1,3-Diaminopropan

1,3-Diaminopropan
	Propan-1,3-diamin
Drugi nazivi	Propandiamin; 1,3-Propilendiamin; Trimetilendiamin ;
Identifikacija
Abrevijacija	TMEDA
CAS registarski broj	109-76-2
PubChem	428
ChemSpider	415
EINECS broj	203-702-7
UN broj	2922
KEGG	C00986
MeSH	trimethylenediamine
ChEBI	15725
ChEMBL	CHEMBL174324
RTECS registarski broj toksičnosti	TX6825000
Bajlštajn	605277
Gmelin Referenca	1298
3DMet	B00214
Jmol-3D slike	Slika 1
SMILES
	NCCCN
InChI
	InChI=1S/C3H10N2/c4-2-1-3-5/h1-5H2 ; Kod: XFNJVJPLKCPIBV-UHFFFAOYSA-N
Svojstva
Molekulska formula	C3H10N2
Molarna masa	74.12 g mol−1
Agregatno stanje	Bezbojna tečnost
Miris	Ima miris ribe, amonijaka
Gustina	888 mg mL−1
Tačka topljenja	-12 °C, 261.15 K, 10 °F
Tačka ključanja	140 °C, 413.2 K, 284 °F
log P	−1,4
Napon pare	<1,1 kPa (na 20 °C)
Indeks prelamanja (nD)	1,458
Opasnost
EU-klasifikacija	T C
R-oznake	R10, R22, R24, R35
S-oznake	S26, S36/37/39, S45
Tačka paljenja	51 °C
Tačka spontanog paljenja	350 °C
Eksplozivni limiti	2,8–15,2%
LD50	177 mg kg−1 (dermalno, zec); 700 mg kg−1 (oralno, pacov);
Srodna jedinjenja
Srodna alkanamini	Etilamin; Etilendiamin; Propilamin; Izopropilamin; 1,2-Diaminopropan; Izobutilamin; tert-Butilamin; n-Butilamin; sec-Butilamin; Putrescin;
Srodna jedinjenja	2-Metil-2-nitrozopropan
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

1,3-Diaminopropan je jednostavni amin. Kalijumova so se koristi u alkin ziper reakciji, objavljenoj 1975.^[6]

Reference uredi

↑ 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
↑ 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.
↑ 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
↑ C. A. Brown and A. Yamashita (1975). „Saline hydrides 2and superbases in organic reactions. IX. Acetylene zipper. Exceptionally facile contrathermodynamic multipositional isomeriazation of alkynes with potassium 3-aminopropylamide”. J. Am. Chem. Soc. 97 (4): 891–892. DOI:10.1021/ja00837a034.

[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] C. A. Brown and A. Yamashita (1975). „Saline hydrides 2and superbases in organic reactions. IX. Acetylene zipper. Exceptionally facile contrathermodynamic multipositional isomeriazation of alkynes with potassium 3-aminopropylamide”. J. Am. Chem. Soc. 97 (4): 891–892. DOI:10.1021/ja00837a034.

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