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o-Toluene Sulfonamide (OTSA),

  • CAS:88-19-7
  • MF:C7H9NO2S
  • Purity:99%
  • Molecular Weight:171.22
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Product Details

  • CAS: 88-19-7
  • MF: C7H9NO2S
  • Appearance: white to light yellow crystal powder
  • High Quality Chinese Factory supply 88-19-7 o-Toluene Sulfonamide (OTSA),

    • Molecular Formula:C7H9NO2S
    • Molecular Weight:171.22
    • Appearance/Colour:white to light yellow crystal powder 
    • Vapor Pressure:0-0.008Pa at 25℃ 
    • Melting Point:155 °C 
    • Refractive Index:1.6100 (estimate) 
    • Boiling Point:330.2 °C at 760 mmHg 
    • PKA:10.17±0.60(Predicted) 
    • Flash Point:153.5 °C 
    • PSA:68.54000 
    • Density:1.271 g/cm3 
    • LogP:2.42350 

    2-Methylbenzene-1-sulfonamide(Cas 88-19-7) Usage

    Safety Profile

    Suspected carcinogen with experimental tumorigenic data. Mildly toxic by ingestion. Experimental reproductive effects. Mutation data reported. An eye irritant. When heated to decomposition it emits very toxic fumes of NOx and SOx. Used as a chemical intermediate in the production of saccharin.

    Purification Methods

    Crystallise the amide from hot H2O (m 153o), then from EtOH or Et2O/pet ether. The N-o-toluenesulfonylphthalimide has m 182o (from EtOH). [Evans & Dehn J Am Chem Soc 51 3652 1929, Beilstein 11 H 86, 11 I 23, 11 II 39, 11 III 167, 11 IV 229.]

    General Description

    Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. o-Toluenesulfonamide is a major impurity in artificial sweetening substances containing saccharin.

    InChI:InChI=1/C7H9NO2S/c1-6-4-2-3-5-7(6)11(8,9)10/h2-5H,1H3,(H2,8,9,10)

    88-19-7 Relevant articles

    Primary Sulfonamide Synthesis Using the Sulfinylamine Reagent N-Sulfinyl- O-(tert-butyl)hydroxylamine, t-BuONSO

    Davies, Thomas Q.,Hall, Adrian,Skolc, David,Tilby, Michael J.,Willis, Michael C.

    supporting information, p. 9495 - 9499 (2020/12/21)

    Sulfonamides have played a defining role...

    One-pot aerobic oxidative sulfonamidation of aromatic thiols with ammonia by a dual-functional β-MnO2 nanocatalyst

    Hayashi, Eri,Yamaguchi, Yui,Kita, Yusuke,Kamata, Keigo,Hara, Michikazu

    supporting information, p. 2095 - 2098 (2020/02/26)

    High-surface-area β-MnO2 (β-MnO2-HS) nan...

    Rational Design, synthesis and biological evaluation of novel triazole derivatives as potent and selective PRMT5 inhibitors with antitumor activity

    Zhu, Kongkai,Shao, Jingwei,Tao, Hongrui,Yan, Xue,Luo, Cheng,Zhang, Hua,Duan, Wenhu

    , p. 775 - 785 (2019/07/22)

    Protein arginine methyltransferase 5 (PR...

    Sulfonamide compound and synthesis method and application thereof

    -

    Paragraph 0094-0097, (2019/04/02)

    The invention discloses a synthesis meth...

    88-19-7 Process route

    2-methyl-2-(toluene-2-ylsulfonylamino)propionic acid

    2-methyl-2-(toluene-2-ylsulfonylamino)propionic acid

    methyl 2-(aminosulfonyl)benzoate
    88-19-7

    methyl 2-(aminosulfonyl)benzoate

    Conditions
    Conditions Yield
    With oxygen; copper(II) oxide; In dimethyl sulfoxide; at 100 ℃; for 8h;
    93%
    2-methylphenyl diazonium tetrafluoroborate
    2093-46-1

    2-methylphenyl diazonium tetrafluoroborate

    methyl 2-(aminosulfonyl)benzoate
    88-19-7

    methyl 2-(aminosulfonyl)benzoate

    Conditions
    Conditions Yield
    With sodium metabisulfite; sodium azide; tetrabutylammomium bromide; triphenylphosphine; In water; acetonitrile; at 80 ℃; for 12h; Inert atmosphere;
    70%
    With sodium metabisulfite; sodium azide; tetrabutylammomium bromide; triphenylphosphine; In water; acetonitrile; at 80 ℃; for 12h; Inert atmosphere; Schlenk technique;
    70%

    88-19-7 Upstream products

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      2-methylbenzenesulfonyl isocyanate

    88-19-7 Downstream products

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    • 24535-66-8
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      N-butyl-N'-(o-tolylsulfonyl)urea

    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

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