1,3-Butadien

1,3-Butadien
1,3-Butadiene	1,3-Butadiene
IUPAC ime
Drugi nazivi	Bietilen; Eritren; Divinil; Viniletilen
Identifikacija
CAS registarski broj	106-99-0
PubChem	7845
ChemSpider	7557
UNII	JSD5FGP5VD
UN broj	1010
KEGG	C16450
ChEBI	39478
ChEMBL	CHEMBL537970
RTECS registarski broj toksičnosti	EI9275000
Jmol-3D slike	Slika 1
Svojstva
Molekulska formula	C4H6
Molarna masa	54.0916
Agregatno stanje	bezbojni gas; ili ohlađena tečnost
Gustina	0.64 g/cm3 na -6 °C, tečnost
Tačka topljenja	-108.9 °C, 164.3 K, -164.0 °F
Tačka ključanja	-4.4 °C, 269 K, 24 °F
Rastvorljivost u vodi	735 ppm
Viskoznost	0.25 cP ma 0 °C
Opasnost
Podaci o bezbednosti prilikom rukovanja (MSDS)	ECSC 0017
Opasnost u toku rada	zapaljiv, iritant, karcinogen
R-oznake	R45 R46 R12
S-oznake	S45 S53
Tačka paljenja	-85 °C
Srodna jedinjenja
Srodna alkeni; i dieni	Izopren; hloropren
Srodna jedinjenja	Butan
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

1,3-Butadien je jednostavan konjugovani dien sa formulom C₄H₆.^[6]^[7] On je važna industrijska hemikalija koja se koristi kao monomer u produkciji sintetičke gume. Reč butadien se najčešće odnosi na 1,3-butadien.

Kratke činjenice Identifikacija, Svojstva ...

Zatvori

Ime butadien se takođe može odnosi na izomer, 1,2-butadien, međutim taj alen se teško priprema i nema industrijski značaj.

[1]
Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
[2]
Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
[3]
Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
[4]
Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
[5]
Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
[6]
Clayden Jonathan, Nick Greeves, Stuart Warren, Peter Wothers (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.
[7]
Smith, Michael B.; March, Jerry (2007). Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th izd.). New York: Wiley-Interscience. ISBN 0-471-72091-7.

Ciklobutadien
Polibutadien

Portal Hemija

1,3-Butadien
Inventar zagađivača Arhivirano 2003-12-22 na Wayback Machine-u

[1] [1]
Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] [2]
Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] [3]
Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] [4]
Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.

[5] [5]
Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[Clayden1st-6] [6]
Clayden Jonathan, Nick Greeves, Stuart Warren, Peter Wothers (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.

[March6th-7] [7]
Smith, Michael B.; March, Jerry (2007). Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th izd.). New York: Wiley-Interscience. ISBN 0-471-72091-7.

[6]

[7]

[1]

[2]

[3]

[4]

[5]

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