

Even if this is diluted to hell, evaporation of hydrazoic acid followed by condensation will make it explosive all over. It does not require oxygen or a spark to explode.

So anyway, azides are fun :)

[tenth-sentence]

Oxidation numbers calculated by the rules on p. 491 can have fractional values (for example, the nitrogen atoms in the ionic compound sodium azide, NaN3 (see figure 12.2), have an oxidation number of -⅓).

"Chemistry" 2e - Blackman, A., Bottle, S., Schmid, S., Mocerino, M., Wille, U.

[whats-in-a-sentence]

The MoFe protein can then reduce the l numerous substrates (Table 13.4), although under natural conditions it reacts only with N2 and H+.

"Plant Physiology and Development" int'l 6e - Taiz, L., Zeiger, E., Møller, I.M., Murphy, A.

[lady-menrva]

PJO Meta (1 of ??)

DISCLAIMER: I don't mean to offend anyone. I am a ship and let ship person. Please note that criticism =/= hate. Lastly, if you're a solangelo shipper who doesn't wish to hear any criticism regarding their ship, please scroll away.

Ever since it's first appearance, solangelo has been a massive fan favourite. I, however, don't have a favourable opinion of the ship. Here is a brief explanation of my reasons for the same. (I apologise for my inarticulation)

Characterization:-

Nico-

Honestly Nico's writing in the trials of Apollo was terrible even by the usual character assassination standards- in the hidden oracle, he legitimately read as a gag charater who served no purpose apart from being "Will Solace's Goth/Emo Boyfriend". Things were hardly better in Tower of Nero, where he was basically just "Will Solace's traumatized Goth/Emo Boyfriend" who happens to be lazy PTSD rep.

Will Solace-

Can't say much. He was never a character of his own, and probably never will be. His substance as a character is comparable to the quantitative mass of an electron in Kilograms (9.11x 1/10³¹) i.e, negligible.

Nico's Healing Arc (or lack of the same )-

After what was essentially two series worth of fanfic-esque trauma bombing, Nico should have received a proper healing arc. Unfortunately, there was no such arc for him (courtesy of solangelo), because Rick has this earth-shattering, inspired-by-Disney idea that relationships can fix everything. So guess what? Nico's years' worth of emotional baggage, pain and trauma simply volatalize into oblivion .

Some shippers may argue "Oh but he got better off page"-but that it is bad writing per se; Nico's struggles, grief, fears, unhealthy coping mechanisms etc. are more pivotal and relevant to his character than a nascent, one dimensional relationship with an insignificant side character. He is much more than just his sexuality, after all.

Cliché and one dimensional:-

Solangelo is firmly rooted in the "opposites attract" trope, which is simply unrealistic in nature.

Also, newsflash: "Opposites attract" is a law specific to physics and chemistry; It's all fun and games till people who are poles apart sit down to take serious decisions, or share opinions. Friction between them can be rather intense.

(Oh! wait... I think Nico was described to be a Nitride anion {or was he Azide? No, I think he was Nitride} and Will was a Tungsten cation. So, they are basically Tungsten Nitride... Boy! They have so much chemistry between them/s)

Anyways, I totally understand why people prefer jasico, valdangelo, percico, nicobaster etc...

[thecrazyalchemist]

(this post is edited from time to time, some stuff may be outdated) [last edited: sunday, December 8th, 2024]

---

Stuff to get out of the way:

I AM A MINOR. PORN BLOGS FOLLOWING *WILL* BE BLOCKED.

I am Israeli. I am tired. If you want Israel wiped away, if you want Jews killed - please get away from my blog and don't come back.

Post relating to my opinion on Zionism and current affairs <- this is a link to the post, please read!

Post relating to fundraisers and charities about the current conflict <- this is a link to the post

I want my blog to be a safe place for me first and foremost, and then a safe space for others. Not the other way around. I just came here to be silly.

This is my bubble. I'll post some stuff about chemistry from time to time (PASSED ORGANIC CHEMISTRY!!!! GOT A 97!!!! SO EXCITED), stuff from fandoms I like, reblog quite a lot maybe definitely too much (as @bettinalevyisdetermined said [I think]: "I abuse the fast-reblog button"), and generally random stuff my dopamine dependant fueled machine likes.

BEWARE: CHRONICALLY ONLINE

You're quite welcome to ask for random hugs! I have plenty - will take ions to run out of stock

Hug gif: (wanted to put it here because it's so good)

Sideblogs:

@randomshowerpoems - poetry sideblog!

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@thecrazyalchemist2 - clone if I have been cursed by the post limit

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Not gonna reblog every single post from there to here, don't wanna hit the post limit too often. Wanna know what's in there? Go look!

Also do please express your opinion about what I write! I appreciate it immensely 🥺

Some information bout me:

Current timezone: whatever the time in Greenwich is

Online name: Nick F. but you can call me Nick (you can also call me Crazy Al ;] | or Arsenic/Arsenick if you want - courtesy of @givemeasong-singamelody )

Nickolasnames: Quackamole Ferret (bestowed upon me by the amazing @annotated-catastrophe), alchemy buddy (bestowed upon me by the magnificent @alchemicalwerewolf), Alchenick (bestowed upon me by the awesome @anxious-alyssia)

Titles: Attraction stealer - beware (bestowed upon me by the amazing @thebookshelflord)

I'm a cis guy

Pronouns: He/Him, although I don't really care

Sexuality: bisexual & aroma(n)tic (aroflux) (I think - basically arospec)

Favorite color: blue-green

Favorite molecule: Azidoazide Azide

Taste of my ceiling - chalky

I prefer tea over coffee

Preference order: jackets>hoodies>sweaters

What I think about when I hear the word cozy: sitting on a yellow couch reading a book (preferably next to a crackling fireplace), while thunderstorm, inside a library

If you have anything else you want me to add to here, just ask/comment/message/send in a vision/transport in an ancient bottle/come to me in a dream/however you want, but please be clear about it cause I'm a bit of a dum-dum

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Reminder: if you want to be added/removed, just say so! Preferably comment/reblog the tag list you want to be added to/removed from to notify me

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Tags:

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---

(this post is edited from time to time, some stuff may be outdated) [last edited: Sunday, December 8th, 2024]

Picture Stuff

Halloween 2024 Achievements:

[dynmghts]

I am putting my whole brain through chemistry hell with what little I remember from high school chemistry to understand how nitroglycerin works (thanks to one whole thread that's just meant to be silly and goofy, and also ignoring that the substance he makes is described as "nitroglycerin-like"). And man, when I tell you... Katsuki simply has to be built different to deal with his Quirk.

For one, it's a good thing that the nitroglycerin only produces from his hands. For two, remember that nitroglycerin is only slightly soluble with water - which also checks out with how Horikoshi draws the sweat beads sometimes, because they're not exactly combining with the nitroglycerin he makes.

But that likely means the nitroglycerin Katsuki makes is... Quite literally pure.

(This got long, so the rest is under the read more!)

Basic fundamentals to understand about nitroglycerin: it is both flammable and combustible. Wikipedia (bc this shit is the only thing making it make sense) says that "flammable applies to combustible materials that ignite easily and thus are more dangerous and more highly regulated". This is because of nitroglycerin's extremely reactive nature, prone to explosion via shock, friction, heat, and flame.

It is a class A explosive under OSHA, which is defined as: "possessing, detonating, or otherwise maximum hazard; such as dynamite, nitroglycerin, picric acid, lead azide, fulminate of mercury, black powder, blasting caps, and detonating primers".

Its HMIS diamond scaffold is as follows (based on this):

Health: 2 (can cause temporary incapacitation or residual injury)

Flammability: 3 (can be ignited under almost all ambient temperature conditions)

Instability: 4 (readily capable of detonation or explosive decomposition or explosive reaction at normal temperatures and pressures)

Special: N/A

Solid nitroglycerin (at 13°C or lower) will destabilise and explode if melted too quickly. A bottle of pure liquid nitroglycerin (14°C-50°C) will explode if it's dropped on the ground. It will begin to decompose at 50-60°C and explode at a temperature of 218°C. Its decomposition has an exothermic reaction, thus it can literally ignite itself. Nitroglycerin does not need oxygen to explode, because it has enough oxygen molecules in its chemical formula.

Its chemical formula in question is C3H5N3O9. The products after exploding are 3 CO2 + 2.5 H2O + 1.5 N2 + 0.5O...

A clean equation looks something like:

4 C3H5N3O9 -> 12 CO2 + 10 H20 + 6 N2 + O2.

Heat liberated from a nitroglycerin explosion exceeds temperatures of 5,000°C. the detonation wave from this reaction reaches a velocity of 7,280-7,700 metres per second, and creates the development of 20,000 atmospheres of pressure. Its explosive energy density sits at about 6.23 kJ/g, which is one of the higher power outputs in terms of explosive molecules.

So what does this mean for Bakugou Katsuki?

Well, simply put, he does not need a substantial amount of nitroglycerin on his palms to create detonations. The tiny sparks he creates are arguably miniscule doses of nitroglycerin that he's spontaneously igniting.

The method of ignition is thankfully obvious: he can heat his palms. He can shock the nitroglycerin on his palms with this rapid heat, thus spurring the molecules into the desired reaction.

It also explains how Katsuki needs to store sweat so he may create larger explosions later on - it's likely that he doesn't typically produce enough nitroglycerin from his palms to immediately justify any large-scale detonations that he desires. So, to achieve this, he has to work harder and sweat more to garner enough of the substance for the result he's after.

In the realm of BNHA, it's pretty clear that Katsuki's explosions don't exhibit the exothermal properties of nitroglycerin, or we would be seeing some very devastating burns left behind. While I think that he is ultimately capable of heat-related damage, his explosions overall are more force-based. I think his ultimate moves (Howitzer in particular) utilise the full force of nitroglycerin's reaction... Maybe, sometimes, reduced to varying degrees depending on the person he's fighting (plus the use of support items, skill, etc.).

For instance, compare his standard Howitzer Impact used against Todoroki in the sports festival to the Cluster-boosted Howitzer against Shigaraki in the final war:

While it was an ultimate move used on Todoroki, he was less experienced at the time, likely hindering its effectiveness. (I want to say he dialled it back so it wouldn't, you know, cause irreparable damage... But it's possible that inexperience trumped its overall power, because he wanted to win with everything he had.)

Then, against Shigaraki, it was so much force that it quite literally moved floating U.A. across the sky. He combined his support gear, his experience, and the amount of nitroglycerin stored to achieve this level of force.

As a further note, because of nitroglycerin's extreme reactivity and explosive properties, it cannot really produce a flame of its own. Because Katsuki's explosions seem to be more force-based on top of that, he is not necessarily capable of setting things alight... (Seen in the training camp arc, where he tried and failed to start a fire, instead just exploding the wood.)

As for Katsuki's natural resistances to his own Quirk (of which I have described before, but I want to reiterate):

Larger explosion sound levels can be anywhere between 120 decibels and 210 decibels... And a human's "safe hearing" level is about 85 decibels. In my headcanon, Katsuki has a natural adaptation which means he can withstand higher decibels than others, but that does not make him immune - so while he can tolerate large-scale explosion sounds in an open area, especially with him at the centre point, he would suffer if it were the same explosion in an enclosed area.

The aforementioned heating on his palms are only a part of Katsuki's adaptation to his Quirk; the skin is also significantly thicker on his palms and fingers, making his tolerance for touching hot things at a higher level. Like... Much, much higher. It accommodates for when nitroglycerin requires 218°C to explode in a controlled environment. It's why he can handle hot things out of the oven, and why he doesn't know what burns on his hands feel like.

The musculature on his arms and shoulders also have a natural level of strength to withstand the force of his quirk, but this isn't impervious either. He's had to train hard and build on that natural strength to best withstand the higher outputs of force.

Exposure to pure nitroglycerin for any individual is ill-advised, but with manga logic and creative liberties, I don't think anyone who wants to hold Katsuki's hand should have to worry. (I'm 99% sure that he washes his hands thoroughly after working out, anyway.) As for Katsuki himself, I think he does exhibit some symptoms of a nitroglycerin overdose when he's pushed himself way past his limit... But these episodes are incredibly rare, and often very short-lived.

The final notes:

Constant detonation of nitroglycerin means Katsuki has a bit of a smoky smell. Past that, there is also a faint caramel smell.

Also do not taste the nitroglycerin (for whatever reason there is to lick his hand or something? Which Katsuki will literally kill you for doing that, because what the fuck). It does not taste as nice as it smells.

[mandizo]

this is it. you are not immune to my chemist spokeishere propaganda!!!!!!

hes literally a chemist why hasnt anyone thought of this yet?? like,, the creature plays around with explosives like they're lego bricks. thats literally what we do. except that he does it better , bc he puts having fun with his deadly kaboom stuff first and safety last

i hereby present to you my meticulously constructed hc that is totally based on facts and logical reasoning. not because i want them to be exactly like me . open the fold to die instantly!

spoke is an awesome 😎 chemist, in the sense that he doesn't wear goggles, doesn't put on a lab coat, or have any sort of ppe in general, he runs his reactions in glass bottles other people use for brewing and he even stores his energetic end products in glassware. without labels ofc. sure enough if the stuff in it just decides to explode one day the bottle will be reduced to countless glass shards flying everywhere but that has never happened. in fact spoke never got hurt synthesising energetic compounds (i should really stop calling them that it just means explosives) no matter how insane the reaction setup looks. he'll stir the mixture wit h his own fingers and the reaction still runs smoothly

crossover with the most hc of all time, spoke cant read , he just cant, but that doesn't really affect doing chemistry does it? dont really have to know how to read. just look at the hexagons with goofy faces on them. he also has an experiment journal like any other chemist. but since he cant read he doesn't actually write anything down. there r only his doodles of withers blowing stuff up and the energetic crystals he makes in there. also some pages are just covered in azides and peroxides. the entire thing is just a gigantic safety hazard. the cover and a couple of pages are gone bc one time parrot was looking through his stuff and took the notebook out of a chest. the book detonated on the spot and the cover and some pages were blown off. parrot lost a heart but spoke is still pretty mad at him since one of the missing pages has a drawing of these reeeaaally pretty S4N4 crystals he made one time.

he draws stuff with d-p backbonding as double bonds (hes literally me!!!) and instead of drawing benzene like a hexagon with a depressed face in it he draws a ^_^ in. look at the example youll get what I mean

also he doesn't know how to do retrosynthesis. when he has to design a route he works from the start to the end. and hes pretty good at it

miscellaneous stuff below

⬆️ the brainrot hit when i was taking the math exam ive been talking abt im failing so hard lol

⬆️ S4N4 crystals from tom’s vid on it

uh thats it actually. im aware that there are some key details i need to work out but i think im just gonna enjoy what i already have for now. um. idk. listen to austenyo? lol

[calversstudy]

i've just leared that my chemistry ia may be fatal or cause permament damage to my genetic material... what a wonderful day to be alive!

tbh i am not going anywhere near sodium azide, 7 in chemistry isn't worth it

[jesus-died-for-mycins]

Back at it again with another funky way to make funky peptides, gotta admit I have a type. The authors didn't provide a scheme but I whipped one up anyways :)

This time the approach is to forgo the traditional cyclisation methods (chemical ligation or disulphide bridging) and instead cyclise the peptide via a click reaction. So, what is a click reaction and why bother? Well click chemistry is the nickname given to a series of biorthogonal (meaning it doesn’t interfere with biological systems) azide-alkyne coupling reactions developed by Bertozzi, Meldal and Sharpless, its kinda a big deal and those folks won the 2022 Nobel prize for their work. There are a few reasons it would be useful to cyclise a peptide with click chemistry, a) its an orthogonal reaction which means that previously inaccessible functional groups could be included in cyclic peptides, b) a lot of ink has been spilled optimising, developing and expanding click chemistry so there’s a massive array of options and flexibility for future development, c) the click reaction produces a far more stable product that disulphide bridging and d) its not confined to the N/C terminus like chemical ligation usually is.

So with the background out of the way, what did these folks actually do? Well the paper is describes a protocol for creating cyclic peptide probes; i.e. a cyclic peptide that will bind to a target and is functionalised with a reactive handle so it can be visualised via a fluorophore. The paper is detailing a quite specific protocol, and what I think likely happened is that these folks were trying to create probes for their other research, but they realised the method they came up with was so effective that they should really publish it as a protocol (this would not be unusual).

But anyways, onto the chemistry. To create cyclic probes the researchers incorporated 2 orthogonal click reactivities into the linear sequence, a thiol-ene reaction to generate the cycle and a classical azide-alkyne for the probe functionality. The scheme does all the talking really (and was a bitch to draw) but nonetheless I think that it’s a neat demonstration of the expanding tools available for synthesising tricky peptides and versatility of click chemistry.

References:

LeValley PJ , Ovadia EM , Bresette CA , Sawicki LA , Maverakis E , Bai S , Kloxin AM . Design of functionalized cyclic peptides through orthogonal click reactions for cell culture and targeting applications. Chem Commun (Camb). 2018 Jun 19;54(50):6923-6926. doi: 10.1039/c8cc03218a. PMID: 29863200; PMCID: PMC7433322.

[metrocity123]

Alkyne PEG | Glycomindsynth Glycomindsynth is high purity Alkyne PEG with multifunctional groups for your research. Alkyne PEG (Polyethylene Glycol) linkers are specialized compounds used in chemical and biological research. Here's a breakdown of their key aspects and uses: Structure and Chemistry: PEG (Polyethylene Glycol): A hydrophilic polymer that is often used to increase solubility, stability, and reduce immunogenicity of compounds. Alkyne Group: A functional group featuring a carbon-carbon triple bond (–C≡C–). This group is commonly used in click chemistry reactions due to its ability to react with azides in a highly selective and efficient manner.To know more, please visit our website: https://glycomindsynth.com/sub_cat_list/Alkyne%20PEG/PEG%20Linkers Call on : 9766253311 Address - Glyco Mindsynth Pvt Ltd 3rd floor, Plot No 144A, Sector 7, PCNTDA MIDC, Bhosari, Pune-411026 (Maharashtra) INDIA

[healthcarehubhh]

Growing Antibody-Drug Conjugates Market Owing to Rising Demand for Targeted Cancer Therapy.

Antibody-drug conjugates (ADCs) are a type of bioconjugate consisting of monoclonal antibodies that are attached by chemical linkers to highly potent anti-cancer payloads. ADCs selectively target antigens that are highly expressed on tumor cells while sparing normal tissues through the use of antibodies. Linkers attached between the antibody and cytotoxic drug allow for the drug to be delivered unchanged until it reaches the intended tumor site, minimizing harm to healthy cells. ADCs have demonstrated clinical efficacy in treating various cancers including lymphoid malignancies, breast cancer, and solid tumors.

The Global Antibody-Drug Conjugates Market is estimated to be valued at US$ 5.38 Bn in 2024 and is expected to exhibit a CAGR of 14% over the forecast period 2023 to 2030. Key Takeaways: Key players operating in the Antibody-Drug Conjugates are AstraZeneca PLC, Daiichi Sankyo Company, Limited, Novasep, ADC Therapeutics SA, Alentis Therapeutics AG, F. Hoffmann-La Roche, Gilead Sciences, Inc., AbbVie Inc., Biosion USA, Inc., Astellas Pharma Inc., Duality Biologics (Suzhou) Co. Ltd., BioNTech SE, LaNova Medicines Ltd., Bliss Biopharmaceutical, Eisai Co., Ltd., ProfoundBio, Pfizer, Inc., ImmunoGen Inc., Mersana Therapeutics Inc., Sorrento Therapeutics Inc., Oxford BioTherapeutics Ltd, and Takeda Pharmaceutical Company Ltd. Growing demand for targeted cancer therapy with minimal side effects is expected to drive significant growth of the ADC market over the forecast period. Additionally, ongoing technological advancements in linker chemistry, increasing pipeline products and approvals are further fueling the market growth. Market Trends: The ADC market is witnessing increasing adoption of cleavable linkers that are stable in circulation but rapidly release the drug payload intracellularly upon internalization into target tumor cells. Additionally, the development of novel conjugation technologies such as DBCO-azide click chemistry is allowing for site-specific conjugation without effect on bioactivity and efficacy of ADCs. Market Opportunities: The significant opportunities in the ADC market are in developing ADCs for liquid and solid tumor indications with unmet medical needs. Additionally, optimization of physiochemical properties of molecules to improve pharmacokinetics is another key area that ADC developers are increasingly focusing on to enhance therapeutic index and efficacy of ADCs.

[universalnewspoint]

Alfa Chemistry Newly Announces Offering of Click Chemistry Reagents: Azides, Terminal Alkynes, and Copper-Chelating Ligands

http://dlvr.it/T1Gg6N

[desmoinesnewsdesk]

Alfa Chemistry Newly Announces Offering of Click Chemistry Reagents: Azides, Terminal Alkynes, and Copper-Chelating Ligands

http://dlvr.it/T1GbvF

[eduebookstore]

Organic Chemistry: 100 Must-know Mechanisms by Roman Valiulin, ISBN-13: 978-3110608304 [PDF eBook eTextbook] Publisher: ‎ De Gruyter (April 20, 2020) Language: ‎ English 230 pages ISBN-10: ‎ 3110608308 ISBN-13: ‎ 978-3110608304 Organic chemistry at a glance: straightforward and easy-to-grasp depiction of 100 crucial mechanisms in organic chemistry. This book summarizes 100 essential mechanisms in organic chemistry ranging from classical such as the Reformatsky Reaction from 1887 to recently elucidated mechanism such as the copper(I)-catalyzed alkyne-azide cycloaddition. The reactions are easy to grasp, well-illustrated and underpinned with explanations and additional information. Audience: Students, Organic Chemists. Author information: Roman Valiulin, Cambridge, USA. What makes us different? • Instant Download • Always Competitive Pricing • 100% Privacy • FREE Sample Available • 24-7 LIVE Customer Support

[thecrazyalchemist]

A beautiful molecule with a beautiful name: Azidoazide Azide

Molecular formula: C2N14

(Blue - Nitrogen, Gray - Carbon)

It explodes if:

Touched

Moved

Dispersed in solution

Exposed to bright light

Or even if

Left undisturbed on a glass plate

Source:

[lifetein]

Enzyme-Degradable Peptides in Click Chemistry Drug Delivery

https://www.lifetein.com/blog/enzyme-degradable-peptides-in-click-chemistry-drug-delivery/ As methods of medicine advance, targeted drug delivery becomes a more appealing and achievable option over its non-selective counterpart. It can focus solely on increasing therapeutic concentration in the target area while greatly eliminating any exposure to healthy tissue, and thus drastically lowering side effects as well. The effective and simple mechanisms of click chemistry are a great way to design payloads for these targeted drug delivery methods. With the use of enzyme-degradable peptides in click chemistry drug delivery, lasting therapeutics can remain in the system for local sustained release over time as well. Enzyme-degradable peptides for sustained drug delivery The team at Rutgers focused on a two-phase method to set up the targeted drug delivery. First, ROS-sensitive PEGDA and acrylate-PEG-azide are aimed at the target area, driven by elevated free radical levels. Once the pretargeting is complete, a payload tethered to DBCO is delivered and captured via azide-DBCO reactions. Enzyme-degradable peptides were provided by LifeTein and incorporated into both steps for ongoing release of the captured payloads. The results showed success in the models tested, with the initial dosage still effective in capturing the payload several days later. This system demonstrated the versatility of a two-phase method, where long term effects are even avoided further by the incorporation of enzyme degradable peptides. The proof of concept displayed here has great promise for the future of drug delivery, and just goes to show how applicable click chemistry is to even more fields. Emily T. DiMartini, Kelly Kyker-Snowman & David I. Shreiber (2023) A click chemistry-based, free radical-initiated delivery system for the capture and release of payloads, Drug Delivery, 30:1, DOI: 10.1080/10717544.2023.2232952