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    CAS No. 78-70-6 Price $30 / 20mg
    Catalog No.CFN99582Purity>=98%
    Molecular Weight154.25Type of CompoundMonoterpenoids
    FormulaC10H18OPhysical DescriptionOil
    Download Manual    COA    MSDSSimilar structuralComparison (Web)
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    Biological Activity
    Description: Linalool, is a competitive antagonist of NMDA receptors, which has anti-inflammatory, antinociceptive, anti-anxiety, local anaesthetic, anti-leishmanicidal, and insecticidal properties. Linalool has dose-dependent marked sedative effects at the central nervous system (CNS), including hypnotic, anticonvulsant and hypothermic properties, it also has an inhibitory effect on the acetylcholine (ACh) release and on the channel open time in the mouse neuromuscular junction. The purified linalool fraction is only inhibitory for C. albicans.
    Targets: IL Receptor | TNF-α | IkB | p38MAPK | JNK | IKK
    In vitro:
    Antimicrob. Agents Ch., 2003, 47(6):1895-901.
    Antileishmanial activity of a linalool-rich essential oil from Croton cajucara.[Pubmed: 12760864 ]
    The in vitro leishmanicidal effects of a Linalool-rich essential oil from the leaves of Croton cajucara against Leishmania amazonensis were investigated.
    Morphological changes in L. amazonensis promastigotes treated with 15 ng of essential oil per ml were observed by transmission electron microscopy; leishmanial nuclear and kinetoplast chromatin destruction, followed by cell lysis, was observed within 1 h. Pretreatment of mouse peritoneal macrophages with 15 ng of essential oil per ml reduced by 50% the interaction between these macrophages and L. amazonensis, with a concomitant increase by 220% in the level of nitric oxide production by the infected macrophages. Treatment of preinfected macrophages with 15 ng of essential oil per ml reduced by 50% the interaction between these cells and the parasites, which led to a 60% increase in the amount of nitric oxide produced by the preinfected macrophages.
    These results provide new perspectives on the development of drugs with activities against Leishmania, as Linalool-rich essential oil is a strikingly potent leishmanicidal plant extract (50% lethal doses, 8.3 ng/ml for promastigotes and 8.7 ng/ml for amastigotes) which inhibited the growth of L. amazonensis promastigotes at very low concentrations (MIC, 85.0 pg/ml) and which presented no cytotoxic effects against mammalian cells.
    Oral Microbiol Immunol. 2005 Apr;20(2):101-5.
    Antimicrobial activity of Croton cajucara Benth linalool-rich essential oil on artificial biofilms and planktonic microorganisms.[Pubmed: 15720570 ]
    We have previously demonstrated that a Linalool-rich essential oil from Croton cajucara Benth presents leishmanicidal activity.
    In the present study, we demonstrate that this essential oil inhibits the growth of reference samples of Candida albicans, Lactobacillus casei, Staphylococcus aureus, Streptococcus sobrinus, Porphyromonas gingivalis and Streptococcus mutans cell suspensions, all of them associated with oral cavity disease. The purified Linalool fraction was only inhibitory for C. albicans. Microbes of saliva specimens from human individuals with fixed orthodontic appliances, as well as the reference strains, were used to construct an artificial biofilm which was exposed to Linalool or to the essential oil. As in microbial suspensions, the essential oil was toxic for all the microorganisms, while the purified Linalool fraction mainly inhibited the growth of C. albicans. The compounds of the essential oil were separated by thin layer chromatography and exposed to the above-cited microorganisms. In this analysis, the proliferation of the bacterial cells was inhibited by still uncharacterized molecules, and Linalool was confirmed as the antifungal component of the essential oil.
    The effects of Linalool on the cell biology of C. albicans were evaluated by electron microscopy, which showed that Linalool induced a reduction in cell size and abnormal germination. Neither the crude essential oil nor the purified Linalool fraction is toxic to mammalian cells, which suggests that the essential oil or its purified components may be useful to control the microbial population in patients with fixed orthodontic appliances.
    Pharmacol Res. 2000 Aug;42(2):177-82.
    Linalool modifies the nicotinic receptor-ion channel kinetics at the mouse neuromuscular junction.[Pubmed: 10887049 ]
    Linalool is a monoterpene compound reported to be a major component of essential oils in various aromatic species. Several Linalool-producing species are used in traditional medical systems. Among these is Aeolanthus suaveolens G. Dom (Labiatae) which is used as an anticonvulsant in the Brazilian Amazon. Psychopharmacological in vivo evaluation of Linalool showed that this compound has dose-dependent marked sedative effects at the central nervous system (CNS), including hypnotic, anticonvulsant and hypothermic properties. It has been suggested that these neurochemical effects might be ascribed to the local anaesthetic activity of Linalool.
    The present study reports an inhibitory effect of Linalool on the acetylcholine (ACh) release and on the channel open time in the mouse neuromuscular junction. These findings could provide a rational basis to confirm the traditional medical use of Linalool-producing plant species.
    Indeed, our data demonstrate some interactions in the modulation of the ACh release at the mouse neuromuscular junction, which are well correlated with the suggested molecular mechanisms. Linalool induced a reduction of the ACh-evoked release. The possibility that this effect could be ascribed to some interaction with pre-synaptic function is noteworthy. Moreover, the inhibitory effect induced on the kinetics of the miniature end-plate current decay demonstrates a local anaesthetic action, either on the voltage or on the receptor-activated channels.
    Food Chem Toxicol. 2009 Jan;47(1):260-6.
    Protective effect of linalool, myrcene and eucalyptol against t-butyl hydroperoxide induced genotoxicity in bacteria and cultured human cells.[Pubmed: 19049815 ]
    We studied the protective effect of monoterpenes myrcene, eucalyptol and Linalool against t-butyl hydroperoxide (t-BOOH) induced genotoxicity in reverse mutation assay with Escherichia coli WP2 IC185 strain and its oxyR mutant IC202, and with the comet assay in human hepatoma HepG2 and human B lymphoid NC-NC cells.
    The monoterpenes were tested in concentration ranges 0.05-1.5 mg/plate and 0.01-1.0 microg/ml in bacteria and mammalian cells, respectively. Suppression of t-BOOH induced mutagenesis was detected only in IC202 strain, and correlated with the observed inhibition of lipid peroxidation by the three monoterpenes. Linalool and myrcene strongly suppressed t-BOOH induced mutagenesis. Eucalyptol, in addition to moderate suppression of t-BOOH induced mutagenesis, suppressed also spontaneous mutagenesis. In NC-NC cells Linalool and myrcene reduced t-BOOH induced DNA damage by about 50% at 0.01 microg/ml, while eucalyptol was less efficient (about 50% reduction at 1.0 microg/ml). In HepG2 cells Linalool and eucalyptol reduced DNA damage by 30% and 40%, respectively, while myrcene was ineffective. The repair of t-BOOH induced DNA damage, studied in HepG2 cells, was not affected by monoterpenes.
    The results indicate that Linalool, eucalyptol and myrcene have substantial protective effect against oxidant induced genotoxicity, which is predominately mediated by their radical scavenging activity.
    In vivo:
    J Surg Res. 2013 Mar;180(1):e47-54.
    Anti-inflammatory effects of linalool in RAW 264.7 macrophages and lipopolysaccharide-induced lung injury model.[Pubmed: 23228323 ]
    Inflammation, characterized by redness, swelling, pain and a sensation of heat, is one of the body's self-defense systems. Although the inflammation response has an important role in host survival, it also leads to chronic inflammatory diseases. Linalool is a natural compound of the essential oils in several aromatic plants species. It possesses anti-inflammatory, antinociceptive, and other bioactive properties. In the present study, we investigated the protective effects of Linalool on inflammation in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells and an LPS-induced in vivo lung injury model. Linalool attenuated the production of LPS-induced tumor necrosis-α and interleukin-6 both in vitro and in vivo. Furthermore, phosphorylation of IκBα protein, p38, c-Jun terminal kinase, and extracellular signal-regulated kinase in LPS-stimulated RAW 264.7 cells was blocked by Linalool. Our in vivo study also found that Linalool attenuated lung histopathologic changes in mouse models. CONCLUSIONS: The results suggest that Linalool inhibits inflammation both in vitro and in vivo, and may be a potential therapeutic candidate for the treatment of inflammatory diseases.
    Phytomedicine. 2010 Jul;17(8-9):679-83.
    Effects of inhaled Linalool in anxiety, social interaction and aggressive behavior in mice.[Pubmed: 19962290 ]
    Aromatherapy uses essential oils (EOs) for several medical purposes, including relaxation. The association between the use of aromas and a decrease in anxiety could be a valuable instrument in managing anxiety in an ever increasing anxiogenic daily life style. Linalool is a monoterpene commonly found as the major volatile component of EOs in several aromatic plant species.
    Adding to previously reported sedative effects of inhaled Linalool, the aim of this study was to investigate the effects of inhaled Linalool on anxiety, aggressiveness and social interaction in mice. Additionally, we investigated the effects of inhaled Linalool on the acquisition phase of a step-down memory task in mice. Inhaled Linalool showed anxiolytic properties in the light/dark test, increased social interaction and decreased aggressive behavior; impaired memory was only seen the higher dose of Linalool.
    These results strengthen the suggestion that inhaling Linalool rich essential oils can be useful as a mean to attain relaxation and counteract anxiety.
    Linalool Description
    Source: The leaves of Cinnamomum camphora
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

    After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

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    doi: 10.1016/j.cell.2017.12.019.

    PMID: 29328914

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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 6.483 mL 32.4149 mL 64.8298 mL 129.6596 mL 162.0746 mL
    5 mM 1.2966 mL 6.483 mL 12.966 mL 25.9319 mL 32.4149 mL
    10 mM 0.6483 mL 3.2415 mL 6.483 mL 12.966 mL 16.2075 mL
    50 mM 0.1297 mL 0.6483 mL 1.2966 mL 2.5932 mL 3.2415 mL
    100 mM 0.0648 mL 0.3241 mL 0.6483 mL 1.2966 mL 1.6207 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Cell Research:
    Int J Mol Sci. 2015 Dec; 16(12): 28169–28179.
    Linalool Induces Cell Cycle Arrest and Apoptosis in Leukemia Cells and Cervical Cancer Cells through CDKIs[Pubmed: 26703569]
    Cell lines:U937 cells
    Concentrations: 1.30, 1.94, 3.24, and 6.48 μM
    Incubation Time: 24 h
    Water-soluble tetrazolium salts (WST-1) analysis is used to determine inhibition of cell growth by varying the concentrations (1.30, 1.94, 3.24, and 6.48 μM) of Linalool administered to U937 cells (1.2 × 105/mL) and activating for 24 h.
    Animal Research:
    Phytother Res. 2012 Sep;26(9):1399-404.
    Effect of linalool on morphine tolerance and dependence in mice.[Pubmed: 22318903 ]
    Animal Models:Adult male albino mice
    Formulation: Saline
    Dosages:50, 75 and 100 mg/kg
    Administration: i.p.