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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 |
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