Tripropylamine

Tripropylamine
Names
IUPAC name
N,N-Dipropylpropan-1-amine
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.002.771
EC Number
  • 203-047-7
101540
UNII
UN number 2260
  • InChI=1S/C9H21N/c1-4-7-10(8-5-2)9-6-3/h4-9H2,1-3H3
    Key: YFTHZRPMJXBUME-UHFFFAOYSA-N
  • 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:[1]
GHS05: CorrosiveGHS06: ToxicGHS07: Exclamation markGHS08: Health hazard
Danger
H226, H301, H311, H314, H332, H335
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)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
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

  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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