1073-05-8

  • Product Name:propylene sulfate
  • Molecular Formula:C3H6 O4 S
  • Purity:99%
  • Molecular Weight:138.144
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Product Details

  • CasNo: 1073-05-8
  • Molecular Formula: C3H6 O4 S
  • Appearance: White Crystal Powder
  • Cost-effective and customizable propylene sulfate 1073-05-8 factory

    • Molecular Formula:C3H6 O4 S
    • Molecular Weight:138.144
    • Appearance/Colour:White Crystal Powder 
    • Vapor Pressure:0.0589mmHg at 25°C 
    • Melting Point:58-62ºC 
    • Refractive Index:1.5500 (estimate) 
    • Boiling Point:240.4ºC at 760 mmHg 
    • Flash Point:99.2ºC 
    • PSA:60.98000 
    • Density:1.452 g/cm3 
    • LogP:0.74890 

    1,3,2-DIOXATHIANE 2,2-DIOXIDE(Cas 1073-05-8) Usage

    Flammability and Explosibility

    Notclassified

    General Description

    Bacillus sp. CCZU11-1 catalyzed biotransformation of 1,3-propanediol cyclic sulfate (1,3-PDS) and its derivatives has been proposed. It can undergo biocatalyzed transformation to diols by Rhodococcus sp.

    InChI:InChI=1/C3H6O4S/c4-8(5)6-2-1-3-7-8/h1-3H2

    1073-05-8 Relevant articles

    Concentration of hydrophobic organic compounds and extraction of protein using alkylammoniosulfate zwitterionic surfactant mediated phase separations (cloud point extractions)

    Saitoh, Tohru,Hinze, Willie L.

    , p. 2520 - 2525 (1991)

    The zwitterionic surfactants 3-[nonyl- (...

    Preparation method of propylene sulfate

    -

    Paragraph 0056-0077, (2020/06/16)

    The invention discloses a preparation me...

    METHOD OF OXIDIZING USING CALCIUM HYPOCHLORIDE AND MANUFACTURING FOR SULFONE OR SULFIDE

    -

    Paragraph 0111-0114; 0116; 0117; 0131, (2020/06/11)

    Is a process for preparing a sulphone or...

    Sulfate preparation method

    -

    Paragraph 0074; 0075; 0076; 0077, (2018/09/11)

    The invention relates to the field of or...

    Preparation method of cyclic sulfate

    -

    Paragraph 0086; 0087; 0088; 0089; 0090, (2018/03/28)

    The invention relates to the field of or...

    1073-05-8 Process route

    trimethyleneglycol
    504-63-2

    trimethyleneglycol

    1,3,2-dioxathiane 2,2-dioxide
    1073-05-8

    1,3,2-dioxathiane 2,2-dioxide

    Conditions
    Conditions Yield
    trimethyleneglycol; With thionyl chloride; In tetrachloromethane; for 1.5h; Heating;
    With ruthenium trichloride; sodium periodate; In water; acetonitrile; at 20 ℃; for 1.5h; Further stages.;
    87%
    trimethyleneglycol; With sodium methylate; In toluene; for 15h; Reflux;
    With fluorosulfonyl fluoride; In dichloromethane; toluene; at -10 - 0 ℃; for 2h; Autoclave; Inert atmosphere;
    82.7%
    trimethyleneglycol; With fluorosulfonyl fluoride; sodium sulfate; cetyltrimethylammonim bromide; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 5 - 10 ℃; for 1.5h; Inert atmosphere;
    With 15-crown-5; 18-crown-6 ether; Reflux;
    68%
    With ruthenium trichloride; sodium periodate; thionyl chloride; Yield given. Multistep reaction; 1) CCl4, 45 min, reflux, 2) H2O, CCl4, acetonitrile, RT, 2 h;
    With sodium periodate; thionyl chloride; ruthenium trichloride; Yield given. Multistep reaction;
    sulfuric acid mono-(3-hydroxy-propyl) ester

    sulfuric acid mono-(3-hydroxy-propyl) ester

    1,3,2-dioxathiane 2,2-dioxide
    1073-05-8

    1,3,2-dioxathiane 2,2-dioxide

    Conditions
    Conditions Yield
    With modified ZSM-5 molecular sieve catalyst; In toluene; at 105 - 115 ℃; Temperature; Solvent; Reagent/catalyst; Inert atmosphere; Sealed tube;
    92%

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    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

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