115-95-7
115-95-7
Chemical Structure
Linalyl acetate
- CAS. Nr.: 115-95-7
- Formula:C12H20O2
- Molecular Weight:196.29
IUPAC Name: 3,7-dimethylocta-1,6-dien-3-yl acetate
InChIKey: UWKAYLJWKGQEPM-UHFFFAOYSA-N
SMILES: CC(OC(CC/C=C(C)\C)(C)C=C)=O
Biological Activity: Linalyl acetate is the principal components of many plant essential oils. Linalyl acetate exhibits anti-anxiety, anti-inflammatory, anti-diabetic, anti-stress, and cardiovascular-regulatory effects. Linalyl acetate is orally active[1][2][3][4].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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Linalyl acetate | 98.80% | Linalyl acetate is the principal components of many plant essential oils. Linalyl acetate exhibits anti-anxiety, anti-inflammatory, anti-diabetic, anti-stress, and cardiovascular-regulatory effects. Linalyl acetate is orally active. | ||||||||||||||||||||
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Linalyl acetate (Standard) | ≥98% | Linalyl acetate (Standard) is the analytical standard of Linalyl acetate. This product is intended for research and analytical applications. Linalyl acetate is the principal components of many plant essential oils. Linalyl acetate exhibits anti-anxiety, anti-inflammatory, anti-diabetic, anti-stress, and cardiovascular-regulatory effects. Linalyl acetate is orally active. | ||||||||||||||||||||
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Linalyl acetate-d6 | Linalyl acetate-d6 is deuterated labeled Linalyl acetate (HY-N6948). Linalyl acetate is the principal components of many plant essential oils. Linalyl acetate exhibits anti-anxiety, anti-inflammatory, anti-diabetic, anti-stress, and cardiovascular-regulatory effects. Linalyl acetate is orally active. | |||||||||||||||||||||
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L-Linalool | 98.0% | L-Linalool ((-)-Linalool) is a naturally derived monoterpene alcohol with oral activity, possessing neuroprotective, anti-inflammatory, and antioxidant activities. L-Linalool is a 5-HT3 receptor inhibitor and a benzodiazepine-responsive GABAA receptor enhancer. L-Linalool reduces nitrite and lipid peroxidation in the brain and partially prevents the decrease of striatal dopamine, DOPAC, and HVA. L-Linalool exhibits neuroprotective effects in hemiparkinsonian rats, cortical oxygen-glucose deprivation injury, and Alzheimer's disease models. L-Linalool prevents the decrease in tyrosine hydroxylase and dopamine transporter expression. L-Linalool can be used in research related to diseases such as Parkinson's disease and Alzheimer's disease. | ||||||||||||||||||||
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(-)-Lavandulyl acetate | (-)-Lavandulyl acetate is a nature product that can be found in Lavandula angustifolia. (-)-Lavandulyl acetate shows toxicity for mosquito vectors. (-)-Lavandulyl acetate can be used as mosquito larvicide. | |||||||||||||||||||||
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(±)-Lavandulyl acetate (Standard) | ≥98% | (±)-Lavandulyl acetate (Standard) is the analytical standard of (±)-Lavandulyl acetate (HY-117419A). This product is intended for research and analytical applications. (±)-Lavandulyl acetate is an isomer of (-)-Lavandulyl acetate (HY-117419). (-)-Lavandulyl acetate is a nature product that can be found in Lavandula angustifolia. (-)-Lavandulyl acetate shows toxicity for mosquito vectors. (-)-Lavandulyl acetate can be used as mosquito larvicide. | ||||||||||||||||||||
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Linalool (Standard) | 97.16% | Linalool (Standard) is the analytical standard of Linalool. This product is intended for research and analytical applications. Linalool is natural monoterpene in essential olis of coriander, acts as a competitive antagonist of Nmethyl d-aspartate (NMDA) receptor, with anti-tumor, anti-cardiotoxicity activity.Linalool is a PPARα ligand that reduces plasma TG levels and rewires the hepatic transcriptome and plasma metabolome. | ||||||||||||||||||||
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(S)-Menthiafolic acid | (S)-Menthiafolic acid is a component found in wines and grape juices. (S)-Menthiafolic acid can be generated from the grape-derived (S)-menthiafolic acid glucose ester during alcoholic and malolactic fermentation, thereby influencing the aroma components of wine. | |||||||||||||||||||||
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10-Carboxylinalool | 10-Carboxylinalool is a metabolite compound isolated from the genus Pseudomonasin in a mineral salt medium. | |||||||||||||||||||||
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Geranyl acetate (Standard) | ≥98% | Geranyl acetate (Standard) is the analytical standard of Geranyl acetate. This product is intended for research and analytical applications. Geranyl acetate, an acyclic monoterpene ester derived from geraniol, is widely used in the cosmetics industry due to its pleasant scent. Geranyl acetate can induces cell apoptosis. | ||||||||||||||||||||
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Neryl acetate (Standard) | ≥98% | Neryl acetate (Standard) is the analytical standard of Neryl acetate. This product is intended for research and analytical applications. Neryl acetate is an essential oil component. Neryl acetate upregulates genes associated with epidermal differentiation, skin barrier formation and ceramide synthesis; it also increases filaggrin expression, total lipid and ceramide contents. Neryl acetate acts as the core driver mediating the skin barrier-forming and antibacterial effects of Helichrysum italicum essential oil. | ||||||||||||||||||||
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(S)-Linalool | 99.71% | (S)-Linalool is the enantiomer of Linalool (HY-N0368). (S)-Linalool can be used in the production of fragrances and flavorings. | ||||||||||||||||||||
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Linalyl formate | 94.01% | Linalyl formate, an ester derivative of Linalool (HY-N0368), is one of the four main volatile substances in fresh blueberry juice | ||||||||||||||||||||
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References
- [1]. A.T. Peana, et al. Anti-inflammatory activity of linalool and linalyl acetate constituents of essential oils,Phytomedicine. 2002 Dec;9(8):721-6. [Content Brief]
- [2]. Rani M, et al. Evaluation of antianxiety activity of Linalyl acetate in Swiss albino Mice[J]. Ann Romanian Soc Cell Biol, 2022, 26(1): 3470-3482.
- [3]. Kim JR, et al., Cardiovascular effects of linalyl acetate in acute nicotine exposure. Environ Health Prev Med. 2017 Apr 24;22(1):42. [Content Brief]
- [4]. Seo E, et al., Linalyl acetate as a potential preventive agent against muscle wasting in rheumatoid arthritis rats chronically exposed to nicotine. J Pharmacol Sci. 2021 Sep;147(1):27-32. [Content Brief]
