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Digestion of rice protein
Interesting, I don't have the equipment to autoclave a protein sample. Perhaps and extended reflux w ... |
10-1-2014 at 13:53
by: mnick12 |
Digestion of rice protein
Sorry this got put on hold for finals.
The bromelain arrived and I tried out the enzymes on a boi ... |
14-12-2013 at 12:39
by: mnick12 |
Formaldehyde => Paraformaldehyde
By far the simplest way is by vacuum distillation. Pour you formalin solution into a large rbf, setu ... |
4-12-2013 at 21:28
by: mnick12 |
Organic cmpd draw and ID software
I have one called "Chemsketch", the freeware version, if you draw a structure there is an internet ... |
9-11-2013 at 21:48
by: mnick12 |
Pretty Pictures (2)
Pumping down an air sensitive ligand:
[file]27332[/file]
A few mg of the the same ligand coor ... |
6-11-2013 at 22:25
by: mnick12 |
redductive alkylations
Without references or experimental this should be in beginnings, but that is not up to me.
To cla ... |
3-11-2013 at 21:28
by: mnick12 |
Digestion of rice protein
I have product called "yeast nutrient" it is a mix of urea and ammonium phosphate, it is recommended ... |
2-11-2013 at 22:00
by: mnick12 |
Digestion of rice protein
My goal is to turn rice into a completely fermentable media, so that I can grow large amounts of yea ... |
2-11-2013 at 10:35
by: mnick12 |
Digestion of rice protein
A brief update:
Two cups ( 170g) of brown rice was cooked on the stove top per the instructions o ... |
1-11-2013 at 18:36
by: mnick12 |
Digestion of rice protein
Hello everyone,
It has been a while since I have done any home chemistry, but I have a few questi ... |
30-10-2013 at 13:46
by: mnick12 |
Meta-Escaline via Ullmann on Bourbonal
5-iodovanillin is more reactive in nucleophilic substitutions than the 5-bromo compound, but the 5-b ... |
9-8-2013 at 14:57
by: mnick12 |
just wanna ask about nital acid
Nital should only be made with very dilute nitric acid ( usually <%5). In such cases it is quite ... |
25-7-2013 at 09:00
by: mnick12 |
Bromination of Vanillin without bromine
What makes you think AcOH is capable of reacting with potassium bromide to form HBr? You have the an ... |
9-6-2013 at 17:11
by: mnick12 |
Bromination of Vanillin without bromine
Which reaction? I used it to form HBr in situ with the potassium bromide. |
8-6-2013 at 20:52
by: mnick12 |
possible to perform Grignard with no solvent?
An ether is necessary in most cases because it coordinates the magnesium metal center. However not a ... |
2-5-2013 at 20:28
by: mnick12 |
non-reactive carrier liquid for fumed silica
So you mean a suspension of fumed silica in some solvent that could be later used to thicken water? ... |
10-4-2013 at 16:38
by: mnick12 |
entropy51 memorial
That is unfortunate,
While sometimes a bit abrasive, entropy51 had a lot of knowledge to share a ... |
10-4-2013 at 16:34
by: mnick12 |
non-reactive carrier liquid for fumed silica
That is really general, could you please be more specific? What reaction are you trying to carry out ... |
10-4-2013 at 16:31
by: mnick12 |
I just made some Rheosmin, what is pure, but has no odor.
For a while I was fooling around with rheosmin and zingerone derivatives. I found that the "clean" ( ... |
9-4-2013 at 14:29
by: mnick12 |
Amino acid chemistry
There are all sorts of neet things you can do with cheap amino acids, for example:
http://www.org ... |
18-3-2013 at 09:03
by: mnick12 |
redox active ligands
Hello everyone,
I have been fortunate enough to have the chance to do some undergrad research on ... |
7-3-2013 at 20:48
by: mnick12 |
Acetic anhydride preparation
Yeah,
The acetyl chloride and sodium acetate method has been mentioned here and quite a few other ... |
7-3-2013 at 20:36
by: mnick12 |
thiourea synthesis
There is a product sold in the US at many hardware stores called "Tarn-X" it is a solution of thiour ... |
26-2-2013 at 12:09
by: mnick12 |
thiourea synthesis
You are not dealing with cyanide when you decompose NH4SCN, it is ammonium thiocyanate which is very ... |
26-2-2013 at 11:59
by: mnick12 |
Grow plants in aqueous carbonic acid.
I think you have that backwards, most plants DO like a slightly acidic growing environment. The nutr ... |
14-2-2013 at 15:58
by: mnick12 |
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