CAS 64-69-7
:Iodoacetic acid
Description:
Iodoacetic acid is an organic compound with the molecular formula C2H2I2O2. It is a halogenated acetic acid derivative, characterized by the presence of iodine atoms, which significantly influence its chemical properties and reactivity. This compound typically appears as a white to off-white crystalline solid and is soluble in water and organic solvents. Iodoacetic acid is known for its role as a reagent in organic synthesis, particularly in the introduction of iodine into various organic molecules. It exhibits strong electrophilic characteristics due to the presence of the iodine atoms, making it useful in nucleophilic substitution reactions. Additionally, it has applications in biochemistry, particularly as a reagent for modifying proteins and enzymes, as it can react with thiol groups. However, it is important to handle iodoacetic acid with care due to its potential toxicity and irritant properties. Proper safety measures should be observed when working with this compound in laboratory settings.
Formula:C2H3IO2
InChI:InChI=1S/C2H3IO2/c3-1-2(4)5/h1H2,(H,4,5)
InChI key:InChIKey=JDNTWHVOXJZDSN-UHFFFAOYSA-N
SMILES:C(CI)(O)=O
Synonyms:- 2-Iodoacetic acid
- Acetic acid, 2-iodo-
- Acetic acid, iodo-
- Acide iodoacetique
- Acido Iodoacetico
- Ai3-52119
- Brn 1739079
- CH<sub>2</sub>ICOOH
- Ccris 667
- Ch2Icooh
- Hsdb 4008
- IA
- Iodessigsaure
- Iodoacetate
- Iodoacetates
- Jodessigsaeure
- Kyselina jodoctova
- Kyselina jodoctova [Czech]
- MIA
- Monoiodine acetate
- Monoiodoacetate
- Monoiodoacetic acid
- Nsc 2125
- Iodoacetic acid
- See more synonyms
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Found 7 products.
Iodoacetic acid, 97+%
CAS:<p>Iodoacetic acid is used as a reagent for the modification of sulfhydryl groups in organic synthesis. It reacts with cysteine moiety in proteins to prevent the re-formation of disulfide bonds during protein sequencing. It is also used as a general reagent in acylation reactions as well as in glycopep</p>Formula:C2H3IO2Purity:97+%Color and Shape:White to yellow to orange-brown or pale cream to cream, Powder or crystalline powder or crystals or flakesMolecular weight:185.95Iodoacetic acid
CAS:<p>Iodoacetic acid</p>Formula:C2H3IO2Purity:97%Color and Shape:SolidMolecular weight:185.95g/molIodoacetic acid
CAS:Formula:ICH2CO2HPurity:≥ 97.0%Color and Shape:White to yellow or brown powder or flakesMolecular weight:185.95Iodoacetic Acid
CAS:Controlled Product<p>Applications Used as a general reagent in acylation reactions. A byproduct formed in treated waters, and found in marine life.<br> E0<br>References Zuckermann, R.N. et al.; J. Am. Chem. Soc., 115, 10646 (1992); Bull, R., et al.: Toxicol. Appl. Pharmacol., 182, 55 (2002), Mitch, W., et al.: Water Sci. Technol., 2, 191 (2002),<br></p>Formula:C2H3IO2Color and Shape:AmberMolecular weight:185.95Iodoacetic Acid 2-13C
CAS:Controlled Product<p>Applications Iodoacetic Acid 2-13C is labelled Iodoacetic Acid (I685520) which is used as a general reagent in acylation reactions. It is also a byproduct formed in treated waters, and found in marine life.<br>References Zuckermann, R.N. et al.; J. Am. Chem. Soc., 115, 10646 (1992); Bull, R., et al.: Toxicol. Appl. Pharmacol., 182, 55 (2002); Mitch, W., et ;l.: Water Sci. Technol., 2, 191 (2002)<br></p>Formula:CCH3IO2Color and Shape:NeatMolecular weight:186.941Iodoaceticacid
CAS:<p>Iodoacetic acid is a non-steroidal anti-inflammatory drug that is used to relieve pain and reduce inflammation. It reduces the production of prostaglandin E2, which is a chemical mediator of inflammation. Iodoacetic acid has been shown to have no significant effects on energy metabolism or response element activity in human polymorphonuclear leukocytes. Iodoacetic acid has shown to be an effective inhibitor of the enzyme form that converts dinucleotide phosphate (NAD) into NADH (NADase). This compound is stable in sephadex g-100, which allows for easy separation by high-performance liquid chromatography (HPLC). The analytical method for iodoacetic acid involves adding the compound to a buffer solution containing sephadex g-100 and measuring the decrease in light transmission at 236 nm over time.</p>Formula:C2H3IO2Purity:Min. 95%Molecular weight:185.95 g/mol





