| Weight | 102.133 g/mol |
|---|---|
| Formula | C5H10O2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
ISOVALERIC ACID (35915-22-1, 503-74-2)
3-methylbutyrate · 3-methylbutyric acid
Score:
#601 in Biochemistry
,
#1747 in Biology
,
#2065 in Chemistry
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- Genetic Elucidation of Human Hyperosmia to Isovaleric Acid (PLOS Biology, 2007)
- Conversion of l-Leucine to Isovaleric Acid by Propionibacterium freudenreichii TL 34 and ITGP23 (Applied and Environmental Microbiology, 2002)
- Identification of -hydroxyisovaleric acid in the urine of a patient with isovaleric acidemia (Biochimica et Biophysica Acta, 1968)
- The genetic basis for specific anosmia to isovaleric acid in the mouse (Cell, 1995)
- Microdetermination of methylmalonic acid and other short chain dicarboxylic acids by gas chromatography: Use in prenatal diagnosis of methylmalonic acidemia and in studies of isovaleric acidemia (Clinica Chimica Acta, 1976)
- Synthesis, biodistribution and micro-PET imaging of a potential cancer biomarker carbon-11 labeled MMP inhibitor (2R)-2-[[4-(6-fluorohex-1-ynyl)phenyl]sulfonylamino]-3-methylbutyric acid [11C]methyl ester (Nuclear Medicine and Biology, 2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-methylbutyrate
- 3-methylbutyric acid
-
SMILESCC(C)CC(=O)O
-
InChIKeyGWYFCOCPABKNJV-UHFFFAOYSA-N
- Pubchem - ISOVALERIC ACID
- Wikipedia - isovaleric acid
3-Methylbutanoic acid, also known as -methylbutyric acid or more commonly isovaleric acid, is an organic compound with the formula (CH3)2CHCH2CO2H. It is sometimes classified as a fatty acid. It is a colourless liquid that is sparingly soluble in water, but highly soluble in most common organic solvents.
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