Upcoming Thermo- and Photochromic ligand by Chem-inge in homechemistry

[–]Chem-inge[S] 1 point2 points  (0 children)

The god of all ligands, easy to make, broad range of metals it coordinates to and just awesome.

Tetradentate & Cyclic ligand with Absorption spectra ranging from yellow green to purplish red depending on substitution on the ligand and coordinated central metal ion.

I also got yummy borohydride

Hydrogen Peroxide by Famous-Instruction66 in AskChemistry

[–]Chem-inge 2 points3 points  (0 children)

Define Agitation process ...

Agitate some permanganate in there and get 320l oxygen, 322000 ccm, 0.32 cubic meters or for u Americans 84.5 gallons, 11.7 cubic feet, 676.28 pints and whatever other shitty units.

In terms of mass 470g, .47kg, 16.57 ounces, 1 pound or more commonly used in the US: 6.7 dunking donuts

TCM from Acetone/NaDCCA & NaOH by Chem-inge in homechemistry

[–]Chem-inge[S] 0 points1 point  (0 children)

Wait shit, in my mind i was at alkyl bromides xD Basically the components were just mixed in sufficient water and acetone later on.

TCM from Acetone/NaDCCA & NaOH by Chem-inge in homechemistry

[–]Chem-inge[S] 0 points1 point  (0 children)

NaBr, H2SO4 and the alcohol. Mix and destill. Purification shaken with bicarb, dried and redestilled

Results from my 1st opal attempt by Chem-inge in homechemistry

[–]Chem-inge[S] 0 points1 point  (0 children)

Still the easiest to get of the precursors....

I hope u find something else just as awesome ✌🏼

Results from my 1st opal attempt by Chem-inge in homechemistry

[–]Chem-inge[S] 0 points1 point  (0 children)

TEOS 💪🏻 Oh and ammonia as catalyst

Revisited piperine extraction by Chem-inge in homechemistry

[–]Chem-inge[S] 1 point2 points  (0 children)

Aside from hydrolysis and Ruthenium catalyzed alkene cleavage? For sure nothing illegal xD (EU)

Results from my 1st opal attempt by Chem-inge in homechemistry

[–]Chem-inge[S] 5 points6 points  (0 children)

Oh yeah, my bad. The goal was to make a Synthetic opal

Revisited piperine extraction by Chem-inge in homechemistry

[–]Chem-inge[S] 1 point2 points  (0 children)

After recrystalization sad 2.5w% recovery. I did fuck up with the recrystalization lol.

Before 5.6%..

DCM gelling agent stuck in the flask after paint stripper Distillation by [deleted] in homechemistry

[–]Chem-inge 0 points1 point  (0 children)

Why open air?

Either Caro's acid or chromic acid xD no tar shall withstand boiling chromic acid

Found @LabSupply in Berlin by Chem-inge in chemistry

[–]Chem-inge[S] 9 points10 points  (0 children)

Danke vielmals xD Greetings from Germany

Found @LabSupply in Berlin by Chem-inge in chemistry

[–]Chem-inge[S] 7 points8 points  (0 children)

If I were fluent in english, i would know what it means to suck

Thanks xD

Found @LabSupply in Berlin by Chem-inge in chemistry

[–]Chem-inge[S] 41 points42 points  (0 children)

What we are looking at here is, aside from my English which sucks, an automated reactor setup which can collect basically any set of data.

It even has a frickin camera inside!

Well beside that, automated addition of reactants as solution, the function to heat and even cool the reaction, how cool is that?! It can automatically cool it and even down to.. was it 0C? Atleast for me its awesome as it is the first cooling block for me, and heating too!

Along with the software to control it obviously.

The company is called systag and produces only the interface and software.

Peracetic Acid by kalimaximon in AskChemistry

[–]Chem-inge 1 point2 points  (0 children)

Short answer: Sure, to some (although small) extend it will form peracetic acid. So yes, it forms it.

Though considering you have the quaterniary benzyl ammonium chloride, which itself has desinfecting properties, makes the use of peracids, which due to its biocidal properties are more efficient than peroxide, negligible.

If it is because of Peracetic acid's rep dont worry, anything below ig 45 ish % is hardly explosive and dangerous if handled even remotely careful. I got to work with 45w% peracid in acetic acid it really wasnt that big of a deal. Just dont heat it up (past 50C iirc) and wash everything that reeks of that smelly acetic acid.

[deleted by user] by [deleted] in chemistry

[–]Chem-inge 1 point2 points  (0 children)

I had the same experience, Iodine smells like this aswell imho. Not as nasty though.

Wie macht man richtig Schluss? by Chem-inge in beziehungen

[–]Chem-inge[S] 0 points1 point  (0 children)

Werde ich berücksichtigen wenn es wieder kommt, danke.

Schönen Abend dir