| Search |
| [Next Page] |
N2O dissolved in H2O2
N2O is fairly inert except at combustion temperatures, it is not going to be oxidized. N2O has very ... |
17-9-2010 at 15:44
by: Anders2 |
Grouping of compatible chemicals for storage
I had my own idea for categories:
1. Oxidizing Acids
2. Reducing Acids (such as HBr or acetic)
(a ... |
17-9-2010 at 15:31
by: Anders2 |
Assorted Extreme Reactions
"Boron triperchlorate did not form an adduct with trimethylamine but did form a somewhat stable addu ... |
17-9-2010 at 15:21
by: Anders2 |
What is 1,3-diisonitrosoacetone guanidinium salt
"results indicate that the rearrangement from nitrosomethane to more stable trans-formaldoxime" , EX ... |
17-9-2010 at 15:15
by: Anders2 |
Diisonitrosoacetone
Let me refer your attention to the same topic in the organic chem section:
"diisonitrosoacetone can ... |
17-9-2010 at 14:47
by: Anders2 |
Calcium Carbide and Methylene Chloride ?
Chloroform does not react at room temperature with, or dissolve in, CaC2. |
17-9-2010 at 14:43
by: Anders2 |
Dinitroacetylene from the Diiodo-
Let me refer your attention to the prepublication section:
http://www.sciencemadness.org/talk/viewt ... |
17-9-2010 at 14:29
by: Anders2 |
Diiodoacetylene
"There will also be a few nitrites stuck on in place of the nitro group, such an arrangement is prob ... |
17-9-2010 at 14:26
by: Anders2 |
Haloalkane synthesis help
I obviously agree with everything above, I just thought the process would go without saying, so I di ... |
17-9-2010 at 13:51
by: Anders2 |
HI reductions, no red P
Interestingly Hydrogen Iodide will react with Acetone, if the proportions are correct, to form 1-Iod ... |
17-9-2010 at 13:36
by: Anders2 |
RDX easy synthesis
I wonder if H2O2 can oxidize this nitrosamine to the nitramine, potentially forming RDX?
I read i ... |
17-9-2010 at 13:28
by: Anders2 |
Synthesis of Diisopropyl-ether
Wow, bromopropane supposedly has a much greater liquid range than water! So much for water being "un ... |
16-9-2010 at 19:46
by: Anders2 |
Haloalkane synthesis help
Okay then,
What about acetic acid, condense with Analine to form the imine, CH3C(=NPh)NH(Ph), then ... |
16-9-2010 at 19:25
by: Anders2 |
Haloalkane synthesis help
Perhaps you meant PhCH2C(=O)CH2CH3 would result?
Now I am getting a little desperate, but perhaps ... |
16-9-2010 at 19:15
by: Anders2 |
Isopropylamine and Diisopropylamine from Acetone
I meant if you used plain ammonia on a ketone, you would need a high pH, not if you used some other ... |
16-9-2010 at 18:52
by: Anders2 |
Haloalkane synthesis help
"The aldehyde you mention is not something that will fall into your hands easily. It's a mere oxidat ... |
16-9-2010 at 18:44
by: Anders2 |
Isopropylamine and Diisopropylamine from Acetone
Here is a relevent link:
http://www.organic-chemistry.org/synthesis/N1H/reductionsimines.shtm
A ... |
16-9-2010 at 18:37
by: Anders2 |
Haloalkane synthesis help
I might be able to provide a suggestion. I read somewhere that heating toluene and CH2O can form CH3 ... |
16-9-2010 at 18:12
by: Anders2 |
HMX
An alternative is just to condense MEDINA with CH2O, guaranteeing absolutely no RDX will contaminate ... |
15-9-2010 at 19:09
by: Anders2 |
Help !!!! Hg-Thermometer broken !!!!
Hg, interestingly enough reacts with sulfur powder, just sprinkle S on it.
This raises an interesti ... |
15-9-2010 at 19:05
by: Anders2 |
Hydrochloric acid hydrogen peroxide mix
I have tried this, no chlorine is produced. I can tell you that you certainly will not be able to ge ... |
15-9-2010 at 18:50
by: Anders2 |
Anyone got ideas? MCPA to 2,5-dihydroxytoluene...
Treat MCPA with a strong base at high temperatures. Chlorobenzene can be converted to phenol in this ... |
15-9-2010 at 18:33
by: Anders2 |
Isopropylamine and Diisopropylamine from Acetone
A better method might be to use NaOH on solid Aluminum.
Not only will this eleminate the requiremen ... |
15-9-2010 at 18:12
by: Anders2 |
What is 1,3-diisonitrosoacetone guanidinium salt
diisonitrosoacetone can condense with hydroxylamine to form
1,2-dinitroso-propyl,2-oxime.
It is ... |
15-9-2010 at 18:08
by: Anders2 |
Synthesis of Diisopropyl-ether
Isobromopropane might react with anhydrous Isopronanol to make the Ether.
bromopropane could be mad ... |
15-9-2010 at 17:53
by: Anders2 |
| [Next Page] |
