Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.1849 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)CCCC(O)=O
InChI
InChIKey=MHPUGCYGQWGLJL-UHFFFAOYSA-N
InChI=1S/C7H14O2/c1-6(2)4-3-5-7(8)9/h6H,3-5H2,1-2H3,(H,8,9)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Ion-exclusion chromatographic separations of C1-C6 aliphatic carboxylic acids on a sulfonated styrene-divinylbenzene co-polymer resin column with 5-methylhexanoic acid as eluent. | 2003 May 16 |
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| Inhibition of luteinizing hormone secretion by testosterone in men requires aromatization for its pituitary but not its hypothalamic effects: evidence from the tandem study of normal and gonadotropin-releasing hormone-deficient men. | 2008 Mar |
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| Hypertrophy is induced during the in vitro chondrogenic differentiation of human mesenchymal stem cells by bone morphogenetic protein-2 and bone morphogenetic protein-4 gene transfer. | 2009 |
|
| Patterns of cerebral activation during olfactory and trigeminal stimulations. | 2009 Mar |
Patents
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JECFA EVALUATION |
5-METHYLHEXANOIC ACID
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628-46-6
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N1AK4X34C2
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12344
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1075
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SUBSTANCE RECORD
