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4-iodophthalic acid

Product Name
4-iodophthalic acid
CAS No.
6301-60-6
Chemical Name
4-iodophthalic acid
Synonyms
Einecs 228-594-9;4-iodophthalic acid;1,2-BENZENEDICARBOXYLIC ACID,4-IODO;4-Iodo-1,2-benzenedicarboxylic acid
CBNumber
CB4937698
Molecular Formula
C8H5IO4
Formula Weight
292.03
MOL File
6301-60-6.mol
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4-iodophthalic acid Property

Melting point:
180-184 °C
Boiling point:
431.1±40.0 °C(Predicted)
Density 
2.138±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
2.90±0.10(Predicted)
Appearance
White to off-white Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Activate Scientific
Product number
AS110541
Product name
4-Iodophthalic acid
Purity
97%
Packaging
1g
Price
$67
Updated
2026/06/04
Activate Scientific
Product number
AS110541
Product name
4-Iodophthalic acid
Purity
97%
Packaging
5g
Price
$188
Updated
2026/06/04
Synthonix
Product number
K47827
Product name
4-Iodophthalic acid
Purity
97%
Packaging
100mg
Price
$17
Updated
2026/05/06
Synthonix
Product number
K47827
Product name
4-Iodophthalic acid
Purity
97%
Packaging
250mg
Price
$23
Updated
2026/05/06
Synthonix
Product number
K47827
Product name
4-Iodophthalic acid
Purity
97%
Packaging
1g
Price
$40
Updated
2026/05/06
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4-iodophthalic acid Chemical Properties,Usage,Production

Synthesis Reference(s)

The Journal of Organic Chemistry, 16, p. 1275, 1951 DOI: 10.1021/jo50002a014

Synthesis

31599-61-8

6301-60-6

The general procedure for the synthesis of 4-iodophthalic acid from 3,4-dimethyl iodobenzene was as follows: 3,4-dimethyl iodobenzene (31 mL, 0.22 mol) was co-dissolved with pyridine (125 mL) in water (375 mL), and potassium permanganate (205 g, 1.3 mol) was slowly added at 60°C and reacted for 16 h under continuous stirring. After completion of the reaction, the temperature was maintained at 60°C and the filtrate was filtered through diatomaceous earth to remove solid impurities. After cooling the filtrate to room temperature, it was acidified by adjusting the pH to 2 with 6N hydrochloric acid and subsequently extracted with ethyl acetate. After purification by column chromatography, the target product 4-iodophthalic acid (44 g, 69% yield) was concentrated.

References

[1] Patent: KR2015/60183, 2015, A. Location in patent: Paragraph 0101; 0102; 0103
[2] European Journal of Organic Chemistry, 2015, vol. 2015, # 27, p. 5919 - 5924

4-iodophthalic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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4-iodophthalic acid Suppliers

Nanjing Norris-Pharm Technology Co., Ltd
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18652989687
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+86-25-52131256
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sales@norris-pharm.com
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China
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Zhengzhou TRIZ Pharmaceutical Technology Co., Ltd.
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19943855286
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0371-53392065
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triz-4@trizpharma.cn
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China
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1936
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Cool Pharm, Ltd
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50966098
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Shanghai YuanYe Biotechnology Co., Ltd.
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021-61312847; 18021002903
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Amadis Chemical Company Limited
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Aikon International Limited
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Henan's chemical products co., LTD
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6301-60-6, 4-iodophthalic acid Related Search:


  • 4-iodophthalic acid
  • Einecs 228-594-9
  • 4-Iodo-1,2-benzenedicarboxylic acid
  • 1,2-BENZENEDICARBOXYLIC ACID,4-IODO
  • 6301-60-6