461642-78-4

  • Product Name:2-(Dodecylsulfanylthiocarbonylsulfanyl)-2-Methylpropionic Acid
  • MF:C17H32O2S3
  • Purity:99%
  • Molecular Weight:364.638
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Product Details

Buy high quality and low price 2-(Dodecylsulfanylthiocarbonylsulfanyl)-2-Methylpropionic Acid 461642-78-4 now

  • Molecular Formula:C17H32O2S3
  • Molecular Weight:364.638
  • Appearance/Colour:pale yellow solid 
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:62-64℃ (hexane ) 
  • Boiling Point:505.984°C at 760 mmHg 
  • PKA:2.89±0.10(Predicted) 
  • Flash Point:259.81°C 
  • PSA:119.99000 
  • Density:1.083g/cm3 
  • LogP:6.52180 

2-(DODECYLSULFANYLTHIOCARBONYLSULFANYL)-2-METHYLPROPIONIC ACID(Cas 461642-78-4) Usage

General Description

Need help choosing the correct RAFT Agent? Please consult the RAFT Agent to Monomer compatibility table.

Industrial uses

The trithiocarbonates have a structure that contains three sulfur atoms. All three sulfur atoms can participate in bonding to the mineral surfaces. Philips Petroleum Company did most of the development of this class of collectors. Monoalkyl trithiocarbonate (Orfom 800 series) is used as a collector in flotation of copper and copper–lead ores.

InChI:InChI=1/C17H32O2S3/c1-4-5-6-7-8-9-10-11-12-13-14-21-16(20)22-17(2,3)15(18)19/h4-14H2,1-3H3,(H,18,19)

461642-78-4 Relevant articles

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Preparation of thermoresponsive polymers bearing amino acid diamide derivatives via RAFT polymerization

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Nanocrystalline cellulose grafted random copolymers of N- isopropylacrylamide and acrylic acid synthesized by RAFT polymerization: Effect of different acrylic acid contents on LCST behavior

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Isothermal LCST transitions triggered by bioreduction of single polymer end-groups

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METHOD FOR PRODUCING A GRAFTED RUBBER AND TIRE COMPRISING THE GRAFTED RUBBER

-

Page/Page column 7, (2020/01/24)

The present invention relates to a metho...

461642-78-4 Process route

carbon disulfide
75-15-0,12122-00-8

carbon disulfide

chloroform
67-66-3,8013-54-5

chloroform

acetone
67-64-1

acetone

1-dodecylthiol
112-55-0

1-dodecylthiol

2-dodecylsulfanylthiocarbonylsulfanyl-2-methyl-propionic acid
461642-78-4

2-dodecylsulfanylthiocarbonylsulfanyl-2-methyl-propionic acid

Conditions
Conditions Yield
carbon disulfide; acetone; 1-dodecylthiol; With sodium hydroxide; Aliquat 336; trimethyloctadecylammonium chloride; In water; for 0.333333h;
chloroform; With sodium hydroxide; In water; at 15 - 20 ℃;
With hydrogenchloride; In water;
85%
1-dodecylthiol; With Aliquat 336; sodium hydroxide; In water; acetone; at 10 ℃; for 0.666667h; Inert atmosphere;
carbon disulfide; acetone; In water; at 10 ℃; for 0.5h; Inert atmosphere;
chloroform; Further stages;
85%
1-dodecylthiol; With sodium hydroxide; In acetone; at 20 ℃; for 0.5h;
carbon disulfide; acetone; In acetone; at 20 ℃; for 0.166667h;
chloroform; With sodium hydroxide; at 20 - 25 ℃;
48%
1-dodecylthiol; With tetrabutylammomium bromide; sodium hydroxide; In water; acetone; at 10 ℃; for 0.583333h; Inert atmosphere;
carbon disulfide; In acetone; for 0.5h;
chloroform; acetone; Further stages;
1-dodecylthiol; With sodium hydroxide; In water; acetone; at 10 ℃; for 0.5h;
carbon disulfide; In water; acetone; for 0.5h;
chloroform; acetone; With sodium hydroxide; In water;
55.2 g
acetone; 1-dodecylthiol; With Aliquat 336; sodium hydroxide; at 10 ℃; for 0.583333h; Inert atmosphere;
carbon disulfide; for 0.5h; Inert atmosphere;
chloroform; Inert atmosphere;
carbon disulfide
75-15-0,12122-00-8

carbon disulfide

2-bromo-2-methylpropionic acid
2052-01-9

2-bromo-2-methylpropionic acid

1-dodecylthiol
112-55-0

1-dodecylthiol

2-dodecylsulfanylthiocarbonylsulfanyl-2-methyl-propionic acid
461642-78-4

2-dodecylsulfanylthiocarbonylsulfanyl-2-methyl-propionic acid

Conditions
Conditions Yield
carbon disulfide; 1-dodecylthiol; With potassium phosphate; In acetone; for 0.666667h;
2-bromo-2-methylpropionic acid; In acetone; at 20 ℃;
65%
1-dodecylthiol; With potassium phosphate; In acetone;
carbon disulfide; In acetone; at 0 ℃;
2-bromo-2-methylpropionic acid; In acetone; at 20 ℃; for 24h;
60%
1-dodecylthiol; With sodium hydroxide; In water; acetone; at 10 ℃; for 0.166667h;
carbon disulfide; In water; acetone; for 0.166667h;
2-bromo-2-methylpropionic acid; In water; acetone; at 20 ℃; for 24h;
47.3%
1-dodecylthiol; With potassium phosphate; In acetone; for 0.166667h;
carbon disulfide; In acetone; for 0.166667h;
2-bromo-2-methylpropionic acid; In acetone; at 20 ℃; for 13h; Inert atmosphere;
43%
1-dodecylthiol; With potassium phosphate; In acetone; for 0.166667h;
carbon disulfide; In acetone; for 0.5h;
2-bromo-2-methylpropionic acid; at 20 ℃; for 14h;
37%
carbon disulfide; 1-dodecylthiol; With potassium phosphate; In acetone; at 0 ℃; for 0.166667h;
2-bromo-2-methylpropionic acid; In acetone; at 20 ℃;
35.8%
carbon disulfide; 1-dodecylthiol; With potassium hydroxide; In water; acetone; at 20 ℃; for 3h; Cooling with ice;
2-bromo-2-methylpropionic acid; In water; acetone;
33%
1-dodecylthiol; With potassium phosphate; In acetone; for 0.5h;
carbon disulfide; In acetone; for 0.333333h;
2-bromo-2-methylpropionic acid; In acetone; for 21h;
32.4%
With potassium phosphate; In acetone; at 20 ℃; for 20h;
1-dodecylthiol; With potassium phosphate; In acetone; at 20 ℃;
carbon disulfide; In acetone; at 20 ℃;
2-bromo-2-methylpropionic acid; In acetone; at 20 ℃; for 24h;

461642-78-4 Upstream products

  • 75-15-0
    75-15-0

    carbon disulfide

  • 67-66-3
    67-66-3

    chloroform

  • 67-64-1
    67-64-1

    acetone

  • 112-55-0
    112-55-0

    1-dodecylthiol

461642-78-4 Downstream products

  • 1174764-26-1
    1174764-26-1

    S-dodecyl-S'-(α,α-dimethylpentafluorophenyl acetate)trithiocarbonate

  • 1204502-18-0
    1204502-18-0

    C31H48O7S3

  • 1292766-77-8
    1292766-77-8

    C35H45O2PS3

  • 1334532-10-3
    1334532-10-3

    2-(dodecylthiocarbonothioylthio)-2-methylpropanoic acid 2-phenoxyethyl ester