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Revision as of 19:35, 7 July 2011 editNReitzel (talk | contribs)Extended confirmed users539 edits Alternate chemical formula depiction← Previous edit Latest revision as of 11:12, 14 September 2024 edit undoAnomieBOT (talk | contribs)Bots6,551,034 editsm Dating maintenance tags: {{Missing information}} 
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{{Missing information|it's basic chemical information|date=September 2024}}
{{chembox {{chembox
| Verifiedfields = changed
| verifiedrevid = 356944564
| Watchedfields = changed
| ImageFile1 = methylammonium nitrate.png
| verifiedrevid = 438290095
| ImageSize1 = 220px
| ImageFileL2 = Methylammonium-3D-balls.png | ImageFile1 = methylammonium nitrate.png
| ImageFileL2 = Methylammonium-3D-balls.png
| ImageSizeL2 = 120px
| ImageNameL2 = Ball-and-stick model of the methylammonium cation | ImageNameL2 = Ball-and-stick model of the methylammonium cation
| ImageFileR2 = Nitrate-3D-balls.png | ImageFileR2 = Nitrate-3D-balls.png
| ImageNameR2 = Ball-and-stick model of the nitrate anion
| ImageSizeR2 = 100px
| IUPACName=methylammonium nitrate
| ImageNameR2 = Ball-and-stick model of the nitrate anion
| OtherNames=Methylamine nitrate<BR />Monomethylamine nitrate<BR />Monomethylammonium nitrate<BR />MMAN
|IUPACName=methanamine; nitric acid
|OtherNames=Methylamine nitrate; Mono-methylamine nitrate; MMAN
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo=22113-87-7 | CASNo=22113-87-7
| PubChem=159924 | PubChem = 10887831
| SMILES=CN.(=O)(O)
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 9063095
| SMILES = C.(=O)()
| InChI = 1/CH5N.NO3/c1-2;2-1(3)4/h2H2,1H3;/q;-1/p+1
| InChIKey = WPHINMYYTFDPIA-IKLDFBCSAW
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/CH5N.NO3/c1-2;2-1(3)4/h2H2,1H3;/q;-1/p+1
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = WPHINMYYTFDPIA-UHFFFAOYSA-O

}} }}
|Section2={{Chembox Properties |Section2={{Chembox Properties
| Formula=CH<sub>6</sub>N<sub>2</sub>O<sub>3</sub> | Formula=CH<sub>6</sub>N<sub>2</sub>O<sub>3</sub>
| MolarMass=94.07 g/mol | MolarMass=94.07 g/mol
| Appearance= | Appearance=
| Density= | Density=
| MeltingPt= | MeltingPt=
| BoilingPt= | BoilingPt=
| Solubility= | Solubility=
}} }}
|Section3={{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards=
| FlashPt= | FlashPt=
| AutoignitionPt =
| Autoignition=
}} }}
|Section8={{Chembox Related |Section8={{Chembox Related
| OtherCations=]<br>] | OtherCations=]<br>]<br>]
}} }}
}} }}


'''Methylammonium nitrate''' is an explosive chemical with the molecular formula CH<sub>6</sub>N<sub>2</sub>O<sub>3</sub>, alternately CH<sub>3</sub>NH<sub>3</sub><sup>+</sup>NO<sub>3</sub><sup>-</sup>. It is the ] formed by the neutralization of ] with ]. This substance is also known as methylamine nitrate and monomethylamine nitrate, not to be confused with methyl nitramine or monomethyl nitramine. '''Methylammonium nitrate''' is an explosive chemical with the molecular formula CH<sub>6</sub>N<sub>2</sub>O<sub>3</sub>, alternately CH<sub>3</sub>NH<sub>3</sub><sup>+</sup>NO<sub>3</sub><sup></sup>. It is the ] formed by the neutralization of ] with ]. This substance is also known as methylamine nitrate and monomethylamine nitrate, not to be confused with methyl nitramine or monomethyl nitramine.


Methylammonium nitrate was first used as an explosive ingredient by the Germans during ].<ref>Urbanski, ''The Chemistry and Technology of Explosives'', Volume 2</ref> It was originally called mono-methylamine nitrate, a name that has largely stuck among chemists who formulate energetic materials. Methylammonium nitrate was first used as an explosive ingredient by the Germans during ].<ref>Urbanski, ''The Chemistry and Technology of Explosives'', Volume 2</ref> It was originally called mono-methylamine nitrate, a name that has largely stuck among chemists who formulate energetic materials.


Methylammonium nitrate is somewhat similar in explosive properties to ] (AN) which yields 85% of the power of ] when the ammonium nitrate is incorporated into an explosive. The addition of the carbon-containing ] in methylammonium nitrate imparts better explosive properties and helps create a more favorable oxygen balance. Methylammonium nitrate is somewhat similar in explosive properties to ] (AN) which yields 85% of the power of ] when the ammonium nitrate is incorporated into an explosive. The addition of the carbon-containing ] in methylammonium nitrate imparts better explosive properties and helps create a more favorable oxygen balance.


Following World War Two, relative to less costly ammonium nitrate, methylammonium nitrate was largely ignored by explosives manufacturers. Ammonium nitrate fuel-oil mixtures (ANFO) were sufficient for most large-diameter explosives uses. After World War II, methylammonium nitrate was largely ignored by explosives manufacturers, in favor of less-costly ammonium nitrate. Ammonium nitrate-fuel oil mixtures (]) were sufficient for most large-diameter explosives uses.


Methylammonium nitrate saw a resurgence when ], seeking to lower the cost of its TNT-based "Tovex" water gels, incorporated a mixture of methylammonium nitrate with ammonium nitrate which served as a basis for DuPont's water gels manufactured under the names "Tovex" "Extra" and "Pourvex" "Extra". Methylammonium nitrate, also known as PR-M (which stands for "Potomac River - Mono-methylamine nitrate") soon was seen as the possible path toward creating a low cost blasting agent (water gel explosives) that might replace the explosives based on nitroglycerin (dynamites). Methylammonium nitrate saw a resurgence when E. I. du Pont de Nemours and Company (]), seeking to lower the cost of its TNT-based ] ]s, incorporated a mixture of methylammonium nitrate with ammonium nitrate which served as a basis for DuPont's water-gels manufactured under the names "Tovex Extra" and "Pourvex Extra". Methylammonium nitrate, also known as PR-M (which stands for "Potomac River—Mono-methylamine nitrate") soon was seen as the possible path toward creating a low-cost blasting agent (water gel explosives) that might replace the explosives based on nitroglycerin (dynamites).


In late 1973, DuPont started to phase out dynamite and replace it with water gels based on PR-M. However, PR-M proved to have unusual "mass effects". That is, if there was sufficient mass, under certain conditions, PR-M could explode without warning. On August 6, 1974, a tank car containing PR-M blew up in Wenatchee, Washington, rail yard, killing two and injuring 66 others.<ref> </ref> On July 4, 1976, a PR-M storage with 60,000 pounds of PR-M detonated at DuPont's Potomac River Works at Martinsburg, WV. Though there was no loss of life, there were many injuries and a substantial loss of property. Within two years, DuPont moved out of water gel explosives. In late 1973, DuPont started to phase out dynamite and replace it with water-gels based on PR-M. However, PR-M proved to have unusual "mass effects". That is, if there was sufficient mass, under certain conditions, PR-M could explode without warning. On August 6, 1974, a tank car containing PR-M blew up in Wenatchee, Washington, rail yard, killing two and injuring 66 others.<ref></ref> On July 4, 1976, a PR-M storage with 60,000 pounds (approximately 27,200Kg) of PR-M detonated at DuPont's Potomac River Works at Martinsburg, WV. Though there was no loss of life, there were many injuries and a substantial loss of property.


== References == ==References==
{{reflist}} {{reflist}}


==External links== ==External links==
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