TETRAHYDROMYRCENOL
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TETRAHYDROMYRCENOL ??
- ???
- -1.53°C (estimate)
- ?? ?
- 197-201 °C(lit.)
- ??
- 0.823 g/mL at 25 °C(lit.)
- ???
- 9.3Pa at 24℃
- ???
- n
20/D 1.4335(lit.)
- ???
- 185 °F
- ?? ?? (pKa)
- 15.33±0.29(Predicted)
- ??
- ??? ??.
- ??
- 100.00%??. ???? ??? ??? ?? ??? ??
- ?? ??
- ???
- ???
- 281.9mg/L at 24℃
- Henry's Law Constant
- 2.7×10-2 mol/(m3Pa) at 25℃, Yaws (2003)
- ??? ?? ??
- PERFUMING
- LogP
- 3.2 at 25℃
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ?? ???? ?? | 52/53 | ||
|---|---|---|---|
| ????? | 61 | ||
| WGK ?? | 2 | ||
| TSCA | TSCA listed | ||
| ?? | Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg (Wohl, 1974). | ||
| ???? ?? | KE-11633 |
| ????(GHS): |
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| ?? ?: | Warning | |||||||||||||||||||||
| ??·?? ??: |
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TETRAHYDROMYRCENOL C??? ??, ??, ??
??
Has apparently not been reported to occur in nature.??
Tetrahydromuguol finds extensive use as a soap perfume chemical (mixture) and as a base for many types of floral fragrances, Muguet, Lilac, Rose, Lily, etc. It blends excellently with the conventional “rose materials”, alifatic aldehydes, Decenol, Amylcinnamic aldehyde, Butylcyclohexanyl acetate, etc. for such purposes.?? ??
From allo-ocimene, via allo-ocimenol followed by hydrogenation (Arctander, 1969). Uses: Use in fragrances in the USA amounts to approximately 35,000 lb/yr.TETRAHYDROMYRCENOL ?? ?? ? ???
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TETRAHYDROMYRCENOL ?? ??
???( 78)?? ??
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