Ethanamine - Revision history

Etienne Robillard at 15:27, 23 February 2013

Etienne Robillard — Sat, 23 Feb 2013 15:27:45 GMT

←Older revision		Revision as of 15:27, 23 February 2013
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	* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]		* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]
-	* When [[Chloroform]] or [[DCM]] is used as a reactant gas, unstable ethanamine species may be converted to '''HN3''' vapors in situ via the Schmidt route. [2, 3, 4~~, 5~~]	+	* When [[Chloroform]] or [[DCM]] is used as a reactant gas, unstable ethanamine species may be converted to '''HN3''' vapors in situ via the Schmidt route. [2, 3, 4]
	* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3		* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3

Etienne Robillard: /* References */

Etienne Robillard — Sat, 23 Feb 2013 15:26:39 GMT

References

←Older revision		Revision as of 15:26, 23 February 2013
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	# Investigations into the Chemistry of Thermodynamically Unstable Species. The Direct Polymerization of Vinyl Alcohol, the Enolic Tautomer of Acetaldehyde. Anna K. Cederstav and Bruce M. Novak. Journal of the American Chemical Society, 1994, Volume 116, Pages 4073-4074		# Investigations into the Chemistry of Thermodynamically Unstable Species. The Direct Polymerization of Vinyl Alcohol, the Enolic Tautomer of Acetaldehyde. Anna K. Cederstav and Bruce M. Novak. Journal of the American Chemical Society, 1994, Volume 116, Pages 4073-4074
-	~~# http://en.wikipedia.org/wiki/Schmidt_reaction~~
	# http://www2.chemistry.msu.edu/faculty/reusch/VirtTxtjml/rearrang.htm		# http://www2.chemistry.msu.edu/faculty/reusch/VirtTxtjml/rearrang.htm
	# http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html		# http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html
	# https://www.sciencemadness.org/whisper/viewthread.php?tid=15190		# https://www.sciencemadness.org/whisper/viewthread.php?tid=15190

Etienne Robillard at 11:47, 15 February 2013

Etienne Robillard — Fri, 15 Feb 2013 11:47:19 GMT

←Older revision		Revision as of 11:47, 15 February 2013
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	* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]		* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]
-	* When [[Chloroform]] or [[DCM]] is used as a reactant gas, unstable ethanamine species may be converted to '''HN3''' vapors in situ via the Schmidt route. [2, 3, 4]	+	* When [[Chloroform]] or [[DCM]] is used as a reactant gas, unstable ethanamine species may be converted to '''HN3''' vapors in situ via the Schmidt route. [2, 3, 4, 5]
	* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3		* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3

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	# http://www2.chemistry.msu.edu/faculty/reusch/VirtTxtjml/rearrang.htm		# http://www2.chemistry.msu.edu/faculty/reusch/VirtTxtjml/rearrang.htm
	# http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html		# http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html
		+	# https://www.sciencemadness.org/whisper/viewthread.php?tid=15190

Etienne Robillard at 10:57, 15 February 2013

Etienne Robillard — Fri, 15 Feb 2013 10:57:12 GMT

←Older revision		Revision as of 10:57, 15 February 2013
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	* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]		* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]
-	* When [[Chloroform]] or [[DCM]] is used as a reactant gas, unstable ethanamine species may be converted to '''HN3''' vapors in situ via the Schmidt route. [2]	+	* When [[Chloroform]] or [[DCM]] is used as a reactant gas, unstable ethanamine species may be converted to '''HN3''' vapors in situ via the Schmidt route. [2, 3, 4]
	* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3		* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3

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	# Investigations into the Chemistry of Thermodynamically Unstable Species. The Direct Polymerization of Vinyl Alcohol, the Enolic Tautomer of Acetaldehyde. Anna K. Cederstav and Bruce M. Novak. Journal of the American Chemical Society, 1994, Volume 116, Pages 4073-4074		# Investigations into the Chemistry of Thermodynamically Unstable Species. The Direct Polymerization of Vinyl Alcohol, the Enolic Tautomer of Acetaldehyde. Anna K. Cederstav and Bruce M. Novak. Journal of the American Chemical Society, 1994, Volume 116, Pages 4073-4074
	# http://en.wikipedia.org/wiki/Schmidt_reaction		# http://en.wikipedia.org/wiki/Schmidt_reaction
		+	# http://www2.chemistry.msu.edu/faculty/reusch/VirtTxtjml/rearrang.htm
	# http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html		# http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html

Etienne Robillard at 10:49, 15 February 2013

Etienne Robillard — Fri, 15 Feb 2013 10:49:57 GMT

←Older revision		Revision as of 10:49, 15 February 2013
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	* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]		* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]
-	* When [[Chloroform]] is used~~, the compound is known~~ as a '''~~Nitrogen Mustard (HN-3) derivative~~'''. [~~http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html~~ 2]	+	* When [[Chloroform]] or [[DCM]] is used as a reactant gas, unstable ethanamine species may be converted to '''HN3''' vapors in situ via the Schmidt route. [2]
	* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3		* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3

	== See also ==		== See also ==

-	* [~~http://openwetware.org/wiki/~~Glutaraldehyde_(Pentanedial) Glutaraldehyde]	+	* [[Glutaraldehyde_(Pentanedial) Glutaraldehyde]]
	* [[Chloroform]]		* [[Chloroform]]
		+	* [[Phosgene]]

	== References ==		== References ==

	# Investigations into the Chemistry of Thermodynamically Unstable Species. The Direct Polymerization of Vinyl Alcohol, the Enolic Tautomer of Acetaldehyde. Anna K. Cederstav and Bruce M. Novak. Journal of the American Chemical Society, 1994, Volume 116, Pages 4073-4074		# Investigations into the Chemistry of Thermodynamically Unstable Species. The Direct Polymerization of Vinyl Alcohol, the Enolic Tautomer of Acetaldehyde. Anna K. Cederstav and Bruce M. Novak. Journal of the American Chemical Society, 1994, Volume 116, Pages 4073-4074
		+	# http://en.wikipedia.org/wiki/Schmidt_reaction
		+	# http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html

Etienne Robillard at 11:18, 7 February 2013

Etienne Robillard — Thu, 07 Feb 2013 11:18:12 GMT

←Older revision		Revision as of 11:18, 7 February 2013
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	== See also ==		== See also ==

-	* [[http://openwetware.org/wiki/Glutaraldehyde_(Pentanedial) Glutaraldehyde]]	+	* [http://openwetware.org/wiki/Glutaraldehyde_(Pentanedial) Glutaraldehyde]
	* [[Chloroform]]		* [[Chloroform]]
		+
		+	== References ==
		+
		+	# Investigations into the Chemistry of Thermodynamically Unstable Species. The Direct Polymerization of Vinyl Alcohol, the Enolic Tautomer of Acetaldehyde. Anna K. Cederstav and Bruce M. Novak. Journal of the American Chemical Society, 1994, Volume 116, Pages 4073-4074

Etienne Robillard: Minor precision about dicholoromethane based blister agents..

Etienne Robillard — Thu, 07 Feb 2013 08:11:55 GMT

Minor precision about dicholoromethane based blister agents..

←Older revision		Revision as of 08:11, 7 February 2013
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	* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]		* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]
-	* When [[Chloroform]] is used, the compound is known as Nitrogen Mustard (NH-3). [http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html 2]	+	* When [[Chloroform]] is used, the compound is known as a '''Nitrogen Mustard (HN-3) derivative'''. [http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html 2]
	* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3		* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3

	== See also ==		== See also ==

-	* Glutaraldehyde	+	* [[http://openwetware.org/wiki/Glutaraldehyde_(Pentanedial) Glutaraldehyde]]
		+	* [[Chloroform]]

Etienne Robillard at 07:53, 7 February 2013

Etienne Robillard — Thu, 07 Feb 2013 07:53:24 GMT

←Older revision		Revision as of 07:53, 7 February 2013
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-	* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name	+	* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]
-	is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]	+
	* When [[Chloroform]] is used, the compound is known as Nitrogen Mustard (NH-3). [http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html 2]		* When [[Chloroform]] is used, the compound is known as Nitrogen Mustard (NH-3). [http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html 2]
	* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3		* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3

Etienne Robillard: New page: * Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InCh...

Etienne Robillard — Thu, 07 Feb 2013 07:50:25 GMT

New page: * Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InCh...

New page

* Ethanamine is the tautomeric form of PVA (PVOH), a acetaldehyde derived imine group... An alternative name
is "aminoacetaldehyde dimethyl acetal". [http://webbook.nist.gov/cgi/inchi/InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3 1]
* When [[Chloroform]] is used, the compound is known as Nitrogen Mustard (NH-3). [http://www.cdc.gov/niosh/ershdb/EmergencyResponseCard_29750012.html 2]
* InChI=1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3

== See also ==

* Glutaraldehyde