baratron: (goggles)
I finally came up with a chemistry pun to explain how my gender works.

I've felt for a while like the cis/trans binary doesn't work for me. Despite being female assigned at birth, I'm not really cis because some of the time I don't feel female. But nor do I feel like I can call myself trans because I'm happy with my body at other times.

So I'm cis but prone to radical isomerisation.

It works because cis/trans isomerisation is a radical mechanism, but also because "radical" has a meaning in English outside of science.
baratron: (science genius girl)
Woo. I feel clever. I worked out that a certain molecule had to be put together in cells by polyketide synthesis. And the mechanism I sketched the other day appears to be basically correct, except I didn't know about a particular gene carrying out selective reductions.

I am recording this since research involves many episodes of feeling like you are the most stupid person on the planet and no one could possibly be as awful as you, and it's nice to celebrate those occasional moments when you get to feel pleased with yourself :)

In other and mostly unrelated news, I am Annoyed with the Pain Management Clinic at Kingston Hospital for failing to get back to me regarding the results of the MRI I had on 5th August. I have been chasing them up since last Friday. The receptionist suggested that the pain management doctor might call me at the end of his clinic on Monday, but he hasn't and - to be honest - nor did I expect him to. I just want to know what's supposed to be happening next, you know? Do I continue taking more and more gabapentin? Is there something obviously physically wrong that they might be able to treat?
baratron: (gaming)
It's Wednesday, and I have actually READ BOOKS THIS WEEK (!). So I should do that Wednesday reading meme thing. Unfortunately I'm exhausted and have lost coherence, AND still have another 2 hours before I can go to bed. Gods damnit.

So have some links that have been sitting in my browser for weeks:

people say I'm gonna regret this, I say fuck you. A Reddit thread in which a user boasts about his tattoo of an illegal drug... which turns out to be so not the molecule he thought it was that it would make anyone with A-level chemistry laugh their arses off. Mmm. Yeah. Benzene rings are tricky little buggers, aren't they?

On similar lines (perhaps), A Simple and Convenient Synthesis of Pseudoephedrine From N-Methylamphetamine. "In recent years it has become increasingly difficult to obtain psuedoephedrine in many states because of its use as a precursor for the illegal drug N-methylamphetamine (also known under various names including crystal meth, meth, ice, etc.)" "A quick search of several neighborhoods of the United States revealed that while pseudoephedrine is difficult to obtain, N-methylamphetamine can be procured at almost any time on short notice and in quantities sufficient for synthesis of useful amounts of the desired material." Given that it's published in the Journal of Apocryphal Chemistry, somehow I doubt this is real... But any organic synthesis route can be reversed, so... I dunno. I laughed anyway.

Groovy glasses. "Ok let's see if that thing with glasses chicks suddenly becoming super weird feminine when they whip off their glasses works". You kinda have to go all the way to the end to find the really funny pictures.

Introducing 'SheZow,' The 'Transgender' Superhero Cartoon That Will Destroy America And/Or Entertain Some Children. I liked this review. Haven't bothered watching any of the cartoon clips though.

How I Lost Faith in the “Pro-Life” Movement. I have a vague feeling I may have linked to this before, but it's worth reading if you have enough spare time to read the whole, very long, article, and are not already in a stabby mood.
baratron: (rainbow chemistry geek)
Who wants to buy me this for Christmas/Yule/Newtonmas?
baratron: (wolfy)
Pink Science, '50s-Style. Interesting comparison of a "Lab Technician Set For Girls" to the hideously gendered "Chemistry" kits of today.

What Milgram’s Shock Experiments Really Mean: Replicating Milgram's shock experiments reveals not blind obedience but deep moral conflict, from Scientific American.

Maps of the 2012 US presidential election results, organised in a number of ways. Interesting but slightly freaky.

Positive pregnancy test diagnoses man's cancer. From Reddit, apparently.

BEST VIDEO OF THE ENTIRE YEAR!!! Two very good dogs teach you chemistry. This is beyond amazing. If you have ANY interest in chemistry or dogs, or even if you don't but you don't actively dislike dogs, WATCH THIS VIDEO.
baratron: (test tube)
I need some brilliant people to come up with a solution to stop me hurting my back.

It's true that I am a lazy git who's been failing to do her physiotherapist-prescribed exercises for months on end, but the main reason my back is showing off now is because I've been doing things in the lab which are normal for chemists but not sensible for me. Specifically I've been standing up for too long, and bending down awkwardly to look at the meniscus of measuring cylinders.

Standing up for too long can be addressed - leaning on things to try to stay standing is putting too much strain on some parts of my spine. There are plenty of lab stools with back support in the lab. I just need to stop being embarrassed about the fact that I can only really stand up for a few (< 5) minutes at a time without pain.

But figuring out is some way of reading measuring cylinders without bending down is more complicated. I could get a "glamorous assistant" who doesn't have a bad back to read them for me (and have to trust that they're competent and have read it properly). My Disabled Students Allowance provides funding for lab assistance BUT I only need someone to help me for a few minutes at a time. I don't want to waste my funding paying for someone to be with me for 3 or 4 hours a day, when I only need help for about 15 minutes out of that. And not 15 minutes all in one go, either. There are other tasks later when I'll need an assistant with me all the time, and I'd rather save the funding for then.

A shelf, or box, would be a solution except that the meniscus that needs to be read at eye height is in a different place every time, since it's rarely the same quantity of liquid that I need to measure.

Can anyone think of something better than simply using a standard chemistry laboratory clamp stand to raise the height of the measuring cylinder? I don't want to do that because it's hard to clamp things perfectly perpendicularly, leading to parallax errors, and the extra clamping and unclamping is more effort on my hands. I'm sure there exist sturdy stands that can be slowly concertinaed up and down... except they probably cost a small fortune. Anyway, something like that, perhaps.
baratron: (test tube)
I have been quite spectacularly busy the past few days. Have been to the Paralympics twice, about which I will write more later. (Though I shall note that Richard & I were at the Athletics event described in section "You can come second and set a new world record", and had to puzzle out how that was possible.)

Today I was supposed to be at College setting up my first organic synthesis in something like 16 years, but my body decided to give out on me entirely and I spent the day asleep. I will be making a chalcone on Friday instead, and am getting progressively more anxious. Since it does not go back as far as 1996, my livejournal does not relate the story of Evil Pink Stuff, which was the last organic synthesis I ever did. It was supposed to be o-benzoylbenzoic acid. Absolutely none of the starting, intermediate, or final compounds are pink. Neither was the catalyst I put in & am pretty sure removed correctly. Yet pink was what I obtained. Pink, gelatinous precipitate, instead of a fine white powder. Gods only know what it was. I'm not sure I had enough time to do all the tests to find out. And I'm traumatised enough by other happenings that year not to want to poke into the box of Here Be Dragons that contains, among other things, my second year lab reports - though definitely curious enough to consider it.

Another point: my phone is being strangely evil of late. I used to frequently comment on livejournal (and deadjournal) from it, but for some reason when I type now, I keep hitting the full stop key by mistake. So I end up with Sentences. That. Look. Like. This., which look terrible and require lots of painful correction (since I don't get on with touchscreens), unless I take the artificial and non-ergonomic step of only hitting the space bar with my left thumb. This slows down my typing, and is actively uncomfortable, and as a result I'm not commenting on anything anywhere near as much as I used to. I've got to figure out if it's me or my keyboard at fault. (Hand positioning, or sticky keys? Or some sort of software "upgrade" that's making the keyboard more sensitive?). Anyway, it means I'm not replying to things when I want to, since I mostly do "social" internet from my phone. But I still love you & care about things in your lives.

Go, IUPAC!

Jul. 7th, 2012 05:01 pm
baratron: (science genius girl)
If you're a certain kind of geek, this is awesome: the new, 2011 definition of the hydrogen bond. Turns out all those school definitions involving a hydrogen covalently bonded to an oxygen, nitrogen or fluorine atom forming a second, weak bond with the lone pair of electrons on another oxygen, nitrogen or fluorine don't go anywhere near far enough...
baratron: (rainbow chemistry geek)
[11:17] <baratron> i never understand how so many stupid Mac users have their machines open when they're staying in a hotel
[11:17] <baratron> i can see 9 other Macs here
[11:18] <baratron> and since the default name for a computer is Firstname Lastname's Mac, i know who owns them
[11:18] <baratron> *mine* is locked down so it doesn't appear on public networks
[11:18] <DysTuvai> good grief, the apples are metastasing. >>
[11:18] <baratron> and is in any case called Praesodymium
[11:19] <DysTuvai> ... that is an awesome name for a computer.
[11:19] <baratron> Macs have to be named after f-block elements *nods sagely*
[11:19] <baratron> Silicon Graphics machines have to be named after d-block elements
[11:20] <DysTuvai> ... that's... an interesting way to look at it
[11:20] <DysTuvai> XD
[11:20] <Teapot> you're such a scientist. :p
[11:20] <DysTuvai> I'm not quite sure what is the connection
[11:20] <DysTuvai> But it's just another one of those awesome HL things
[11:20] <DysTuvai> ^^
[11:25] <baratron> it's how the computers at college were named
[11:25] <baratron> we did not have PCs
[11:26] <baratron> i suppose they'd have to be s- or p-block elements
[11:27] <DysTuvai> All I can say
[11:27] <DysTuvai> Is that this degree of geekery is pure unrefined awesome. XD
[11:27] <Teapot> And also quite likely to make a Mac's trendy aluminium head explode. ;D
[11:28] <baratron> the lecture theatre we had for our final-year lectures had each seat named after an element, in order
[11:28] <baratron> i usually sat in Copper or Cobalt
[11:28] <Teapot> that is brilliant
[11:28] <baratron> the building does not exist any longer :(
[11:29] <DysTuvai> It was too awesome to exist.
baratron: (face only)
'Cos three things make a post, right? (This is actually four).

[21:41] My ovary (or whatever) is really flippin' hurting again. I want to know when i'm supposed to be getting it scanned.

[22:53] I used the Hyperbole & a Half Pain Scale to determine if I needed to take my ovary to hospital. I decided it was about a "5", as in "Why is this happening to me??". It's not time to get it prodded in A&E until it's up to a 6 or 7 (I'm pretty sure I have to be crying with pain before it's worth going to the hospital in the middle of the night). I seriously need to chase up that scan though.


[01:49] I don't mind molecules with a whole load of different names, but it gets positively insulting when there are a whole load of NUMBERING schemes. Geldanamycin is case in point - what IUPAC thinks is carbon 19 is what people using the old/ biochemistry/ natural product name think is carbon 17. Given that the IUPAC name is hideous then referring to it as geldanamycin makes sense - but it gets ever so confusing when you have names of derivatives based on adding and removing groups from carbon 17 - when the "official" name calls that carbon 19!

And I've just found a molecule (Radicicol) that can be numbered from 1-18 consecutively OR from 1-6 (round the benzene ring) and then from 1' to 12' (round the rest of it).

Mind you, if you ever want to have a fit of the vapours, try looking up the official IUPAC name for plain old glucose.


[04:25] Gods, the weather here has been VILE for HOURS. Driving wind and rain non-stop since about 9pm (it's now nearly 4.30 am)


[04:39] Did I mention that I'm wearing a pair of Richard's socks? The stupid boy was supposed to get my socks out of the washing machine & pair them & hang them on the line on FRIDAY. Today, I went downstairs with a load of dirty sheets and found them all still in the machine, smelling really revolting since they'd been damp since Friday. So I've had to rewash them, which meant I was completely out of clean socks.

Richard's socks are horrible & scratchy, & make my feet itch.
baratron: (pokemon scientist)
A question for you at 4.30am:

Why on earth is the compound with formula Na2S2O4 called sodium HYDROsulfite when there's no sign of hydrogen anywhere near it? (It's also called sodium dithionate and sodium sulfoxylate, both of which are more sensible names). I'd think it was a typo for sodium hyposulfite if it wasn't so damned prevalent on the web. But sodium hyposulfite appears to be an old name for sodium thiosulphate, Na2S2O3.

Damn you, atoms with too many oxidation states for sensible names to work! (See also: nitrogen).
baratron: (flasks)
Of the reaction mechanisms I drew last night:
2 were completely right
1 was almost completely right (SN2 instead of SN1, something which I wouldn't have known because the textbook says that particular reagent, unusually, almost always goes via SN1 despite being primary)
1 would have been right if I'd trusted my instincts
and the last was bollocks only because I'd produced an extra C=C bond from nowhere and got myself confused. Without that, it would have made sense and I'd have been able to finish it.

Apparently I am not actually stupid at organic chemistry. I just need a lot more practice so that I trust myself in unfamiliar cases.
baratron: (science genius girl)
Too tired for personal update. It's Techniques Week, which means several days of sitting through lectures, and two early morning starts. (10 am at College means leaving the house before 9, which means getting up at *mumble*...)

Instead, have some pictures which will make geeks laugh, weep, or both: Signs on chemistry labs at Georgia Tech in Atlanta.

What IS wrong with the picture? )
baratron: (rainbow chemistry geek)
Having given up and gone to bed two and a half hours ago, work is now happening. Well, WHATEVER - I don't care what time the clock says if I have a concentration span and am able to get useful work done. However, I am now reading an article by this man who is obsessed with the word physicochemical, and it's annoying me greatly. I'm not joking about his obsession - on the same page, we have:
"the physicochemical features of protein folding"
"the physicochemical basis of protein folding"
"the same physicochemical features of the polypeptide chains" and
"under the physicochemical conditions found in the living systems".

The reason it's annoying me is that physicochemical is a horrible kludge of a word. Technically, it means "relating to physics and chemistry"; but in practice, the features that are being described are entirely physical - as in "relating to physics". But they don't use the word "physical" in these papers for two reasons:

1) Virtually no one reading the paper would describe themselves as a physicist. You'll get a lot of Physical Chemists, a few Chemical Physicists, and a few Biophysicists - but no unmodified Physicists. (Also, the word "physicist" now looks like it's spelled wrongly through having been typed too many times, hmmm). The author doesn't want to alienate readers by implying that these mysterious but very important properties are all to do with physics - even though they are! (We're talking about very basic properties such as electrostatics, here - opposite charges attracting and same charges repelling. Electrostatics cover at least 90% of the "physicochemical" features being referred to in this context).

2) When people read the word "physical" next to "features", many people will jump to thinking in terms of what the molecules look like. After all, my physical features include brown eyes and long hair. Non-physicists don't immediately associate the word "physical" with physics!

So instead, this horrible made-up word appears to try to stop biologists and biochemists* freaking out at/being confused by the mention of physics.

Have I mentioned recently how much I hate the division of science into three main and a handful of ancillary subjects? There's a huge amount of physics in chemistry, a huge amount of chemistry in biology, and even quite a bit of physics in biology (though I'm not sure there's too much biology in physics); while materials science crosses over everything. Students tell me "I love biology" / "I hate physics" without being aware of how much of one subject is in the other. Tell me you hate a topic - I'll happily accept "I hate electricity" / "I hate Newtonian mechanics". But don't tell me you hate an entire discipline until you've learned how much nifty cell biology and functioning of the nervous system is due to basic physics.

This rant has been brought to you by the letter P for physicochemical, and the letter C for cold. Which it is. 2.4 deg C outside right now, brrr!

* Interesting note: I no longer know what I am. I used to be a Physical Chemist. Then I was either an Atmospheric Physicist or an Environmental Chemist. Now I could be a Biochemist or a Molecular Biologist or a Chemical Biologist or a Medicinal Chemist... Woo, interdisciplinary!
baratron: (rainbow chemistry geek)
Two HSP90 ligands I found today: NP4 and NP5.

What's wrong with them? Well, "normal" sizes for rings in organic chemistry are 3, 5, 6 and 7 carbon atoms. 3 carbons form a triangle, which is thermodynamically unstable because of the strain in the bonds (carbon atoms with all single bonds usually have bond angles around 109.5 degrees, and in a triangle they're closer to 60 degrees) - but common in nature, especially if stabilised by some other rings adjacent. 5, 6 and 7 carbon atoms are stable because there is no ring strain, and form very easily because it's a relatively small number of carbons to have to wrap around to form the ring. As the number of carbon atoms increases, the probability of ring formation decreases, because it's too far for the first and last carbons to "find" each other.

By the time you're up to a single ring of 13 carbon atoms, the molecule looks quite ludicrous. It looks to me like a normal molecule with two 6-membered rings, where someone's taken one of the rings and pumped it up with a cycle pump!
baratron: (Default)
Three snippets of recent conversation:

Richard (getting dressed & pulling clean underwear out of a drawer): "I think these pants have had it. Look at the elastic! It's not elastic any more, it's undergoing plastic deformation!".

Me: "Hooke's Law in action!"


Tim (coming into our room as we were getting up): "Oh, you've got the big bear in bed with you!".

Richard (rolling over sleepily): "This is my bed! I always sleep here!".

Tim: "Perhaps I should have said 'the big bear (white)', to distinguish him from any big bears (brown)".


Peter (talking about somewhere they'd eaten recently): "It's quite a smart pub. They have games. We drank a bottle of wine and played Scrabble."

Tim: "Only the pieces were muddled up like they came from several different sets."

Peter: "So you could draw a Q and put it on the board, and then draw another Q."

Tim: "There was one tile which was the same size as a normal Scrabble tile, but had letters on both sides. And another one which was 1/4 of the size of a normal Scrabble tile, with the number 4 on it."

Richard: "For all of those words with a 4 in, obviously."

Tim: Maybe it was from a set of Chemistry Scrabble!

Richard: "You could have double and triple atom score, and double and triple bond score..."

Tim: "But would you be allowed free radicals? That's the question."

Me: "I don't think so. Anything can be a radical - CH3 dot would be too cheaty. It would have to be actual molecules and compounds only."

Richard: "You'd be screwed if you drew helium, though."

Me: "I guess it would have to be no Noble Gases."

Richard: "It would be even better if it used organic notation with all those zigzag lines. You'd be able to add a benzene ring to the end of any atom on the board!"
baratron: (lego)
I've been speed-reading academic papers for a couple of days. This is because I am working on my dissertation. Actually, "dissertation" isn't a good name for this piece of coursework. Normally a dissertation is a presentation of your own research, whereas this is more of a literature report - read a load of papers and condense them into a coherent piece in your own words with references. Anyway, you know what academic style is like, and reading too many papers all in one go does break your brain rather.

Thus it becomes incredibly funny when I find sentences like this in the middle of an article: Several therapeutically used drugs bind to more than one receptor and are correspondingly termed "promiscuous" ligands.
baratron: (rainbow chemistry geek)
Analgesics (painkillers) that I have personally taken - with bonus educational bits! Big image. Read more... )

Molecules!

Mar. 20th, 2009 02:37 am
baratron: (science genius girl)
I have ChemDraw! The standard price for ChemDraw Pro is £640.00, but students can buy it for £90. Yay.

To celebrate this, I have drawn the structures of every psychoactive drug I have ever taken. Big picture )

When more time exists, I will draw the structures of every painkiller and antibiotic I've ever taken. Opioids have incredibly weird structures which will test my understanding of the software. (I think they're a bit beyond me today.)

Yay hexagons!
baratron: (rainbow chemistry geek)
Richard just brought in a couple of tetrapaks of "So Organic chick peas". Apparently Sainsbury's have decided that tetrapaks are more environmentally-friendly than cans - I'm guessing because the mass of the tetrapak is much less than that of a steel can, so less energy is needed to transport food in tetras. Anyway, on the back they say:
Ingredients: Chick Peas, Water.
Of the ingredients that can be organic, 100% are organic. Water cannot be organic.

Sainsbury's, you are absolutely right - but probably not for the reason you think.

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