Tetraetil pirofosfat

Tetraetil pirofosfat
	tetraetil difosfat
Identifikacija
CAS registarski broj	107-49-3
PubChem	7873
ChemSpider	7585
ChEMBL	CHEMBL293787
Jmol-3D slike	Slika 1
SMILES
	O=P(OP(=O)(OCC)OCC)(OCC)OCC
InChI
	InChI=1S/C8H20O7P2/c1-5-11-16(9,12-6-2)15-17(10,13-7-3)14-8-4/h5-8H2,1-4H3 ; Kod: IDCBOTIENDVCBQ-UHFFFAOYSA-N InChI=1/C8H20O7P2/c1-5-11-16(9,12-6-2)15-17(10,13-7-3)14-8-4/h5-8H2,1-4H3; Kod: IDCBOTIENDVCBQ-UHFFFAOYAI
Svojstva
Molekulska formula	C8H20O7P2
Molarna masa	290.19 g mol−1
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Tetraetil pirofosfat (TEPP) je organofosfatno jedinjenje. Ono se koristi kao pesticid.

Ovo jedinjenje je čista, bezbojna tečnost. Ono je rastvorno u vodi, ali se brzo hidrolizuje.^[5] TEPP je prvi sintetisao Filip de Klermont. Ovo jedinjenje se može pripremiti koristeći dva ekvivalenta dietil hlorofosfata sa jednim ekvivalentom vode u prisustvu piridina da sakupi formirani hlorovodonik:^[6]

Reference

↑ 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
↑ 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.
↑ 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
↑ 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 21948863. edit
↑ Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. 2005.
↑ Toy, A. D. F. (1948). „The Preparation of Tetraethyl Pyrophosphate and Other Tetraalkyl Pyrophosphates”. J. Am. Chem. Soc. 70 (11): 3882. DOI:10.1021/ja01191a104.

[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] 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 21948863. edit

[Ullmann-5] Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. 2005.

[6] Toy, A. D. F. (1948). „The Preparation of Tetraethyl Pyrophosphate and Other Tetraalkyl Pyrophosphates”. J. Am. Chem. Soc. 70 (11): 3882. DOI:10.1021/ja01191a104.

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