http://dbpedia.org/ontology/abstract
|
Triacetonamine is an organic compound with … Triacetonamine is an organic compound with the formula OC(CH2CMe2)2NH (where Me = CH3). It is a colorless or white solid that melts near room temperature. The compound is an intermediate in the preparation of 2,2,6,6-tetramethylpiperidine, a sterically hindered base and precursor to the reagent called TEMPO. Triacetonamine is formed by the poly-aldol condensation of acetone in the presence of ammonia and calcium chloride: 3 (CH3)2CO + NH3 → OC(CH2CMe2)2NH + 2 H2O Reductive amination of triacetonamine gives 4-amino-2,2,6,6-tetramethylpiperidine. It is primarily used as a stabilizer for plastics, typically via its conversion to number of hindered amine light stabilizers, but also finds use as a chemical feedstock. It is used to prepare the hindered amine 2,2,6,6-tetramethylpiperidine, CH2[CH2C(CH3)2]2NH, as well as the radical oxidizer 4-Hydroxy-TEMPO.l as the radical oxidizer 4-Hydroxy-TEMPO.
, トリアセトンアミン(triacetone amine)は、アセトンとアンモニアの縮合反応で得られる化合物である。 3 CH3C(O)CH3 + NH3 → OC(CH2C(CH3)2)2NH + 2 H2O 立体障害をもつアミン:2,2,6,6-テトラメチルピペリジンの合成に使われる。
, Triacetonamin ist eine chemische Verbindung und ein tetramethyliertes .
|
http://dbpedia.org/ontology/alternativeName
|
Triacetone amine
|
http://dbpedia.org/ontology/iupacName
|
2,2,6,6-Tetramethylpiperidin-4-one
|
http://dbpedia.org/ontology/thumbnail
|
http://commons.wikimedia.org/wiki/Special:FilePath/Triacetonamine-Structural_formula_V1.svg?width=300 +
|
http://dbpedia.org/ontology/wikiPageID
|
7890927
|
http://dbpedia.org/ontology/wikiPageLength
|
3873
|
http://dbpedia.org/ontology/wikiPageRevisionID
|
1116589663
|
http://dbpedia.org/ontology/wikiPageWikiLink
|
http://dbpedia.org/resource/Reductive_amination +
, http://dbpedia.org/resource/2%2C2%2C6%2C6-Tetramethylpiperidine +
, http://dbpedia.org/resource/Steric_hindrance +
, http://dbpedia.org/resource/Piperidine +
, http://dbpedia.org/resource/TEMPO +
, http://dbpedia.org/resource/Hindered_amine_light_stabilizers +
, http://dbpedia.org/resource/Category:Piperidines +
, http://dbpedia.org/resource/Organic_compound +
, http://dbpedia.org/resource/Aldol_condensation +
, http://dbpedia.org/resource/4-Amino-2%2C2%2C6%2C6-tetramethylpiperidine +
, http://dbpedia.org/resource/Calcium_chloride +
, http://dbpedia.org/resource/Category:Cyclic_ketones +
, http://dbpedia.org/resource/4-Hydroxy-TEMPO +
|
http://dbpedia.org/property/imagefile
|
Triacetonamine-Structural formula V1.svg
|
http://dbpedia.org/property/name
|
Triacetone amine
|
http://dbpedia.org/property/othernames
|
Triacetone amine
|
http://dbpedia.org/property/pin
|
2266
|
http://dbpedia.org/property/verifiedfields
|
changed
|
http://dbpedia.org/property/verifiedrevid
|
470612896
|
http://dbpedia.org/property/watchedfields
|
changed
|
http://dbpedia.org/property/wikiPageUsesTemplate
|
http://dbpedia.org/resource/Template:H-phrases +
, http://dbpedia.org/resource/Template:Chembox_Structure +
, http://dbpedia.org/resource/Template:Cascite +
, http://dbpedia.org/resource/Template:Chemspidercite +
, http://dbpedia.org/resource/Template:GHS05 +
, http://dbpedia.org/resource/Template:GHS07 +
, http://dbpedia.org/resource/Template:Chembox_Identifiers +
, http://dbpedia.org/resource/Template:Chembox_Hazards +
, http://dbpedia.org/resource/Template:Ebicite +
, http://dbpedia.org/resource/Template:Chembox_Properties +
, http://dbpedia.org/resource/Template:Chembox +
, http://dbpedia.org/resource/Template:Stdinchicite +
, http://dbpedia.org/resource/Template:P-phrases +
, http://dbpedia.org/resource/Template:Chembox_Related +
|
http://purl.org/dc/terms/subject
|
http://dbpedia.org/resource/Category:Cyclic_ketones +
, http://dbpedia.org/resource/Category:Piperidines +
|
http://www.w3.org/ns/prov#wasDerivedFrom
|
http://en.wikipedia.org/wiki/Triacetonamine?oldid=1116589663&ns=0 +
|
http://xmlns.com/foaf/0.1/depiction
|
http://commons.wikimedia.org/wiki/Special:FilePath/Triacetonamine-Structural_formula_V1.svg +
|
http://xmlns.com/foaf/0.1/isPrimaryTopicOf
|
http://en.wikipedia.org/wiki/Triacetonamine +
|
http://xmlns.com/foaf/0.1/name
|
Triacetone amine
|
owl:sameAs |
http://fa.dbpedia.org/resource/%D8%AA%D8%B1%DB%8C%E2%80%8C%D8%A7%D8%B3%D8%AA%D9%88%D9%86_%D8%A2%D9%85%DB%8C%D9%86 +
, http://sr.dbpedia.org/resource/Triaceton_amin +
, http://sh.dbpedia.org/resource/Triaceton_amin +
, http://www.wikidata.org/entity/Q6120732 +
, http://ja.dbpedia.org/resource/%E3%83%88%E3%83%AA%E3%82%A2%E3%82%BB%E3%83%88%E3%83%B3%E3%82%A2%E3%83%9F%E3%83%B3 +
, http://azb.dbpedia.org/resource/%D8%AA%D8%B1%DB%8C%E2%80%8C%D8%A7%D8%B3%D8%AA%D9%88%D9%86_%D8%A2%D9%85%DB%8C%D9%86 +
, http://de.dbpedia.org/resource/Triacetonamin +
, https://global.dbpedia.org/id/4oL3v +
, http://dbpedia.org/resource/Triacetonamine +
|
rdf:type |
http://www.wikidata.org/entity/Q11173 +
, http://dbpedia.org/ontology/ChemicalCompound +
, http://www.ontologydesignpatterns.org/ont/dul/DUL.owl#ChemicalObject +
, http://dbpedia.org/ontology/ChemicalSubstance +
|
rdfs:comment |
Triacetonamine is an organic compound with … Triacetonamine is an organic compound with the formula OC(CH2CMe2)2NH (where Me = CH3). It is a colorless or white solid that melts near room temperature. The compound is an intermediate in the preparation of 2,2,6,6-tetramethylpiperidine, a sterically hindered base and precursor to the reagent called TEMPO. Triacetonamine is formed by the poly-aldol condensation of acetone in the presence of ammonia and calcium chloride: 3 (CH3)2CO + NH3 → OC(CH2CMe2)2NH + 2 H2O Reductive amination of triacetonamine gives 4-amino-2,2,6,6-tetramethylpiperidine.ves 4-amino-2,2,6,6-tetramethylpiperidine.
, Triacetonamin ist eine chemische Verbindung und ein tetramethyliertes .
, トリアセトンアミン(triacetone amine)は、アセトンとアンモニアの縮合反応で得られる化合物である。 3 CH3C(O)CH3 + NH3 → OC(CH2C(CH3)2)2NH + 2 H2O 立体障害をもつアミン:2,2,6,6-テトラメチルピペリジンの合成に使われる。
|
rdfs:label |
トリアセトンアミン
, Triacetonamine
, Triacetonamin
|