(+)-NerolidolCAS# 142-50-7 |
- Nerolidol
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Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 142-50-7 | SDF | Download SDF |
| PubChem ID | 5356544 | Appearance | Powder |
| Formula | C15H26O | M.Wt | 222.4 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Synonyms | d-Nerolidol;(s)-nerolidol | ||
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (3S,6Z)-3,7,11-trimethyldodeca-1,6,10-trien-3-ol | ||
| SMILES | CC(=CCCC(=CCCC(C)(C=C)O)C)C | ||
| Standard InChIKey | FQTLCLSUCSAZDY-QKXCFHHRSA-N | ||
| Standard InChI | InChI=1S/C15H26O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h6,9,11,16H,1,7-8,10,12H2,2-5H3/b14-11-/t15-/m1/s1 | ||
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
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| About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
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| Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. | ||
(+)-Nerolidol Dilution Calculator
(+)-Nerolidol Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 4.4964 mL | 22.482 mL | 44.964 mL | 89.9281 mL | 112.4101 mL |
| 5 mM | 0.8993 mL | 4.4964 mL | 8.9928 mL | 17.9856 mL | 22.482 mL |
| 10 mM | 0.4496 mL | 2.2482 mL | 4.4964 mL | 8.9928 mL | 11.241 mL |
| 50 mM | 0.0899 mL | 0.4496 mL | 0.8993 mL | 1.7986 mL | 2.2482 mL |
| 100 mM | 0.045 mL | 0.2248 mL | 0.4496 mL | 0.8993 mL | 1.1241 mL |
| * Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. | |||||
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Chemotype diversity of Psidium guajava L.[Pubmed:29913321]
Phytochemistry. 2018 Sep;153:129-137.
The essential oil of Psidium guajava L. has been studied for pharmacological and industrial purposes, without considering the plant's genotype regarding the heterogeneity of its composition. The present study aimed to characterize the chemotype diversity of the essential oil extracted from the leaves of 22 genotypes of P. guajava grown in two different environments in the state of Espirito Santo, Brazil, and to identify the different chemical markers present in these plants. Essential oil from the leaves of the P. guajava genotypes was extracted by hydrodistillation, and its chemical composition was analyzed by gas chromatography-flame ionization detection (GC-FID) and gas chromatography-mass spectrometry (GC-MS). Thirty-three compounds were identified, comprising 87.5-99.0% of the total composition, with a prevalence of sesquiterpenes in all samples. The major compounds identified consisted of (E)-trans-Caryophyllene, alpha-Humulene, trans-Nerolidol, beta-Bisabolene, beta-Bisabolol, and Hinesol, the first of which was identified as a possible chemical marker for the species. Multivariate factor analysis of the chemical composition of P. guajava oil identified three chemotypes: Commercial - PAL, SEC, PS, PET, C7, C11, and C17MI, characterized by high levels of beta-Selinene, alpha-Selinene, Hinesol, and 14-hydroxy-epi-(E)-caryophyllene, with beta-Selinene and alpha-Selinene as the chemical markers; C10 and C13, exhibiting high levels of Elemol, trans-Nerolidol, trans-beta-Eudesmol, and (2Z, 6Z)-Farnesol, which were indicated as chemical markers, and Cortibel - C1, C2, C3, C4, C5, C6, C8, C9, C12, C14, C15, C16, C17LI, which retained high levels of alpha-Cedrene, cis-alpha-Bergamotene, alpha-Humulene, Humulene epoxide, epi-alpha-Cadinol, beta-Bisabolol, and alpha-Bisabolol, with beta-Bisabolol and alpha-Bisabolol as the chemical markers. The use of guava genotypes with different chemotypes, that are agronomically favorable to fruit production and essential oil exploitation adds value to the crop and renders it more sustainable. Given guava crops produce large amounts of leaf biomass, resulting from successive prunings, the extraction of their essential oil, which retains commercially valuable compounds, can be feasible.
