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Catalog Number:
31960
CAS Number:
35453-19-1
Ácido 5-amino-2,4,6-triyodoisoftálico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido 5-amino-2,4,6-triyodobenceno-1,3-dicarboxílico
Documents
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Tamaño
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Product Information

Mantener el envase bien cerrado en un lugar seco y bien ventilado.

Synonyms
Ácido 5-amino-2,4,6-triyodobenceno-1,3-dicarboxílico
CAS Number
35453-19-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C8H4I3NO4
Molecular Weight
558.84
MDL Number
MFCD00190167
PubChem ID
3015783
Melting Point
265 - 270 ?C
Appearance
Polvo de color marrón ligeramente amarillento o blanco.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 5-amino-2,4,6-triyodobenceno-1,3-dicarboxílico
CAS Number
35453-19-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C8H4I3NO4
Molecular Weight
558.84
MDL Number
MFCD00190167
PubChem ID
3015783
Melting Point
265 - 270 ?C
Appearance
Polvo de color marrón ligeramente amarillento o blanco.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Amino-2,4,6-triiodoisophthalic acid is widely utilized in research focused on:

  • Medical Imaging: This compound is used as a contrast agent in various imaging techniques, particularly in enhancing the visibility of tissues during X-ray and CT scans, improving diagnostic accuracy.
  • Radiopharmaceuticals: It plays a crucial role in the development of radiopharmaceuticals for targeted cancer therapies, allowing for precise delivery of radioactive isotopes to tumor sites.
  • Polymer Chemistry: The compound is employed in synthesizing specialized polymers that exhibit unique properties, such as increased thermal stability and enhanced mechanical strength, beneficial for various industrial applications.
  • Environmental Monitoring: It is used in the detection and quantification of iodine in environmental samples, aiding in pollution control and ensuring compliance with safety regulations.
  • Research in Biochemistry: The compound serves as a valuable tool in biochemical assays, helping researchers study enzyme activities and interactions due to its reactive functional groups.

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