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ChemicalBook--->CAS DataBase List--->93-28-7

93-28-7

93-28-7 Structure

93-28-7 Structure
IdentificationMore
[Name]

EUGENOL ACETATE
[CAS]

93-28-7
[Synonyms]

1,3,4-EUGENOL ACETATE
1-ACETOXY-2-METHOXY-4-ALLYLBENZENE
4-ALLYL-2-METHOXYPHENOL ACETATE
4-ALLYL-2-METHOXYPHENYL ACETATE
ACETOEUGENOL
ACETYL EUGENOL
EUGENOL ACETATE
EUGENYL ACETATE
FEMA 2469
PHENOL, 4-ALLYL-2-METHOXY:ACETATE
1-acetoxy-4-allyl-2-methoxy-benzene
2-methoxy-4-(2-propenyl)-phenoacetate
2-methoxy-4-(2-propenyl)-phenol,acetate
4-allyl-2-methoxy-phenoacetate
Aceteugenol
aceticacid4-allyl-2-methoxy-phenylester
eugenyl
Phenol,2-methoxy-4-(2-propenyl)-,acetate
EUGENYL ACETATE 98+% FCC
EUGENOL ACETATE 98+%
[EINECS(EC#)]

202-235-6
[Molecular Formula]

C12H14O3
[MDL Number]

MFCD00026191
[Molecular Weight]

206.24
[MOL File]

93-28-7.mol
Chemical PropertiesBack Directory
[Appearance]

liquid
[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℃
[FEMA ]

2469
[refractive index ]

n20/D 1.518(lit.)
[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
[Stability:]

Stable. Combustible. Incompatible with strong oxidizing agents.
[Odor Type]

spicy
[Water Solubility ]

407mg/L at 20℃
[JECFA Number]

1531
[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)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R38:Irritating to the skin.
[Safety Statements ]

S36:Wear suitable protective clothing .
[WGK Germany ]

2
[RTECS ]

SJ4550000
[HS Code ]

29147000
[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.
[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).
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Eugenol
[Preparation Products]

3-METHOXY-DL-TYROSINE
Hazard InformationBack Directory
[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.
[Chemical Properties]

liquid
[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.
[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.
[Definition]

ChEBI: Acetyleugenol is a member of phenols and a benzoate ester.
[Preparation]

By direct acetylation of eugenol using acetic anhydride.
[Flammability and Explosibility]

Notclassified
Spectrum DetailBack Directory
[Spectrum Detail]

EUGENOL ACETATE(93-28-7)MS
EUGENOL ACETATE(93-28-7)1HNMR
EUGENOL ACETATE(93-28-7)13CNMR
EUGENOL ACETATE(93-28-7)IR1
EUGENOL ACETATE(93-28-7)Raman
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

93-28-7(sigmaaldrich)
[TCI AMERICA]

Eugenol Acetate,>98.0%(GC)(93-28-7)
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