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LINALOOL


CAS NO:78-70-6
EC NO:201-134-4; 245-083-6


Linalool refers to two enantiomers of a naturally occurring terpene alcohol found in many flowers and spice plants. 
Linalool has multiple commercial applications, the majority of which are based on its pleasant scent (floral, with a touch of spiciness).
Linalool is a colorless oil. 
Linalool is classified as an acyclic monoterpenoid. licareol and (S)-(+)-linalool is also known as coriandrol.


Properties
Chemical formula        C10H18O
Molar mass        154.253 g·mol−1
Density        0.858 to 0.868 g/cm3
Melting point        < −20 °C (−4 °F; 253 K)
Boiling point        198 to 199 °C (388 to 390 °F; 471 to 472 K)
Solubility in water        1.589 g/l


Linalool Occurrence


Both enantiomeric forms are found in nature: (S)-linalool is found, for example, as a major constituent of the essential oils of coriander (Coriandrum sativum L.), cymbopogon (Cymbopogon martini var. martinii), and sweet orange (Citrus sinensis) flowers. (R)-linalool is present in lavender (Lavandula officinalis), bay laurel (Laurus nobilis), and sweet basil (Ocimum basilicum), among others.


Each enantiomer evokes different neural responses in humans, so are classified as possessing distinct scents. (S)-(+)-Linalool is perceived as sweet, floral, petitgrain-like (odor threshold 7.4 ppb) and the (R)-form as more woody and lavender-like (odor threshold 0.8 ppb).


Over 200 species of plants produce linalool, mainly from the families Lamiaceae (mint and other herbs), Lauraceae (laurels, cinnamon, rosewood), and Rutaceae (citrus fruits), but also birch trees and other plants, from tropical to boreal climate zones.


Lavandula
Cinnamomum tamala
Cannabis sativa
Basil
Solidago
Artemisia vulgaris (mugwort)
Humulus lupulus
Linalool was first synthesized in the laboratory of Leopold Ružička in 1919.


Biosynthesis
The biosynthesis of linalool in higher plants starts at the condensation of dimethylallyl diphosphate (DMAPP) and isopentenyl diphosphate (IPP) to form geranyl pyrophosphate (GPP).With the aid of linalool synthase (LIS), water attacks to form the chiral center.
 LIS appears to show a limonene synthase-type catalysis through a simplified "metal-cofactor-binding domain [where the majority] of the residues involved in substrate...binding [are] in the C-terminal part of the protein" suggesting stereoselectivity and the reasoning behind why some plants have varying levels of each enantiomer.


Uses of Linalool
Linalool is used as a scent in 60% to 80% of perfumed hygiene products and cleaning agents including soaps, detergents, shampoos, and lotions.
Linalool exhibits antifungal properties.


Linalool is also used as a chemical intermediate. One common downstream product of linalool is vitamin E.
In addition, linalool is used as an insecticide against flea, fruit fly, and cockroach. 
Linalool can also be used as a method of pest control for codling moths. 
Linalool creates a synergistic effect with the codling moth's pheromone called codlemone, which increases attraction of males.
Linalool is used in some mosquito-repellent products; however, the U.S. EPA notes that "a preliminary screen of labels for products containing Linalool (as the sole active ingredient) indicates that efficacy data on file with the Agency may not support certain claims to repel mosquitos."


Linalool is a monoterpenoid that is octa-1,6-diene substituted by methyl groups at positions 3 and 7 and a hydroxy group at position 3. 
Linalool has been isolated from plants like Ocimum canum. 
Linalool has a role as a plant metabolite, a volatile oil component, an antimicrobial agent and a fragrance. 
Linalool is a tertiary alcohol and a monoterpenoid.


Linalool Industry Uses        
Intermediates
Odor agents


Linalool Consumer Uses        
Air care products
Cleaning and furnishing care products
Laundry and dishwashing products
Non-TSCA use
Personal care products
Plastic and rubber products not covered elsewhere
aroma chemicals


Linalool Industry Processing Sectors
All other basic organic chemical manufacturing
All other chemical product and preparation manufacturing
Miscellaneous manufacturing
Plastic material and resin manufacturing
Soap, cleaning compound, and toilet preparation manufacturing


Linalool has been estimated that it is present in 90% of all fine fragrances.
Linalool (3,7-dimethyl-1,6-octadien-3-ol) is an important fragrance chemical, frequently used in scented products because of its fresh, flowery odor. 
Linalool is an unsaturated hydrocarbon and is therefore susceptible to oxidation in the presence of air. The primary oxidation products, that is, hydroperoxides, formed in the autoxidation process, are reactive compounds that can be suspected to act as sensitizers.


Linalool is a floral and spicy terpene alcohol. 
Linalool is found in over 200 plants such as citrus fruits and lavender. Concentrations of linalool above 20 ppb have been shown to give a fruity hoppy aroma to beer.
Linalool is generally used as a starting material in the total synthesis of agelasine E analogs and vitamin E derivatives.


Physicochemical Information
Density        0.86 g/cm3 (293.15 °C)
Explosion limit        0.9 - 5.2 %(V)
Flash point        77.2 °C
Ignition temperature        235 °C
Melting Point        <-100 °C
pH value        4.5 (1.45 g/l, H₂O, 25 °C)
Vapor pressure        0.27 hPa (25 °C)
Solubility        1.45 g/l


What Is Linalool?


 Like menthol, linalool is a monoterpene alcohol. A monoterpene is a molecule with a backbone made of 10 carbons. An alcohol is an oxygen atom bonded to both a hydrogen atom and a carbon atom in that backbone. (Check out the doTERRA Chemistry Handbook to learn more.) While Lavender essential oil has one of the highest amounts of linalool, you can also find linalool in Coriander, Cilantro, Basil, and Petitgrain essential oils.


Benefits of Linalool


Through research, scientists have found that linalool has a lot to offer.


Topical Use Benefits
Possesses cleansing properties based on experimental research.1-3


Aromatic Use Benefits
May help to promote feelings of calmness and relaxation based on experimental research.4,5


Internal Use Benefits
May help to promote a healthy circulatory system based on experimental research.
In vivo research indicates that linalool-rich lavender may be beneficial to the immune system. While more research is required, internal use of an oil containing linalool might lend support to this body system


APPEARANCE AT 20°C Clear mobile liquid 
COLOR Colorless to pale yellow 
ODOR Floral, woody notes, fresh 
OPTICAL ROTATION (°) 0 / 0 
DENSITY AT 20°C (G/ML)) 0,856 - 0,868 
REFRACTIVE INDEX ND20 1,4590 - 1,4680 
FLASHPOINT (°C) 75 
SOLUBILITY 1:4 v/v ethanol 60º - 1,45g/l in water 
ASSAY (% GC) > 96 
ACID VALUE (MG KOH/G) < 0,5


Linalool is an aromatic compound classified among the 26 allergens regulated by Europe. 
Linalool is present naturally in the essential oils of thyme, lavender, lavandin, Scots pine or peppermint ... 
Linalool is also found in many extracts (lemon, orange, verbena ...).


Its functions (INCI)
Deodorant : Reduces or masks unpleasant body odors
Perfuming : Used for perfume and aromatic raw materials


Linalool is a fragrant, natural compound that occurs naturally in many essential oils.
Linalool has a soft, floral and citrusy scent and can be found in tangerine, spearmint, rose, cypress, lemon, cinnamon and ylang ylang, among other plants.


Linalool is a monoterpene compound present in many plants. The enantiomer naturally occurring in essentiaI oils is (-)- linalool. Many reports have described the racemate form of this monoterpene and its effect on the brain neurotransmitters glutamic acid, -y-aminobutyric acid (GASA),acetylcholine and dopamine.


Linalool is a super common fragrance ingredient. 
Linalool’s kind of everywhere - both in plants and in cosmetic products. 
Linalool’s part of 200 natural oils including lavender, ylang-ylang, bergamot, jasmine, geranium and it can be found in 90-95% of prestige perfumes on the market. 


The problem with linalool is, that just like limonene it oxidises on air exposure and becomes allergenic. That’s why a product containing linalool that has been opened for several months is more likely to be allergenic than a fresh one.


Linalol is an aromatic substance, naturally present in the essential oils of lavender and lavandin, woodland pine or peppermint or in many vegetable extracts.


Appearance
Clear colorless liquid


 


Applications
Fragrance (Odor profile)
Fresh floral, herbal, lavender, rosewood, petitgrain, bergamot
Flavor (Taste profile)
Floral, fruity, lavender, herbal, bergamot


Linalool is a super common fragrance piece.
Linalool's ubiquitous, both in herbs and in cosmetics.
Linalool is part of 200 natural essential oils, including lavender, ylang-ylang, bergamot, jasmine, geranium, and is found in 90-95% of prestige perfumes on the market.
The problem with linalo is that it oxidizes and becomes pre-conceived.
Linalool will be more likely to occur in some way.
Linalool is found in a product above a certain amount, it must also be specified as an ingredient on the label.


Linalool is a common synthetic aroma ingredient with intense floral, lavender and sweet notes at room temperature. 
Linalool is used as a scent in 60–80% of perfumed hygiene products including soaps, detergents, shampoos, and lotions. 
Linalool also finds applications in the formulation of aftershave lotions, skin care, hair care products, cosmetics, home care and laundry care. 
Linalool comes as clear, colourless liquid.


Formula: C10H18O / (CH3)2C=CH(CH2)2C(CH3)(OH)CH=CH2
Molecular mass: 154.2
Boiling point: 198-200°C
Relative density (water = 1): 0.9
Solubility in water, g/100ml at 25°C: 0.16
Vapour pressure, Pa at 25°C: 21
Flash point: 75°C
Auto-ignition temperature: 235°C
Octanol/water partition coefficient as log Pow: 2.97 


Linalool occurs naturally in many of the essential oils we use. 
As an ingredient, Linalool 's used in floral fragrances. 
This colorless liquid occurs naturally in many essential oils, such as tangerine, spearmint, rose, cypress, lemon, cinnamon and ylang ylang. 
Linalool  has a soft, sweet scent.


Linalool is a bioactive component and utilized as a functional and nutraceutical tool in different foodstuffs. 
Linalool (3,7-dimethyl-1,6-octadien-3-ol) is a volatile compound present in diverse plant tissues such as leaves, fruits and flowers, respectively. 
Linalool and its esters are the mostly used in perfumery substances, and the odor of (R)- and (S)-linalool known as lavender-like and petitgrain. Owing to their phytochemical profile, it prevents from the lipid oxidation and enhances the shelf life of the food. 
Linalool, a monoterpene alcohol is also present in essential oils of various medicinal plants along with diverse health promoting activities such as prevention from cancer insurgence, preventive role in diabetes complications, protection from microbial growth and inflammations.


Keywords: Phytochemical, coriander, linalool, diet-based therapy, functional aspects


Linalool has two imperative forms generally known as R (-)-linalool (licareol)and S (π)-linalool (coriandrol) and these two forms varied in different plants depending upon nature and agro-climatic conditions. 
Linalool oil is extracted from the coriander seeds through steam distillation and further also quantified by gas chromatography-mass spectrometry.


Linalool is tertiary alcohol and monoterpenoid. 
Linalool  is mainly a component of volatile oils obtained from various spices and flowers such as cinnamon, mint, birch trees and citrus fruits, also some trees and fungi. 
Linalool  is one of the ingredients, which is responsible for providing fragrance. 
Linalool  is naturally widely found and at the same time synthetically produced.
Linalool  appears as a colorless to very pale yellow liquid with a floral scent.


Linalool can be referred to as a volatile oil substitute, plant metabolite, antimicrobial agent and a fragrance ingredient. The terpenoids are usually antimicrobial in nature since they have certain molecules in their structure which can bind to bacterial enzymes and render them ineffective. Because of antimicrobial properties, Linalool  can be used in any cleansing products such as house cleaning products, facial cleaning and toiletries. 
When any ingredient has antimicrobial properties, it also affects the harmful bacteria which cause body odor and P. acne – an acne-causing bacterium as well. 
So, it can be used to combat body odor. 
Linalool is used in bath products, bubble baths, cleansing products, hair care shampoos, lipsticks, moisturizers, skincare products and suntan products.


Linalool is a natural chemical: it naturally occurs within lots of different essential oils (over 200 in total) but as some people are allergic to it, it is often confused with a non-natural ingredients so   to clear up any confusion.


Linalool is classified as :
Deodorant
Perfuming


Linalool is a so-called tertiary alcohol of myrcene—a classification based on the molecule’s carbon arrangement. 
Linalool is a potent odorant in hops and beer. As an alcohol, it is considered part of the oxygenated fraction of hop oils and consequently is more soluble in wort and beer than its counterpart myrcene. 
Linalool has a distinctive floral aroma reminiscent of rose as well as lavender and/or bergamot.
Linalool also has citrusy and woody notes. 
Linalool is found at low levels of perhaps 10 to 100 ppm in hop oils, but it has an extremely low odor threshold for humans—down to 2 ppb in most lagers, for instance. This means it can be a very noticeable component in a beer’s aroma.
Linalool is commonly present in regularly hopped beers at a range of 1 to 30 ppb, but it may reach as much as 100 ppb or more in dry-hopped beers. 
Agronomically, linalool concentration in hop oil can vary significantly within the same variety, even in the same hop yard, but from different years—sometimes by as much as a factor of 2. Some researchers believe that linalool serves as a marker for hop aroma in beer, especially when German lagers are flavored with German aroma hops, simply because higher levels of linalool in beer tend to correlate with hoppier aromas in lagers. Nevertheless, linalool is only one of many hop aroma components derived from the many different essential oils in hops.


What Is It?
Linalool is a colorless to very pale yellow liquid with a floral smell similar to that of bergamot oil and French lavender. 
Linalool is a naturally occurring substance that is used to make fragrances and flavors. In cosmetics and personal care products, Linalool is used in the formulation of aftershave lotions, bath products, bubble baths, cleansing products, hair care products, lipsticks, moisturizers, perfumes and colognes, shampoos, skin care products and suntan products.


Why is it used in cosmetics and personal care products?
Linalool functions as a fragrance ingredient.


Scientific Facts: 
Linalool is a naturally occurring fragrance substance produced by a wide variety of plants such as mint, cinnamon, citrus fruits, and birch trees. 
Linalool can also be produced synthetically.


Linalool is not exactly a lily scent, but it is a floral fragrance with a lily-like appearance, in the form of enantiomers in many plants. For example, 60-70% of coriander oil consists of the (+)- enantiomer of linalool. Like its enantiomers, it is a colorless liquid with a lily-like, fresh floral odour. There is a slight odor difference between its enantiomers. Along with its ester forms, linalool is one of the most commonly used fragrances.


Products & Informations
Linalool is a monoterpenoid that found in many plants, mainly in Brazilian rose and Chinese camphor. 
Linalool appears colorless transparent liquid with floral odor. 
Linalool is divided into (+) – linalool isomer and (-) – linalool isomer. 
Linalool can be extracted from essential oils. And it can also be prepared by the hydrogenation of a-pinene. 
Linalool is mainly used in fragrance formulation of daily chemical products.


APPLICATIONS & USES
1. Linalool used as fragrance ingredient for floral type personal care products
2. Linalool used as flavoring agent for peach, mango, passion flower, resp berry,tropic fruit, tea scents
3. Linalool used as intermediate for vitamin synthesis
4.Linalool used as ingredient of deodorization
5.Linalool used as biobased ingredient for pest control
6. Linalool used as broad-spectrum bacteriostasis
7. Linalool used as pharmaceutical raw material
8.Linalool used as decay resistant agent


Benefits
Linalool is an anxiolytic agent, which means that it has powerful anti-stress effects. There are two mechanisms by which linalool improves sleep – firstly, the relaxing, anti-stress effects, and secondly through a direct sedative impact.
Linalool can help to reduce general inflammation and pain. 
Linalool is a powerful anti-inflammatory.


History of Linalool
Linalool and its esters are distributed in a vast number of essential oils from trace up to major amounts. 
Linalool is early production was accomplished in 1875 by isolation from Cayenne Bois de Rose oil from French Guiana. A Frenchman by the name of Licare was so involved with the oil’s production that Iinalool was initially called Licareol. Subsequent production shifted to Brazil (Bois de Rose oil) and Mexico (Linaloe oil) and more recently from Ho-leaf and Ho-wood oil (Taiwan, China and Japan). Availability of natural linalool has remained fairly constant since 1925. The volume of supply of natural product, however, has been dwarfed by the supply of synthetic product. The demand for linalool cannot be met by the production of natural oils.


Linalool is a naturally occurring terpene alcohol chemical found in many flowers and spice plants. 
Linalool has a number of commercial applications. 
Linalool is obtained by the steam fractional distillation of basil oil.
Linalool is a colourless liquid, with a characteristic herbaceous odour. 
Linalool is used in flavour and fragrance formulations.


Chemical Properties
 Linalool is colorless liquid with fragrance similar with bergamot. 
 Linalool is insoluble in water, but miscible with ethanol and ether.


Uses


1.  Linalool is used for the preparation of cosmetics, soaps, detergents, food and other flavors.
2. GB 276011996 states it is classified into food flavor allowed for temporary use. 
 Linalool is mainly used for the preparation of flavors or aromatic seasoning of pineapple, peach, and chocolate.
3.  Linalool is widely presented in flowers, fruits, stems, leaves, roots and green Rosa Chinensis viridiflora. 
 Linalool has a wide range of application, not only for all the floral flavors, such as sweet bean curd, jasmine, Convallaria majalis, lilac, etc., it can also be applied in fruit flavor type, Fen-flavor type, wood flavor type, aldehyde flavor type, oriental flavor type, amber scent type, chypre type, fern-type and other non-flower type of flavor. 
 Linalool can also be used in formulating orange leaf, bergamot, lavender, and some kinds of artificial oils such as hybrid lavender oil. 
 Linalool is mostly used in soap or flavor. 
 Linalool can be used for food flavor.
4. Linalool is a kind of important spices and is the blending raw materials for producing various kinds of artificial oil, also used extensively for the manufacturing of various esters of linalool. 
Linalool has an important position in the ester-type perfumes and other cosmetic formulations.
 Linalool can generate citral through oxidation and can also be used for the synthesis of many other kinds of spices.


Linalool is a kind of terpene alcohols and is one kind of famous perfume compounds. It is the mixture of two isomers (α-linalool and β-linalool). 
Linalool is extracted from camphor oil (from camphor tree) or synthesized from the α-pinene or β-pinene contained in turpentine. 
Linalool is colorless oily liquid with sweet and tender fresh flowers and a fragrance of Convallaria majalis. 
Linalool is easily soluble in organic solvents such as ethanol, ethylene glycol and diethyl ether but insoluble in water and glycerol. 
Linalool is easily subject to isomerization and is relatively stable in alkali. 
Linalool has a density (25 ℃) of 0.860~0.867, the refractive index (20 ℃) of ​​1.4610~1.4640, optical rotation (20 ℃) of ​​-12 ° ~-18 °, the boiling point being 197~199 ℃, and the flash point (open ended) of 78 ℃. 
Linalool with alcohol content higher than 95% is an important spices for floral fragrance used for perfumes, soaps and other fragrance industry. 
Linalool is also widely used in flowers oils of lending lily, lilac, sweet pea, and orange blossom as well as the compound perfume of amber incense, oriental fragrance, and aldehyde-type fragrance, cosmetics perfumes and food flavor. 
Linalool can also be used as the spices of lemon, lime, orange, grape, apricot, pineapple, plum, peach, cardamom, cocoa, and chocolate. Drug containing 92.5% alcohol content is used as the raw material drugs in the pharmaceutical industry for producing isophytol which is an important intermediate in the preparation of vitamin E. 
Linalool can also be used as raw material for producing valuable spices linalyl acetate and some other esters. Linalool belongs to open chain terpene tertiary alcohol. 
It has two double bonds. However, it contains an asymmetric carbon atom, so it has three kinds of optical isomers. In Nature, all three kinds of isomers are present with the amount of I-body being the highest, accounting for 70% to 80% of the total amount of the three. 
I-body is mostly presented in linalool oil (containing about 80 to 90%), champa, lavender oil, lime oil, neroli oil, clary sage oil, aloeswood oil, lemon oil, rose oil, cananga orodrata oil and some other kinds of essential oil; its d-body is mostly presented in coriander oil (containing about 60% to 70%), sweet orange oil, nutmeg oil, palmarosa oil and other kinds of essential oil; its dl-form is mainly presented in the essential oils of clary sage and jasmine.


Linalool is used as a scent in 60-80% of perfumed hygiene products and cleaning agents including soaps, detergents, shampoos, and lotions. as a scent in 60-80% of perfumed hygiene products and cleaning agents including soaps, detergents, shampoos, and lotions.


Linalool is a naturally occurring terpene alcohol chemical found in many flowers and spice plants with many commercial applications, the majority of which are based on its pleasant scent (floral, with a touch of spiciness).
Linalool is used as a scent in 60–80% of perfumed hygiene products and cleaning agents including soaps, detergents, shampoos, and lotions.


About this substance
Helpful information
Linalool is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.


Linalool is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Consumer Uses
Linalool is used in the following products: washing & cleaning products, biocides (e.g. disinfectants, pest control products), polishes and waxes, air care products, cosmetics and personal care products, perfumes and fragrances, anti-freeze products and inks and toners.
Other release to the environment of Linalool is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.


Article service life
Other release to the environment of Linalool is likely to occur from: indoor use as processing aid and indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints).
Linalool is intended to be released from scented: clothes, eraser, toys, paper products and CDs.


Widespread uses by professional workers
Linalool is used in the following products: washing & cleaning products and polishes and waxes.
Linalool is used in the following areas: mining.
Linalool is used for the manufacture of: textile, leather or fur, wood and wood products, chemicals and furniture.
Other release to the environment of Linalool is likely to occur from: indoor use as processing aid and outdoor use as processing aid.


Formulation or re-packing
Linalool is used in the following products: perfumes and fragrances, washing & cleaning products, cosmetics and personal care products, polishes and waxes and air care products.
Release to the environment of Linalool can occur from industrial use: formulation of mixtures.


Uses at industrial sites
Linalool is used in the following products: washing & cleaning products, polishes and waxes and perfumes and fragrances.
Linalool has an industrial use resulting in manufacture of another substance (use of intermediates).
Linalool is used in the following areas: mining.
Linalool is used for the manufacture of: chemicals.
Release to the environment of Linalool can occur from industrial use: in processing aids at industrial sites and as an intermediate step in further manufacturing of another substance (use of intermediates).


Manufacture
Release to the environment of Linalool can occur from industrial use: manufacturing of the substance.


IUPAC names
(3S)-3,7-dimethylocta-1,6-dien-3-ol
(S)-3,7-Dimethyl-1,6-octadien-3-ol
- 3,7-dimethylocta-1,6-dien-3-ol
1,6-Octadien-3-ol, 3,7-dimethyl-
1,6-Octadien-3-ol,3,7-dimethyl
2,6-Dimethyl-2,7-Octadien-6-ol
2,6-Dimethyl-2,7-octadiene-3-ol
3,7- dimethyl octa-1,6-dien-3-ol
3,7-dimethtlocta-1,6-dien-3-ol
3,7-Dimethyl octa-1,6-diene-3-ol
3,7-Dimethyl octa-1,6-diene-3-ol  
3,7-Dimethyl-1,6-octadien-3-ol
3,7-dimethyl-1,6-octadien-3-ol
3,7-Dimethylocta-1,6-dien-3-ol
3,7-dimethylocta-1,6-dien-3-ol
3,7-dimethylocta-1,6-dien-3-ol
Ho Oil
linalol
LINALOOL
Linalool
linalool
LInalool
Linalool
linalool
Linalool synthetic
Natural linalool


SYNONYMS:
(±)-3,7-Dimethyl-1,6-octadien-3-ol
(±)-3,7-Dimethyl-3-hydroxy-1,6-octadiene
(±)-Linalool
(±)-Linalool
(�)-Linalool
1,6-Octadien-3-ol, 3,7-dimethyl- [ACD/Index Name]
245-083-6 [EINECS]
3,7-Dimethyl-1,6-octadien-3-ol [ACD/IUPAC Name]
3,7-Dimethyl-1,6-octadien-3-ol [German] [ACD/IUPAC Name]
3,7-Diméthyl-1,6-octadién-3-ol [French] [ACD/IUPAC Name]
3,7-Dimethylocta-1,6-dien-3-ol
78-70-6 [RN]
allo-Ocimenol
dl-Linalool
Linalool [Wiki]
LINALOOL, (-)-
LINALOOL, (+)-
LINALOOL, (±)-
Linalool, β
linalyl alcohol
β-linalool
β-Linalool
(±)-Linalool
(±)-Linalool|3,7-dimethyl-1,6-octadien-3-ol
(±)-Linalool-d3
1, 6-Octadien-3-ol, 3,7-dimethyl-, (-)-
1,1,2-Trideuterio-3,7-dimethylocta-1,6-dien-3-ol
1,6-Octadien-3-ol,3,7-Dimethyl-
1,6-Octadien-3-ol,3,7-dimethyl-, (3R)-
1,6-Octadien-3-ol,3,7-dimethyl-, (3S)-


 

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