LINALYL PHENYL ACETATE
- CAS No.
- 7143-69-3
- Chemical Name:
- LINALYL PHENYL ACETATE
- Synonyms
- Linalylphenylacetat;linalylalpha-toluate;LINALYL PHENYL ACETATE;3,7-dimethylocta-1,6-dien-3-yl 2-phenylacetate;aceticacid,phenyl-,1,5-dimethyl-1-vinyl-4-hexenylester;Phenylacetic acid 3,7-dimethyl-1,6-octadiene-3-yl ester;Benzeneaceticacid,1-ethenyl-1,5-dimethyl-4-hexenylester;benzeneaceticacid,1,5-dimethyl-1-ethenyl-4-hexenylester;Benzeneacetic acid, 1-ethenyl-1,5-dimethyl-4-hexen-1-yl ester
- CBNumber:
- CB2345785
- Molecular Formula:
- C18H24O2
- Molecular Weight:
- 272.38
- MOL File:
- 7143-69-3.mol
- Modify Date:
- 2023/5/25 18:01:03
| Boiling point | 375.44°C (rough estimate) |
|---|---|
| Density | 1.0134 (rough estimate) |
| refractive index | 1.5510 (estimate) |
| FEMA | 3501 | LINALYL PHENYLACETATE |
| color | A colourless or pale straw-coloured viscous liquid |
| Odor | at 100.00 %. rose sweet honey sick neroli rose |
| Odor Type | floral |
| JECFA Number | 1019 |
| LogP | 5.64 |
| EPA Substance Registry System | Benzeneacetic acid, 1-ethenyl-1,5-dimethyl-4-hexenyl ester (7143-69-3) |
SAFETY
Risk and Safety Statements
| Toxicity | Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg(Moreno, 1974). |
|---|
LINALYL PHENYL ACETATE Chemical Properties,Uses,Production
Description
Linalyl phenylacetate has a mildly floral, intensely sweet Neroli rose type odor. May be synthesized from dehydrolinalool and methyl phenylacetate in the presence of sodium methylate catalyst, followed by hydrogenation of the ester, or by any other suitable means.
Chemical Properties
Linalyl phenylacetate has a mildly floral, intensely sweet Neroli rose–type odor.
Occurrence
Has apparently not been reported to occur in nature
Preparation
From dehydrolinalool and methyl phenylacetate in the presence of sodium methylate catalyst, followed by hydrogenation of the ester, or by any other suitable means.
Metabolism
Open-chain olefinic terpene esters are presumably hydrolysed to the alcohol and the acid (Fassett, 1963). Open-chain terpenes are metabolized in the rabbit by ω-oxidation and by reduction of an a,B-double bond (Williams, 1959)
LINALYL PHENYL ACETATE Preparation Products And Raw materials
Raw materials
Preparation Products
LINALYL PHENYL ACETATE Suppliers
| Supplier | Tel | Country | ProdList | Advantage | Inquiry |
|---|---|---|---|---|---|
| Pfaltz & Bauer, Inc. | (800) 225-5172 | United States | 6830 | 72 | Inquiry |
| 3B Scientific Corporation | 847.281.9822 | United States | 6744 | 47 | Inquiry |
| CARBONE SCIENTIFIC CO.,LTD | +44(0)870 486 8629 | United Kingdom | 6682 | 30 | Inquiry |
| Shanghai wencai New Material Technology Co., Ltd. | 15721586846 | China | 2796 | 58 | Inquiry |
| Penta International Corporation | (973) 740-2300 | United States | 5043 | 58 | Inquiry |
| Penta Manufacturing Company | 973 740 2300 | United States | 5077 | 65 | Inquiry |
| Shaanxi Dideu Newmaterial Co., Ltd. | 029-63373950 15353716720 | China | 10011 | 58 | Inquiry |
| TCI (Shanghai) Chemical Trading Co., Ltd. | 021-021-61109150 | China | 31163 | 58 | Inquiry |
| BOC Sciences | USA | 0 | 65 | Inquiry |
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