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MedKoo Cat#: 535041 | Name: Iomorinic acid

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Iomorinic acid is a bioactive chemical.

Chemical Structure

Iomorinic acid
Iomorinic acid
CAS#51934-76-0

Theoretical Analysis

MedKoo Cat#: 535041

Name: Iomorinic acid

CAS#: 51934-76-0

Chemical Formula: C17H20I3N3O4

Exact Mass: 710.8588

Molecular Weight: 711.08

Elemental Analysis: C, 28.72; H, 2.84; I, 53.54; N, 5.91; O, 9.00

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Iomorinic acid
IUPAC/Chemical Name
2-Methyl-N-(2,4,6-triiodo-3-((1-morpholinoethylidene)amino)benzoyl)-beta-alanine
InChi Key
APLUDQKQBHQBHR-LSHDLFTRSA-N
InChi Code
InChI=1S/C17H20I3N3O4/c1-9(7-13(24)25)21-17(26)14-11(18)8-12(19)16(15(14)20)22-10(2)23-3-5-27-6-4-23/h8-9H,3-7H2,1-2H3,(H,21,26)(H,24,25)/b22-10+
SMILES Code
O=C(O)CC(C)NC(C1=C(I)C=C(I)C(/N=C(N2CCOCC2)\C)=C1I)=O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 711.08 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Singhvi M, Zendo T, Sonomoto K. Free lactic acid production under acidic conditions by lactic acid bacteria strains: challenges and future prospects. Appl Microbiol Biotechnol. 2018 Jul;102(14):5911-5924. doi: 10.1007/s00253-018-9092-4. Epub 2018 May 26. PMID: 29804138. 2: Hao X, Chen B, An T. [Pathway modification of industrial microorganisms to improve acid-stress tolerance]. Sheng Wu Gong Cheng Xue Bao. 2015 Aug;31(8):1151-61. Chinese. PMID: 26762037. 3: Luo Q , Zhan W , Boom RM , Janssen AEM . Interactions between acid and proteins under in vitro gastric condition - a theoretical and experimental quantification. Food Funct. 2018 Oct 17;9(10):5283-5289. doi: 10.1039/c8fo01033a. PMID: 30250956. 4: Kim SJ, Baek JH, Koh JS, Bae MI, Lee SJ, Shin MK. The effect of physically applied alpha hydroxyl acids on the skin pore and comedone. Int J Cosmet Sci. 2015 Oct;37(5):519-25. doi: 10.1111/ics.12244. Epub 2015 Jun 26. PMID: 26032934. 5: Naseeruddin S, Desai S, Venkateswar Rao L. Selection of suitable mineral acid and its concentration for biphasic dilute acid hydrolysis of the sodium dithionite delignified Prosopis juliflora to hydrolyze maximum holocellulose. Bioresour Technol. 2016 Feb;202:231-7. doi: 10.1016/j.biortech.2015.12.025. Epub 2015 Dec 14. PMID: 26716889. 6: Rabbani KA, Charles W, Kayaalp A, Cord-Ruwisch R, Ho G. Biofilter for generation of concentrated sulphuric acid from H2S. Environ Sci Pollut Res Int. 2016 Aug;23(16):16781-9. doi: 10.1007/s11356-016-6858-z. Epub 2016 May 18. PMID: 27189453. 7: Shelor CP, Dasgupta PK. Automated programmable pressurized carbonic acid eluent ion exclusion chromatography of organic acids. J Chromatogr A. 2017 Nov 10;1523:300-308. doi: 10.1016/j.chroma.2017.05.036. Epub 2017 May 16. PMID: 28549716. 8: Sai M, Yamamoto H. Chiral Brønsted Acid as a True Catalyst: Asymmetric Mukaiyama Aldol and Hosomi-Sakurai Allylation Reactions. J Am Chem Soc. 2015 Jun 10;137(22):7091-4. doi: 10.1021/jacs.5b04168. Epub 2015 May 27. PMID: 26017677. 9: Ono M, Oda S, Yasuda S, Mineno T, Okawa M, Kinjo J, Miyashita H, Yoshimitsu H, Nohara T, Miyahara K. Acylated Glycosidic Acid Methyl Esters Generated from the Convolvulin Fraction of Rhizoma Jalapae Braziliensis by Treatment with Indium(III) Chloride in Methanol. Chem Pharm Bull (Tokyo). 2017;65(1):107-111. doi: 10.1248/cpb.c16-00673. PMID: 28049906. 10: Palma M, Sá-Correia I. Physiological Genomics of the Highly Weak-Acid- Tolerant Food Spoilage Yeasts of Zygosaccharomyces bailii sensu lato. Prog Mol Subcell Biol. 2019;58:85-109. doi: 10.1007/978-3-030-13035-0_4. PMID: 30911890. 11: Yanai H. Chemistry of Fluorinated Carbon Acids: Synthesis, Physicochemical Properties, and Catalysis. Chem Pharm Bull (Tokyo). 2015;63(9):649-62. doi: 10.1248/cpb.c15-00487. PMID: 26329858. 12: Fukuda Y, Kataoka Y, Sano Y, Takizawa K, Watanabe T, Teshima R. [Development and Applicability of Analytical Methods for Quantifying Cyanide and Bromic Acid in Mineral Waters]. Shokuhin Eiseigaku Zasshi. 2015;56(6):256-62. Japanese. doi: 10.3358/shokueishi.56.256. PMID: 26699274. 13: Toda Y, Pink M, Johnston JN. Brønsted acid catalyzed phosphoramidic acid additions to alkenes: diastereo- and enantioselective halogenative cyclizations for the synthesis of C- and P-chiral phosphoramidates. J Am Chem Soc. 2014 Oct 22;136(42):14734-7. doi: 10.1021/ja5088584. Epub 2014 Oct 14. PMID: 25336273; PMCID: PMC4210055. 14: Uysal A, Tuncer D, Kir E, Koseoglu TS. Recovery of nutrients from digested sludge as struvite with a combination process of acid hydrolysis and Donnan dialysis. Water Sci Technol. 2017 Nov;76(9-10):2733-2741. doi: 10.2166/wst.2017.450. PMID: 29168713. 15: Zatta L, Ramos LP, Wypych F. Acid activated montmorillonite as catalysts in methyl esterification reactions of lauric acid. J Oleo Sci. 2012;61(9):497-504. doi: 10.5650/jos.61.497. PMID: 22975784. 16: Ogiso K, Shimizu Y, Watanabe K, Tonosaki K. Possible involvement of undissociated acid molecules in the acid response of the chorda tympani nerve of the rat. J Neurophysiol. 2000 May;83(5):2776-9. doi: 10.1152/jn.2000.83.5.2776. PMID: 10805675. 17: Agrawal A, Sahu KK. An overview of the recovery of acid from spent acidic solutions from steel and electroplating industries. J Hazard Mater. 2009 Nov 15;171(1-3):61-75. doi: 10.1016/j.jhazmat.2009.06.099. Epub 2009 Jun 25. PMID: 19632040. 18: Zheng A, Liu SB, Deng F. Acidity characterization of heterogeneous catalysts by solid-state NMR spectroscopy using probe molecules. Solid State Nucl Magn Reson. 2013 Oct-Nov;55-56:12-27. doi: 10.1016/j.ssnmr.2013.09.001. Epub 2013 Sep 20. PMID: 24094848. 19: Abedinia A, Ariffin F, Huda N, Nafchi AM. Extraction and characterization of gelatin from the feet of Pekin duck (Anas platyrhynchos domestica) as affected by acid, alkaline, and enzyme pretreatment. Int J Biol Macromol. 2017 May;98:586-594. doi: 10.1016/j.ijbiomac.2017.01.139. Epub 2017 Feb 4. PMID: 28174080. 20: Viers J, Grande JA, Zouiten C, Freydier R, Masbou J, Valente T, Torre ML, Destrigneville C, Pokrovsky OS. Are Cu isotopes a useful tool to trace metal sources and processes in acid mine drainage (AMD) context? Chemosphere. 2018 Feb;193:1071-1079. doi: 10.1016/j.chemosphere.2017.11.133. Epub 2017 Nov 23. PMID: 29874734.