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Cinnamyl alcohol Basic information |
Product Name: | Cinnamyl alcohol |
Synonyms: | (2E)-3-Phenyl-2-propen-1-ol;1-Phenyl-1-propen-3-ol;2-Propen-1-ol,3-phenyl-;3-Fenyl-2-propen-1-ol;3-phenyl-2-propen-1-o;3-Phenyl-2-propenol;3-phenyl-prop-2-en-1-ol;3-phenylprop-2-en-1-ol |
CAS: | 104-54-1 |
MF: | C9H10O |
MW: | 134.18 |
EINECS: | 203-212-3 |
Product Categories: | Pharmaceutical Intermediates;Benzhydrols, Benzyl & Special Alcohols;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Cosmetics |
Mol File: | 104-54-1.mol |
Cinnamyl alcohol Chemical Properties |
Melting point | 30-33 °C(lit.) |
Boiling point | 250 °C(lit.) |
density | 1.044 g/mL at 25 °C(lit.) |
vapor density | 4.6 (vs air) |
vapor pressure | <0.01 mm Hg ( 25 °C) |
refractive index | 1.5819 |
FEMA | 2294 | CINNAMYL ALCOHOL |
Fp | >230 °F |
storage temp. | 2-8°C |
solubility | H2O: soluble |
form | Fused Low Melting Crystalline Solid |
color | White |
Water Solubility | 1.8 g/L (20 ºC) |
Merck | 14,2302 |
BRN | 1903999 |
Stability: | Stable. Incompatible with strong oxidizing agents. |
CAS DataBase Reference | 104-54-1(CAS DataBase Reference) |
NIST Chemistry Reference | 2-Propen-1-ol, 3-phenyl-(104-54-1) |
EPA Substance Registry System | 2-Propen-1-ol, 3-phenyl-(104-54-1) |
Safety Information |
Hazard Codes | Xn |
Risk Statements | 22-36/38-43-36 |
Safety Statements | 26-36/37-37/39-24-24/25 |
RIDADR | 2811 |
WGK Germany | 2 |
RTECS | GE2200000 |
F | 10-23 |
TSCA | Yes |
Hazardous Substances Data | 104-54-1(Hazardous Substances Data) |
Cinnamyl alcohol Usage And Synthesis |
Description |
As an organic compound, Cinnamic alcohol has a very distinct sweet, spicy, hyacinth odour that is found in resins, balsams and cinnamon leaves. It is used commonly in the fragrance industry due to its distinctive odour, which can be applied as a deodorant, fragrance and additive in cosmetic products and in the formulation of bath products, body and hand products, such as soaps, toothpaste, deodorants, etc. Besides, it also finds application as a food additive in chewing gum, bakery products, candy and soft drinks. Naturally, Cinnamyl alcohol is occurrent only in small amount, thus its industrial demand is usually fulfilled by chemical synthesis starting from the reduction of cinnamaldehyde. Cinnamyl alcohol has been found to have a sensitising effect on some particular people, thus it is also considered as a Standardized Chemical Allergen. The physiologic effect of cinnamyl alcohol is caused by the Increased Histamine Release and cell-mediated Immunity. |
References |
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Chemical Properties | colourless solid |
Uses | Cinnamyl alcohol was used to study the alkylation of 2,4-di-tert-butylphenol by cinnamyl alcohol using aluminum-containing mesoporous ethane-silica catalyst. It was used to study gold nanoparticles supported on titanium dioxide catalysed oxidative coupling of alcohols and amines to form the corresponding imines. |
Uses | In perfumery; as deodorant in 12.5% solution in glycerol. |
Definition | ChEBI: A primary alcohol comprising an allyl core with a hydroxy substituent at the 1-position and a phenyl substituent at the 3-position (geometry of the C2C bond unspecified). |
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