- Dihydromyrcenol
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- $5.00 / 1KG
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2025-05-26
- CAS:18479-58-8
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10000kg
- Dihydromyrcenol
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- $120.00 / 1kg
-
2025-04-15
- CAS:18479-58-8
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 20ton
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| | Dihydromyrcenol Basic information |
| | Dihydromyrcenol Chemical Properties |
| Boiling point | 84 °C10 mm Hg(lit.) | | density | 0.784 g/mL at 25 °C(lit.) | | vapor pressure | 20Pa at 25℃ | | refractive index | n20/D 1.443(lit.) | | Fp | 170 °F | | pka | 15.31±0.29(Predicted) | | form | liquid | | color | A colourless viscous liquid. | | Odor | at 100.00 %. fresh citrus lime floral clean cologne weedy | | Odor Type | citrus | | biological source | synthetic | | Water Solubility | 939mg/L at 20℃ | | Major Application | flavors and fragrances | | Cosmetics Ingredients Functions | FRAGRANCE
PERFUMING | | InChI | 1S/C10H20O/c1-5-9(2)7-6-8-10(3,4)11/h5,9,11H,1,6-8H2,2-4H3 | | InChIKey | XSNQECSCDATQEL-UHFFFAOYSA-N | | SMILES | CC(CCCC(C)(C)O)C=C | | LogP | 3.25 at 40℃ | | CAS DataBase Reference | 18479-58-8(CAS DataBase Reference) | | NIST Chemistry Reference | 7-Octen-2-ol, 2,6-dimethyl-(18479-58-8) | | EPA Substance Registry System | Dihydromyrcenol (18479-58-8) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38-36-36/38 | | Safety Statements | 26-36/37 | | WGK Germany | 1 | | RTECS | RH3420000 | | TSCA | TSCA listed | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2 | | toxicity | The acute oral LD50 value in rats was reported as 5.3 g/kg (4.5-6.1 g/kg) (Moreno, 1972). The acute dermal LD50 value in rabbits exceeded 5 g/kg (Moreno, 1972) |
| | Dihydromyrcenol Usage And Synthesis |
| Chemical Properties | Dihydromyrcenol is a colorless liquid with a
fresh citrus-like odor and a lavender note. It is obtained from 3,7-dimethyl-1,6-
octadiene (citronellene), the pyrolysis product of cis-pinane and can be prepared by three different processes: (i) by addition of hydrogen chloride and
subsequent hydrolysis of the resulting 2,6-dimethyl-2-chloro-7-octene; or
(ii) by addition of formic acid and subsequent saponification of the resulting
dihydromycrenyl formate; or (iii) by direct hydroxylation with 60–80%
sulfuric acid.Dihydromyrcenol is used in fine fragrances as well as in soap and detergent perfumes
for fresh lime and citrus-like floral notes. | | Occurrence | Found in the leaf oils of Barosma venusta and in the oil of hops (Gildemeister & Hoffman, 1960) | | Uses | Dihydromyrcenol is used in the fragrance industry for its fresh lime and citrus-like odor.
Dihydromyrcenol is a fragrance ingredient used in cosmetics, fine fragrances, shampoos, toilet soaps, and other toiletries as well as in non-cosmetic products such as household cleaners and detergents. Its worldwide use is greater than >1000 metric tons per year (IFRA, 2004). A colorless, somewhat viscous liquid that is a mixture of approximately 50% 2,6-dimethyl-7-octen-2-ol and 50% 2,6-dimethyl-7-octen-2-yl formate. It has apparently not been reported to occur in nature. | | Uses | Dihydromyrcenol was used in the synthesis of bioamphiphilic polymers based on the hydrophilic dextran and the hydrophobic terpenes as renewable resources. | | Preparation | Dihydromyrcenol is prepared by adding hydrogen chloride to myrcene followed by hydrolysis under mild conditions.(Bedoukian, 1967) | | Definition | ChEBI: A monoterpenoid that is oct-7-en-2-ol substituted by methyl groups at positions 2 and 6 respectively. | | General Description | Methoxycarbonylation of dihydromyrcenol catalyzed by [PdCl2(PPh3)2]-SnCl2·2H2O-2PPh3 has been investigated. Dihydromyrcenol is a widely used fragrance ingredient and has been evaluated for developmental toxicity in pregnant Sprague-Dawley rats. | | Flammability and Explosibility | Not classified | | Solubility in organics | Practically
insoluble in water, soluble in alcohol and oils. |
| | Dihydromyrcenol Preparation Products And Raw materials |
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