Tripropylamine

Tripropylamine
Names
	IUPAC name N,N-Dipropylpropan-1-amine
Identifiers
CAS Number	102-69-2 [EPA];
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:38880;
ChemSpider	7334;
ECHA InfoCard	100.002.771
EC Number	203-047-7;
Gmelin Reference	101540
PubChem CID	7616;
UNII	06S624V3U2;
UN number	2260
CompTox Dashboard (EPA)	DTXSID9021849 ;
	InChI InChI=1S/C9H21N/c1-4-7-10(8-5-2)9-6-3/h4-9H2,1-3H3 Key: YFTHZRPMJXBUME-UHFFFAOYSA-N;
	SMILES CCCN(CCC)CCC;
Properties
Appearance	colorless liquid
Density	0.7558 g/cm3
Melting point	−93.5 °C (−136.3 °F; 179.7 K)
Boiling point	156 °C (313 °F; 429 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H226, H301, H311, H314, H332, H335
Precautionary statements	P210, P233, P240, P241, P242, P243, P260, P261, P262, P264, P264+P265, P270, P271, P273, P280, P301+P316, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P319, P321, P330, P361+P364, P363, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)	2 2 0
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Tripropylamine is an organic compound with the formula (CH₃CH₂CH₂)₃N. It is classified as a tertiary amine. It is a colorless liquid with a "fishy" odor.^[2]

It has been used in electrochemiluminescence as a coreactant.^[3]

Synthesis method

References

^ "Tripropylamine". pubchem.ncbi.nlm.nih.gov.
^ Eller, Karsten; Henkes, Erhard; Rossbacher, Roland; Höke, Hartmut (2000). "Amines, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a02_001. ISBN 9783527303854.
^ Hanif, Saima; Han, Shuang; John, Peter; Gao, Wenyue; Kitte, Shimeles Addisu; Xu, Guobao (April 2016). "Electrochemiluminescence of Luminol-Tripropylamine System". Electrochimica Acta. 196: 245–251. doi:10.1016/j.electacta.2016.02.175.

[1] "Tripropylamine". pubchem.ncbi.nlm.nih.gov.

[2] Eller, Karsten; Henkes, Erhard; Rossbacher, Roland; Höke, Hartmut (2000). "Amines, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a02_001. ISBN 9783527303854.

[3] Hanif, Saima; Han, Shuang; John, Peter; Gao, Wenyue; Kitte, Shimeles Addisu; Xu, Guobao (April 2016). "Electrochemiluminescence of Luminol-Tripropylamine System". Electrochimica Acta. 196: 245–251. doi:10.1016/j.electacta.2016.02.175.

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[2]

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