| Identification | Back Directory | [Name]
ETHYL LINALOOL | [CAS]
10339-55-6 | [Synonyms]
ETHYL LINALOOL
Ethyl Linanlool
METHYL LINALOOL
Rhodinol (Nature)
3,7-dimethylnona-
Ethyllinalool Technical
3,7-dimethylnona-1,6-dien
3,7-dimethyl-6-nonadien-3-ol
3,7-dimethylnona-1,6-dien-3-ol
6-Nonadien-3-ol,3,7-dimethyl-1
3,7-dimethyl-1,6-nonadien-3-ol
1,6-Nonadien-3-ol, 3,7-dimethyl-
6-NONADIEN-3-OL, 3,7-DIMETHYL-1,85% | [EINECS(EC#)]
233-732-6 | [Molecular Formula]
C12H22O | [MDL Number]
MFCD00135350 | [MOL File]
10339-55-6.mol | [Molecular Weight]
182.3 |
| Chemical Properties | Back Directory | [Boiling point ]
132℃ (86 Torr) | [density ]
0.857±0.06 g/cm3 (20 ºC 760 Torr) | [vapor pressure ]
18Pa at 25℃ | [refractive index ]
1.4603 (589.3 nm 25℃) | [Fp ]
90.9±15.0℃ | [pka]
14.45±0.29(Predicted) | [color ]
Colourless slightly oily liquid. | [Odor]
at 100.00 %. fresh bois de rose herbal wet green lavender bergamot | [Odor Type]
floral | [Water Solubility ]
656mg/L at 20℃ | [Cosmetics Ingredients Functions]
PERFUMING
FRAGRANCE | [InChI]
InChI=1S/C11H20O/c1-5-10(3)8-7-9-11(4,12)6-2/h6,8,12H,2,5,7,9H2,1,3-4H3 | [InChIKey]
KRLBLPBPZSSIGH-UHFFFAOYSA-N | [SMILES]
C=CC(C)(O)CCC=C(C)CC | [LogP]
3.3 | [EPA Substance Registry System]
1,6-Nonadien-3-ol, 3,7-dimethyl- (10339-55-6) |
| Hazard Information | Back Directory | [Chemical Properties]
Clear colorless to pale yellowish liquid. | [Physical properties]
Colorless slightly oily liquid. Very slightly
soluble in Mater, soluble in alcohol and oils. | [Occurrence]
Has apparently not been reported to occur in nature. | [Uses]
Ethyl Linalool is fresh bois de rose herbal wet green lavender bergamot. It has a floral, fresh, bergamot character and is sweeter and less agrestic than Linalool. As with Linalool, it is used in a wide variety of notes for floral bouquets. | [Preparation]
From methyl ethyl ketone and acetylene through a series of reactions (Bedoukian, 1967). | [Metabolism]
Tertiary alcohols are not readily metabolized and may be excreted in the urine both unchanged and highly conjugated with glucuronic acid. In rabbits, carbon-carbon double bonds make little difference to the extent of conjugation of terf-hexyl alcohols (Williams, 1959). |
| Questions And Answer | Back Directory | [Aroma]
Floral, only slightly woody-green, soft odor
of moderate tenacity. The odor type compared
to Linalool indicates that "Ethyl Iinalool" is
softer, more waxy, less volatile, less woodygrecn and overall more floral. It is more
Coriander-like, less Bois-de-Rose-like. | [Uses in Perfume]
Ethyl linalool has been suggested for use in
perfume compositions as a modifier for LinaIool with certain advantages over that marerial. Ethyl Iinalool has a somewhat slower rate
of evaporation and is easier to work with, needs
only normal fixation, and blends with more
materials. It introduces softer, more floralwoody, less citrusy notes, according to the
composition in which it is used. Along with
Ethyl Iinalyl acetate, it forms a pleasant
Bergamot-type background note even in soap
perfumes, a combination which is more stable
than Bergamot oil itself.
The alcohol is also an interesting item in
Muguet, Lilac, Lily, Appleblossom, etc. as
well as in fantasy creations. |
|
| Company Name: |
jiliang chemicals
|
| Telephone: |
21-62165282 |
| Website: |
http://www.jiliangchem.com |
| Company Name: |
Rhawn Reagent
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| Telephone: |
400-400-1332688 18019345275 |
| Website: |
http://www.rhawn.cn |
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