- Eugenol acetate
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- $61.00 / 5g
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2026-02-01
- CAS:93-28-7
- Min. Order:
- Purity: 98.66%
- Supply Ability: 10g
- Eugenol Acetate
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- $30.00 / 1KG
-
2025-06-27
- CAS:93-28-7
- Min. Order: 50KG
- Purity: 99%
- Supply Ability: 500000kg
- EUGENOL ACETATE
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- $130.00 / 1kg
-
2025-05-26
- CAS:93-28-7
- Min. Order: 10kg
- Purity: 99%
- Supply Ability: 100000kg
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| | EUGENOL ACETATE Basic information |
| | EUGENOL ACETATE Chemical Properties |
| Melting point | 26°C | | Boiling point | 281-286 °C(lit.) | | density | 1.079 g/mL at 25 °C(lit.) | | vapor pressure | 0.041Pa at 20℃ | | refractive index | n20/D 1.518(lit.) | | FEMA | 2469 | EUGENYL ACETATE | | Fp | 230 °F | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | solubility | Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Slightly) | | form | Colourless to Light Yellow Oil to Semi-Solid | | color | White or Colorless to Light yellow | | Odor | at 100.00 %. fresh sweet woody clove floral carnation malt spice | | Odor Type | spicy | | biological source | synthetic | | Water Solubility | 407mg/L at 20℃ | | JECFA Number | 1531 | | Stability: | Stable. Combustible. Incompatible with strong oxidizing agents. | | Major Application | cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care | | Cosmetics Ingredients Functions | FRAGRANCE | | InChI | 1S/C12H14O3/c1-4-5-10-6-7-11(15-9(2)13)12(8-10)14-3/h4,6-8H,1,5H2,2-3H3 | | InChIKey | SCCDQYPEOIRVGX-UHFFFAOYSA-N | | SMILES | COc1cc(CC=C)ccc1OC(C)=O | | LogP | 2.8 at 25℃ | | CAS DataBase Reference | 93-28-7(CAS DataBase Reference) | | NIST Chemistry Reference | Phenol, 2-methoxy-4-(2-propenyl)-, acetate(93-28-7) | | EPA Substance Registry System | Phenol, 2-methoxy-4-(2-propenyl)-, acetate (93-28-7) |
| Hazard Codes | Xn | | Risk Statements | 22-38 | | Safety Statements | 36 | | WGK Germany | 2 | | RTECS | SJ4550000 | | TSCA | TSCA listed | | HS Code | 29147000 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Acute Tox. 4 Oral
Skin Sens. 1B | | toxicity | The acute oral LD50 value in rats was reported as 1.67 g/kg (Jenner, Hagan, Taylor, Cook & Fitzhugh, 1964) and as 2.6 g/kg (2.3-2.9 g/kg) (Moreno, 1972b). The acute dermal LD50 value in rabbits exceeded 5 g/kg (Moreno, 1972a). |
| | EUGENOL ACETATE Usage And Synthesis |
| Chemical Properties | Eugenol Acetate occurs in clove
oil, together with eugenol. It is a crystalline solid (mp 29°C) or yellowish liquid
with a slightly fruity, clove odor. Eugenol acetate is prepared by acetylation of
eugenol with acetic anhydride and is used in floral compositions to accentuate
floral, spicy characters. | | Chemical Properties | Eugenyl acetate has a characteristic odor reminiscent of clove oil, with a burning, aromatic favor. | | Occurrence | Reported found in the essential oils of Laurus nobilis, clove buds and leaves, cassia leaf and cinnamon leaf, root and bark | | Uses | Eugenol Acetate is a constituent of Clove oil, an essential oil from the clove plant, Syzygium aromaticum. Clove oil is a natural analgaesic and antiseptic used primarily in dentistry for its main ingredient Eugenol. Clove oil can also be purchased in pharmacies over the counter, as a home remedy for dental pain relief, mainly toothache; it is also often found in the aromatherapy section of health food stores. | | Preparation | By direct acetylation of eugenol using acetic anhydride. | | Definition | ChEBI: Acetyleugenol is a member of phenols and a benzoate ester. | | Application |
Mild and sweet-spicy, balsamic-fruity odour, reminiscent of carnation. Earthy-fresh notes or leafy-floral notes are not uncommon. Used in perfumes to emphasize floralness in carnation, along with iso-eugenol, Amyl oxy-iso-eugenol, etc. Fresher than these, but also milder. Not stable in white soap or alkali. It is in flavors for berry, fruit, mint, spice, and vanilla types.
| | Flammability and Explosibility | Not classified | | Safety Profile | Moderately toxic by
ingestion. A skin irritant. Combustible
liquid. When heated to decomposition it
emits acrid smoke and irritating fumes. See
also EUGENOL, ALLYL COMPOUNDS,
and ESTERS. |
| | EUGENOL ACETATE Preparation Products And Raw materials |
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