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About: Nitrile
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class="bi-box-arrow-up-right"></i> Sparql Endpoint </a> </li> </ul> </div> </div> </nav> <div style="margin-bottom: 60px"></div> <!-- /navbar --> <!-- page-header --> <section> <div class="container-xl"> <div class="row"> <div class="col"> <h1 id="title" class="display-6"><b>About:</b> <a href="http://dbpedia.org/resource/Nitrile">Nitrile</a> </h1> </div> </div> <div class="row"> <div class="col"> <div class="text-muted"> <span class="text-nowrap">An Entity of Type: <a href="http://www.w3.org/2002/07/owl#Thing">Thing</a>, </span> <span class="text-nowrap">from Named Graph: <a href="http://dbpedia.org">http://dbpedia.org</a>, </span> <span class="text-nowrap">within Data Space: <a href="http://dbpedia.org">dbpedia.org</a></span> </div> </div> </div> <div class="row pt-2"> <div class="col-xs-9 col-sm-10"> <p class="lead">In organic chemistry, a nitrile is any organic compound that has a −C≡N functional group. The prefix cyano- is used interchangeably with the term nitrile in industrial literature. Nitriles are found in many useful compounds, including methyl cyanoacrylate, used in super glue, and nitrile rubber, a nitrile-containing polymer used in latex-free laboratory and medical gloves. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons.</p> </div> <div class="col-xs-3 col-sm-2"> <a href="#" class="thumbnail"> <img src="http://commons.wikimedia.org/wiki/Special:FilePath/Nitrile_Structural_Formulae_V.1.png?width=300" alt="thumbnail" class="img-fluid" /> </a> </div> </div> </div> </section> <!-- page-header --> <!-- property-table --> <section> <div class="container-xl"> <div class="row"> <div class="table-responsive"> <table class="table table-hover table-sm table-light"> <thead> <tr> <th class="col-xs-3 ">Property</th> <th class="col-xs-9 px-3">Value</th> </tr> </thead> <tbody> <tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/ontology/abstract"><small>dbo:</small>abstract</a> </td><td class="col-10 text-break"><ul> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="ar" >النتريلات عبارة عن صنف من المركبات العضوية والتي تحوي على المجموعة الوظيفية C≡N- والتي تدعى بمجموعة النتريل. توجد هناك رابطة ثلاثية في مجموعة النتريل بين الكربون والنتروجين. تستخدم السابقة سيانو في تسمية المركبات الكيميائية الحاوية على مجموعة النتريل في البنية الجزيئية للمركب.هناك طريقتين للتسسميه اما ذكر سيانيد ثم السلسلة الهيدروكربونيهأو نبدل مقطع (ويك) من الحمض الكربوكسيلي المناظر واضافه مقطع نيتريل يصبح:اسيتو نيتريل.</span><small> (ar)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="cs" >Jako nitril se označuje jakákoli organická sloučenina obsahující funkční skupinu -C≡N. Skupina -C≡N se nazývá nitrilová skupina (též jen nitril). Ve skupině -CN jsou uhlíkový a dusíkový atom vázány trojnou vazbou. V chemickém názvosloví se pro indikaci přítomnosti nitrilové skupiny v molekule používá také prefix kyan. Kyanidový iont má záporný náboj a vzorec CN−. Skupina -CN se někdy, méně přesně, označuje také jako kyanidová skupina nebo kyanoskupina a sloučeniny ji obsahující jako kyanidy. Nitrily někdy uvolňují vysoce toxický kyanidový aniont CN−. Viz článek kyanid pro informace o biologických účincích a toxicitě.</span><small> (cs)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="ca" >Un nitril és una classe de composts químics orgànics que presenten un grup funcional format per un àtom de carboni unit a un àtom de nitrogen per un triple d'enllaç, amb fórmula .</span><small> (ca)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="el" >Νιτρίλιο (nitrile) είναι οποιαδήποτε οργανική ένωση που έχει τη χαρακτηριστική ομάδα −C≡N. Το πρόθεμα κυανο- (cyano-) χρησιμοποιείται εναλλακτικά με τον όρο νιτρίλιο στη βιομηχανική βιβλιογραφία. Τα νιτρίλια βρίσκονται σε πολλές χρήσιμες ενώσεις, που συμπεριλαμβάνουν το κυανοακρυλικό μεθύλιο (methyl cyanoacrylate), που χρησιμοποιείται στην υπερκόλλα (super glue) και το ελαστικό νιτριλίου (nitrile rubber), ένα πολυμερές που περιέχει νιτρίλιο και χρησιμοποιείται στα εργαστηριακά και στα ιατρικά γάντια. Το ελαστικό νιτριλίου χρησιμοποιείται επίσης πλατιά για τη στεγανοποίηση αυτοκινήτων και άλλων υλικών, επειδή αντιστέκεται σε καύσιμα και έλαια. Οι οργανικές ενώσεις που περιέχουν πολλαπλές νιτριλομάδες είναι γνωστές ως κυανοανθρακούχες (cyanocarbons). Οι ανόργανες ενώσεις που περιέχουν την ομάδα −C≡N δεν ονομάζονται νιτρίλια, αλλά κυανίδια. Αν και τα νιτρίλια και τα κυανίδια μπορούν να παραχθούν από κυανιούχα άλατα, τα περισσότερα νιτρίλια δεν είναι καθόλου τοξικά.</span><small> (el)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="eo" >Nitrilo aŭ R-C≡N estas organika komponaĵo enhavanta la funkcian grupon aŭ C≡N. La prefikso ciano uzatas interŝanĝe kun la nitrila grupo en la industria literaturo. Nitriloj trovatas en pluraj utilaj kombinaĵoj, inklude de "metila cianoakrilato", uzata en super gluaĵoj, kaj "nitrila kaŭĉuko", ia polimero nitrilenhava uzata en laboratorioj kaj medicinaj gantoj. La nitrila kaŭĉuko ankaŭ uzatas kiel aŭtaj sigelringoj pro ĝia rezistemo al brulaĵoj kaj oleoj. Organikaj komponaĵoj enhavantaj multoblajn nitrilajn grupojn konatas kiel cianokarbonaĵoj. Neorganikaj kombinaĵoj enhavanta la grupon cianon R-C≡N ne nomatas nitrilooj, sed cianidoj. Kvankam nitriloj kaj cianidoj povas deriviĝi el cianidaj saloj, la plejmulto el la nitriloj ne estas tiel toksaj. Industrie, la ĉefa metodo por produktado de nitriloj estas la amoniaka oksidado kaj cianidigo. Ambaŭ procezoj estas medisubteneblaj pro tio ke ili ne generas stekiometriajn kvantojn de saloj.</span><small> (eo)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="de" >Nitrile sind eine Gruppe chemischer Verbindungen mit der allgemeinen Formel R–C≡N. Die funktionelle Gruppe aus Kohlenstoff und dreifach gebundenem Stickstoff wird als Nitril- oder Cyanogruppe bezeichnet. Die Nitrile leiten sich formal von der Blausäure (HCN) durch Austausch des Wasserstoffatoms gegen einen organischen Rest ab. Die Isomere mit der Formel R–N≡C nennt man Isonitrile. Nitril-Polymere sind chemisch sehr beständig und haben gummiähnliche Eigenschaften, weshalb sie z. B. für Schutzhandschuhe verwendet werden.</span><small> (de)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="eu" >Nitriloa egituran -C≡N taldea (nitrilo taldea) duen konposatu organikoa da. aurkitu zituen nitriloak 1834an. Azido karboxilikoen deribatuak dira. Uretan ez dira urtzen, eta usain berezia dute. Besteak beste, amidak deshidratatuz eta metalen zianuroak alkil erreakzionaraziz lortzen dira. Nitrilo garrantzitsuenen artean akrilonitriloa (H2C=CH-C≡N) eta azetonitriloa (CH3-C≡N) daude. Biak sukoiak dira, eta polimeroen eta kopolimeroen ekoizpenean nahiko garrantzi handia dute, lehenengoak bereziki. bat (kautxu nitriloa) akrilonitriloaren eta butadienoaren kopolimerizazioz lortzen da. Nitriloak toxikoak izaten dira gehienetan.</span><small> (eu)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="es" >Los nitrilos son compuestos orgánicos que poseen un grupo de cianuro (-C≡N) como grupo funcional principal. Son derivados orgánicos del cianuro de los que el hidrógeno ha sido sustituido por un radical alquilo.</span><small> (es)</small></span></li> <li><span class="literal"><span property="dbo:abstract" lang="en" >In organic chemistry, a nitrile is any organic compound that has a −C≡N functional group. The prefix cyano- is used interchangeably with the term nitrile in industrial literature. Nitriles are found in many useful compounds, including methyl cyanoacrylate, used in super glue, and nitrile rubber, a nitrile-containing polymer used in latex-free laboratory and medical gloves. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons. Inorganic compounds containing the −C≡N group are not called nitriles, but cyanides instead. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic.</span><small> (en)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="fr" >Le groupement nitrile correspond à ≡N (-C≡N est le groupe cyano ou carbonitrile) et les règles IUPAC de dénomination des nitriles sont claires : par exemple, * CH3-C≡N est l'acétonitrile ou éthanenitrile ou cyanométhane * CH3CH2-C≡N est le propanenitrile ou le cyanoéthane * CH2=CH-C≡N est l'acrylonitrile ou 2-propènenitrile ou cyanoéthène * C6H5-C≡N est le benzonitrile (pas phénonitrile) ou cyanobenzène Les nitriles font partie de la famille des dérivés d'acides carboxyliques. Certains d'entre eux sont toxiques.</span><small> (fr)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="in" >Nitril adalah senyawa organik yang memiliki gugus fungsional −C≡N. Awalan cyano- digunakan secara bergantian dengan istilah nitril dalam literatur industri. Nitril ditemukan dalam senyawa yang banyak berguna, termasuk , digunakan dalam lem super, dan , nitril yang mengandung polimer yang digunakan dalam lateks laboratorium dan . juga banyak digunakan pada otomotif dan segel lainnya karena tahan terhadap bahan bakar dan minyak. Senyawa organik yang mengandung beberapa gugus nitril dikenal sebagai . Senyawa anorganik yang mengandung gugus −C≡N tidak disebut nitril, tetapi sianida. Meskipun nitril dan sianida dapat berasal dari garam sianida, sebagian besar nitril nyaris tidak beracun.</span><small> (in)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="ko" >나이트릴(영어: nitrile)은 −C≡N 작용기를 가지고 있는 모든 유기 화합물을 지칭한다. 접두사 "사이아노-"는 산업 문헌에서 "나이트릴"이라는 용어와 같은 의미로 사용된다. 나이트릴은 순간 접착제에 사용되는 와 라텍스가 없는 실험용 장갑 및 의료용 장갑에 사용되는 나이트릴 함유 중합체인 나이트릴 고무를 비롯한 많은 유용한 화합물에서 발견된다.</span><small> (ko)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="ja" >ニトリル (nitrile) は R−C≡N で表される構造を持つ有機化合物の総称である。カルボン酸やその誘導体と、炭素の酸化数において同等とされる。なお、手袋などの家庭用品によく使われるニトリルは、ニトリルゴム（ブタジエンアクリロニトリル共重合体）のことである。</span><small> (ja)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="it" >I nitrili sono composti organici caratterizzati dal gruppo funzionale −C≡N. Nella letteratura industriale al termine nitrile si preferisce il prefisso ciano-. I nitrili sono costituenti di materiali di uso comune come le colle cianoacriliche e la gomma nitrilica usata in guanti da laboratorio e in sigillanti per uso automobilistico. I composti inorganici contenenti il gruppo −C≡N sono chiamati, invece, cianuri. Sia i nitrili che i cianuri si possono considerare derivati di cianuri salini tipo NaCN e KCN, ma in genere i nitrili sono meno tossici. Il gruppo funzionale −C≡N non va confuso col gruppo −N≡C, caratteristico degli isocianuri.</span><small> (it)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="pl" >Nitryle – organiczne związki chemiczne zawierające grupę nitrylową, pochodne cyjanowodoru, o wzorze ogólnym R−C≡N. Acetonitryl i benzonitryl stosowane są jako rozpuszczalniki, a akrylonitryl jako monomer do otrzymywania poliakrylonitrylu.</span><small> (pl)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="nl" >Een nitril is een organische verbinding met de functionele groep -C≡N. De functionele groep -C≡N heet een nitrilgroep. In de -CN-groep zijn het koolstof- en het stikstofatoom met een drievoudige binding aan elkaar gebonden. Het voorzetsel cyano wordt in de chemische nomenclatuur gebruikt voor het aanduiden van een nitrilgroep in een molecuul. Een cyanide-ion is een negatief geladen ion met de formule CN−. De -CN-groep wordt soms, hoewel niet geheel juist, aangeduid als een cyanidegroep of cyanogroep en stoffen met deze groep soms als cyaniden. Uit nitrilen ontstaat soms het zeer toxische CN−-cyanide-ion. In planten komen cyanogene glycosides voor. Zij vormen een onderdeel van het chemische arsenaal tegen vraat.</span><small> (nl)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="pt" >Nitrilas, também denominadas cianetos, são um composto orgânico que apresentam o seguinte grupo funcional: ─ C ≡ N. De maneira geral, pode-se considerar que as nitrilas são obtidas a partir da substituição do hidrogênio do gás cianídrico (HCN).</span><small> (pt)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="sv" >Ej att förväxla med nitrilgummi som ofta kallas "nitril". Nitriler är kemiska organiska föreningar innehållande cyanogrupp (-C≡N). Om kolkedjan i stället binder till kvävet (-N≡C) fås en . Nitriler kan i en viss mening ses som organiska cyanider och vissa kan under omständigheter frisätta den mycket giftiga cyanidjonen (CN-). Nitriler har många användningsområden och förekommer dels naturligt i flera föreningar från växt- och djurriket samt i av människan syntetiserade föreningar.</span><small> (sv)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="uk" >Нітри́ли — клас органічних сполук, які мають у своїй структурі функціональну групу C≡N. В цій групі атоми Карбону та Нітрогену зв'язані потрійним зв'язком. Щоб показати присутність нітрильної групи в молекулі використовують префікс ціано-. Інколи групу -CN називають ціанідною або ціаногрупою, а сполуки, де вона міститься, — ціанідами. Нітрили можуть утворювати дуже токсичний іон CN−.</span><small> (uk)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="ru" >Нитри́лы — органические соединения общей формулы R—C≡N, формально являющиеся C-замещенными производными синильной кислоты HC≡N. Группа —C≡N называется нитрильной группой.</span><small> (ru)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="zh" >腈 （页面存档备份，存于互联网档案馆）（英語：nitrile），指的是带有C≡N官能团的有机化合物。 C≡N基团称作氰基，在 -CN 基团中碳原子和氮原子通过三键键合在一起。无机化学中带有此官能团者為氰，而不称“腈”。 许多含氰基的化合物都具有高毒性。</span><small> (zh)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/ontology/thumbnail"><small>dbo:</small>thumbnail</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><a class="uri" rel="dbo:thumbnail" resource="http://commons.wikimedia.org/wiki/Special:FilePath/Nitrile_Structural_Formulae_V.1.png?width=300" href="http://commons.wikimedia.org/wiki/Special:FilePath/Nitrile_Structural_Formulae_V.1.png?width=300"><small>wiki-commons</small>:Special:FilePath/Nitrile_Structural_Formulae_V.1.png?width=300</a></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" 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>1486.0</span><small> (dbd:nicaraguanCórdoba)</small></span></li> <li><span class="literal"><span property="dbp:file" lang="en" >N04151</span><small> (en)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/title"><small>dbp:</small>title</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:title" lang="en" >cyanide</span><small> (en)</small></span></li> <li><span class="literal"><span property="dbp:title" lang="en" >nitrile</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/wikiPageUsesTemplate"><small>dbp:</small>wikiPageUsesTemplate</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><a class="uri" rel="dbp:wikiPageUsesTemplate" resource="http://dbpedia.org/resource/Template:X10%5E" href="http://dbpedia.org/resource/Template:X10%5E"><small>dbt</small>:X10^</a></span></li> 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class="col-10 text-break"><ul> <li><span class="literal"><a class="uri" rel="dct:subject" resource="http://dbpedia.org/resource/Category:Nitriles" href="http://dbpedia.org/resource/Category:Nitriles"><small>dbc</small>:Nitriles</a></span></li> <li><span class="literal"><a class="uri" rel="dct:subject" resource="http://dbpedia.org/resource/Category:Functional_groups" href="http://dbpedia.org/resource/Category:Functional_groups"><small>dbc</small>:Functional_groups</a></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://www.w3.org/1999/02/22-rdf-syntax-ns#type"><small>rdf:</small>type</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><a class="uri" rel="rdf:type" resource="http://www.w3.org/2002/07/owl#Thing" href="http://www.w3.org/2002/07/owl#Thing"><small>owl</small>:Thing</a></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://www.w3.org/2000/01/rdf-schema#comment"><small>rdfs:</small>comment</a> </td><td class="col-10 text-break"><ul> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="ar" >النتريلات عبارة عن صنف من المركبات العضوية والتي تحوي على المجموعة الوظيفية C≡N- والتي تدعى بمجموعة النتريل. توجد هناك رابطة ثلاثية في مجموعة النتريل بين الكربون والنتروجين. تستخدم السابقة سيانو في تسمية المركبات الكيميائية الحاوية على مجموعة النتريل في البنية الجزيئية للمركب.هناك طريقتين للتسسميه اما ذكر سيانيد ثم السلسلة الهيدروكربونيهأو نبدل مقطع (ويك) من الحمض الكربوكسيلي المناظر واضافه مقطع نيتريل يصبح:اسيتو نيتريل.</span><small> (ar)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="ca" >Un nitril és una classe de composts químics orgànics que presenten un grup funcional format per un àtom de carboni unit a un àtom de nitrogen per un triple d'enllaç, amb fórmula .</span><small> (ca)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="de" >Nitrile sind eine Gruppe chemischer Verbindungen mit der allgemeinen Formel R–C≡N. Die funktionelle Gruppe aus Kohlenstoff und dreifach gebundenem Stickstoff wird als Nitril- oder Cyanogruppe bezeichnet. Die Nitrile leiten sich formal von der Blausäure (HCN) durch Austausch des Wasserstoffatoms gegen einen organischen Rest ab. Die Isomere mit der Formel R–N≡C nennt man Isonitrile. Nitril-Polymere sind chemisch sehr beständig und haben gummiähnliche Eigenschaften, weshalb sie z. B. für Schutzhandschuhe verwendet werden.</span><small> (de)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="eu" >Nitriloa egituran -C≡N taldea (nitrilo taldea) duen konposatu organikoa da. aurkitu zituen nitriloak 1834an. Azido karboxilikoen deribatuak dira. Uretan ez dira urtzen, eta usain berezia dute. Besteak beste, amidak deshidratatuz eta metalen zianuroak alkil erreakzionaraziz lortzen dira. Nitrilo garrantzitsuenen artean akrilonitriloa (H2C=CH-C≡N) eta azetonitriloa (CH3-C≡N) daude. Biak sukoiak dira, eta polimeroen eta kopolimeroen ekoizpenean nahiko garrantzi handia dute, lehenengoak bereziki. bat (kautxu nitriloa) akrilonitriloaren eta butadienoaren kopolimerizazioz lortzen da. Nitriloak toxikoak izaten dira gehienetan.</span><small> (eu)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="es" >Los nitrilos son compuestos orgánicos que poseen un grupo de cianuro (-C≡N) como grupo funcional principal. Son derivados orgánicos del cianuro de los que el hidrógeno ha sido sustituido por un radical alquilo.</span><small> (es)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="fr" >Le groupement nitrile correspond à ≡N (-C≡N est le groupe cyano ou carbonitrile) et les règles IUPAC de dénomination des nitriles sont claires : par exemple, * CH3-C≡N est l'acétonitrile ou éthanenitrile ou cyanométhane * CH3CH2-C≡N est le propanenitrile ou le cyanoéthane * CH2=CH-C≡N est l'acrylonitrile ou 2-propènenitrile ou cyanoéthène * C6H5-C≡N est le benzonitrile (pas phénonitrile) ou cyanobenzène Les nitriles font partie de la famille des dérivés d'acides carboxyliques. Certains d'entre eux sont toxiques.</span><small> (fr)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="ko" >나이트릴(영어: nitrile)은 −C≡N 작용기를 가지고 있는 모든 유기 화합물을 지칭한다. 접두사 "사이아노-"는 산업 문헌에서 "나이트릴"이라는 용어와 같은 의미로 사용된다. 나이트릴은 순간 접착제에 사용되는 와 라텍스가 없는 실험용 장갑 및 의료용 장갑에 사용되는 나이트릴 함유 중합체인 나이트릴 고무를 비롯한 많은 유용한 화합물에서 발견된다.</span><small> (ko)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="ja" >ニトリル (nitrile) は R−C≡N で表される構造を持つ有機化合物の総称である。カルボン酸やその誘導体と、炭素の酸化数において同等とされる。なお、手袋などの家庭用品によく使われるニトリルは、ニトリルゴム（ブタジエンアクリロニトリル共重合体）のことである。</span><small> (ja)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="pl" >Nitryle – organiczne związki chemiczne zawierające grupę nitrylową, pochodne cyjanowodoru, o wzorze ogólnym R−C≡N. Acetonitryl i benzonitryl stosowane są jako rozpuszczalniki, a akrylonitryl jako monomer do otrzymywania poliakrylonitrylu.</span><small> (pl)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="pt" >Nitrilas, também denominadas cianetos, são um composto orgânico que apresentam o seguinte grupo funcional: ─ C ≡ N. De maneira geral, pode-se considerar que as nitrilas são obtidas a partir da substituição do hidrogênio do gás cianídrico (HCN).</span><small> (pt)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="sv" >Ej att förväxla med nitrilgummi som ofta kallas "nitril". Nitriler är kemiska organiska föreningar innehållande cyanogrupp (-C≡N). Om kolkedjan i stället binder till kvävet (-N≡C) fås en . Nitriler kan i en viss mening ses som organiska cyanider och vissa kan under omständigheter frisätta den mycket giftiga cyanidjonen (CN-). Nitriler har många användningsområden och förekommer dels naturligt i flera föreningar från växt- och djurriket samt i av människan syntetiserade föreningar.</span><small> (sv)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="uk" >Нітри́ли — клас органічних сполук, які мають у своїй структурі функціональну групу C≡N. В цій групі атоми Карбону та Нітрогену зв'язані потрійним зв'язком. Щоб показати присутність нітрильної групи в молекулі використовують префікс ціано-. Інколи групу -CN називають ціанідною або ціаногрупою, а сполуки, де вона міститься, — ціанідами. Нітрили можуть утворювати дуже токсичний іон CN−.</span><small> (uk)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="ru" >Нитри́лы — органические соединения общей формулы R—C≡N, формально являющиеся C-замещенными производными синильной кислоты HC≡N. Группа —C≡N называется нитрильной группой.</span><small> (ru)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="zh" >腈 （页面存档备份，存于互联网档案馆）（英語：nitrile），指的是带有C≡N官能团的有机化合物。 C≡N基团称作氰基，在 -CN 基团中碳原子和氮原子通过三键键合在一起。无机化学中带有此官能团者為氰，而不称“腈”。 许多含氰基的化合物都具有高毒性。</span><small> (zh)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="cs" >Jako nitril se označuje jakákoli organická sloučenina obsahující funkční skupinu -C≡N. Skupina -C≡N se nazývá nitrilová skupina (též jen nitril). Ve skupině -CN jsou uhlíkový a dusíkový atom vázány trojnou vazbou. V chemickém názvosloví se pro indikaci přítomnosti nitrilové skupiny v molekule používá také prefix kyan. Kyanidový iont má záporný náboj a vzorec CN−. Skupina -CN se někdy, méně přesně, označuje také jako kyanidová skupina nebo kyanoskupina a sloučeniny ji obsahující jako kyanidy.</span><small> (cs)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="el" >Νιτρίλιο (nitrile) είναι οποιαδήποτε οργανική ένωση που έχει τη χαρακτηριστική ομάδα −C≡N. Το πρόθεμα κυανο- (cyano-) χρησιμοποιείται εναλλακτικά με τον όρο νιτρίλιο στη βιομηχανική βιβλιογραφία. Τα νιτρίλια βρίσκονται σε πολλές χρήσιμες ενώσεις, που συμπεριλαμβάνουν το κυανοακρυλικό μεθύλιο (methyl cyanoacrylate), που χρησιμοποιείται στην υπερκόλλα (super glue) και το ελαστικό νιτριλίου (nitrile rubber), ένα πολυμερές που περιέχει νιτρίλιο και χρησιμοποιείται στα εργαστηριακά και στα ιατρικά γάντια. Το ελαστικό νιτριλίου χρησιμοποιείται επίσης πλατιά για τη στεγανοποίηση αυτοκινήτων και άλλων υλικών, επειδή αντιστέκεται σε καύσιμα και έλαια. Οι οργανικές ενώσεις που περιέχουν πολλαπλές νιτριλομάδες είναι γνωστές ως κυανοανθρακούχες (cyanocarbons).</span><small> (el)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="eo" >Nitrilo aŭ R-C≡N estas organika komponaĵo enhavanta la funkcian grupon aŭ C≡N. La prefikso ciano uzatas interŝanĝe kun la nitrila grupo en la industria literaturo. Nitriloj trovatas en pluraj utilaj kombinaĵoj, inklude de "metila cianoakrilato", uzata en super gluaĵoj, kaj "nitrila kaŭĉuko", ia polimero nitrilenhava uzata en laboratorioj kaj medicinaj gantoj. La nitrila kaŭĉuko ankaŭ uzatas kiel aŭtaj sigelringoj pro ĝia rezistemo al brulaĵoj kaj oleoj. Organikaj komponaĵoj enhavantaj multoblajn nitrilajn grupojn konatas kiel cianokarbonaĵoj.</span><small> (eo)</small></span></li> <li><span class="literal"><span property="rdfs:comment" lang="en" >In organic chemistry, a nitrile is any organic compound that has a −C≡N functional group. The prefix cyano- is used interchangeably with the term nitrile in industrial literature. Nitriles are found in many useful compounds, including methyl cyanoacrylate, used in super glue, and nitrile rubber, a nitrile-containing polymer used in latex-free laboratory and medical gloves. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons.</span><small> (en)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="in" >Nitril adalah senyawa organik yang memiliki gugus fungsional −C≡N. Awalan cyano- digunakan secara bergantian dengan istilah nitril dalam literatur industri. Nitril ditemukan dalam senyawa yang banyak berguna, termasuk , digunakan dalam lem super, dan , nitril yang mengandung polimer yang digunakan dalam lateks laboratorium dan . juga banyak digunakan pada otomotif dan segel lainnya karena tahan terhadap bahan bakar dan minyak. Senyawa organik yang mengandung beberapa gugus nitril dikenal sebagai .</span><small> (in)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="it" >I nitrili sono composti organici caratterizzati dal gruppo funzionale −C≡N. Nella letteratura industriale al termine nitrile si preferisce il prefisso ciano-. I nitrili sono costituenti di materiali di uso comune come le colle cianoacriliche e la gomma nitrilica usata in guanti da laboratorio e in sigillanti per uso automobilistico. I composti inorganici contenenti il gruppo −C≡N sono chiamati, invece, cianuri. Sia i nitrili che i cianuri si possono considerare derivati di cianuri salini tipo NaCN e KCN, ma in genere i nitrili sono meno tossici.</span><small> (it)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="nl" >Een nitril is een organische verbinding met de functionele groep -C≡N. De functionele groep -C≡N heet een nitrilgroep. In de -CN-groep zijn het koolstof- en het stikstofatoom met een drievoudige binding aan elkaar gebonden. Het voorzetsel cyano wordt in de chemische nomenclatuur gebruikt voor het aanduiden van een nitrilgroep in een molecuul. Een cyanide-ion is een negatief geladen ion met de formule CN−. De -CN-groep wordt soms, hoewel niet geheel juist, aangeduid als een cyanidegroep of cyanogroep en stoffen met deze groep soms als cyaniden.</span><small> (nl)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://www.w3.org/2000/01/rdf-schema#label"><small>rdfs:</small>label</a> </td><td class="col-10 text-break"><ul> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="ar" >نتريل</span><small> (ar)</small></span></li> <li><span class="literal"><span property="rdfs:label" lang="en" >Nitrile</span><small> (en)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="ca" >Nitril</span><small> (ca)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="cs" >Nitril</span><small> (cs)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="de" >Nitrile</span><small> (de)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="el" >Νιτρίλιο</span><small> (el)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="eo" >Nitrilo</span><small> (eo)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="es" >Nitrilo</span><small> (es)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="eu" >Nitrilo</span><small> (eu)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="in" >Nitril</span><small> (in)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="fr" >Nitrile</span><small> (fr)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="it" >Nitrili</span><small> (it)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="ko" >나이트릴</span><small> (ko)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="ja" >ニトリル</span><small> (ja)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="nl" >Nitril</span><small> (nl)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="pl" >Nitryle</span><small> (pl)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="pt" >Nitrila</span><small> (pt)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="ru" >Нитрилы</span><small> (ru)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="sv" >Nitril</span><small> (sv)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="zh" >腈</span><small> (zh)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="uk" >Нітрили</span><small> (uk)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://www.w3.org/2000/01/rdf-schema#seeAlso"><small>rdfs:</small>seeAlso</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><a class="uri" rel="rdfs:seeAlso" resource="http://dbpedia.org/resource/Von_Braun_reaction" href="http://dbpedia.org/resource/Von_Braun_reaction"><small>dbr</small>:Von_Braun_reaction</a></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://www.w3.org/2002/07/owl#differentFrom"><small>owl:</small>differentFrom</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><a class="uri" rel="owl:differentFrom" resource="http://dbpedia.org/resource/Cyanide" href="http://dbpedia.org/resource/Cyanide"><small>dbr</small>:Cyanide</a></span></li> </ul></td></tr><tr class="even"><td 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