2-HYDROXYETHYL-N-OCTYL SULPHIDE

  • Name: 2-HYDROXYETHYL-N-OCTYL SULPHIDE
  • CAS: 3547-33-9
  • Purity: 99%
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Details

Manufacturer supply good quality 2-HYDROXYETHYL-N-OCTYL SULPHIDE 3547-33-9 with stock

  • Molecular Formula: C10H22 O S
  • Molecular Weight: 190.35
  • Appearance/Colour: clear to yellowish liquid 
  • Vapor Pressure: 0mmHg at 25°C 
  • Melting Point: 0°C 
  • Refractive Index: 1.4760 (estimate) 
  • Boiling Point: 180 - 185 C  
  • Flash Point: 77 C 
  • PSA： 45.53000 
  • Density: 0.928 g/cm3 
  • LogP: 3.07240 

2-HYDROXYETHYL-N-OCTYL SULPHIDE(Cas 3547-33-9) Usage

Safety Profile

Mildly toxic by ingestion and skincontact. An insect repellent. When heated todecomposition it emits toxic fumes of SOx.

InChI:InChI=1/C20H42O2S/c1-5-7-9-11-13-19(17(3)21)15-23-16-20(18(4)22)14-12-10-8-6-2/h17-22H,5-16H2,1-4H3

3547-33-9 Relevant articles

Catalytic synthesis method for 2-hydroxyethyl n-octyl sulfide

-

Page/Page column 0023-0047, (2019/02/13)

The invention relates to a catalytic syn...

Method for catalyzing n-octylmercaptan and ethylene carbonate to react through organic tertiary amine

-

Paragraph 0024-0027, (2019/04/13)

The invention provides a method for cata...

A mechanism of alkali metal carbonates catalysing the synthesis of β-hydroxyethyl sulfide with mercaptan and ethylene carbonate

Liu, Dongliang,Thomas, Tiju,Gong, Hong,Li, Fei,Li, Qiang,Song, Lijuan,Azhagan, Tamil,Jiang, Heng,Yang, Minghui

, p. 9367 - 9374 (2019/11/13)

The reaction of β-hydroxyethylation is e...

Sulfur makes the difference: Synthesis and mesomorphic properties of novel thioether-functionalized imidazolium ionic liquid crystals

Mansueto, Markus,Kre?, Katharina Christina,Laschat, Sabine

, p. 6258 - 6264 (2015/03/30)

Novel thioether-linked imidazolium ionic...

3547-33-9 Process route

2-(octylthio)acetic acid
7252-60-0

2-(octylthio)acetic acid

3-thiaundecanol
3547-33-9

3-thiaundecanol

Conditions
Conditions Yield
With dimethylsulfide borane complex; In tetrahydrofuran; at 0 - 18 ℃; for 18h;
80%
2-hydroxyethanethiol
60-24-2

2-hydroxyethanethiol

3-thiaundecanol
3547-33-9

3-thiaundecanol

Conditions
Conditions Yield
With caustic alkali; In butan-1-ol; at 120 ℃; for 6h;
96%

3547-33-9 Upstream products

  • 111-88-6
    111-88-6

    Octanethiol

  • 111-66-0
    111-66-0

    oct-1-ene

  • 60-24-2
    60-24-2

    2-hydroxyethanethiol

  • 107-07-3
    107-07-3

    2-chloro-ethanol

3547-33-9 Downstream products

  • 19155-38-5
    19155-38-5

    2-chloroethyl octyl sulfide

  • 3944-72-7
    3944-72-7

    1-octanesulfonic acid

  • 75-21-8
    75-21-8

    oxirane

  • 18915-86-1
    18915-86-1

    β-hydroxy-γphenoxypropyl-(n-octyl)sulfide

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