Dipropyl sulfide

Available forms:clear colorless liquid

pd_proNo:262595-0754f6f1-f37a-4a55-900e-a8ab4bf8b5ca

pd_productuse:

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Detailed introduction

Purity 99% Min Dipropyl sulfide 111-47-7 Spot Supply with Safe Transportation

  • Molecular Formula:C6H14S
  • Molecular Weight:118.243
  • Appearance/Colour:clear colorless liquid 
  • Vapor Pressure:6.42mmHg at 25°C 
  • Melting Point:-103 °C 
  • Refractive Index:n20/D 1.4487(lit.)  
  • Boiling Point:144.4 °C at 760 mmHg 
  • Flash Point:28.3 °C 
  • PSA:25.30000 
  • Density:0.835 g/cm3 
  • LogP:2.53960 

Propyl sulfide(Cas 111-47-7) Usage

Synthesis Reference(s)

Canadian Journal of Chemistry, 51, p. 1419, 1973 DOI: 10.1139/v73-213Organic Syntheses, Coll. Vol. 2, p. 547, 1943Tetrahedron Letters, 20, p. 3995, 1979

Purification Methods

Wash the sulfide with aqueous 5% NaOH, then water. Dry it with CaCl2 and distil it from Na [Dunstan & Griffiths J Chem Soc 1344 1962]. [Beilstein 1 IV 1452.]

InChI:InChI=1/C6H14S/c1-3-5-7-6-4-2/h3-6H2,1-2H3

111-47-7 Relevant articles

-

Nishimura,Kawamoto

, p. 274,275 (1972)

-

-

Winssinger

, p. 109 (1887)

-

The reaction of (η-C5H5)2Ti(CO)2 with sulfoxides

Chen, T. L.,Shaver, Alan,Chan, T. H.

, p. C5 - C8 (1989)

Sulfoxides are reduced by (η-C5H5)2Ti(CO...

Reactions of Dichloroethenes with Sulfur in the System Hydrazine Hydrate–KОН

Levanova,Nikonova,Grabel’nykh,Russavskaya,Albanov,Rozentsveig,Korchevin

, p. 383 - 388 (2018)

Vinylidene chloride and 1,2-dichloroethe...

Bis(tributyltin) Sulfide: An Effective and General Sulfur-Transfer Reagent

Harpp, David N.,Gingras, Marc,Aida, T.,Chan, T. H.

, p. 1122 - 1124 (1987)

Bis(tributyltin) sulfide acts efficientl...

A process for the preparation of isoflavones propanethiol

-

Paragraph 0052; 0053, (2017/04/03)

The invention discloses a method for syn...

Dithiooxamide as an Effective Sulfur Surrogate for Odorless High-Yielding Carbon-Sulfur Bond Formation in Wet PEG200 as an Eco-Friendly, Safe, and Recoverable Solvent

Firouzabadi, Habib,Iranpoor, Nasser,Gorginpour, Forough,Samadi, Arash

supporting information, p. 2914 - 2920 (2015/05/04)

In this study, we have employed dithioox...

Hydrogenation of sulfoxides to sulfides under mild conditions using ruthenium nanoparticle catalysts

Mitsudome, Takato,Takahashi, Yusuke,Mizugaki, Tomoo,Jitsukawa, Koichiro,Kaneda, Kiyotomi

supporting information, p. 8348 - 8351 (2014/08/18)

The first demonstration of the hydrogena...

111-47-7 Process route

1,4-di(n-propyl)tetrasulfane
52687-98-6

1,4-di(n-propyl)tetrasulfane

1,2-dithiole-3-thione
534-25-8

1,2-dithiole-3-thione

1-thiopropane
107-03-9

1-thiopropane

propyl sulfide
111-47-7

propyl sulfide

Dipropyl disulfide
629-19-6

Dipropyl disulfide

Conditions
Conditions Yield
at 350 ℃;
52%
14%
15%
4%
dipropyl trisulfide*dipropyl tetrasulfide

dipropyl trisulfide*dipropyl tetrasulfide

1,2-dithiole-3-thione
534-25-8

1,2-dithiole-3-thione

1-thiopropane
107-03-9

1-thiopropane

propyl sulfide
111-47-7

propyl sulfide

Dipropyl disulfide
629-19-6

Dipropyl disulfide

Conditions
Conditions Yield
at 350 ℃;
44%
13%
7%
3%

111-47-7 Upstream products

  • 71-23-8
    71-23-8

    propan-1-ol

  • 56-23-5
    56-23-5

    tetrachloromethane

  • 107-03-9
    107-03-9

    1-thiopropane

  • 187737-37-7
    187737-37-7

    propene

111-47-7 Downstream products

  • 17626-99-2
    17626-99-2

    S,S-dipropyl-N-(toluene-4-sulfonyl)-sulfimide

  • 107-03-9
    107-03-9

    1-thiopropane

  • 7789-89-1
    7789-89-1

    1,1,1-trichloropropane

  • 598-03-8
    598-03-8

    propyl sulfone

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