| Identification | Back Directory | [Name]
IOXAGLIC ACID (100 MG) | [CAS]
59017-64-0 | [Synonyms]
p286
D01761
Ioxaglic
hexabrix160
ioxaglicacid
Hexabrix 320
Hexabrix 320 (tn)
Ioxaglic acid CRS
IOXAGLIC ACID (100 MG)
P-286(contrast medium)
Ioxaglic Acid (1345159)
Ioxaglic acid (jan/usp/inn)
Ioxaglic acid, isomer mixture
IOXAGLIC ACID (100 MG) USP/EP/BP
Fosfomycin Trometamol Impurity 28
Ioxaglic acid, isomer mixture in water
benzoicacid,3-((((3-(acetylmethylamino)-2,4,6-triiodo-5-((methylamino)carbony
benzoicacid,3-[[[[3-(acetylmethylamino)-2,4,6-triiodo-5-[(methylamino)carbony
l)benzoyl)amino)acetyl)amino)-5-(((2-hydroxyethyl)amino)carbonyl)-2,4,6-triiod
l]benzoyl]amino]acetyl]amino]-5-[[(2-hydroxyethyl)amino]carbonyl]-2,4,6-triiodo
N-(2-Hydroxyethyl)-2,4,6-triiodo-5-{2-[2,4,6-triiodo-3-(N-methylacetamido)-5-(methylcarbamoyl)benzamido]acetamido}isophthalamic acid
3-((2-hydroxyethyl)carbamoyl)-2,4,6-triiodo-5-(2-(2,4,6-triiodo-3-(N-methylacetamido)-5-(methylcarbamoyl)benzamido)acetamido)benzoic acid
N-(2-Hydroxyethyl)-2,4,6-triiodo-5-[2-[2,4,6-triiodo-3-(N-methylacetylamino)-5-(methylcarbamoyl)benzoylamino]acetylamino]isophthalamic acid
Benzoic acid, 3-[[2-[[3-(acetylmethylamino)-2,4,6-triiodo-5-[(methylamino)carbonyl]benzoyl]amino]acetyl]amino]-5-[[(2-hydroxyethyl)amino]carbonyl]-2,4,6-triiodo-
Benzoic acid, 3-[[[[3-(acetylmethylamino) -2,4,6-triiodo-5-[(methylamino)carbonyl]benzoyl ]amino]acetyl]amino]-5-[[(2-hydroxyethyl)amino]carbony l]-2,4,6-triiodo-
Ioxaglic AcidQ: What is
Ioxaglic Acid Q: What is the CAS Number of
Ioxaglic Acid Q: What is the storage condition of
Ioxaglic Acid Q: What are the applications of
Ioxaglic Acid | [EINECS(EC#)]
261-560-1 | [Molecular Formula]
C24H21I6N5O8 | [MDL Number]
MFCD00867945 | [MOL File]
59017-64-0.mol | [Molecular Weight]
1268.86 |
| Hazard Information | Back Directory | [Chemical Properties]
White or almost white, hygroscopic powder. | [Uses]
Diagnostic aid(radiopaque medium). | [Definition]
ChEBI: A benzenedicarboxamide compound having N-substituted carbamoyl groups at the 1and 3-positions, iodo substituents at the 2-, 4and 6-positions and an acetyl(methyl)amino group at the 5-position. |
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