| Weight | 185.948 g/mol |
|---|---|
| Formula | C2H3IO2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
IODOACETIC ACID (64-69-7)
Monoiodoacetic Acid · Sodium Iodoacetate
Score:
#797 in Biochemistry
,
#2166 in Biology
,
#2665 in Chemistry
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- Sodium Iodoacetate-Induced Experimental Osteoarthritis and Associated Pain Model in Rats (Journal of Veterinary Medical Science, 2003)
- Proteolytic fragmentation of the catalytic subunit of the sodium and potassium adenosine triphosphatase. Alignment of tryptic and chymotryptic fragments and location of sites labeled with ATP and iodoacetate. (Journal of Biological Chemistry, 1979)
- Alterations of ultrastructure and elemental composition in cultured neonatal rat cardiac myocytes after metabolic inhibition with iodoacetic acid. (Laboratory Investigation, 1985)
- INHIBITION OF GLYCERALDEHYDE3PHOSPHATE DEHYDROGENASE IN MAMMALIAN NERVE BY IODOACETIC ACID (Journal of Neurochemistry, 1971)
- Inhibition of Experimental Dental Caries in the Rat by Fluoride and Iodoacetic Acid (Experimental Biology and Medicine, 1938)
- THE REACTION OF IODOACETIC ACID ON MERCAPTANS AND AMINES (Journal of Biological Chemistry, 1934)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H371: May cause damage to organs
Warning Specific target organ toxicity, single exposure - Category 2 - Monoiodoacetic Acid
- Sodium Iodoacetate
-
SMILESC(C(=O)O)I
-
InChIKeyJDNTWHVOXJZDSN-UHFFFAOYSA-N
- Pubchem - IODOACETIC ACID
- Wikipedia - iodoacetic acid
Iodoacetic acid is a derivative of acetic acid. It is a toxic compound, because, like many alkyl halides, it is an alkylating agent. It reacts with cysteine residues in proteins.
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