Iopamidol - ≥98% , CAS No.62883-00-5

CAS: 62883-00-5 Cat. No.: I304202 Molecular Weight: 777.09
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
Bracco 15000|60208-45-9|62883-00-5|D-Iopamidol|N1,N3-Bis(1,3-dihydroxypropan-2-yl)-5-(2-hydroxypropanamido)-2,4,6-triiodoisophthalamide|1-N,3-N-bis(1,3-dihydroxypropan-2-yl)-5-(2-hydroxypropanoylamino)-2,4,6-triiodobenzene-1,3-dicarboxamide|1-N,3-N-bis(1,
Storage
Room temperature,Desiccated
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
250mg
I304202-250mg
2
$9.90
1g
I304202-1g
2
$27.90
5g
I304202-5g
4
$103.90
25g
I304202-25g
5
$246.90
100g
I304202-100g
3
$664.90
500g
I304202-500g
1
$1,218.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Desiccated Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
Bracco 15000 | 60208-45-9 | 62883-00-5 | D-Iopamidol | N1, N3-Bis(1, 3-dihydroxypropan-2-yl)-5-(2-hydroxypropanamido)-2, 4, 6-triiodoisophthalamide | 1-N, 3-N-bis(1, 3-dihydroxypropan-2-yl)-5-(2-hydroxypropanoylamino)-2, 4, 6-triiodobenzene-1, 3-dicarboxamide | 1-N, 3-N-bis(1,
Specifications & Purity
≥98%
Storage
Room temperature, Desiccated
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid488179786
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179786
Canonical SmilesCC(C(=O)NC1=C(C(=C(C(=C1I)C(=O)NC(CO)CO)I)C(=O)NC(CO)CO)I)O
IUPAC Name1-N,3-N-bis(1,3-dihydroxypropan-2-yl)-5-(2-hydroxypropanoylamino)-2,4,6-triiodobenzene-1,3-dicarboxamide
InChIKeyXQZXYNRDCRIARQ-UHFFFAOYSA-N
INCHI1S/C17H22I3N3O8/c1-6(28)15(29)23-14-12(19)9(16(30)21-7(2-24)3-25)11(18)10(13(14)20)17(31)22-8(4-26)5-27/h6-8,24-28H,2-5H2,1H3,(H,21,30)(H,22,31)(H,23,29)
Isomeric SMILES CC(C(=O)NC1=C(C(=C(C(=C1I)C(=O)NC(CO)CO)I)C(=O)NC(CO)CO)I)O
Molecular Weight 777.09
Reaxy-Rn 6773333
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6773333&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentAcylaminobenzoic acid and derivatives
Alternative Parents 2-halobenzoic acids and derivatives  4-halobenzoic acids and derivatives  Anilides  Benzamides  Benzoyl derivatives  N-arylamides  Iodobenzenes  Aryl iodides  Vinylogous halides  Secondary alcohols  Secondary carboxylic acid amides  Organoiodides  Hydrocarbon derivatives  Carbonyl compounds  Organopnictogen compounds  Primary alcohols  Organic oxides  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Acylaminobenzoic acid or derivatives - Halobenzoic acid or derivatives - 4-halobenzoic acid or derivatives - 2-halobenzoic acid or derivatives - Benzamide - Anilide - Benzoyl - N-arylamide - Halobenzene - Iodobenzene - Aryl halide - Aryl iodide - Vinylogous halide - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Organonitrogen compound - Organoiodide - Organohalogen compound - Hydrocarbon derivative - Alcohol - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Primary alcohol - Organic nitrogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDateItem
G2305137Certificate of AnalysisApr 03, 2026 I304202
I2116273Certificate of AnalysisJul 12, 2024 I304202
I2116274Certificate of AnalysisJul 12, 2024 I304202
I2116275Certificate of AnalysisJul 12, 2024 I304202
I2116276Certificate of AnalysisJul 12, 2024 I304202
I2116277Certificate of AnalysisJul 12, 2024 I304202
I2116278Certificate of AnalysisJul 12, 2024 I304202
Chemical and Physical Properties
Flash Point(°C)428.8ºC
Boil Point(°C)785.3ºC
Molecular Weight777.100 g/mol
XLogP3-2.400
Hydrogen Bond Donor Count8
Hydrogen Bond Acceptor Count8
Rotatable Bond Count10
Exact Mass776.854 Da
Monoisotopic Mass776.854 Da
Topological Polar Surface Area188.000 Ų
Heavy Atom Count31
Formal Charge0
Complexity583.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Yurong Gu, Zi Song, Zijun Dong, Feiyun Sun, Chengchun Jiang, Jikun Qi.  (2022)  Efficient degradation and deiodination of iopamidol by UV/sulfite process: Assessment of typical process parameters and transformation paths.  ENVIRONMENT INTERNATIONAL,      [PMID:35952467] [10.1016/j.envint.2022.107383]
2. Jingdong Yang, Yu Li, Zequn Yang, Kaimin Shih, Guang-Guo Ying, Yong Feng.  (2022)  Activation of ozone by peroxymonosulfate for selective degradation of 1,4-dioxane: Limited water matrices effects.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:35739743] [10.1016/j.jhazmat.2022.129223]
3. Shuwei Xiao, Pengchao Wang, Jian Zhao, Zhengyun Ling, Ziyan An, Zhouyang Fu, Weijun Fu, Xu Zhang.  (2021)  Bi-layer silk fibroin skeleton and bladder acellular matrix hydrogel encapsulating adipose-derived stem cells for bladder reconstruction.  Biomaterials Science,  (18): (6169-6182).  [PMID:34346416] [10.1039/D1BM00761K]
4. Chaoqun Tan, Yuhao Guo, Wangqi Yu, Ming Chen, Lianghu Su, Dongsheng Wang.  (2025)  Alkaline regeneration of activated carbon in biological activated carbon filter from drinking water treatment:Adsorption of micropollutant.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2025.118035]
5. Qiang Tan, Zhonglin Chen, Jimin Shen, Pengwei Yan, Jing Kang, Binyuan Wang, Shengxin Zhao, Yang Shen, Yabin Li.  (2025)  In situ construction of ZnFe-layered double oxides on biochar for improving interfacial adsorption-catalysis of ozone achieves efficient water purification.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.135358]
6. Wang Xuesheng, Zhang Fan, Zhou Zhonghan, Fu Qiang, Liao Limin.  (2025)  Comparative study of bladder augmentation using different biomimetic scaffolds: electrospun nanofiber vs. extracellular matrix scaffold with adipose-derived stem cells.  International Journal of Surgery,      [PMID:40788005] [10.1097/JS9.0000000000003152]
7. Jianping Tao, Qiang Wang, Congcong Yang, Lunjie Zhao, Jianyou Xia, Chen Zhang, Fanyang Zhou, Renxi Zhu, Qiang Li, Dong Zhuo, Yujie Xu, Zhenxing Zhang.  (2025)  Magnesium Oxide Nanoparticle-Incorporated Electrospun Nanofiber Scaffolds for Bladder Repair.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.5c04621]
Solution Calculators
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