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Names | |
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Preferred IUPAC name
3-Hydroxypentanoic acid | |
Other names
3-Hydroxyvalerate
3-Hydroxy valeric acid beta-Hydroxyvaleric acid beta-Hydroxypentanoate | |
Identifiers | |
3D model (
JSmol)
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ChemSpider | |
ECHA InfoCard | 100.123.761 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
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Properties | |
C5H10O3 | |
Molar mass | 118.13 g/mol |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
3-Hydroxypentanoic acid is the organic compound with the formula CH3CH2CH(OH)CH2CO2H. It is one of the hydroxypentanoic acids. [1] It is made from odd carbon fatty acids in the liver and rapidly enters the brain. As opposed to 4-carbon ketone bodies, 3-hydroxypentanoic acid is anaplerotic, meaning it can refill the pool of TCA cycle intermediates. The triglyceride triheptanoin is used clinically to produce beta-hydroxypentanoate. [2]
![]() | |
Names | |
---|---|
Preferred IUPAC name
3-Hydroxypentanoic acid | |
Other names
3-Hydroxyvalerate
3-Hydroxy valeric acid beta-Hydroxyvaleric acid beta-Hydroxypentanoate | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.123.761 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C5H10O3 | |
Molar mass | 118.13 g/mol |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
3-Hydroxypentanoic acid is the organic compound with the formula CH3CH2CH(OH)CH2CO2H. It is one of the hydroxypentanoic acids. [1] It is made from odd carbon fatty acids in the liver and rapidly enters the brain. As opposed to 4-carbon ketone bodies, 3-hydroxypentanoic acid is anaplerotic, meaning it can refill the pool of TCA cycle intermediates. The triglyceride triheptanoin is used clinically to produce beta-hydroxypentanoate. [2]