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Preparation of sodium chlorite
I think it must be in the anhydrous state. Theoretic, can KNO3 be used instead of the NaNO3?
1-2-2005 at 14:26
by: Esplosivo
phenol
Yes it can, the phenol product does have a brownish tinge though due to aerial oxidation and polymer ...
30-1-2005 at 07:18
by: Esplosivo
Readily Available Chemicals Website: Version 2
About the 'Surgical spirit', I think it contains some propan-2-ol though I am not complete ...
28-1-2005 at 07:49
by: Esplosivo
Readily Available Chemicals Website: Version 2
The remainder should be water, if the ethanol is sold at a pharmacy. Methanol metabolism can have so ...
27-1-2005 at 12:42
by: Esplosivo
decarboxylation of phenylalanine
Damn, sorry my bad. Thought it was phenylamine not phenylalanine. Sorry again.
23-1-2005 at 21:29
by: Esplosivo
decarboxylation of phenylalanine
First of, the reaction you mention is no decarboxylation. The addition of an ethyl group to the benz ...
23-1-2005 at 12:55
by: Esplosivo
gel electrophoresis
If you are in to experimenting I would try using a mixture of bromophenol blue and methyl orange in ...
18-1-2005 at 06:52
by: Esplosivo
gel electrophoresis
mick, that is the same thing as using ethidium bromide although I don't known if it would work. ...
17-1-2005 at 12:59
by: Esplosivo
gel electrophoresis
onlyus, I cannot understand your post quite well. Do you need a 'marker' or 'tracker ...
17-1-2005 at 12:39
by: Esplosivo
Direct oxidation of toluene to benzaldehyde using chromyl chloride
Chromyl chloride (chromium (VI) dichloride dioxide) is a red, fuming, toxic liquid produced as follo ...
16-1-2005 at 14:28
by: Esplosivo
aniline impurities
For the purification I can answer briefly by saying that it can be carried out by steam distillation ...
11-1-2005 at 06:36
by: Esplosivo
DIY glove box for HBr?
I don't know much about HBr but I would suggest using Teflon gloves and of keeping away metals ...
10-1-2005 at 06:44
by: Esplosivo
xCuSO4 + yCa(OCl)2 ----> ?
Chlorine turns moist red litmus paper red and then bleaches it (if in high enough concentrations).
...
10-1-2005 at 06:33
by: Esplosivo
Hg(OAc)2 ???
A simple double displacement reaction will do the trick. Assuming that you have HgCl2, you could rea ...
3-1-2005 at 07:57
by: Esplosivo
TeACN
[quote][i]Originally posted by quest[/i]
whan i put in outside it dry and all the outside is turnin ...
30-12-2004 at 05:34
by: Esplosivo
Preparation of trinitromethane
Note that the reaction should produce a precipitate of silver iodide, which has a yellowish colour. ...
21-12-2004 at 22:37
by: Esplosivo
Preparation of trinitromethane
Well usually such reactions do not involve the use of much heat, warming is generally carried out. T ...
20-12-2004 at 12:08
by: Esplosivo
Preparation of trinitromethane
According to [url=http://www.jtbaker.com/msds/englishhtml/i3480.htm]this MSDS[/url] Iodoform is said ...
20-12-2004 at 11:11
by: Esplosivo
Decarboxylation of fatty acids to alkanes.
Well at the melting point of the hydroxide which falls in the range of 320 deg celcius the alkane wi ...
19-12-2004 at 13:17
by: Esplosivo
Decarboxylation of fatty acids to alkanes.
'Aliphatic' decarboxylation is usually carried out by fusing the sodium salt of the carbox ...
19-12-2004 at 12:53
by: Esplosivo
Niacin ---> Pyridine (HCl)
If you're about to prepare pyridine, and you're male, I would check out the MSDS. Pyridine ...
14-12-2004 at 23:37
by: Esplosivo
Propellant
Aniline is phenylamine. It is usually prepared in the lab by reducing nitrobenzene with an Sn/HCl mi ...
14-12-2004 at 08:12
by: Esplosivo
Bromine Source and Synthesis
[quote][i]Originally posted by psychokitty[/i]
Neutrino: Cl2 added to water forms hypochlorous aci ...
8-12-2004 at 00:22
by: Esplosivo
Bromine Source and Synthesis
Did the reddish brown substance precipitate or something, or was the reddish brown colour simply in ...
6-12-2004 at 21:39
by: Esplosivo
Pseudonitrosites
Well then I owe some apologies. Give the method I mentioned a try Axt. The one in which rxn of Cu wi ...
5-12-2004 at 06:40
by: Esplosivo
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