Trioctylphosphine See also References Navigation menu4731-53-7Interactive image19625100.022.94020851"Triocylphosphine"expanding ite

Organic compound stubsPhosphines


organophosphorus compoundformulananoparticlestrioctylphosphine oxide



























Trioctylphosphine

Trioctylphosphine.svg
Names

IUPAC name
Trioctylphosphane

Identifiers

CAS Number


  • 4731-53-7


3D model (JSmol)


  • Interactive image


Beilstein Reference

1776995

ChemSpider

  • 19625


ECHA InfoCard

100.022.940


PubChem CID


  • 20851





Properties

Chemical formula


C24H51P

Molar mass
370.635498

Density
0.831 g/mL

Boiling point
284 to 291 °C (543 to 556 °F; 557 to 564 K) at 50 mmHg

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).


Infobox references


Trioctylphosphine is an organophosphorus compound with the formula P(C8H17)3 sometimes abbreviated TOP.[1] It is a common reagent in the chemical synthesis of nanoparticles. Trioctylphosphine reacts with oxygen to form trioctylphosphine oxide.



See also


  • Triphenylphosphine


References




  1. ^ "Triocylphosphine". Chemspider.com..mw-parser-output cite.citationfont-style:inherit.mw-parser-output .citation qquotes:"""""""'""'".mw-parser-output .citation .cs1-lock-free abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-subscription abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registrationcolor:#555.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration spanborder-bottom:1px dotted;cursor:help.mw-parser-output .cs1-ws-icon abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center.mw-parser-output code.cs1-codecolor:inherit;background:inherit;border:inherit;padding:inherit.mw-parser-output .cs1-hidden-errordisplay:none;font-size:100%.mw-parser-output .cs1-visible-errorfont-size:100%.mw-parser-output .cs1-maintdisplay:none;color:#33aa33;margin-left:0.3em.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-formatfont-size:95%.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-leftpadding-left:0.2em.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-rightpadding-right:0.2em








Organic compound stubs, PhosphinesUncategorized

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