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METHYL N-OCTYL SULFIDE


  • CasNo 3698-95-1
  • Purity 99%
Inquery

Perfect Factory Offer Excellent quality METHYL N-OCTYL SULFIDE 3698-95-1 with Safe Shipping

  • Molecular Formula: C9H20S
  • Molecular Weight: 160.324
  • Vapor Pressure: 0.194mmHg at 25°C 
  • Melting Point: -47.39°C (estimate) 
  • Refractive Index: 1.454 
  • Boiling Point: 217.6 °C at 760 mmHg 
  • Flash Point: 89.2 °C 
  • PSA: 25.30000 
  • Density: 0.839 g/cm3 
  • LogP: 3.70990 

METHYL N-OCTYL SULFIDE(Cas 3698-95-1) Usage

General Description

Methyl N-octyl sulfide is a chemical compound with the formula C9H20S. It is a colorless to pale yellow liquid with a characteristic odor, and it is commonly used as a flavor and fragrance ingredient. Methyl N-octyl sulfide is found naturally in a variety of foods and beverages, and it is often used to add a garlic-like aroma to products. It is also used in the manufacturing of chemical products and as a solvent for certain types of materials. In addition, it is a potential skin and eye irritant and should be handled with care. Overall, methyl N-octyl sulfide is a versatile compound with a wide range of applications in the food, fragrance, and chemical industries.

InChI:InChI=1/C9H20S/c1-3-4-5-6-7-8-9-10-2/h3-9H2,1-2H3

3698-95-1 Relevant articles

Methyl-transfer reaction to alkylthiol catalyzed by a simple vitamin B 12 model complex using zinc powder

Pan, Ling,Tahara, Keishiro,Masuko, Takahiro,Hisaeda, Yoshio

, p. 194 - 199 (2011)

The catalytic methyl-transfer reaction f...

Electrochemical methyl-transfer reaction to alkylthiol catalyzed by hydrophobic vitamin B12

Pan, Ling,Shimakoshi, Hisashi,Hisaeda, Yoshio

, p. 26 - 27 (2009)

The catalytic methyl-transfer reaction f...

Synthesis of Aryl Methyl Sulfides from Arysulfonyl Chlorides with Dimethyl Carbonate as the Solvent and C1 Source

Miao, Ren-Guan,Qi, Xinxin,Wu, Xiao-Feng

supporting information, p. 5219 - 5221 (2021/10/19)

A new procedure for the synthesis of ary...

Synthesizing process of flutriafol key intermediate 1-(2-fluorophenyl)-1-(4-fluorophenyl)ethylene oxide

-

Paragraph 0013; 0014, (2019/02/25)

The invention discloses a synthesizing p...

Sulfonium salt type chloramine antibacterial agent and synthetic method thereof

-

Paragraph 0038; 0039, (2018/11/22)

The invention belongs to the technical f...

The energy-transfer-enabled biocompatible disulfide–ene reaction

Teders, Michael,Henkel, Christian,Anh?user, Lea,Strieth-Kalthoff, Felix,Gómez-Suárez, Adrián,Kleinmans, Roman,Kahnt, Axel,Rentmeister, Andrea,Guldi, Dirk,Glorius, Frank

, p. 981 - 988 (2018/08/31)

Sulfur-containing molecules participate ...

3698-95-1 Process route

Octanethiol
111-88-6

Octanethiol

methyl iodide
74-88-4

methyl iodide

methyl octyl sulfide
3698-95-1

methyl octyl sulfide

Conditions
Conditions Yield
With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 4h; Cooling with ice;
70%
With sodium hydroxide; In methanol;
methyl n-octylsulfoxide
3079-27-4

methyl n-octylsulfoxide

methyl octyl sulfide
3698-95-1

methyl octyl sulfide

Conditions
Conditions Yield
With aluminum oxide; sodium tetrahydroborate; cobalt(II) chloride hexahydrate; water; In hexane; at 30 ℃; for 3h;
99%
With hydrogen; In 1,4-dioxane; at 100 ℃; for 1h; under 760.051 Torr; chemoselective reaction;
90%
With titanium(IV) iodide; In acetonitrile; at 0 ℃; for 0.166667h;
84%
With dimethylsulfide; trifluoroacetic anhydride; In dichloromethane;
With isopropyl alcohol; In toluene; at 110 ℃; for 1h; chemoselective reaction; Inert atmosphere; Green chemistry;
> 99 %Chromat.

3698-95-1 Upstream products

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    dithiophosphoric acid O ,O '-diethyl ester S -octyl ester

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    sodium methylate

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    n-chlorooctane

3698-95-1 Downstream products

  • 3079-27-4
    3079-27-4

    methyl n-octylsulfoxide

  • 22438-39-7
    22438-39-7

    1-(methylthio)decane

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    126901-39-1

    octyldimethylsulfonium triflate

  • 7560-60-3
    7560-60-3

    methyloctyl sulfone

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