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How to [recover] dissolved in acid Tin
@Romix: How much tin are we talking about? What acid did you use?
If you're not in a hurry, you m ... |
9-6-2024 at 06:10
by: bnull |
Where can I get bacteria professionally identified?
It may sound a bit odd (or quite bizarre, as it now seems to me) but, are you friendly with any vete ... |
8-6-2024 at 06:24
by: bnull |
How to [recover] dissolved in acid Tin
Did you try electrolysis? |
7-6-2024 at 15:50
by: bnull |
Diethylether (sulfuric acid saving method)
[rquote=693449&tid=160329&author=RU_KLO]So its not an easy task.... (instead of the second H ... |
7-6-2024 at 09:43
by: bnull |
The Short Questions Thread (4)
It is to minimize error. The amount of liquid that gets into the ground glass joint is predictable a ... |
7-6-2024 at 09:14
by: bnull |
What have we got so far
I thought it would be good to condense what has been discussed, what works and what does not.
[li ... |
7-6-2024 at 05:50
by: bnull |
Steel temperature transformation range(s)
[rquote=693423&tid=160361&author=justender]"[u]temperature range[/u] - The temperature at wh ... |
5-6-2024 at 09:14
by: bnull |
Stubborn benzophenone
You would have to do that second distillation anyway.
No, I just thought benzopinacol would be in ... |
4-6-2024 at 06:52
by: bnull |
Pyrazinoate from 2-acetylpyrazine
@jackchem2001: It is pyrazine, with two N in the ring, one opposite the other (https://en.wikipedia. ... |
4-6-2024 at 06:26
by: bnull |
Stubborn benzophenone
I thought a re-distillation would work. It's good to see that it did.
[quote]I put the vial in th ... |
3-6-2024 at 13:14
by: bnull |
Stubborn benzophenone
Did you distill it again?
|
2-6-2024 at 16:12
by: bnull |
Distilling methyl nitrate
Do you really need methyl nitrate? Volatile, toxic, explodes at 64 °C or so (which funnily enough i ... |
2-6-2024 at 08:31
by: bnull |
DIY melting point apparatus
Don't forget the sounds. A bip when the device is turned on, a bip when it is turned off, that kind ... |
1-6-2024 at 04:42
by: bnull |
Stubborn benzophenone
Dissolve some drops of benzophenone in ethanol or ether, spread the solution on a dish to dry and th ... |
31-5-2024 at 12:02
by: bnull |
Failed attempts at oxidation of alcohols with DMSO/P2O5
Well, I'm sadistic enough to offer you some more references. They come from the Encyclopedia of Reag ... |
29-5-2024 at 16:02
by: bnull |
Has anyone ever had a bottle of pool grade calcium hypochlorite burst?
One of the impurities of pool chlorine is calcium chloride, which is hygroscopic. It takes up water ... |
29-5-2024 at 15:40
by: bnull |
Sodium benzoate + ammonium chloride → Ammonium benzoate + Salt?
[rquote=693326&tid=160303&author=clearly_not_atara]Alternative possibilities include heating ... |
29-5-2024 at 09:35
by: bnull |
Sodium benzoate + ammonium chloride → Ammonium benzoate + Salt?
What about ammonium benzoate from ammonium bicarbonate and benzoic acid? There would be no sodium ch ... |
29-5-2024 at 06:22
by: bnull |
Mini- (or micro-) hot plate / stirrer
If it breaks, you can either fix it yourself or use it to house a new circuit. Not bad. |
28-5-2024 at 14:50
by: bnull |
n chloro butylamine
[rquote=693292&tid=160347&author=mr_bovinejony]Is it not mentioned in the first post that py ... |
28-5-2024 at 03:04
by: bnull |
n chloro butylamine
I read the section "N-Halo-de-hydrogenation" from March's Advanced Organic Chemistry (7th), pages 72 ... |
27-5-2024 at 08:50
by: bnull |
n chloro butylamine
BOC looks better. Or maybe you can make an amide. Trityl could end up being chlorinated too; a napht ... |
27-5-2024 at 06:58
by: bnull |
n chloro butylamine
What about protecting the amino group? Protection would reduce reactivity and leave only one hydroge ... |
27-5-2024 at 05:32
by: bnull |
Ca+YF3 bad idea?
I'd say "Don't do that!"
[b]Edit[/b]: OK, I think you deserve an explanation: fluorine is a bitch ... |
26-5-2024 at 12:37
by: bnull |
I cant find a problem of my heating mantle
@Rainwater: 500 W is the heating power, as described in the label (image 4). The resistance of the m ... |
24-5-2024 at 04:49
by: bnull |
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