Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C5H10O3 |
| Molecular Weight | 118.1311 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(O)CCC(O)=O
InChI
InChIKey=FMHKPLXYWVCLME-UHFFFAOYSA-N
InChI=1S/C5H10O3/c1-4(6)2-3-5(7)8/h4,6H,2-3H2,1H3,(H,7,8)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Porphyrins with exocyclic rings. 16. Synthesis and spectroscopic characterization of fluoranthoporphyrins, a new class of highly conjugated porphyrin chromophores. | 2001 May 4 |
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| Development of a process for the biotechnological large-scale production of 4-hydroxyvalerate-containing polyesters and characterization of their physical and mechanical properties. | 2001 Spring |
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| Analysis of GHB and 4-methyl-GHB in postmortem matrices after long-term storage. | 2005 Jan-Feb |
|
| Comparative analysis of gamma-hydroxybutyrate and gamma-hydroxyvalerate using GC/MS and HPLC. | 2007 Mar |
|
| High-titer production of monomeric hydroxyvalerates from levulinic acid in Pseudomonas putida. | 2009 Jan 1 |
Patents
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WIKIPEDIA |
Designer-drugs-.gamma.-Hydroxyvaleric acid
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DTXSID60928958
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114539
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236-884-1
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13532-37-1
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58B139Q3RL
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admin on Sat Dec 16 08:20:36 GMT 2023 , Edited by admin on Sat Dec 16 08:20:36 GMT 2023
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SUBSTANCE RECORD
