3-IODOPHTHALIC ACID

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Company Name: Hebei Yanxi Chemical Co., Ltd.
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CAS:6937-34-4
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Company Name: Hebei Chuanghai Biotechnology Co., Ltd
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Products Intro: Product Name:3-IODOPHTHALIC ACID
CAS:6937-34-4
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Company Name: Hefei Lbao Physical & Chemical Science Co.,Ltd
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Products Intro: Product Name:3-iodophthalic acid
CAS:6937-34-4
Purity:98% Package:1kg;
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Products Intro: Product Name:3-Iodophthalic acid
CAS:6937-34-4
Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:3-Iodophthalic acid
CAS:6937-34-4
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg

3-IODOPHTHALIC ACID manufacturers

  • 3-IODOPHTHALIC ACID
  • 3-IODOPHTHALIC ACID pictures
  • $25.00
  • 2025-06-20
  • CAS:6937-34-4
  • Min. Order: 1kg
  • Purity: 0.99
  • Supply Ability: 10 tons
3-IODOPHTHALIC ACID Basic information
Product Name:3-IODOPHTHALIC ACID
Synonyms:3-IODOPHTHALIC ACID;3-Iodobenzene-1,2-dicarboxylic acid;3-Iodo-1,2-benzenedicarboxylic acid;NSC 42518;3-Iodophthaltc acid;3-Lodophthalic acid;3-Iodophthalic acid 95%;1,2-Benzenedicarboxylic acid, 3-iodo-
CAS:6937-34-4
MF:C8H5IO4
MW:292.03
EINECS:638-780-5
Product Categories:Carboxylic Acids;Pyrazines, Pyrimidines & Pyridazines;Carboxylic Acids;Phenyls & Phenyl-Het;Pyrazines, Pyrimidines & Pyridazines
Mol File:6937-34-4.mol
3-IODOPHTHALIC ACID Structure
3-IODOPHTHALIC ACID Chemical Properties
Melting point 200-204 °C
Boiling point 426.3±40.0 °C(Predicted)
density 2.138±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka1.91±0.10(Predicted)
AppearanceOff-white to yellow Solid
Safety Information
Hazard Codes Xi
Hazard Note Irritant
HS Code 2917399590
MSDS Information
3-IODOPHTHALIC ACID Usage And Synthesis
UsesThe study of the interaction of uranyl ion with 3-Iodophthalic Acid by Calvin-Bjerrum titration technique.
Synthesis
3-AMINOPHTHALIC ACID

5434-20-8

3-IODOPHTHALIC ACID

6937-34-4

3-Aminophthalic acid (5.00 g, 27.6 mmol) was used as raw material and dissolved in 8.4 mol/L hydrochloric acid (60 mL). Under the cooling condition of an ice bath, aqueous sodium nitrate solution (10 mL containing 2.0 g, 29 mmol) was slowly added dropwise and the reaction was kept for 20 minutes. Subsequently, stirring was continued at the same temperature for 3 hours. Next, an aqueous solution (10 mL) of potassium iodide (6.9 g, 41 mmol) and urea (291 mg) pre-dissolved in potassium iodide (6.9 g, 41 mmol) and urea (291 mg) was added dropwise to the reaction mixture and transferred to room temperature and stirred for 20 hours. Upon completion of the reaction, the mixture was quenched by adding 10% aqueous sodium thiosulfate solution to the mixture and the product was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure and the residue was washed with chloroform to give the final 3-iodophthalic acid (5.0 g, 62% yield).

References[1] Patent: EP2108642, 2009, A1. Location in patent: Page/Page column 110
[2] Journal fuer Praktische Chemie (Leipzig), 1896, vol. <2> 53, p. 383
[3] Journal of the Chemical Society, 1914, vol. 105, p. 2480
[4] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 22, p. 6366 - 6379
3-IODOPHTHALIC ACID Preparation Products And Raw materials
Raw materials3-AMINOPHTHALIC ACID-->DIMETHYL 3-IODOPHTHALATE-->Urea-->Hydrochloric acid-->Potassium iodide-->Sodium nitrate
Tag:3-IODOPHTHALIC ACID(6937-34-4) Related Product Information
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