?????????
|
|
????????? ??
- ?? ?
- 174-176 °C/15 mmHg (lit.)
- ??
- 0.95 g/mL at 25 °C (lit.)
- ???
- n
20/D 1.55(lit.)
- ???
- 200 °F
- ?? ??
- -20°C
- ???
- ?: 25°C?? ???0.005g/L
- ??? ??
- ??
- ??
- ?? ???
- ??
- 100.00%??. ??? ??? ?? ??? ?? ??
- ?? ??
- ???
- ???? ??
- synthetic
- JECFA Number
- 686
- ???
- ???
- LogP
- 5.33
- CAS ??????
- 101-86-0(CAS DataBase Reference)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ??? ?? | C,Xi | ||
|---|---|---|---|
| ?? ???? ?? | 36/37/38-34-43-52/53 | ||
| ????? | 26-36/37/39-45-36-36/37-61 | ||
| ????(UN No.) | UN 3265 8/PG 3 | ||
| WGK ?? | 2 | ||
| RTECS ?? | GD6560000 | ||
| HS ?? | 29122990 | ||
| ?? | The acute oral LD50 value in rats was reported as 3.1 g/kg (2.45-3.75 g/kg) (Moreno, 1971). The acute dermal LD50 value in rabbits was reported as > 3 g/kg (Moreno, 1971). | ||
| ???? ?? | KE-28401 |
????????? C??? ??, ??, ??
??
α-Hexylcinnamaldehyde has a jasmine-like odor, particularly on dilution. May be synthesized by condensation of octylaldehyde with benzaldehyde.??? ??
alpha-Hexylcinnamaldehyde is a yellow liquid with a mild, slightly fatty, floral, somewhat herbal odor, and a distinct jasmine note. Similarly to the ??-amyl homolog, ??-hexylcinnamaldehydemust be protected against oxidation by the addition of stabilizers. It is prepared in a manner similar to that of ??-amylcinnamaldehyde by alkaline condensation of excess benzaldehyde with octanal (instead of heptanal). ??-Hexylcinnamaldehyde is widely used in flower compositions (e.g., jasmine and gardenia) and, because of its stability to alkali, in soap perfumes.??
Reported found in cooked, scented rice.??
α-Hexylcinnamaldehyde is characterized by a typical floral scent, which makes them suitable to be used as fragrances in personal care (perfumes, creams, shampoos, etc.) and household products. It has been also used as flavouring additive in food and pharmaceutical industry.??
ChEBI: A member of the class of cinnamaldehydes carrying a hexyl substituent at the alpha-position.?? ??
By condensation of octylaldehyde with benzaldehyde?? ??
Solubilization of α-hexylcinnamaldehyde by the ionic surfactants, sodium dodecyl sulfate and dodecyltrimethylammonium chloride and a non-ionic surfactant such as dodecyl polyoxyethylene ethers has been investigated.???
Combustible.?? ?? ??
Hexyl cinnamic aldehyde is a fragrance allergen. Its presence has to be mentioned by name in cosmetics within the EU.Solubility in organics
Insoluble in Propylene glycol and Glycerin. Soluble in alcohol, miscible with oils.????????? ?? ?? ? ???
???
?? ??
????????? ?? ??
???( 381)?? ??
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????????? ?? ??:
????????? ????????? ??????????? DL-6,8-??? ? ??(??-)?????? ?????? ?????????????? ???? ???? ???? ?????????
3-（trifluoromethyl) Cinnamaldehyde
4-(Dimethylamino)cinnamaldehyde
3-(4-METHYLBENZYLIDENE)CAMPHOR?
Cassia Aurantium P.E Catechins 8% HPLC
TOSLAB 864097
2-(E)-BENZYLIDENE-6-(TRIFLUOROACETYL)CYCLOHEXANONE
TOSLAB 860368