. . "M\u00E9thylvinylc\u00E9tone"@fr . "\u4E01\u70EF\u916E\uFF08MVK\uFF09\uFF0C\u7ED3\u6784\u5F0FCH3COCH\uFF1DCH2\u3002\u662F\u6700\u7B80\u5355\u7684\u03B1,\u03B2-\u4E0D\u9971\u548C\u916E\u3002"@zh . "La m\u00E9thylvinylc\u00E9tone est un compos\u00E9 organique de formule CH3C(O)CH=CH2. C'est la plus simple des \u00E9nones. Elle se pr\u00E9sente sous la forme d'un liquide incolore tr\u00E8s inflammable, susceptible de former des m\u00E9langes explosifs avec l'air, \u00E0 l'odeur piquante d\u00E9sagr\u00E9able. Elle est soluble dans l'eau et les solvants polaires. Sa manipulation est particuli\u00E8rement dangereuse car elle est toxique et corrosive, et a tendance \u00E0 former des peroxydes explosifs et \u00E0 polym\u00E9riser sous l'effet de la lumi\u00E8re. C'est un interm\u00E9diaire utile \u00E0 la synth\u00E8se d'autres compos\u00E9s. Elle est produite industriellement par condensation d'ac\u00E9tone CH3C(O)CH3 et de formald\u00E9hyde HCHO suivie par une d\u00E9shydratation. Elle est \u00E9galement pr\u00E9par\u00E9e par la r\u00E9action de Mannich \u00E0 partir de chlorure de di\u00E9thylammonium [(CH3CH2)2NH2]Cl, ce qui donne l'adduit de Mannich, \u00E0 partir duquel la m\u00E9thylvinylc\u00E9tone est obtenue par chauffage avec lib\u00E9ration de chlorure de di\u00E9thylammonium : CH3C(O)CH3 + HCHO + [(CH3CH2)2NH2]Cl \u27F6 [CH3C(O)CH2CH2N(H)(CH2CH3)2]Cl + H2O ;[CH3C(O)CH2CH2N(H)(CH2CH3)2]Cl \u27F6 CH3C(O)CH=CH2 + [(CH3CH2)2NH2]Cl."@fr . "La m\u00E9thylvinylc\u00E9tone est un compos\u00E9 organique de formule CH3C(O)CH=CH2. C'est la plus simple des \u00E9nones. Elle se pr\u00E9sente sous la forme d'un liquide incolore tr\u00E8s inflammable, susceptible de former des m\u00E9langes explosifs avec l'air, \u00E0 l'odeur piquante d\u00E9sagr\u00E9able. Elle est soluble dans l'eau et les solvants polaires. Sa manipulation est particuli\u00E8rement dangereuse car elle est toxique et corrosive, et a tendance \u00E0 former des peroxydes explosifs et \u00E0 polym\u00E9riser sous l'effet de la lumi\u00E8re. C'est un interm\u00E9diaire utile \u00E0 la synth\u00E8se d'autres compos\u00E9s."@fr . "La butenona,\u200B tambi\u00E9n llamada metil vinil cetona es un compuesto org\u00E1nico del grupo de las cetonas, y m\u00E1s concretamente una enona. Es un l\u00EDquido altamente t\u00F3xico, inflamable e incoloro con un olor acre. Es f\u00E1cilmente soluble en agua, metanol, etanol, acetona, y \u00E1cido ac\u00E9tico."@es . . . . . "Methylvinylketon"@de . . "changed"@en . . "MVK"@en . . "Methyl vinyl ketone"@en . "\u0392\u03BF\u03C5\u03C4\u03B5\u03BD\u03CC\u03BD\u03B7"@el . . "Skeletal formula of methyl vinyl ketone"@en . "\u041C\u0435\u0442\u0438\u043B\u0432\u0438\u043D\u0438\u043B\u043A\u0435\u0442\u043E\u0301\u043D (3-\u0431\u0443\u0442\u0435\u043D-2-\u043E\u043D, \u0432\u0438\u043D\u0438\u043B\u043C\u0435\u0442\u0438\u043B\u043A\u0435\u0442\u043E\u043D, \u041C\u0412\u041A, MVK) \u2014 \u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u043E\u0435 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u0435, \u043A\u0435\u0442\u043E\u043D c \u0445\u0438\u043C\u0438\u0447\u0435\u0441\u043A\u043E\u0439 \u0444\u043E\u0440\u043C\u0443\u043B\u043E\u0439 CH3COCH=CH2. \u0418\u043C\u0435\u0435\u0442 \u0432\u0438\u0434 \u0431\u0435\u0441\u0446\u0432\u0435\u0442\u043D\u043E\u0439 \u0436\u0438\u0434\u043A\u043E\u0441\u0442\u0438 \u0441 \u0440\u0430\u0437\u0434\u0440\u0430\u0436\u0430\u044E\u0449\u0438\u043C \u0437\u0430\u043F\u0430\u0445\u043E\u043C. \u0422\u043E\u043A\u0441\u0438\u0447\u0435\u043D \u0438 \u0440\u0430\u0437\u0434\u0440\u0430\u0436\u0430\u0435\u0442 \u043A\u043E\u0436\u0443. \u041B\u0435\u0433\u043A\u043E \u043F\u043E\u043B\u0438\u043C\u0435\u0440\u0438\u0437\u0443\u0435\u0442\u0441\u044F \u0432 \u043F\u0440\u043E\u0437\u0440\u0430\u0447\u043D\u0443\u044E \u044D\u043B\u0430\u0441\u0442\u0438\u0447\u043D\u0443\u044E \u043C\u0430\u0441\u0441\u0443, \u043F\u0440\u0438\u043C\u0435\u043D\u044F\u0435\u0442\u0441\u044F \u043F\u0440\u0438 \u043F\u043E\u043B\u0443\u0447\u0435\u043D\u0438\u0438 \u043F\u043E\u043B\u0438\u043C\u0435\u0440\u043E\u0432 \u0438 \u0441\u043E\u043F\u043E\u043B\u0438\u043C\u0435\u0440\u043E\u0432, \u0438\u0441\u043F\u043E\u043B\u044C\u0437\u0443\u0435\u0442\u0441\u044F \u0432 \u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u043E\u043C \u0441\u0438\u043D\u0442\u0435\u0437\u0435."@ru . "Butenona"@es . . . "Methyl vinyl ketone molecule ball.png"@en . . . "Methyl vinyl ketone"@en . . . "Butenon"@nl . "160"^^ . . . . "\u041C\u0435\u0442\u0438\u043B\u0432\u0438\u043D\u0438\u043B\u043A\u0435\u0442\u043E\u043D"@ru . . . . . . . "Butenon of methylvinylketon (MVK) is een zeer toxische en reactieve organische verbinding met als brutoformule C4H6O. De stof komt voor als een corrosieve en zeer licht ontvlambare kleurloze vloeistof met een scherpe geur, die zeer goed oplosbaar is in water, ethanol, aceton en azijnzuur. Butenon is het meest eenvoudige enon, een alfa,b\u00E8ta-onverzadigd keton."@nl . "Methylvinylketon (MVK, systematick\u00FD n\u00E1zev butenon), je reaktivn\u00ED organick\u00E1 slou\u010Denina a nejjednodu\u0161\u0161\u00ED enon. Je u\u017Eite\u010Dn\u00FDm meziproduktem p\u0159i synt\u00E9ze dal\u0161\u00EDch slou\u010Denin."@cs . "150"^^ . "La butenona,\u200B tambi\u00E9n llamada metil vinil cetona es un compuesto org\u00E1nico del grupo de las cetonas, y m\u00E1s concretamente una enona. Es un l\u00EDquido altamente t\u00F3xico, inflamable e incoloro con un olor acre. Es f\u00E1cilmente soluble en agua, metanol, etanol, acetona, y \u00E1cido ac\u00E9tico."@es . . . . . "Methylene acetone"@en . "Methylvinylketon"@cs . . . . "\u0397 \u03B2\u03BF\u03C5\u03C4\u03B5\u03BD\u03CC\u03BD\u03B7 \u03AE \u03B2\u03B9\u03BD\u03C5\u03BB\u03BF\u03BC\u03B5\u03B8\u03C5\u03BB\u03BF\u03BA\u03B5\u03C4\u03CC\u03BD\u03B7 \u03B5\u03AF\u03BD\u03B1\u03B9 \u03BC\u03B9\u03B1 \u03B4\u03C1\u03B1\u03C3\u03C4\u03B9\u03BA\u03AE \u03BF\u03C1\u03B3\u03B1\u03B9\u03BA\u03AE \u03AD\u03BD\u03C9\u03C3\u03B7 \u03C0\u03BF\u03C5 \u03C4\u03B1\u03BE\u03B9\u03BD\u03BF\u03BC\u03B5\u03AF\u03C4\u03B1\u03B9 \u03C9\u03C2 (\u03AE \u03BB\u03AF\u03B3\u03BF \u03B3\u03B5\u03BD\u03B9\u03BA\u03CC\u03C4\u03B5\u03C1\u03B1, \u03C9\u03C2 ). \u0395\u03AF\u03BD\u03B1\u03B9 \u03AD\u03BD\u03B1 \u03AC\u03C7\u03C1\u03C9\u03BC\u03BF, \u03B5\u03CD\u03C6\u03BB\u03C1\u03BA\u03C4\u03BF \u03BA\u03B1\u03B9 \u03C0\u03BF\u03BB\u03CD \u03C4\u03BF\u03BE\u03B9\u03BA\u03CC \u03C5\u03B3\u03C1\u03CC \u03BC\u03B5 \u03AD\u03BD\u03C4\u03BF\u03BD\u03B7 \u03BF\u03C3\u03BC\u03AE. \u03A0\u03C1\u03BF\u03BA\u03B1\u03BB\u03B5\u03AF \u03B2\u03AE\u03C7\u03B1, \u03C3\u03C5\u03C1\u03B9\u03B3\u03BC\u03CC \u03BA\u03B1\u03B9 \u03B1\u03C3\u03C6\u03C5\u03BE\u03AF\u03B1 \u03B1\u03C0\u03CC \u03C7\u03B1\u03BC\u03B7\u03BB\u03AE \u03C3\u03C5\u03B3\u03BA\u03AD\u03BD\u03C4\u03C1\u03C9\u03C3\u03B7. \u0395\u03AF\u03BD\u03B1\u03B9 \u03B5\u03CD\u03BA\u03BF\u03BB\u03B1 \u03B4\u03B9\u03B1\u03BB\u03C5\u03C4\u03AE \u03C3\u03C4\u03BF \u03BD\u03B5\u03C1\u03CC, \u03C3\u03C4\u03B7 \u03BC\u03B5\u03B8\u03B1\u03BD\u03CC\u03BB\u03B7, \u03C3\u03C4\u03B7\u03BD \u03B1\u03B9\u03B8\u03B1\u03BD\u03CC\u03BB\u03B7, \u03C3\u03C4\u03B7\u03BD \u03C0\u03C1\u03BF\u03C0\u03B1\u03BD\u03CC\u03BD\u03B7 \u03BA\u03B1\u03B9 \u03C3\u03C4\u03BF \u03B1\u03B9\u03B8\u03B1\u03BD\u03B9\u03BA\u03CC \u03BF\u03BE\u03CD. \u0388\u03C7\u03B5\u03B9 \u03C3\u03CD\u03BD\u03C4\u03BF\u03BC\u03BF \u03C3\u03C5\u03BD\u03C4\u03B1\u03BA\u03C4\u03B9\u03BA\u03CC \u03C4\u03CD\u03C0\u03BF CH2=CHCOCH3. \u03A3\u03C5\u03BD\u03C4\u03BF\u03BC\u03BF\u03B3\u03C1\u03B1\u03C6\u03B9\u03BA\u03AC \u03B1\u03C0\u03BF\u03B4\u03AF\u03B4\u03B5\u03C4\u03B1\u03B9: ViCOMe \u03AE MVK (MethylVinylKetone)."@el . . . . . . . "Methyl vinyl ketone (MVK, IUPAC name: butenone) is the organic compound with the formula CH3C(O)CH=CH2. It is a reactive compound classified as an enone, in fact the simplest example thereof. It is a colorless, flammable, highly toxic liquid with a pungent odor. It is soluble in water and polar organic solvents. It is a useful intermediate in the synthesis of other compounds."@en . . . "\u4E01\u70EF\u916E"@zh . . . . . . . . . . . . . . . . . "\u0397 \u03B2\u03BF\u03C5\u03C4\u03B5\u03BD\u03CC\u03BD\u03B7 \u03AE \u03B2\u03B9\u03BD\u03C5\u03BB\u03BF\u03BC\u03B5\u03B8\u03C5\u03BB\u03BF\u03BA\u03B5\u03C4\u03CC\u03BD\u03B7 \u03B5\u03AF\u03BD\u03B1\u03B9 \u03BC\u03B9\u03B1 \u03B4\u03C1\u03B1\u03C3\u03C4\u03B9\u03BA\u03AE \u03BF\u03C1\u03B3\u03B1\u03B9\u03BA\u03AE \u03AD\u03BD\u03C9\u03C3\u03B7 \u03C0\u03BF\u03C5 \u03C4\u03B1\u03BE\u03B9\u03BD\u03BF\u03BC\u03B5\u03AF\u03C4\u03B1\u03B9 \u03C9\u03C2 (\u03AE \u03BB\u03AF\u03B3\u03BF \u03B3\u03B5\u03BD\u03B9\u03BA\u03CC\u03C4\u03B5\u03C1\u03B1, \u03C9\u03C2 ). \u0395\u03AF\u03BD\u03B1\u03B9 \u03AD\u03BD\u03B1 \u03AC\u03C7\u03C1\u03C9\u03BC\u03BF, \u03B5\u03CD\u03C6\u03BB\u03C1\u03BA\u03C4\u03BF \u03BA\u03B1\u03B9 \u03C0\u03BF\u03BB\u03CD \u03C4\u03BF\u03BE\u03B9\u03BA\u03CC \u03C5\u03B3\u03C1\u03CC \u03BC\u03B5 \u03AD\u03BD\u03C4\u03BF\u03BD\u03B7 \u03BF\u03C3\u03BC\u03AE. \u03A0\u03C1\u03BF\u03BA\u03B1\u03BB\u03B5\u03AF \u03B2\u03AE\u03C7\u03B1, \u03C3\u03C5\u03C1\u03B9\u03B3\u03BC\u03CC \u03BA\u03B1\u03B9 \u03B1\u03C3\u03C6\u03C5\u03BE\u03AF\u03B1 \u03B1\u03C0\u03CC \u03C7\u03B1\u03BC\u03B7\u03BB\u03AE \u03C3\u03C5\u03B3\u03BA\u03AD\u03BD\u03C4\u03C1\u03C9\u03C3\u03B7. \u0395\u03AF\u03BD\u03B1\u03B9 \u03B5\u03CD\u03BA\u03BF\u03BB\u03B1 \u03B4\u03B9\u03B1\u03BB\u03C5\u03C4\u03AE \u03C3\u03C4\u03BF \u03BD\u03B5\u03C1\u03CC, \u03C3\u03C4\u03B7 \u03BC\u03B5\u03B8\u03B1\u03BD\u03CC\u03BB\u03B7, \u03C3\u03C4\u03B7\u03BD \u03B1\u03B9\u03B8\u03B1\u03BD\u03CC\u03BB\u03B7, \u03C3\u03C4\u03B7\u03BD \u03C0\u03C1\u03BF\u03C0\u03B1\u03BD\u03CC\u03BD\u03B7 \u03BA\u03B1\u03B9 \u03C3\u03C4\u03BF \u03B1\u03B9\u03B8\u03B1\u03BD\u03B9\u03BA\u03CC \u03BF\u03BE\u03CD. \u0388\u03C7\u03B5\u03B9 \u03C3\u03CD\u03BD\u03C4\u03BF\u03BC\u03BF \u03C3\u03C5\u03BD\u03C4\u03B1\u03BA\u03C4\u03B9\u03BA\u03CC \u03C4\u03CD\u03C0\u03BF CH2=CHCOCH3. \u03A3\u03C5\u03BD\u03C4\u03BF\u03BC\u03BF\u03B3\u03C1\u03B1\u03C6\u03B9\u03BA\u03AC \u03B1\u03C0\u03BF\u03B4\u03AF\u03B4\u03B5\u03C4\u03B1\u03B9: ViCOMe \u03AE MVK (MethylVinylKetone)."@el . . . . . . . . . "Methyl vinyl ketone (MVK, IUPAC name: butenone) is the organic compound with the formula CH3C(O)CH=CH2. It is a reactive compound classified as an enone, in fact the simplest example thereof. It is a colorless, flammable, highly toxic liquid with a pungent odor. It is soluble in water and polar organic solvents. It is a useful intermediate in the synthesis of other compounds."@en . . . . . . . . . . . . . "But-3-en-2-one"@en . . . "\u30E1\u30C1\u30EB\u30D3\u30CB\u30EB\u30B1\u30C8\u30F3(\u7565\u79F0\uFF1AMVK)\u306F\u3001\u30A8\u30CE\u30F3\u306B\u5206\u985E\u3055\u308C\u308B\u53CD\u5FDC\u6027\u306E\u9AD8\u3044\u6709\u6A5F\u5316\u5408\u7269\u3067\u3042\u308B\u3002\u6D88\u9632\u6CD5\u306B\u5B9A\u3081\u308B\u7B2C4\u985E\u5371\u967A\u7269 \u7B2C1\u77F3\u6CB9\u985E\u306B\u8A72\u5F53\u3059\u308B\u3002"@ja . . . . . . . . . . . "5293027"^^ . . . . . . . . . . . "Metil vinil cetone (MVK, do ingl\u00EAs methyl vinyl ketone) \u00E9 um composto org\u00E2nico reativo classificado como uma enona. \u00C9 um l\u00EDquido incolor, inflam\u00E1vel e altamente t\u00F3xico com odor pungente. \u00C9 facilmente sol\u00FAvel em \u00E1gua, metanol, etanol, acetona e \u00E1cido ac\u00E9tico. MVK tem sido preparado industrialmente pela condensa\u00E7\u00E3o de acetona e formalde\u00EDdo, seguida por desidrata\u00E7\u00E3o. MVK pode atuar como um porque \u00E9 um receptor de Michael efetivo. Esta habilidade de alquila\u00E7\u00E3o \u00E9 tanto a fonte de sua alta toxicidade e a caracter\u00EDstica que a faz um intermedi\u00E1rio \u00FAtil em s\u00EDntese org\u00E2nica. MVK ir\u00E1 polimerizar-se espontaneamente, e \u00E9 usada na produ\u00E7\u00E3o de pol\u00EDmeros pl\u00E1sticos. \u00C9 tamb\u00E9m um intermedi\u00E1rio na s\u00EDntese de ester\u00F3ides e vitamina A. MVK \u00E9 extremamente perigoso por inala\u00E7\u00E3o causando tosse, asma e dificuldade respirat\u00F3ria mesmo em baixas concentra\u00E7\u00F5es. Ela tamb\u00E9m facilmente causa irrita\u00E7\u00E3o da pele, olhos e membranas mucosas."@pt . "3-Buten-2-on (auch Methylvinylketon) ist das einfachste unges\u00E4ttigte Keton, eine stechend riechende Fl\u00FCssigkeit, die leicht polymerisiert."@de . . . . "5505"^^ . . . . . "\u30E1\u30C1\u30EB\u30D3\u30CB\u30EB\u30B1\u30C8\u30F3"@ja . . . "444013203"^^ . . . . . "\u041C\u0435\u0442\u0438\u043B\u0432\u0438\u043D\u0438\u043B\u043A\u0435\u0442\u043E\u0301\u043D (3-\u0431\u0443\u0442\u0435\u043D-2-\u043E\u043D, \u0432\u0438\u043D\u0438\u043B\u043C\u0435\u0442\u0438\u043B\u043A\u0435\u0442\u043E\u043D, \u041C\u0412\u041A, MVK) \u2014 \u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u043E\u0435 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u0435, \u043A\u0435\u0442\u043E\u043D c \u0445\u0438\u043C\u0438\u0447\u0435\u0441\u043A\u043E\u0439 \u0444\u043E\u0440\u043C\u0443\u043B\u043E\u0439 CH3COCH=CH2. \u0418\u043C\u0435\u0435\u0442 \u0432\u0438\u0434 \u0431\u0435\u0441\u0446\u0432\u0435\u0442\u043D\u043E\u0439 \u0436\u0438\u0434\u043A\u043E\u0441\u0442\u0438 \u0441 \u0440\u0430\u0437\u0434\u0440\u0430\u0436\u0430\u044E\u0449\u0438\u043C \u0437\u0430\u043F\u0430\u0445\u043E\u043C. \u0422\u043E\u043A\u0441\u0438\u0447\u0435\u043D \u0438 \u0440\u0430\u0437\u0434\u0440\u0430\u0436\u0430\u0435\u0442 \u043A\u043E\u0436\u0443. \u041B\u0435\u0433\u043A\u043E \u043F\u043E\u043B\u0438\u043C\u0435\u0440\u0438\u0437\u0443\u0435\u0442\u0441\u044F \u0432 \u043F\u0440\u043E\u0437\u0440\u0430\u0447\u043D\u0443\u044E \u044D\u043B\u0430\u0441\u0442\u0438\u0447\u043D\u0443\u044E \u043C\u0430\u0441\u0441\u0443, \u043F\u0440\u0438\u043C\u0435\u043D\u044F\u0435\u0442\u0441\u044F \u043F\u0440\u0438 \u043F\u043E\u043B\u0443\u0447\u0435\u043D\u0438\u0438 \u043F\u043E\u043B\u0438\u043C\u0435\u0440\u043E\u0432 \u0438 \u0441\u043E\u043F\u043E\u043B\u0438\u043C\u0435\u0440\u043E\u0432, \u0438\u0441\u043F\u043E\u043B\u044C\u0437\u0443\u0435\u0442\u0441\u044F \u0432 \u043E\u0440\u0433\u0430\u043D\u0438\u0447\u0435\u0441\u043A\u043E\u043C \u0441\u0438\u043D\u0442\u0435\u0437\u0435."@ru . . . . "Methylene acetone"@en . . . "Metil vinil cetona"@pt . . . . . . . . "3-Buten-2-on"@de . . "Ball-and-stick model of the methyl vinyl ketone molecule"@en . . . . . "Metil vinil cetone (MVK, do ingl\u00EAs methyl vinyl ketone) \u00E9 um composto org\u00E2nico reativo classificado como uma enona. \u00C9 um l\u00EDquido incolor, inflam\u00E1vel e altamente t\u00F3xico com odor pungente. \u00C9 facilmente sol\u00FAvel em \u00E1gua, metanol, etanol, acetona e \u00E1cido ac\u00E9tico. MVK tem sido preparado industrialmente pela condensa\u00E7\u00E3o de acetona e formalde\u00EDdo, seguida por desidrata\u00E7\u00E3o. MVK \u00E9 extremamente perigoso por inala\u00E7\u00E3o causando tosse, asma e dificuldade respirat\u00F3ria mesmo em baixas concentra\u00E7\u00F5es. Ela tamb\u00E9m facilmente causa irrita\u00E7\u00E3o da pele, olhos e membranas mucosas."@pt . . . . . "Methylvinylketon (MVK, systematick\u00FD n\u00E1zev butenon), je reaktivn\u00ED organick\u00E1 slou\u010Denina a nejjednodu\u0161\u0161\u00ED enon. Je u\u017Eite\u010Dn\u00FDm meziproduktem p\u0159i synt\u00E9ze dal\u0161\u00EDch slou\u010Denin."@cs . . . . "Butenon of methylvinylketon (MVK) is een zeer toxische en reactieve organische verbinding met als brutoformule C4H6O. De stof komt voor als een corrosieve en zeer licht ontvlambare kleurloze vloeistof met een scherpe geur, die zeer goed oplosbaar is in water, ethanol, aceton en azijnzuur. Butenon is het meest eenvoudige enon, een alfa,b\u00E8ta-onverzadigd keton."@nl . . . . "\u4E01\u70EF\u916E\uFF08MVK\uFF09\uFF0C\u7ED3\u6784\u5F0FCH3COCH\uFF1DCH2\u3002\u662F\u6700\u7B80\u5355\u7684\u03B1,\u03B2-\u4E0D\u9971\u548C\u916E\u3002"@zh . . . . . . "Methyl vinyl ketone"@en . "MVK"@en . . . "3-Buten-2-on (auch Methylvinylketon) ist das einfachste unges\u00E4ttigte Keton, eine stechend riechende Fl\u00FCssigkeit, die leicht polymerisiert."@de . "But-3-en-2-one"@en . "1081219914"^^ . . . . . . "Structure of methyl vinyl ketone.png"@en . "\u30E1\u30C1\u30EB\u30D3\u30CB\u30EB\u30B1\u30C8\u30F3(\u7565\u79F0\uFF1AMVK)\u306F\u3001\u30A8\u30CE\u30F3\u306B\u5206\u985E\u3055\u308C\u308B\u53CD\u5FDC\u6027\u306E\u9AD8\u3044\u6709\u6A5F\u5316\u5408\u7269\u3067\u3042\u308B\u3002\u6D88\u9632\u6CD5\u306B\u5B9A\u3081\u308B\u7B2C4\u985E\u5371\u967A\u7269 \u7B2C1\u77F3\u6CB9\u985E\u306B\u8A72\u5F53\u3059\u308B\u3002"@ja . . . . . .