(±)9,10-DiHODE
- CAS No.
- 1400693-71-1
- Chemical Name:
- (±)9,10-DiHODE
- Synonyms
- (±)9,10-DiHODE;(±)9,10-DiHODE;(±)9,10-DiHODE(γ);12,15-Octadecadienoic acid, 9,10-dihydroxy-, (9R,10R,12Z,15Z)-
- CBNumber:
- CB714907484
- Molecular Formula:
- C18H32O4
- Molecular Weight:
- 312.44
- MDL Number:
- MOL File:
- 1400693-71-1.mol
- MSDS File:
- SDS
(±)9,10-DiHODE price
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Cayman Chemical | 39907 | (±)9,10-DiHODE(γ) ≥95% | 25μg | $54 | 2026-04-30 | Buy | |
| Cayman Chemical | 39907 | (±)9,10-DiHODE(γ) ≥95% | 50μg | $97 | 2026-04-30 | Buy | |
| Cayman Chemical | 39907 | (±)9,10-DiHODE(γ) ≥95% | 100μg | $184 | 2026-04-30 | Buy | |
| Cayman Chemical | 39907 | (±)9,10-DiHODE(γ) ≥95% | 500μg | $809 | 2026-04-30 | Buy | |
| Cayman Chemical | 35856 | (±)9,10-DiHODE ≥95% | 1400693-71-1 | 25μg | $61 | 2026-04-30 | Buy |
(±)9,10-DiHODE Chemical Properties, Uses, Production
Uses
(±)9,10-DiHODE (compound 4) is a plant oxylipin compound that reduces the carbonyl group of α-ketoalcohols to form adjacent diols. They act as important signaling molecules in plants and play a role in regulating growth and flowering processes[1].
References
[1] Murata A, et al. Enantio-selective reduction of the flowering related compound KODA and its analogues in Pharbitis nil cv. Violet[J]. Tetrahedron, 2012, 68(27-28): 5583-5589.
[2] JAN PHILIPP SCHUCHARDT . Comparison of free serum oxylipin concentrations in hyper- vs. normolipidemic men[J]. Prostaglandins, leukotrienes, and essential fatty acids, 2013, 89 1: Pages 19-29. DOI: 10.1016/j.plefa.2013.04.001
[3] M. SVENVIK . Plasma oxylipin levels associated with preterm birth in preterm labor✰[J]. Prostaglandins, leukotrienes, and essential fatty acids, 2021, 166: Article 102251. DOI: 10.1016/j.plefa.2021.102251
[4] MEGAN P.T. OWEN . Oxylipin concentrations in bovine corpora lutea during maternal recognition of pregnancy[J]. Theriogenology, 2020, 142: Pages 384-389. DOI: 10.1016/j.theriogenology.2019.10.003
