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Iodopanoic acid

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Origin: China

Cas No: 96-83-3

Specification: 99%min

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  • Products Specification
  • Product Description
  • Property

    CAS No.: 96-83-3 Formula: C11H12I3NO2 Molecular Weight: 570.93200

    Description

    Iodopanoic Acid is an iodine-containing radiocontrast medium used in cholecystography. Iodopanoic Acid is a potent inhibitor of thyroid hormone release from thyroid gland.

    Basic Info

    Chemical Name Iodopanoic acid
    Synonyms

    Copanoic;
    Cistobil;
    Telepaque;
    Benzenepropanoic acid, 3-amino-alpha-ethyl-2,4,6-triiodo-;
    2-Ethyl-3-(3-amino-2,4,6-triiodophenyl)propionic acid;
    Colepax;
    Benzenepropanoic acid, 3-amino-α-ethyl-2,4,6-triiodo-;
    Polognost;
    α-Ethyl-β-(3-amino-2,4,6-triiodophenyl)propionic acid;
    Cholevid;
    Iodopanic acid;
    Bilijodon;
    2-(3-Amino-2,4,6-triiodobenzyl)butyric acid;
    Iopagnost;
    Jopagnost;
    3-Amino-α-ethyl-2,4,6-triiodobenzenepropanoic acid;
    Iodopanoic acid;
    2-[(5-Amino-2,4,6-triiodophenyl)methyl]butanoic acid;
    NSC 41706;
    3-Amino-α-ethyl-2,4,6-triiodohydrocinnamic acid;
    Hydrocinnamic acid, 3-amino-α-ethyl-2,4,6-triiodo-;
    Choladine;
    3-(3-Amino-2,4,6-triiodophenyl)-2-ethylpropionic acid;
    Jopanoic acid;
    2-[(3-amino-2,4,6-triiodophenyl)methyl]butanoic acid;
    3-(3-Amino-2,4,6-triiodophenyl)-2-ethylpropanoic acid;
    Iopanoicum;

    CAS No. 96-83-3
    Molecular Formula C11H12I3NO2
    Molecular Weight 570.93200
    PSA 63.32000
    LogP 4.31710

    Properties

    Density 2.426g/cm3
    Boiling Point 529.1ºC at 760mmHg
    Melting Point 153ºC
    Flash Point 273.8ºC
    Refractive Index 1.732
    Storage Condition Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition sources and untrained individuals. Secure and label area. Protect containers/cylinders from physical damage.

    Safety Info

    RTECS NW5075000
    Safety Statements S22; S26; S36/37/39
    HS Code 2922499990
    Risk Statements R20/21/22

    Synthesis Route

    2-[(3-aminophenyl)methyl]butanoic acidIodopanoic acid
    Cinnamic acid, .α.-ethyl-m-nitro-, (E)-Iodopanoic acid

    Precursor

    2-[(3-aminophenyl)methyl]butanoic acid
    Cinnamic acid, .α.-ethyl-m-nitro-, (E)-

    Downstream Product

    ethyl 2-[(3-amino-2,4,6-triiodophenyl)methyl]butanoate

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