Category: fragrance agents
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
Appearance: | colorless to pale yellow clear liquid (est) |
Assay: | 96.00 to 100.00 %
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Food Chemicals Codex Listed: | No |
Specific Gravity: | 0.87850 @ 25.00 °C.
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Refractive Index: | 1.46830 @ 20.00 °C.
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Boiling Point: | 94.00 to 95.00 °C. @ 13.00 mm Hg
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Boiling Point: | 229.00 to 230.00 °C. @ 760.00 mm Hg
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Vapor Pressure: | 0.013000 mmHg @ 25.00 °C. (est) |
Flash Point: | 191.00 °F. TCC ( 88.33 °C. )
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logP (o/w): | 2.665 (est) |
Soluble in: |
| alcohol | | water, 253.2 mg/L @ 25 °C (est) |
Insoluble in: |
| water |
Organoleptic Properties:
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Odor Type: floral |
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Odor Strength: | medium |
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| floral waxy mimosa herbal |
Odor Description: at 100.00 %. | delicate farnesol-like |
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Odor and/or flavor descriptions from others (if found). |
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Cosmetic Information:
Suppliers:
Safety Information:
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Hazards identification |
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Classification of the substance or mixture |
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
None found. |
GHS Label elements, including precautionary statements |
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Pictogram | |
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Hazard statement(s) |
None found. |
Precautionary statement(s) |
None found. |
Oral/Parenteral Toxicity: |
Not determined
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Dermal Toxicity: |
Not determined
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Inhalation Toxicity: |
Not determined
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Safety in Use Information:
Safety References:
References:
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
4- | hexen-1-ol, 2-isopropenyl-5-methyl-, (-)- | 4- | hexen-1-ol, 5-methyl-2-(1-methylethenyl)- | | lavandulol | (±)- | lavandulol | 5- | methyl-2-(1-methyl ethenyl)-4-hexen-1-ol | 5- | methyl-2-(1-methylethenyl)hex-4-en-1-ol | 5- | methyl-2-(prop-1-en-2-yl)hex-4-en-1-ol | 5- | methyl-2-prop-1-en-2-ylhex-4-en-1-ol | iso | propenyl methyl hexenol | 2-iso | propenyl-5-methyl hex-4-en-1-ol | 2-iso | propenyl-5-methyl-4-hexen-1-ol | 2-iso | propenyl-5-methylhex-4-en-1-ol |
Articles:
PubMed: | Transformation of (±)-lavandulol and (±)-tetrahydrolavandulol by a fungal strain Rhizopus oryzae. |
PubMed: | Selective deoxygenation of allylic alcohol: stereocontrolled synthesis of lavandulol. |
PubMed: | One-Pot synthesis of gamma,delta-unsaturated carbonyl compounds from allyl alcohols and vinyl or isopropenyl acetates catalyzed by [IrCl(cod)]2. |
PubMed: | Enzymatic esterification of lavandulol--a partial kinetic resolution of (S)-lavandulol and preparation of optically enriched (R)-lavandulyl acetate. |
PubMed: | The biosynthetic origin of irregular monoterpenes in Lavandula: isolation and biochemical characterization of a novel cis-prenyl diphosphate synthase gene, lavandulyl diphosphate synthase. |
PubMed: | Enzymatic resolution and odor description of both enantiomers of lavandulol, a fragrance of lavender oil. |
PubMed: | Chemical composition and antioxidative activity of Echinophora platyloba DC. essential oil, and its interaction with natural antimicrobials against food-borne pathogens and spoilage organisms. |
PubMed: | Hydrolysis of beta,gamma-Unsaturated Aldehyde Dimethylhydrazones with Copper Dichloride: A New Synthesis of Lavandulol. |
PubMed: | Inhibition by TRPA1 agonists of compound action potentials in the frog sciatic nerve. |
PubMed: | Role of novel terpenes in transcutaneous permeation of valsartan: effectiveness and mechanism of action. |
PubMed: | Development of an attractant-baited trap for Oxythyrea funesta Poda (Coleoptera: Scarabaeidae, Cetoniinae). |
PubMed: | Growth-inhibiting effects of Paeonia lactiflora root steam distillate constituents and structurally related compounds on human intestinal bacteria. |
PubMed: | Antimicrobial Activity and Chemical Composition of Essential Oil From the Seeds of Artemisia aucheri Boiss. |
PubMed: | Components of male aggregation pheromone of strawberry blossom weevil, Anthonomus rubi herbst. (Coleoptera:Curculionidae). |
PubMed: | Male behaviors reveal multiple pherotypes within vine mealybug Planococcus ficus (Signoret) (Hemiptera; Pseudococcidae) populations. |
PubMed: | A DFT analysis of thermal decomposition reactions important to natural products. |
PubMed: | Analysis of the essential oil from aerial parts of Eupatorium cannabinum subsp. corsicum (L.) by gas chromatography with electron impact and chemical ionization mass spectrometry. |
PubMed: | [Not Available]. |
PubMed: | Syntheses and odor descriptions of cyclopropanated compounds, part 6: Analogs of aliphatic monoterpene dienols and non-branched alcohols. |
PubMed: | Development and optimization of methods for using sex pheromone for monitoring the mealybug Planococcus ficus (Homoptera: Pseudococcidae) in California vineyards. |
PubMed: | The monoterpenes of Artemisia tridentata ssp. vaseyana, Artemisia cana ssp. viscidula and Artemisia tridentata ssp. spiciformis. |
PubMed: | Deoxyarteannuin B, dihydro-deoxyarteannuin B and trans-5-hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol from Artemisia anuua. |
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