Your Location:Home >Products >Intermediates >73334-07-3

73334-07-3

  • Product Name:lopromide
  • Molecular Formula:C18H24I3N3O8
  • Purity:99%
  • Molecular Weight:791.117
Get the best price

Product Details

  • CasNo: 73334-07-3
  • Molecular Formula: C18H24I3N3O8
  • Appearance: off-white to white powder
  • Cost-effective and customizable lopromide 73334-07-3 supplier

    • Molecular Formula:C18H24I3N3O8
    • Molecular Weight:791.117
    • Appearance/Colour:off-white to white powder 
    • Vapor Pressure:5E-30mmHg at 25°C 
    • Melting Point:broad (160oC transition) 
    • Refractive Index:1.709 
    • Boiling Point:840.9 °C at 760 mmHg 
    • PKA:10.62±0.70(Predicted) 
    • Flash Point:462.4 °C 
    • PSA:168.66000 
    • Density:2.173 g/cm3 
    • LogP:0.05740 

    Iopromide(Cas 73334-07-3) Usage

    Definition

    ChEBI: A dicarboxylic acid diamide that consists of N-methylisophthalamide bearing three iodo substituents at positions 2, 4 and 6, a methoxyacetyl substituent at position 5 and two 2,3-dihydroxypropyl groups attached to the amide nitrogens. A ater soluble x-ray contrast agent for intravascular administration.

    Brand name

    Ultravist (Berlex).

    General Description

    Iopromide is a low-osmolar,nonionic monomer with 48% bound iodine content. It is indicatedfor use in angiography, excretory urography, andnumerous CT procedures.

    InChI:InChI=1/C18H24I3N3O8/c1-24(4-9(28)6-26)18(31)12-13(19)11(17(30)22-3-8(27)5-25)14(20)16(15(12)21)23-10(29)7-32-2/h8-9,25-28H,3-7H2,1-2H3,(H,22,30)(H,23,29)

    73334-07-3 Relevant articles

    Preparation method and application of iopromide intermediate (by machine translation)

    -

    Paragraph 0102-0104, (2020/07/24)

    The invention relates to a preparation m...

    Preparation method of iopromide

    -

    , (2019/08/01)

    The invention belongs to the technical f...

    Preparation methods of iopromide and intermediate of iopromide

    -

    Paragraph 0105-0107, (2018/03/24)

    The application of the invention relates...

    A method for preparing [...]

    -

    , (2018/12/13)

    The present invention relates to an X-ra...

    73334-07-3 Process route

    5-methoxyacetylamino-2,4,6-triiodoisophthalic acid [(2,3-dihydroxy-N-methylpropyl)-(2,3-diacetoxypropyl)]diamide
    1193076-40-2

    5-methoxyacetylamino-2,4,6-triiodoisophthalic acid [(2,3-dihydroxy-N-methylpropyl)-(2,3-diacetoxypropyl)]diamide

    iopromide
    73334-07-3

    iopromide

    Conditions
    Conditions Yield
    With water; sodium hydroxide; In N,N-dimethyl acetamide; at 20 - 25 ℃; for 10h;
    85%
    With water; sodium hydroxide; at 20 - 25 ℃; for 10h; Industry scale;
    C<sub>26</sub>H<sub>32</sub>I<sub>3</sub>N<sub>3</sub>O<sub>12</sub>

    C26H32I3N3O12

    iopromide
    73334-07-3

    iopromide

    Conditions
    Conditions Yield
    With sodium methylate; In methanol; at 75 ℃; for 8h;
    100%
    C26H32I3N3O12; With sodium hydroxide; at 50 ℃; for 4h;
    With hydrogenchloride; pH=2-3;
    99%

    73334-07-3 Upstream products

    • 40137-22-2
      40137-22-2

      3-methylamino-propane-1,2-diol

    • 7440-44-0
      7440-44-0

      pyrographite

    • 1193076-40-2
      1193076-40-2

      5-methoxyacetylamino-2,4,6-triiodoisophthalic acid [(2,3-dihydroxy-N-methylpropyl)-(2,3-diacetoxypropyl)]diamide

    • 1955-46-0
      1955-46-0

      5-nitro-1,3-benzenedicarboxylic acid, monomethyl ester

    Relevant Products

    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

    Contact Now

    We will contact you as soon as possible


    提交